Cyclic AMIDES formed from aminocarboxylic acids by the elimination of water. Lactims are the enol forms of lactams.
A cyclohexylamido analog of PENICILLANIC ACID.
Four-membered cyclic AMIDES, best known for the PENICILLINS based on a bicyclo-thiazolidine, as well as the CEPHALOSPORINS based on a bicyclo-thiazine, and including monocyclic MONOBACTAMS. The BETA-LACTAMASES hydrolyze the beta lactam ring, accounting for BETA-LACTAM RESISTANCE of infective bacteria.
A frequent complication of drug therapy for microbial infection. It may result from opportunistic colonization following immunosuppression by the primary pathogen and can be influenced by the time interval between infections, microbial physiology, or host resistance. Experimental challenge and in vitro models are sometimes used in virulence and infectivity studies.
Glycosylated compounds in which there is an amino substituent on the glycoside. Some of them are clinically important ANTIBIOTICS.
Substances that reduce the growth or reproduction of BACTERIA.
Nonsusceptibility of an organism to the action of penicillins.
Changing an open-chain hydrocarbon to a closed ring. (McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
Works about clinical trials that involve at least one test treatment and one control treatment, concurrent enrollment and follow-up of the test- and control-treated groups, and in which the treatments to be administered are selected by a random process, such as the use of a random-numbers table.
A 13-amino acid peptide derived from proteolytic cleavage of ADRENOCORTICOTROPIC HORMONE, the N-terminal segment of ACTH. ACTH (1-13) is amidated at the C-terminal to form ACTH (1-13)NH2 which in turn is acetylated to form alpha-MSH in the secretory granules. Alpha-MSH stimulates the synthesis and distribution of MELANIN in MELANOCYTES in mammals and MELANOPHORES in lower vertebrates.
A class of organic compounds containing a ring structure made up of more than one kind of atom, usually carbon plus another atom. The ring structure can be aromatic or nonaromatic.
An interleukin-1 subtype that is synthesized as an inactive membrane-bound pro-protein. Proteolytic processing of the precursor form by CASPASE 1 results in release of the active form of interleukin-1beta from the membrane.
Compounds consisting of glucosamine and lactate joined by an ether linkage. They occur naturally as N-acetyl derivatives in peptidoglycan, the characteristic polysaccharide composing bacterial cell walls. (From Dorland, 28th ed)
The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
An 11-kDa protein associated with the outer membrane of many cells including lymphocytes. It is the small subunit of the MHC class I molecule. Association with beta 2-microglobulin is generally required for the transport of class I heavy chains from the endoplasmic reticulum to the cell surface. Beta 2-microglobulin is present in small amounts in serum, csf, and urine of normal people, and to a much greater degree in the urine and plasma of patients with tubular proteinemia, renal failure, or kidney transplants.
The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds.
The creation of an amine. It can be produced by the addition of an amino group to an organic compound or reduction of a nitro group.
A plant genus of the family CAPPARACEAE that contains cleogynol and 15alpha-acetoxycleomblynol (dammaranes) and 1-epibrachyacarpone (a triterpene), and ISOTHIOCYANATES.
A family of G-protein-coupled receptors that have specificity for MELANOCYTE-STIMULATING HORMONES and ADRENOCORTICOTROPIC HORMONE. There are several subtypes of melanocortin receptors, each having a distinct ligand specificity profile and tissue localization.
One of two major pharmacologically defined classes of adrenergic receptors. The beta adrenergic receptors play an important role in regulating CARDIAC MUSCLE contraction, SMOOTH MUSCLE relaxation, and GLYCOGENOLYSIS.
An integrin beta subunit of approximately 85-kDa in size which has been found in INTEGRIN ALPHAIIB-containing and INTEGRIN ALPHAV-containing heterodimers. Integrin beta3 occurs as three alternatively spliced isoforms, designated beta3A-C.
Imines are organic compounds derived from the condensation of an amine and an aldehyde or ketone, and have potential applications in medicine as ligands for metal ions and in the synthesis of bioactive molecules.
A group of antibiotic aminoglycosides differing only in the number of repeating residues in the peptide side chain. They are produced by Streptomyces and Actinomyces and may have broad spectrum antimicrobial and some antiviral properties.
Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING).
A factor synthesized in a wide variety of tissues. It acts synergistically with TGF-alpha in inducing phenotypic transformation and can also act as a negative autocrine growth factor. TGF-beta has a potential role in embryonal development, cellular differentiation, hormone secretion, and immune function. TGF-beta is found mostly as homodimer forms of separate gene products TGF-beta1, TGF-beta2 or TGF-beta3. Heterodimers composed of TGF-beta1 and 2 (TGF-beta1.2) or of TGF-beta2 and 3 (TGF-beta2.3) have been isolated. The TGF-beta proteins are synthesized as precursor proteins.
The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups.
Unsaturated hydrocarbons of the type Cn-H2n, indicated by the suffix -ene. (Grant & Hackh's Chemical Dictionary, 5th ed, p408)
Organic compounds containing the carboxy group (-COOH). This group of compounds includes amino acids and fatty acids. Carboxylic acids can be saturated, unsaturated, or aromatic.
A genus of bacteria that form a nonfragmented aerial mycelium. Many species have been identified with some being pathogenic. This genus is responsible for producing a majority of the ANTI-BACTERIAL AGENTS of practical value.
Organic compounds containing the -CO-NH2 radical. Amides are derived from acids by replacement of -OH by -NH2 or from ammonia by the replacement of H by an acyl group. (From Grant & Hackh's Chemical Dictionary, 5th ed)
The molecular designing of drugs for specific purposes (such as DNA-binding, enzyme inhibition, anti-cancer efficacy, etc.) based on knowledge of molecular properties such as activity of functional groups, molecular geometry, and electronic structure, and also on information cataloged on analogous molecules. Drug design is generally computer-assisted molecular modeling and does not include pharmacokinetics, dosage analysis, or drug administration analysis.
A class of saturated compounds consisting of two rings only, having two or more atoms in common, containing at least one hetero atom, and that take the name of an open chain hydrocarbon containing the same total number of atoms. (From Riguady et al., Nomenclature of Organic Chemistry, 1979, p31)
An integrin found in FIBROBLASTS; PLATELETS; MONOCYTES, and LYMPHOCYTES. Integrin alpha5beta1 is the classical receptor for FIBRONECTIN, but it also functions as a receptor for LAMININ and several other EXTRACELLULAR MATRIX PROTEINS.
Peptides whose amino and carboxy ends are linked together with a peptide bond forming a circular chain. Some of them are ANTI-INFECTIVE AGENTS. Some of them are biosynthesized non-ribosomally (PEPTIDE BIOSYNTHESIS, NON-RIBOSOMAL).
Also known as CD104 antigen, this protein is distinguished from other beta integrins by its relatively long cytoplasmic domain (approximately 1000 amino acids vs. approximately 50). Five alternatively spliced isoforms have been described.
An analytical technique for resolution of a chemical mixture into its component compounds. Compounds are separated on an adsorbent paper (stationary phase) by their varied degree of solubility/mobility in the eluting solvent (mobile phase).
This intrgrin is a key component of HEMIDESMOSOMES and is required for their formation and maintenance in epithelial cells. Integrin alpha6beta4 is also found on thymocytes, fibroblasts, and Schwann cells, where it functions as a laminin receptor (RECEPTORS, LAMININ) and is involved in wound healing, cell migration, and tumor invasiveness.
Integrin beta chains combine with integrin alpha chains to form heterodimeric cell surface receptors. Integrins have traditionally been classified into functional groups based on the identity of one of three beta chains present in the heterodimer. The beta chain is necessary and sufficient for integrin-dependent signaling. Its short cytoplasmic tail contains sequences critical for inside-out signaling.
A 44-kDa highly glycosylated plasma protein that binds phospholipids including CARDIOLIPIN; APOLIPOPROTEIN E RECEPTOR; membrane phospholipids, and other anionic phospholipid-containing moieties. It plays a role in coagulation and apoptotic processes. Formerly known as apolipoprotein H, it is an autoantigen in patients with ANTIPHOSPHOLIPID ANTIBODIES.
Aza compounds are a class of organic compounds containing a nitrogen atom bonded to a carbon atom, with potential applications in the medical field.
Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures.
Integrin alpha4beta1 is a FIBRONECTIN and VCAM-1 receptor present on LYMPHOCYTES; MONOCYTES; EOSINOPHILS; NK CELLS and thymocytes. It is involved in both cell-cell and cell- EXTRACELLULAR MATRIX adhesion and plays a role in INFLAMMATION, hematopoietic cell homing and immune function, and has been implicated in skeletal MYOGENESIS; NEURAL CREST migration and proliferation, lymphocyte maturation and morphogenesis of the PLACENTA and HEART.
Unstable isotopes of indium that decay or disintegrate emitting radiation. In atoms with atomic weights 106-112, 113m, 114, and 116-124 are radioactive indium isotopes.
The characteristic three-dimensional shape of a molecule.

Mechanisms of beta-lactam resistance amongst Pseudomonas aeruginosa isolated in an Italian survey. (1/1422)

The mechanisms of resistance to beta-lactam antibiotics in 325 isolates of Pseudomonas aeruginosa were examined. These isolates were selected because of their resistance to meropenem and imipenem (breakpoint, >4 mg/L), carbenicillin (>128 mg/L), ceftazidime (>8 mg/L), piperacillin and ticarcillin/clavulanate (>64 mg/L). The most frequent mechanism of resistance was beta-lactamase-independent, so called 'intrinsic resistance', which was found in 183 isolates and was probably due to impermeability and/or efflux mechanisms. beta-Lactamase-mediated resistance was demonstrated in 111 strains (11.1%). Derepression of Ambler Class C chromosomal beta-lactamase was detected in 64 isolates, most of which were resistant to ceftazidime and piperacillin but susceptible to meropenem, whereas secondary plasmid-encoded beta-lactamases were found in 34 isolates, all of them resistant to carboxypenicillins and ureidopenicillins and susceptible to carbapenems. Twelve strains showed more than one plasmid-encoded beta-lactamase plus derepression of chromosomal Class C enzyme. Resistance to carbapenems was independent of resistance to other beta-lactam antibiotics, indicating a different mechanism of resistance, probably due to the loss of the D2 porin. In total, 32 strains were resistant to carbapenems: 24 only to imipenem and eight to both imipenem and meropenem.  (+info)

Comparison of activities of broad-spectrum beta-lactam compounds against 1,128 gram-positive cocci recently isolated in cancer treatment centers. (2/1422)

We report the in vitro activities of broad-spectrum beta-lactam antimicrobials tested against 1,128 gram-positive pathogens recently isolated from cancer patients. Cefepime and imipenem were more active than ceftazidime and ceftriaxone against these organisms. Only vancomycin demonstrated reliable activity against oxacillin-resistant staphylococci, Enterococcus spp., and Corynebacterium spp. The spectrum of gram-positive organisms against which cefepime and imipenem have activity provides an advantage over ceftazidime as empiric therapy for cancer patients, potentially reducing the need for the empiric addition of glycopeptides.  (+info)

Clavulanic acid inhibition of beta-lactamase I from Bacillus cereus 569/H. (3/1422)

Inactivation of beta-lactamase I by clavulanic acid was investigated. Clavulanic acid induced inhibition of the enzyme was found to be progressive with time. Benzylpenicillin provided protection against the adverse effects of the inhibitor initially, however, the enzyme was irreversibly inhibited in a progressive manner even in the presence of substrate. Reaction of beta-lactamase I with clavulanic acid, in the presence of ampicillin, led to a very rapid inactivation of the enzyme.  (+info)

Kinetic properties and metal content of the metallo-beta-lactamase CcrA harboring selective amino acid substitutions. (4/1422)

The crystal structure of the metallo-beta-lactamase CcrA3 indicates that the active site of this enzyme contains a binuclear zinc center. To aid in assessing the involvement of specific residues in beta-lactam hydrolysis and susceptibility to inhibitors, individual substitutions of selected amino acids were generated. Substitution of the zinc-ligating residue Cys181 with Ser (C181S) resulted in a significant reduction in hydrolytic activity; kcat values decreased 2-4 orders of magnitude for all substrates. Replacement of His99 with Asn (H99N) significantly reduced the hydrolytic activity for penicillin and imipenem. Replacement of Asp103 with Asn (D103N) showed reduced hydrolytic activity for cephaloridine and imipenem. Deletion of amino acids 46-51 dramatically reduced both the hydrolytic activity and affinity for all beta-lactams. The metal binding capacity of each mutant enzyme was examined using nondenaturing electrospray ionization mass spectrometry. Two zinc ions were observed for the wild-type enzyme and most of the mutant enzymes. However, for the H99N, C181S, and D103N enzymes, three different zinc content patterns were observed. These enzymes contained two zinc molecules, one zinc molecule, and a mixture of one or two zinc molecules/enzyme molecule, respectively. Two enzymes with substitutions of Cys104 or Cys104 and Cys155 were also composed of mixed enzyme populations.  (+info)

OXA-17, a further extended-spectrum variant of OXA-10 beta-lactamase, isolated from Pseudomonas aeruginosa. (5/1422)

Pseudomonas aeruginosa isolates 871 and 873 were isolated at Hacettepe University Hospital in Ankara and were highly resistant to ceftazidime (MIC, 128 microg/ml). Each produced three beta-lactamases, with pIs of 5.3, 6.1, and 7.9. The beta-lactamase with a pI of 5.3 was previously shown to be PER-1 enzyme. The antibiograms of the isolates were not entirely explained by production of PER-1 enzyme, insofar as ceftazidime resistance was incompletely reversed by clavulanate. The enzymes with pIs of 6.1 and 7.9 were therefore investigated. The enzyme with a pI of 6.1 proved to be a novel mutant of OXA-10, which we designated OXA-17, and had asparagine changed to serine at position 73 of the protein. When cloned into Escherichia coli XL1-blue, OXA-17 enzyme conferred greater resistance to cefotaxime, latamoxef, and cefepime than did OXA-10, but it had only a marginal (two- to fourfold) effect on the MIC of ceftazidime. This behavior contrasted with that of previous OXA-10 mutants, specifically OXA-11, -14, and -16, which predominately compromise ceftazidime. Extracted OXA-17 enzyme had relatively greater activity than OXA-10 against oxacillin, cloxacillin, and cefotaxime but, in terms of kcat/Km, it had lower catalytic efficiency against most beta-lactams. The enzyme with a pI of 7.9 was shown by gene sequencing to be OXA-2.  (+info)

Activities of beta-lactams and macrolides against Helicobacter pylori. (6/1422)

A continuous-culture system (chemostat) was used to study the activities of beta-lactam antimicrobial agents, clarithromycin, and 14-OH-clarithromycin against slowly growing Helicobacter pylori NCTC 11637. H. pylori was grown to steady state before exposure to these antimicrobial agents at x8 the MIC. The bactericidal actions of combinations of amoxicillin and clarithromycin were also studied. Viable counts (numbers of CFU per milliliter) were determined at 2-h intervals for 12 h and at 20 h after the addition of antibiotics. The effects of pH changes (6.5 to 7.4) on the activities of amoxicillin, clarithromycin, and the combination of these against H. pylori NCTC 11637 were also studied. Viable counts following exposure to ampicillin, cefixime, ceftazidime, cefuroxime, cefotaxime, azlocillin, and piperacillin at 20 h showed bacteriostatic activity. Imipenem, meropenem, amoxicillin, clarithromycin, and 14-OH-clarithromycin reduced the viable counts by 3 log10 CFU/ml (>/=99.9% killing). Imipenem was the most rapidly bactericidal against H. pylori NCTC 11637. Results of the pH experiments showed that amoxicillin was bactericidal at pHs 6.5 to 7. 4. Clarithromycin was bactericidal at pH 7.0 to 7.4 but was bacteriostatic at pH 6.5. The combination of amoxicillin and clarithromycin was bactericidal at pHs 6.5 and 7.0. A batch culture (flask system) was also used to investigate 12 strains of H. pylori for their susceptibilities to beta-lactams, clarithromycin, and/or 14-OH-clarithromycin in order to determine whether results from the chemostat model can be reproduced with batch cultures. Results of the chemostat time-kill kinetic study were reproducible in our batch culture flask system. The role of carbapenems in the eradication of H. pylori should be investigated.  (+info)

In vivo efficacies of combinations of beta-lactams, beta-lactamase inhibitors, and rifampin against Acinetobacter baumannii in a mouse pneumonia model. (7/1422)

The effects of various regimens containing combinations of beta-lactams, beta-lactam inhibitor(s), and rifampin were assessed in a recently described mouse model of Acinetobacter baumannii pneumonia (M. L. Joly-Guillou, M. Wolff, J. J. Pocidalo, F. Walker, and C. Carbon, Antimicrob. Agents Chemother. 41:345-351, 1997). Two aspects of the therapeutic response were studied: the kinetics of the bactericidal effect (treatment was initiated 3 h after intratracheal inoculation, and bacterial counts were determined over a 24-h period) and survival (treatment was initiated 8 h after inoculation, and the cumulative mortality rate was assessed on day 5). Two clinical strains were used: a cephalosporinase-producing strain (SAN-94040) and a multiresistant strain (RCH-69). For SAN-94040 and RCH-69, MICs and MBCs (milligrams per liter) were as follows: ticarcillin, 32, 64, 256, and >256, respectively; ticarcillin-clavulanate, 32, 64, and 512, and >512, respectively; imipenem, 0.5, 0.5, 8, and 32, respectively; sulbactam, 0.5, 0.5, 8, and 8, respectively; and rifampin, 8, 8, 4, and 4, respectively. Against SAN-94040, four regimens, i.e., imipenem, sulbactam, imipenem-rifampin, and ticarcillin-clavulanate (at a 25/1 ratio)-sulbactam produced a true bactericidal effect (>/=3-log10 reduction of CFU/g of lung). The best survival rate (i.e., 93%) was obtained with the combination of ticarcillin-clavulanate-sulbactam, and regimens containing rifampin provided a survival rate of >/=65%. Against RCH-69, only regimens containing rifampin and the combination of imipenem-sulbactam had a true bactericidal effect. The best survival rates (>/=80%) were obtained with regimens containing rifampin and sulbactam. These results suggest that nonclassical combinations of beta-lactams, beta-lactamase inhibitors, and rifampin should be considered for the treatment of nosocomial pneumonia due to A. baumannii.  (+info)

Inhibition of beta-lactamase in Neisseria gonorrhoeae by sodium clavulanate. (8/1422)

Sodium clavulanate at subinhibitory concentrations affected the activity of penicillin G, ampicillin, or amoxicillin on beta-lactamase-positive strains of Neisseria gonorrhoeae as demonstrated by marked reduction in the minimal inhibitory concentrations of the drugs for the organisms. The compound did not affect the activity of these penicillins on beta-lactamase-negative strains of N. gonorrhoeae. It also had no effect on the activity of cefoxitin against either beta-lactamase-negative or -positive strains. The reduction in minimal inhibitory concentrations of the penicillins for the beta-lactamase-positive organisms brought about by sodium clavulanate is probably due to inhibition of the beta-lactamase by the compound.  (+info)

Lactams are a class of organic compounds that contain a six-membered ring with an amide group (-CONH-) attached to one of the carbon atoms. They are commonly found in nature and are also synthesized in the laboratory for use in medicine. In the medical field, lactams are used as antibiotics to treat a variety of bacterial infections. The most well-known lactam antibiotics are penicillins, which contain a beta-lactam ring. Other examples of lactam antibiotics include cephalosporins, monobactams, and carbapenems. Lactams are effective against a wide range of bacteria, including gram-positive and gram-negative bacteria. They work by inhibiting the production of cell walls in bacteria, leading to cell lysis and death. However, like all antibiotics, lactams can also have side effects and can lead to the development of antibiotic resistance if not used properly.

Cyclacillin is an antibiotic medication that is used to treat a variety of bacterial infections. It is a member of the penicillin group of antibiotics and works by inhibiting the growth of bacteria. Cyclacillin is typically used to treat infections of the skin, respiratory tract, and urinary tract, as well as certain types of meningitis and sepsis. It is usually administered intravenously or intramuscularly, and may be used alone or in combination with other antibiotics. Cyclacillin is contraindicated in patients with a history of penicillin allergy or certain other medical conditions.

Beta-Lactams are a class of antibiotics that are derived from the beta-lactam ring structure. They are one of the most widely used classes of antibiotics and are effective against a broad range of bacterial infections. The beta-lactam ring is a six-membered ring with a beta-hydroxy group and an amide group. The beta-lactam antibiotics work by inhibiting the synthesis of the bacterial cell wall, which leads to cell lysis and death. There are several subclasses of beta-lactam antibiotics, including penicillins, cephalosporins, monobactams, and carbapenems. Each subclass has its own unique properties and is effective against different types of bacteria. Beta-lactam antibiotics are often used to treat a variety of bacterial infections, including pneumonia, urinary tract infections, skin infections, and infections of the respiratory, gastrointestinal, and genitourinary tracts. They are generally well-tolerated and have a low risk of side effects, although allergic reactions can occur in some people.

Superinfection is a medical term used to describe the occurrence of a secondary infection in a patient who is already infected with a primary pathogen. This can happen when the immune system is weakened or compromised, making it easier for a new pathogen to enter the body and establish an infection. Superinfections can occur in a variety of ways, including through exposure to a new pathogen, through the use of antibiotics or other medications that disrupt the normal balance of microorganisms in the body, or through the spread of a pathogen from one part of the body to another. Superinfections can be serious and may require prompt medical attention. They can also complicate the treatment of the primary infection, as the new pathogen may be resistant to the same medications that are effective against the primary pathogen.

Aminoglycosides are a class of antibiotics that are commonly used to treat a variety of bacterial infections, including pneumonia, urinary tract infections, and meningitis. They work by binding to the ribosomes of bacterial cells, which are responsible for protein synthesis, and interfering with this process, leading to the death of the bacteria. Aminoglycosides are typically administered intravenously, although some may also be given by mouth or injection. They are often used in combination with other antibiotics to increase their effectiveness and reduce the risk of bacterial resistance. However, aminoglycosides can also have serious side effects, including hearing loss, kidney damage, and neuromuscular disorders. As a result, they are typically reserved for use in severe infections and are administered with caution, under close medical supervision.

Anti-bacterial agents, also known as antibiotics, are medications that are used to treat bacterial infections. They work by killing or inhibiting the growth of bacteria, thereby preventing the spread of the infection. There are several types of anti-bacterial agents, including: 1. Penicillins: These are the first antibiotics discovered and are effective against a wide range of bacteria. 2. Cephalosporins: These are similar to penicillins and are effective against many of the same types of bacteria. 3. Macrolides: These antibiotics are effective against bacteria that are resistant to other antibiotics. 4. Tetracyclines: These antibiotics are effective against a wide range of bacteria and are often used to treat acne. 5. Fluoroquinolones: These antibiotics are effective against a wide range of bacteria and are often used to treat respiratory infections. It is important to note that antibiotics are only effective against bacterial infections and are not effective against viral infections such as the common cold or flu. Additionally, overuse or misuse of antibiotics can lead to the development of antibiotic-resistant bacteria, which can be more difficult to treat.

In the medical field, cyclization refers to a chemical reaction in which a molecule undergoes a rearrangement to form a ring structure. This process can occur naturally in the body as part of metabolic pathways, or it can be induced artificially in the laboratory to synthesize new compounds with specific properties. Cyclization reactions are important in the synthesis of many drugs and other bioactive molecules, as they can be used to create molecules with specific shapes and chemical properties that are necessary for their biological activity. For example, the synthesis of many antibiotics involves cyclization reactions to create the ring structures that are essential for their activity against bacteria. In addition to their use in drug synthesis, cyclization reactions are also important in the study of biological molecules such as proteins and nucleic acids. Cyclization can occur naturally in these molecules as part of their structure, and understanding the mechanisms of cyclization can provide insights into the function and regulation of these molecules.

Alpha-melanocyte-stimulating hormone (α-MSH) is a peptide hormone that is produced by the pituitary gland and the melanocytes (pigment-producing cells) in the skin. It plays a role in regulating the production of melanin, the pigment that gives skin its color, and also has effects on appetite, mood, and the immune system. α-MSH is a 13-amino acid peptide that is derived from the pro-opiomelanocortin (POMC) precursor protein. It is composed of two smaller peptides, α-MSH and β-MSH, which have different functions. α-MSH is the more potent of the two and is primarily responsible for its effects on melanin production and appetite regulation. In the medical field, α-MSH is sometimes used to treat conditions such as vitiligo, a skin disorder characterized by the loss of pigmentation, and anorexia nervosa, an eating disorder characterized by a lack of appetite and a distorted body image. It is also being studied for its potential use in the treatment of other conditions, such as depression and cancer.

In the medical field, "Heterocyclic Compounds, 1-Ring" refers to a class of organic compounds that contain at least one nitrogen atom (or other heteroatom such as oxygen, sulfur, or phosphorus) in a ring of six or fewer carbon atoms. These compounds are often used as pharmaceuticals, as they can interact with biological molecules in various ways to produce therapeutic effects. Examples of heterocyclic compounds include pyridine, imidazole, and thiazole, which are commonly used as anti-inflammatory, anti-cancer, and anti-bacterial agents, respectively.

Interleukin-1beta (IL-1β) is a type of cytokine, which is a signaling molecule that plays a crucial role in the immune system. It is produced by various types of immune cells, including macrophages, monocytes, and dendritic cells, in response to infection, injury, or inflammation. IL-1β is involved in the regulation of immune responses, including the activation of T cells, B cells, and natural killer cells. It also promotes the production of other cytokines and chemokines, which help to recruit immune cells to the site of infection or injury. In addition to its role in the immune system, IL-1β has been implicated in a variety of inflammatory and autoimmune diseases, including rheumatoid arthritis, inflammatory bowel disease, and multiple sclerosis. It is also involved in the pathogenesis of certain types of cancer, such as breast cancer and ovarian cancer. Overall, IL-1β is a key mediator of inflammation and immune responses, and its dysregulation has been linked to a range of diseases and conditions.

In the medical field, muramic acids are a type of amino acid that are found in the peptidoglycan layer of bacterial cell walls. Peptidoglycan is a complex polymer made up of sugars and amino acids that provides structural support to the bacterial cell wall. Muramic acids are important components of the peptidoglycan layer because they play a role in the cross-linking of the polymer, which helps to strengthen the cell wall and provide protection against external stresses. In addition, muramic acids are also involved in the recognition and binding of antibiotics, such as penicillin, which target the peptidoglycan layer of bacterial cells. In summary, muramic acids are a key component of the peptidoglycan layer of bacterial cell walls and play an important role in the structure and function of these cells.

Beta 2-Microglobulin (β2M) is a small protein that is produced by most cells in the body, including immune cells such as T cells and B cells. It is a component of the major histocompatibility complex (MHC) class I molecules, which are found on the surface of most cells and are responsible for presenting antigens (foreign substances) to the immune system. In the medical field, β2M is often used as a marker of kidney function. High levels of β2M in the blood can indicate kidney damage or failure, as the kidneys are responsible for removing β2M from the bloodstream. In addition, high levels of β2M have been associated with an increased risk of certain types of cancer, including multiple myeloma and prostate cancer. β2M is also used as a diagnostic tool in the laboratory to help identify and monitor certain diseases and conditions, such as multiple myeloma, autoimmune disorders, and viral infections. It is also used as a component of some types of cancer treatments, such as immunotherapy.

In the medical field, "amination" typically refers to the process of administering a medication or treatment that contains an amine, which is a type of organic compound containing a nitrogen atom bonded to two hydrogen atoms. For example, amine medications such as dopamine, norepinephrine, and epinephrine are commonly used in the treatment of various medical conditions, including hypertension, heart failure, and shock. These medications work by stimulating the release of certain hormones and neurotransmitters in the body, which can help to regulate blood pressure, heart rate, and other vital functions. Amination may also refer to the process of adding an amine group to a molecule, which can alter its chemical properties and potentially make it more effective as a medication or therapeutic agent. This process is often used in the development of new drugs and treatments.

Cleome is a genus of flowering plants in the family Cleomaceae, commonly known as spider flowers or bindweeds. In the medical field, Cleome species are used for various medicinal purposes, including: 1. Antimicrobial activity: Some Cleome species have been found to have antimicrobial properties, making them useful in the treatment of infections caused by bacteria, fungi, and viruses. 2. Anti-inflammatory activity: Cleome species have been shown to have anti-inflammatory properties, making them useful in the treatment of inflammatory conditions such as arthritis, rheumatism, and gout. 3. Antioxidant activity: Cleome species contain antioxidants that can help protect the body against damage caused by free radicals, which are unstable molecules that can damage cells and contribute to the development of chronic diseases such as cancer and heart disease. 4. Anticancer activity: Some Cleome species have been found to have anticancer properties, making them useful in the treatment of various types of cancer, including breast cancer, prostate cancer, and lung cancer. 5. Diuretic activity: Cleome species have been found to have diuretic properties, making them useful in the treatment of conditions such as edema, high blood pressure, and kidney disease. It is important to note that the use of Cleome species for medicinal purposes should be done under the guidance of a qualified healthcare professional, as some species may have toxic effects or interact with other medications.

Receptors, Melanocortin are a family of G protein-coupled receptors that are expressed in various tissues throughout the body. They are activated by melanocortin peptides, which are produced by the pituitary gland and the adrenal gland. Melanocortin receptors play a role in regulating a variety of physiological processes, including metabolism, appetite, stress response, and immune function. They are also involved in the development of skin pigmentation and the regulation of body temperature. In the medical field, the study of melanocortin receptors and their ligands is important for understanding the pathophysiology of various diseases, including obesity, diabetes, and skin disorders.

Receptors, Adrenergic, beta (β-adrenergic receptors) are a type of protein found on the surface of cells in the body that bind to and respond to signaling molecules called catecholamines, including adrenaline (epinephrine) and noradrenaline (norepinephrine). These receptors are part of the adrenergic signaling system, which plays a critical role in regulating a wide range of physiological processes, including heart rate, blood pressure, metabolism, and immune function. There are three main types of β-adrenergic receptors: β1, β2, and β3. Each type of receptor is found in different tissues and has different functions. For example, β1 receptors are primarily found in the heart and are responsible for increasing heart rate and contractility. β2 receptors are found in the lungs, blood vessels, and muscles, and are involved in relaxing smooth muscle and increasing blood flow. β3 receptors are found in adipose tissue and are involved in regulating metabolism. Activation of β-adrenergic receptors can have a variety of effects on the body, depending on the specific receptor subtype and the tissue it is found in. For example, activation of β2 receptors in the lungs can cause bronchodilation, which can help to open up airways and improve breathing in people with asthma or other respiratory conditions. Activation of β1 receptors in the heart can increase heart rate and contractility, which can help to improve blood flow and oxygen delivery to the body's tissues. Activation of β3 receptors in adipose tissue can increase metabolism and help to promote weight loss. β-adrenergic receptors are important therapeutic targets for a variety of medical conditions, including heart disease, asthma, and diabetes. Drugs that target these receptors, such as beta blockers and beta agonists, are commonly used to treat these conditions.

Integrin beta3, also known as CD18, is a protein that plays a crucial role in the immune system and blood clotting. It is a subunit of integrin receptors, which are transmembrane proteins that mediate cell-cell and cell-extracellular matrix interactions. In the context of the immune system, integrin beta3 is expressed on the surface of various immune cells, including neutrophils, monocytes, and platelets. It helps these cells to adhere to the endothelium (inner lining of blood vessels) and migrate through the blood vessel walls to sites of inflammation or infection. In the context of blood clotting, integrin beta3 is expressed on the surface of platelets. It plays a critical role in platelet aggregation, which is the process by which platelets stick together to form a plug at the site of a blood vessel injury. Integrin beta3 also helps to activate platelets and promote the formation of a fibrin clot, which stabilizes the platelet plug and prevents further bleeding. Mutations in the gene encoding integrin beta3 can lead to various bleeding disorders, such as Glanzmann thrombasthenia, a rare inherited bleeding disorder characterized by impaired platelet aggregation.

In the medical field, imines are organic compounds that contain a nitrogen atom bonded to two carbon atoms. They are formed by the reaction of an amine with an aldehyde or ketone, and are often used as intermediates in the synthesis of other organic compounds. Imines have a variety of applications in medicine, including as antifungal agents, antiviral agents, and as inhibitors of enzymes involved in the metabolism of drugs. They are also used as ligands in metal complexes, which can be used in the treatment of diseases such as cancer and inflammatory disorders. One example of a medical application of imines is the use of the drug amphotericin B, which is an antifungal agent that contains an imine group. Amphotericin B is used to treat serious fungal infections, such as cryptococcal meningitis and aspergillosis. Overall, imines play an important role in the development of new drugs and therapies in the medical field, and continue to be an active area of research.

Streptothricins are a group of antibiotics that are produced by certain species of Streptomyces bacteria. They are used to treat a variety of bacterial infections, including those caused by gram-positive and gram-negative bacteria. Streptothricins work by inhibiting the growth of bacteria by interfering with their ability to synthesize proteins. They are typically administered intravenously or intramuscularly, and are often used in combination with other antibiotics to treat severe or resistant infections.

Transforming Growth Factor beta (TGF-β) is a family of cytokines that play a crucial role in regulating cell growth, differentiation, and migration. TGF-βs are secreted by a variety of cells, including immune cells, fibroblasts, and epithelial cells, and act on neighboring cells to modulate their behavior. TGF-βs have both pro-inflammatory and anti-inflammatory effects, depending on the context in which they are released. They can promote the differentiation of immune cells into effector cells that help to fight infections, but they can also suppress the immune response to prevent excessive inflammation. In addition to their role in immune regulation, TGF-βs are also involved in tissue repair and fibrosis. They can stimulate the production of extracellular matrix proteins, such as collagen, which are essential for tissue repair. However, excessive production of TGF-βs can lead to fibrosis, a condition in which excessive amounts of connective tissue accumulate in the body, leading to organ dysfunction. Overall, TGF-βs are important signaling molecules that play a critical role in regulating a wide range of cellular processes in the body.

In the medical field, alkenes are a type of organic compound that contain at least one carbon-carbon double bond. They are unsaturated hydrocarbons, which means they have fewer hydrogen atoms than the maximum possible number for their molecular formula. Alkenes are commonly used in the production of various medical products, including drugs, plastics, and synthetic rubber. They are also used as solvents in some medical procedures and as components in medical devices. One example of an alkene used in medicine is propylene glycol, which is a common ingredient in many medications and medical devices. It is used as a solvent, a preservative, and a stabilizer. Another example is ethylene oxide, which is used as a sterilizing agent for medical equipment and as a precursor for the production of various medical products. Overall, alkenes play an important role in the medical field and are used in a variety of applications to improve patient care and medical technology.

Carboxylic acids are a class of organic compounds that contain a carboxyl functional group (-COOH). In the medical field, carboxylic acids are often used as drugs or as intermediates in the synthesis of drugs. They have a wide range of biological activities and can be used to treat a variety of conditions, including infections, inflammation, and pain. Some examples of carboxylic acids that are used in medicine include aspirin, ibuprofen, and naproxen. These drugs are commonly used to relieve pain, reduce inflammation, and lower fever. Carboxylic acids can also be used to synthesize other drugs, such as antibiotics and anti-cancer agents.

In the medical field, amides are a class of organic compounds that contain a nitrogen atom bonded to two carbon atoms. They are commonly used as drugs and are often referred to as "amide derivatives." One example of an amide derivative used in medicine is acetaminophen, which is commonly sold under the brand name Tylenol. It is used to relieve pain and reduce fever. Another example is aspirin, which is also an amide derivative and is used to relieve pain, reduce fever, and thin the blood. Amides can also be used as local anesthetics, such as lidocaine, which is used to numb the skin and nerves during medical procedures. They can also be used as muscle relaxants, such as succinylcholine, which is used to relax muscles during surgery. Overall, amides play an important role in medicine as they have a wide range of therapeutic applications and are often used to treat various medical conditions.

In the medical field, "Bicyclo Compounds, Heterocyclic" refers to a class of organic compounds that contain two rings of carbon atoms, with one or more heteroatoms (atoms other than carbon) such as nitrogen, oxygen, or sulfur, incorporated into the structure. These compounds are often used as pharmaceuticals or as intermediates in the synthesis of drugs. They can exhibit a wide range of biological activities, including analgesic, anti-inflammatory, anticonvulsant, and antitumor effects. Examples of bicyclo compounds include the anti-inflammatory drug ibuprofen and the anticonvulsant drug phenytoin.

Integrin alpha5beta1, also known as vitronectin receptor (VNR) or fibronectin receptor (FnR), is a transmembrane protein complex that plays a crucial role in cell adhesion, migration, and signaling. It is composed of two subunits, alpha5 and beta1, which are encoded by separate genes and assemble into a heterodimeric complex. Integrin alpha5beta1 is expressed on the surface of many different cell types, including fibroblasts, endothelial cells, and immune cells. It binds to extracellular matrix (ECM) proteins such as fibronectin, vitronectin, and laminin, which are essential for tissue development, wound healing, and angiogenesis. In the medical field, integrin alpha5beta1 is of great interest due to its role in various diseases and conditions. For example, it has been implicated in cancer progression, as its overexpression is often associated with increased tumor invasion and metastasis. It is also involved in the development of fibrotic diseases such as idiopathic pulmonary fibrosis and liver cirrhosis. Targeting integrin alpha5beta1 has been proposed as a potential therapeutic strategy for these diseases. Several drugs that block the interaction between integrin alpha5beta1 and its ECM ligands are currently in preclinical or clinical development for the treatment of cancer and fibrotic diseases.

In the medical field, peptides are short chains of amino acids that are linked together by peptide bonds. Cyclic peptides are a type of peptide in which the amino acids are linked in a ring-like structure, rather than in a linear chain. These cyclic peptides can have a variety of biological activities, including antimicrobial, antiviral, and anti-inflammatory effects. They are being studied for their potential use in the development of new drugs and therapies.

Integrin beta4 is a protein that plays a crucial role in the formation and maintenance of blood vessels, skin, and other tissues in the human body. It is a component of integrin receptors, which are cell surface proteins that mediate cell-cell and cell-matrix interactions. In the medical field, integrin beta4 is often studied in the context of cancer. It has been found to be overexpressed in many types of cancer, including breast, ovarian, and lung cancer, and is thought to contribute to tumor growth and metastasis. In addition, integrin beta4 has been shown to play a role in the development of certain skin conditions, such as psoriasis and atopic dermatitis. Targeting integrin beta4 has been proposed as a potential therapeutic strategy for cancer and other diseases. For example, drugs that block the interaction between integrin beta4 and its ligands have shown promise in preclinical studies as potential cancer treatments.

Chromatography, Paper is a method of separating and analyzing compounds based on their ability to interact with a stationary phase and a mobile phase. In this method, a small amount of a sample is applied to a piece of paper or a thin layer of adsorbent material, such as silica gel or alumina. The paper or adsorbent material is then placed in a container filled with a mobile phase, such as a solvent or a gas. As the mobile phase flows over the stationary phase, the compounds in the sample are separated based on their chemical properties, such as their polarity, size, or charge. The separated compounds are then visualized by adding a colorimetric or fluorometric reagent to the paper or adsorbent material, which allows the compounds to be seen as colored or fluorescent bands. Chromatography, Paper is a simple and inexpensive method that is commonly used in the medical field for the analysis of small samples, such as blood, urine, or tissue. It is particularly useful for the detection and quantification of drugs, hormones, and other biomolecules in biological samples.

Integrin alpha6beta4 is a protein complex that plays a crucial role in the development and maintenance of various tissues in the human body. It is a transmembrane protein that is expressed on the surface of cells and is involved in cell adhesion, migration, and signaling. In the medical field, integrin alpha6beta4 is of particular interest because it is involved in the development and progression of several diseases, including cancer. In particular, integrin alpha6beta4 is overexpressed in many types of cancer, including breast, ovarian, and pancreatic cancer, and is thought to play a role in the growth and spread of these tumors. Integrin alpha6beta4 is also involved in the development of other diseases, including inflammatory bowel disease, psoriasis, and alopecia areata. In these conditions, the expression of integrin alpha6beta4 is altered, leading to abnormal cell behavior and tissue damage. Overall, integrin alpha6beta4 is a key protein in the regulation of cell behavior and tissue function, and its role in various diseases is an active area of research in the medical field.

Integrin beta chains are one of the subunits that make up integrins, which are transmembrane proteins found on the surface of most cells. Integrins are responsible for mediating cell-cell and cell-extracellular matrix interactions, and play a crucial role in a variety of physiological processes, including cell adhesion, migration, and signaling. There are 18 different integrin beta chains that have been identified, each of which pairs with a different alpha chain to form a specific integrin heterodimer. These integrin heterodimers have distinct binding specificities for various extracellular matrix proteins, such as fibronectin, laminin, and vitronectin. Integrin beta chains are encoded by different genes, and mutations in these genes can lead to various diseases and disorders, such as leukocyte adhesion deficiency, platelet function defects, and cancer. Therefore, understanding the structure and function of integrin beta chains is important for developing new therapeutic strategies for these diseases.

Beta 2-Glycoprotein I (β2-GPI) is a plasma protein that plays a crucial role in the coagulation cascade and the regulation of blood clotting. It is a member of the phospholipid-binding protein family and is composed of 544 amino acids. β2-GPI is a cofactor for the activation of factor X and the inactivation of factor Va and VIIIa, which are essential components of the coagulation cascade. It also binds to phospholipids, which are important components of cell membranes and are involved in the formation of blood clots. In addition to its role in coagulation, β2-GPI has been implicated in several medical conditions, including antiphospholipid syndrome (APS), a disorder characterized by the formation of blood clots and pregnancy complications. In APS, antibodies against β2-GPI can bind to phospholipids and activate the coagulation cascade, leading to the formation of blood clots. β2-GPI is also a target of autoantibodies in systemic lupus erythematosus (SLE), an autoimmune disorder that can affect multiple organs and systems in the body. In SLE, autoantibodies against β2-GPI can cause inflammation and damage to various tissues, including the kidneys, joints, and brain. Overall, β2-GPI is a critical protein involved in the regulation of blood clotting and has been implicated in several medical conditions, including APS and SLE.

In the medical field, "aza compounds" refers to a class of organic compounds that contain a nitrogen atom (N) in place of a carbon atom (C) in their molecular structure. These compounds are often used as drugs or as intermediates in the synthesis of drugs. Aza compounds can be further classified based on the functional groups present in their structure. For example, aza analogs of carboxylic acids are called aza acids, while aza analogs of alcohols are called aza alcohols. Some common examples of aza compounds used in medicine include azithromycin (an antibiotic), azacitidine (a chemotherapy drug), and azelaic acid (a skin care product). Aza compounds are often used in medicine because they can interact with biological molecules in unique ways, leading to new therapeutic effects. For example, azithromycin is effective against a wide range of bacterial infections because it inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. Azacitidine, on the other hand, works by inhibiting DNA methyltransferases, which are enzymes involved in the regulation of gene expression.

Integrin alpha4beta1, also known as very late antigen-4 (VLA-4), is a cell surface protein that plays a crucial role in the adhesion and migration of immune cells, particularly leukocytes, to the endothelium of blood vessels. It is composed of two subunits, alpha4 and beta1, which are encoded by different genes. In the context of the immune system, integrin alpha4beta1 is involved in the homing of immune cells to specific tissues, such as the lymph nodes, spleen, and bone marrow. It also plays a role in the activation and differentiation of immune cells, as well as in the regulation of inflammation and immune responses. In addition to its role in the immune system, integrin alpha4beta1 has been implicated in various diseases, including cancer, autoimmune disorders, and infectious diseases. For example, it has been shown to be involved in the metastasis of certain types of cancer cells, as well as in the pathogenesis of multiple sclerosis and rheumatoid arthritis. Overall, integrin alpha4beta1 is a key regulator of immune cell function and has important implications for the development and treatment of various diseases.

Indium radioisotopes are radioactive isotopes of the element indium that are used in medical imaging and therapy. These isotopes emit radiation that can be detected by medical imaging equipment, such as single-photon emission computed tomography (SPECT) or positron emission tomography (PET) scanners. Indium radioisotopes are used in a variety of medical applications, including: 1. Diagnostic imaging: Indium-111 is commonly used in diagnostic imaging to detect infections, tumors, and other abnormalities in the body. It is often used in conjunction with antibodies or other targeting agents to help locate specific cells or tissues. 2. Radiation therapy: Indium-111 is also used in radiation therapy to treat certain types of cancer. It is administered to the patient in the form of a radioactive compound that is taken up by cancer cells, where it emits radiation that damages the cancer cells and slows their growth. Overall, indium radioisotopes play an important role in medical imaging and therapy, allowing doctors to diagnose and treat a wide range of conditions with greater accuracy and effectiveness.

A beta-lactam (β-lactam) ring is a four-membered lactam. A lactam is a cyclic amide, and beta-lactams are named so because the ... The Breckpot β-lactam synthesis produces substituted β-lactams by the cyclization of beta amino acid esters by use of a ... Synthesis of β-lactams (Articles with short description, Short description matches Wikidata, Beta-lactams, Four-membered rings) ... β-lactams are significant structural units of medicines as manifested in many β-lactam antibiotics Up to 1970, most β-lactam ...
β-lactam antibiotics (beta-lactam antibiotics) are antibiotics that contain a beta-lactam ring in their chemical structure. ... List of β-lactam antibiotics ATC code J01C Beta-lactam antibacterials, penicillins ATC code J01D Other beta-lactam ... β-lactams are classified according to their core ring structures. β-lactams fused to saturated five-membered rings: β-lactams ... β-lactams fused to unsaturated five-membered rings: β-lactams containing 2,3-dihydrothiazole rings are named penems. β-lactams ...
... is an American independent record label founded by Chris McBeth in 2000.The label relocated from its ... Textura Review: Three Beta-lactam Ring Records Releases; August 2008; accessed online Archived September 3, 2008, at the ...
Miller, M. T.; Bachmann, B. O.; Townsend, C. A.; Rosenzweig, A. C. (2002). "The catalytic cycle of beta -lactam synthetase ... In enzymology, a (carboxyethyl)arginine β-lactam-synthase (EC 6.3.3.4) is an enzyme that catalyzes the chemical reaction ATP + ... Bachmann BO, Li R, Townsend CA (1998). "β-Lactam synthetase: A new biosynthetic enzyme". Proc. Natl. Acad. Sci. 95 (16): 9082-6 ...
Unlike the Staudinger β-lactam synthesis, the umpolung ketene in the Lectka β-lactam synthesis behaves as the nucleophile ... asymmetric synthesis of beta-lactams". J. Am. Chem. Soc. 124 (23): 6626-6635. doi:10.1021/ja0258226. PMID 12047183. France, S ... Mechanistic evidence for imine activation working in tandem with chiral enolate formation in the synthesis of beta-lactams". J ... Achiral ketenes and imines, in the presence of a chiral nucleophilic catalyst, are allowed to react to make β-lactams in high ...
Gin A, Dilay L, Karlowsky JA, Walkty A, Rubinstein E, Zhanel GG (June 2007). "Piperacillin-tazobactam: a beta-lactam/beta- ... as the beta-lactam ring is hydrolyzed by the bacteria's beta-lactamase. It was patented in 1974 and approved for medical use in ... Page MG (2012). "Beta-Lactam Antibiotics". In Dougherty TJ, Pucci MJ (eds.). Antibiotic Discovery and Development. Boston, MA: ... However, the co-administration of tazobactam does not confer activity against MRSA, as penicillin (and most other beta lactams ...
... shielding more potent beta-lactams such as ampicillin. Sulbactam itself contains a beta-lactam ring, and has weak antibacterial ... Singh GS (January 2004). "Beta-lactams in the new millennium. Part-II: cephems, oxacephems, penams and sulbactam". Mini Reviews ... Beta-lactamase inhibitors, Lactams, Sulfones, Carboxylic acids, All stub articles, Antibiotic stubs). ... This drug is given in combination with β-lactam antibiotics to inhibit β-lactamase, an enzyme produced by bacteria that ...
... or carbonyl groups to form beta-lactones. With imines, beta-lactams are formed. This is the Staudinger synthesis, a facile ... The example shows the synthesis of a β-lactam by the reaction of a ketene with an imine (see Staudinger synthesis): Ketenes are ... lactams. This system has a broad substrate scope and can be applied to various combinations of carbene precursors, nucleophiles ...
Like all beta-lactam antibiotics, ertapenem is bactericidal. It inhibits cross-linking of the peptidoglycan layer of bacterial ... "Beta lactam antibiotics". StatPearls. 2020. PMID 31424895. Cushnie TP, O'Driscoll NH, Lamb AJ (December 2016). "Morphological ... Like all carbapenem antibiotics, ertapenem has a broader spectrum of activity than other beta-lactams like penicillins and ... to other beta-lactam antibiotics in the past. Common side effects are diarrhoea (in 5% of people receiving ertapenem), nausea ( ...
It is a narrow-spectrum beta-lactam antibiotic of the penicillin class. It is similar in effect to cloxacillin and ... ISBN 978-1-4614-1399-8. Page MG (2012). "Beta-Lactam Antibiotics". Antibiotic Discovery and Development. pp. 79-117. doi: ... Like other β-lactam antibiotics, flucloxacillin acts by inhibiting the synthesis of bacterial cell walls. It inhibits cross- ... Despite flucloxacillin being insensitive to beta-lactamases, some organisms have developed resistance to it and other narrow- ...
Beta-lactam antibiotics mimic the D-Ala-D-Ala site, thereby irreversibly inhibiting PBP crosslinking of peptidoglycan. ... Overall, the research shows that all beta lactams have the intrinsic hazard of very serious hazardous reactions in susceptible ... "5.1.2 Cephalosporins and other beta-lactams". British National Formulary (56 ed.). London: BMJ Publishing Group Ltd and Royal ... Pandey, Neelanjana; Cascella, Marco (2020). "Beta Lactam Antibiotics". StatPearls. StatPearls. PMID 31424895. Dash, C. H. (1 ...
Beta-lactam antibiotics). ... A penem is a type of β-lactam with an unsaturated five-member ... This molecule has no substitution at the above position, but has a bulky group attached to the β-lactam ring, and it displays ... One possible consequence of these structural differences of penems from other β-lactams may be reduced immunogenicity and ... heterocycle containing a sulfur atom fused to the β-lactam ring. Penems do not occur naturally; all are synthetic. Related to ...
Pandey N, Cascella M (March 2020). "Beta Lactam Antibiotics". StatPearls. PMID 31424895. Bardal SK, Waechter JE, Martin DS ( ... All β-lactam antibiotics (except for tabtoxinine-β-lactam, which inhibits glutamine synthetase) bind to PBPs, which are ... The β-lactam ring is a structure common to all β-lactam antibiotics. Penicillin core. Filamentation (top right of electron ... When they bind to penicillin, the β-lactam amide bond is ruptured to form a covalent bond with the catalytic serine residue at ...
"New Products: Randox Laboratories' Beta-Lactams Array; Ingenuity Systems' iReport". BioArray News. GenomeWeb. January 24, 2012 ... "Ingenuity Preps New NGS Variant Analysis Tool, Signs Translational Oncology Group as Beta Tester". BioInform. GenomeWeb. ...
Tidwell, Thomas T. (2017). "Beta-Lactams from ketene- Imine Cycloadditins: An Update". In Banik, Bimal K. (ed.). Beta-Lactams: ... Beta-lactam Carbene Hypervalent molecule Polyoxymethylene Pyrethrin Triphenylphosphine phenylimide Heidegger and Nazism: ...
However, mecA codes for PBP2a that has a lower affinity for beta-lactams, which keeps the structural integrity of the cell wall ... The latter forms a therapeutic target to improve the ability of beta-lactams to prevent cell wall synthesis in resistant S. ... For example, epicatechin gallate, a compound found in green tea, has shown signs of lowering the resistance to beta-lactams, to ... Severin A, Wu SW, Tabei K, Tomasz A (October 2005). "High-level (beta)-lactam resistance and cell wall synthesis catalyzed by ...
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Bentley, Ronald (2009). "Different roads to discovery; Prontosil (hence sulfa drugs) and penicillin (hence beta-lactams)". ...
Synthesis of alpha,beta-unsaturated delta-valerolactones and -lactams". Org. Lett. 1 (4): 641-4. doi:10.1021/ol9907217. PMID ...
Thykaer J, Nielsen J (January 2003). "Metabolic engineering of beta-lactam production". Metabolic Engineering. 5 (1): 56-69. ... The glycerol enters glycolysis and the fatty acids are broken down by beta oxidation to release acetyl-CoA, which then is fed ... Steroids are also broken down by some bacteria in a process similar to beta oxidation, and this breakdown process involves the ...
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Antibiotics Containing the Beta-Lactam Structure. Berlin, Heidelberg: Springer Berlin Heidelberg. ISBN 3-642-81966-4. {{cite ...
... is a beta-lactam antibiotic. It is a phenyl derivative of carbenicillin, acting as a prodrug. Basker MJ, Comber KR ...
James, C.W.; Gurk-Turner, C. (January 2001). "Cross-reactivity of beta-lactam antibiotics". Baylor University Medical Center ... β-lactam penicillins became the most widely used antibiotics in the world. Amoxicillin, a semisynthetic penicillin developed by ... 6-APA was found to constitute the core nucleus of penicillin (and subsequently many β-lactam antibiotics) and was easily ... The usefulness of the β-lactam ring was such that related antibiotics, including the mecillinams, the carbapenems and, most ...
Reading C, Cole M (1977). "Clavulanic Acid: a Beta-Lactamase-Inhibiting Beta-Lactam from Streptomyces clavuligerus". Antimicrob ... Non-β-lactam antibiotics include holomycin and an antibiotic complex, MM 19290, related to tunicamycin; a beta-lactamase- ... nov., a beta-lactam antibiotic producer". International Journal of Systematic Bacteriology. 21 (4): 326-31. doi:10.1099/ ... S. clavuligerus produces over 20 secondary metabolites, including many beta-lactam antibiotics such as clavulanic acid, ...
July 1979). "Synthetic studies on beta-lactam antibiotics. Part 101. Synthesis of 7beta-[2-carboxy-2-(4-hydroxyphenyl)acetamido ... Narisada M, Onoue H, Nagata W (1977). "Synthetic Studies on b-Lactam Antibiotics. Part 5. A Synthesis of 7b-Acylamino-3-methyl- ... Lactams, Ethers, Propionamides, Phenols, Oxygen heterocycles, All stub articles, Antibiotic stubs). ... and introduction of a 7-methoxyl group analogous to that which is present in cephamycins and gives them the enhanced beta- ...
Because of the unfused beta-lactam ring there is somewhat lower cross-reactivity between aztreonam and many other beta-lactam ... There is a much lower risk of cross-sensitivity between aztreonam and other beta-lactam antibiotics than within other beta- ... James CW, Gurk-Turner C (January 2001). "Cross-reactivity of beta-lactam antibiotics". Proceedings. 14 (1): 106-107. doi: ... Terico AT, Gallagher JC (December 2014). "Beta-lactam hypersensitivity and cross-reactivity". Journal of Pharmacy Practice. 27 ...
Solomon, edited by Arnold L. Demain, Nadine A. (1983). Antibiotics Containing the Beta-Lactam Structure. Berlin, Heidelberg: ... Corbett, David F.; Eglington, A. John; Howarth, T. Trefor (1977). "Structure elucidation of MM 17880, a new fused β-lactam ... antibiotic isolated from Streptomyces olivaceus; a mild β-lactam degradation reaction". J. Chem. Soc., Chem. Commun. (24): 953- ...
6-Aminopenicillanic acid (6-APA) is a compound derived from penicillin G. 6-APA contains the beta-lactam core of penicillin G, ... The β-lactam ring is itself fused to a five-membered thiazolidine ring. The fusion of these two rings causes the β-lactam ring ... β-Lactamase inhibitors irreversibly bind to β-lactamase preventing it from breaking down the beta-lactam rings on the ... James CW, Gurk-Turner C (January 2001). "Cross-reactivity of beta-lactam antibiotics". Proceedings. 14 (1): 106-7. doi:10.1080/ ...
Beta-lactams with beta-lactamase inhibitors can also be used; examples include ampicillin/sulbactam, piperacillin/tazobactam, ...
Antibiotics, beta-lactams. Class Summary. The beta-lactam used to treat patients with H pylori infection is stable in an acid ...
CTX-M-14 Class A Beta-LactamasePOTASSIUM ION[(1,2,3,4,5-eta)-1-(4-{[(4-carboxy-5,5-dimethyl-1,3-thiazolidin-2-yl)methyl]amino}- ... 4XXR: Atomic Resolution X-Ray Crystal Structure of a Ruthenocene Conjugated Beta-Lactam Antibiotic in Complex with CTX-M-14 ...
The beta-lactam and beta-lactamase inhibitors market is expected to exhib... ... Beta-lactam and beta-lactamase inhibitors are chemical compounds of natural or semi-synthetic or synthetic origin. They inhibit ... The beta-lactam and beta-lactamase inhibitors market is expected to exhibit significant growth during the forecast period due ... The beta-lactam and beta-lactamase inhibitors market is expected to exhibit significant growth during the forecast period due ...
Beta-Lactams - Etiology, pathophysiology, symptoms, signs, diagnosis & prognosis from the MSD Manuals - Medical Professional ... Beta-Lactamases Beta-lactamases are a diverse class of enzymes produced by bacteria that break open the beta-lactam ring, ... Beta-lactams are antibiotics that have a beta-lactam ring nucleus. Subclasses include ... which can inactivate all beta-lactam antibiotics except for aztreonam Monobactams Monobactams are parenteral beta-lactam ...
The significance of beta-lactam allergy cross reactivity is then mentioned. She goes on to explain how beta-lactam allergy ... Ward begins her presentation by reviewing the impact of beta-lactam allergies on the healthcare system. She then discusses the ... Lastly, she identifies strategies to improve the documentation of beta-lactam allergy reporting. ...
Tags Antibiotics, Beta lactam antibiotics, Beta lactam compound classification, classification of Beta lactam drugs, Definition ... classification of beta-lactam drugs:. classification of Beta-lactam drugs. Make sure check azaming article: What are ... Beta-Lactam antibiotics. Antibiotic containing the beta-lactam (alpha-4 membraned cyclic amide) ring structure constitute the ... beta-lactam antibiotic are a broad class of antibiotic, the structure having a lactam group with a heteroatom structure ...
Give The Beta-Lactam Before the Vanc. / SOAP Note, ID / By Brown Med-Peds ... A 2022 study in Clinical Infectious Diseases looked at whether administration of a broad-spectrum β-lactam (e.g., cefepime, ... Administration of vancomycin prior to a β-lactam was not associated with improved survival in the subgroup of 524 patients with ... The prevalence of bacterial pathogens causing BSIs susceptible to broad spectrum β-lactams is higher than the prevalence of ...
SPERANCA, Paulo Augusto; GOMES, Alice da Silva and PRAZERES, Claudia Maria Guerra. Sensitivity of S. aureus to beta-lactam and ... Keywords : beta-lactam Glycopeptidies; Staphylococcus aureus; amoxicillin. · abstract in Portuguese · text in Portuguese · pdf ... with the aim of this study was to compare in vitro the degree of effectiveness of beta-lactam antibiotics and glycopeptide in ...
Beta-lactams. 102 (94). 60 (94). 42 (95). Amoxicillin/clavulanic acid. 9 (9). 6 (10). 3 (7). ...
Beta-lactam. mecA. Disclaimer:. The resistance mechanisms listed were identified by analysis of whole genome sequence using the ...
The objective of this study was to investigate the genetic basis for declining susceptibility to penicillin and other β-lactams ... This study found that a growing trend of isolates displayed reduced susceptibility to β-lactams including penicillin, ... of which 18 substitutions were most statistically associated with reduced β-lactams susceptibility. Almost all the S. suis ... that there was genetically widespread presence of PBPs substitutions associated with reduced susceptibility to β-lactam ...
Synthetic, Enterome partner to study effects of beta-lactam antibiotics on gastrointestinal microflora Synthetic Biologics, Inc ... today announced that they have entered into an agreement to conduct metagenomic research on the effects of beta-lactam ... the Companys investigational oral beta-lactamase enzyme designed to protect the microbiome and prevent C. difficile infection ...
In the nursing home setting, treatment should consist of an antipneumococcal fluoroquinolone alone or either a high-dose beta- ... lactam/beta-lactamase inhibitor or a second- or third-generation cephalosporin, in combination with azithromycin. Treatment of ... An antipseudomonal cephalosporin, an antipseudomonal carbapenem, or an extended-spectrum beta-lactam/beta-lactamase inhibitor ... alone or either a high-dose beta-lactam/beta-lactamase inhibitor (e.g., amoxicillin/clavulanate [Augmentin]) or a second- or ...
Compounding beta lactams under FDAs recent new guidance document Compounding Thyroid USP in light of FDAs recent letters to ...
Combination of beta-Lactam Antibiotics and beta-Lactamase Inhibitors. Amoxicillin is a semisynthetic beta-lactam antibiotic, an ... Combination of beta-Lactam Antibiotics and beta-Lactamase Inhibitors. The New Macrolides. Initial Treatment Regimens. ... Beta-lactam antibiotics penetrate poorly into mammalian cells, and this characteristic may limit the effectiveness of these ... These include amikacin, quinolones, rifamycin derivatives, clofazimine, and beta-lactams (9). None of these agents has been ...
In a clinical isolate of E. coli, plasmid clearance and re-sensitization to five beta-lactams were achieved. Reusability of ... You Are Here:Exploring the CRISPR-Cas9 potential to revert beta-lactam resistance in clinically relevant gram-negative bacteria ... You Are Here: Exploring the CRISPR-Cas9 potential to revert beta-lactam resistance in clinically relevant gram-negative ... Exploring the CRISPR-Cas9 potential to revert beta-lactam resistance in clinically relevant gram-negative bacteria. * ...
beta-Lactam Resistance / drug effects * beta-Lactam Resistance / genetics * beta-Lactams / pharmacology ... Resistant strains selected by treatment with β-lactams express variants of the target enzymes that do not recognize the drugs ... Until now, the crucial transpeptidase activity that is inhibited by β-lactams was not amenable to in vitro investigation with ...
Most antibiotics used to treat community-acquired aspiration pneumonia (eg, beta-lactam/beta-lactamase inhibitor) are highly ... A beta-lactam (ampicillin plus sulbactam 1.5-3 g every 6 hours or cefotaxime 1-2 g every 8 hours or ceftriaxone 1-2 g daily or ... Beta-lactams (ampicillin/sulbactam 1.5-3 g every 6 hours or ceftriaxone 1-2 g daily or cefotaxime 1-2 g every 8 hours or ... Beta-lactam (amoxicillin/clavulanate 2 g/125 mg twice daily or 500 mg/125 mg three times daily or 875 mg/125 mg twice daily, ...
Secondary outcomes included documentation of previously tolerated beta-lactams, modification of non-beta-lactam therapy, ... and among patients receiving a non-beta-lactam, a greater percentage was subsequently switched to a beta-lactam (11.4% vs 25.7 ... allergy history documentation and increase the use of beta-lactams when appropriate in patients with a reported beta-lactam ... Confronting the Challenge of Beta-Lactam Allergies: A Quasi-Experimental Study Assessing Impact of Pharmacy-Led Interventions. ...
Beta-lactam Ring. Baker, Aidan. Sea Swells A Bit. A Silent Place. ...
Antibiotics - narrow spectrum beta-lactams. Antihistamines. Antimalarials. Bangyong Technology. Bangyong Technology Co.,Ltd. ...
Typhoid is a bacterial infection that can lead to a high fever, diarrhea, and vomiting. It can be fatal. It is caused by the bacteria Salmonella typhi. The...
... beta-Lactams); EC 3.5.2.6 (beta-Lactamases); OID: NLM: PMC3346353; 2012/03/09 [aheadofprint]; ppublish ... In this study, we focused on evaluating the occurrence of extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli in ... Characterization of extended-spectrum beta-lactamase genes found among Escherichia coli isolates from duck and environmental ...
Potential cross contamination with non-antibacterial beta-lactam drug substance Scynexis, Inc. ...
Older beta-lactams were lower risk (penicillin AOR, 1.8; amoxicillin, 2.0; cephalexin, 2.9; cefadroxil, 2.8). The lowest-risk ... not only showing a wide variation among beta-lactam antibiotics but also indicating that the risk associated with ...
Nordmann P. Trends in beta-lactam resistance among Enterobacteriaceae. Clin Infect Dis. 1998 Aug. 27 Suppl 1:S100-6. [QxMD ... Extended-spectrum beta-lactamase-producing Enterobacteriaceae: an emerging public-health concern. Lancet Infect Dis. 2008 Mar. ... The outbreak strain was typed as an enteroaggregative Shiga-toxin-producing E coli O104:H4, producing extended-spectrum beta- ... Melzer M, Petersen I. Mortality following bacteraemic infection caused by extended spectrum beta-lactamase (ESBL) producing E. ...
... beta-lactam antibiotics such as penicillin or amoxicillin (Amoxil, Larotid, Moxatag); any other medications, or any of the ... Tazobactam is in a class called beta-lactamase inhibitor. It works by preventing bacteria from destroying piperacillin. ...
Songs of Eta Carinae (Beta-lactam). Review by Aaron Shaul.. The Black Heart Procession. Music Reviews • February 6, 2007. ...
Oral beta-lactams provide noninferior postdischarge pyelonephritis treatment Publish date: October 5, 2019 ...
  • Beta-lactams are antibiotics that have a beta-lactam ring nucleus. (msdmanuals.com)
  • Classification of antibiotics and beta-lactam compound. (pharmacygyan.com)
  • Objective: The indiscriminate use of antibiotics has led to the creation of resistant microorganisms, with the aim of this study was to compare in vitro the degree of effectiveness of beta-lactam antibiotics and glycopeptide in the inhibition of Staphylococcus aureus by comparing its effectiveness in surgical wound infection. (bvsalud.org)
  • Resistant strains selected by treatment with β-lactams express variants of the target enzymes that do not recognize the drugs but retain their activity in cell wall building, despite the antibiotics being mimics of the natural substrate. (nih.gov)
  • Secondary outcomes included documentation of previously tolerated beta-lactams, modification of non-beta-lactam therapy, discharge antibiotics, and adverse reactions. (wustl.edu)
  • Penicillin-allergic women who do not have a history suggestive of IgE-mediated reaction, (pruritic rash, urticaria (hives), immediate flushing, hypotension, angioedema, or respiratory distress) recurrent reactions to administration of a beta-lactam antibiotic, reactions to multiple beta-lactam antibiotics, positive penicillin allergy test, or a history of rare delayed onset cutaneous or systemic reactions following administration of a penicillin or a cephalosporin should receive cefazolin for GBS intrapartum prophylaxis. (cdc.gov)
  • However, development of antibiotic resistance, driven by misuse of beta-lactam and beta-lactamase inhibitors and the time taken for the regulatory approval is projected to impede the market growth. (pharmiweb.com)
  • Beta-lactamases are a diverse class of enzymes produced by bacteria that break open the beta-lactam ring, inactivating the beta-lactam antibiotic. (msdmanuals.com)
  • Antibiotic containing the beta-lactam (alpha-4 membraned cyclic amide) ring structure constitute the dominant class of agents currently employed for the chemotherapy of bacterial infections. (pharmacygyan.com)
  • beta-lactam antibiotic are a broad class of antibiotic, the structure having a lactam group with a heteroatom structure consisting of the cyclic amide with 3 carbon atoms and one nitrogen atom. (pharmacygyan.com)
  • A 2022 study in Clinical Infectious Diseases looked at whether administration of a broad-spectrum β-lactam (e.g., cefepime, piperacillin-tazobactam, etc.) before the infusion of vancomycin, as the first dose of antibiotic therapy, is protective against mortality in the first 7 days for hospitalized patients with BSIs. (brownmedpedsresidency.org)
  • Of 3376 eligible patients across 5 hospitals, 2685 (79.5%) received a β-lactam and 691 (20.5%) received vancomycin as their initial antibiotic. (brownmedpedsresidency.org)
  • Synthetic Biologics, Inc., a developer of pathogen-specific therapies for serious infections and diseases, with a focus on protecting the microbiome, today announced the initiation of a Phase 2a clinical trial to evaluate the gastrointestinal (GI) antibiotic-degrading effects and the safety of SYN-004, the Company's investigational oral beta-lactamase enzyme designed to protect the microbiome and prevent C. difficile infection (CDI). (news-medical.net)
  • CONCLUSION: Multidisciplinary education and local guideline implementation led by pharmacists may improve allergy documentation and antibiotic selection in patients with reported beta-lactam allergies. (wustl.edu)
  • Combination segment is further categorized into penicillin/beta lactamase inhibitors, cephalosporins/beta lactamase inhibitors, and carbapenems/beta lactamase inhibitors. (pharmiweb.com)
  • All beta-lactams bind to and inactivate enzymes required for bacterial cell wall synthesis. (msdmanuals.com)
  • Beta-lactamase production is among the most clinically important mechanisms of resistance for gram-negative bacterial pathogens. (msdmanuals.com)
  • Exploring the CRISPR-Cas9 potential to revert beta-lactam resistance in clinica. (rwth-aachen.de)
  • The global emergence of carbapenemase-producing organisms is a public health emergency because these enzymes confer resistance to nearly all Beta-lactam drugs and are often associated with multidrug or pandrug resistance. (cdc.gov)
  • OXA beta-lactamases primarily hydrolyze narrow spectrum penicillins but certain OXA variants such as the plasmid encoded OXA 48 can hydrolyze carbapenems, even while leaving many cephalosporins active. (msdmanuals.com)
  • Dr. Ward begins her presentation by reviewing the impact of beta-lactam allergies on the healthcare system. (idpodcasts.net)
  • Confronting the Challenge of Beta-Lactam Allergies: A Quasi-Experimental Study Assessing Impact of Pharmacy-Led Interventions. (wustl.edu)
  • In the nursing home setting, treatment should consist of an antipneumococcal fluoroquinolone alone or either a high-dose beta-lactam/beta-lactamase inhibitor or a second- or third-generation cephalosporin, in combination with azithromycin. (aafp.org)
  • Nonhospitalized nursing home patients requiring treatment for pneumonia should be treated with an antipneumococcal fluoroquinolone, or either a high-dose beta-lactam/beta-lactamase inhibitor or a second- or third-generation cephalosporin, in combination with azithromycin (Zithromax). (aafp.org)
  • Tazobactam is in a class called beta-lactamase inhibitor. (medlineplus.gov)
  • The significance of beta-lactam allergy cross reactivity is then mentioned. (idpodcasts.net)
  • She goes on to explain how beta-lactam allergy testing is performed. (idpodcasts.net)
  • Lastly, she identifies strategies to improve the documentation of beta-lactam allergy reporting. (idpodcasts.net)
  • OBJECTIVE: To improve allergy history documentation and increase the use of beta-lactams when appropriate in patients with a reported beta-lactam allergy. (wustl.edu)
  • Plasmid-encoded AmpC expression is also constitutive and may be spread among bacteria usually lacking this beta-lactamase, such as Escherichia coli , Klebsiella pneumoniae , and Proteus mirabilis . (msdmanuals.com)
  • The prevalence of bacterial pathogens causing BSIs susceptible to broad spectrum β-lactams is higher than the prevalence of pathogens not susceptible to broad-spectrum β-lactams. (brownmedpedsresidency.org)
  • The beta-lactam and beta-lactamase inhibitors market is expected to exhibit significant growth during the forecast period due to increased consumption in low and middle-income countries (LMICs) and rise in prevalence of infectious diseases. (pharmiweb.com)
  • This study determined the prevalence of MDR A. baumannii isolates from intensive care units in a large tertiary-care hospital in Ismailia, Egypt, and the occurrence of different beta-lactamases in these isolates. (who.int)
  • Classes A, C, and D have a serine residue at the active site, whereas class B enzymes have zinc at the active site, ie, metallo-beta-lactamases (MBLs). (msdmanuals.com)
  • These enzymes are not inhibited by currently available beta-lactamase inhibitors. (msdmanuals.com)
  • Until now, the crucial transpeptidase activity that is inhibited by β-lactams was not amenable to in vitro investigation with enzymes from Gram-positive organisms, including streptococci, staphylococci, or enterococci pathogens. (nih.gov)
  • The beta-lactam used to treat patients with H pylori infection is stable in an acid environment, binds to proteins within bacterial cell walls, induces direct wall lysis, and inhibits cell-wall synthesis. (medscape.com)
  • Understanding the most common types of beta-lactamases produced by different pathogens can help with susceptibility interpretation, therapeutic decision making, and infection control practices. (msdmanuals.com)
  • Although the organism was not extensively resistant, it was resistant to all Beta-lactam drugs tested, including ertapenem. (cdc.gov)
  • ment of these beta-lactamase-resistant then incubated aerobically at 37° C are now recognized to play a consider- non-fermenting bacilli. (who.int)
  • Beta-lactam and Beta-lactamase Inhibitors Market Like to. (pharmiweb.com)
  • Pune, Maharashtra, India, February 22 2021 (Wiredrelease) Allied Analytics -:Beta-lactam and beta-lactamase inhibitors are chemical compounds of natural or semi-synthetic or synthetic origin. (pharmiweb.com)
  • In addition, development of novel approaches for new beta-lactam and beta-lactamase inhibitors for treating bacterial infections and a large number of clinical trials, further supplement the market growth. (pharmiweb.com)
  • The cephalosporin segment accounted more than two-fifths of the total beta-lactam and beta-lactamase inhibitors market share in 2018. (pharmiweb.com)
  • Asia-Pacific was the leading revenue contributor to the global beta-lactam and beta-lactamase inhibitors market in 2018, and is expected to remain dominant throughout the forecast period. (pharmiweb.com)
  • The report provides a comprehensive analysis of the key players operating in the global beta-lactam and beta-lactamase inhibitors market industry, namely, Abbott Laboratories, Allergan Plc. (pharmiweb.com)
  • U.S. generated the highest revenue in the global beta-lactam and beta-lactamase inhibitors in 2018, accounting more than one-fifth of the global market in 2018. (pharmiweb.com)
  • AmpC beta-lactamase may be chromosome- or plasmid-encoded. (msdmanuals.com)
  • Worldwide dissemination of the Klebsiella pneumoniae , VIM, OXA, and New Delhi metallo-Beta-lactamase type carbapenemases among humans has been facilitated by intercontinental passenger travel, but the role of the global food trade in this dissemination has not been investigated. (cdc.gov)
  • Among the isolates, 6 isolates were carbapenemase producers, 2 were AmpC beta-lactamase producers and no isolates were metallo-beta- lactamase producers. (who.int)
  • It groups beta-lactamases by class on the basis of molecular homology. (msdmanuals.com)
  • Administration of vancomycin prior to a β-lactam was not associated with improved survival in the subgroup of 524 patients with MRSA BSI (aOR 0.93 [95% CI 0.33-2.63]), supporting the overall study findings of prioritizing β-lactam therapy when there is a heightened suspicion for BSI. (brownmedpedsresidency.org)
  • In sum, for patients likely to be experiencing BSI, prioritizing administration of a β-lactam over vancomycin appears to reduce early mortality, underscoring the significant impact of a relatively simple practice change on improving patient survival. (brownmedpedsresidency.org)
  • Primary outcomes were documentation of reaction type and percentage of patients receiving non-beta-lactam therapy. (wustl.edu)
  • No significant differences were observed between the before versus after groups in the percentage of patients with documentation of reaction type (90.1% vs 89.8%, P = .940) or the overall percentage of patients receiving non-beta-lactams (86.8% vs 84.1%, P = .605). (wustl.edu)
  • However, significantly more patients in the after phase had documentation of previously tolerated beta-lactams (8.8% vs 28.4%, P = .001), and among patients receiving a non-beta-lactam, a greater percentage was subsequently switched to a beta-lactam (11.4% vs 25.7%, P = .022). (wustl.edu)
  • En Égypte, des isolats prélevés sur les tubulures d'appareils d'aspiration et de respiration artificielle (A8) et sur les cuvettes (A7) étaient liés à ceux prélevés chez les patients ayant ces antibiotypes. (who.int)
  • Beta-lactamases are a diverse class of enzymes produced by bacteria that break open the beta-lactam ring, inactivating the beta-lactam antibiotic. (msdmanuals.com)
  • Amoxicillin is a broad-spectrum beta-lactam antibiotic. (nel.edu)
  • Beta-lactamase production is among the most clinically important mechanisms of resistance for gram-negative bacterial pathogens. (msdmanuals.com)
  • Structural basis for the beta lactam resistance of PBP2a from methicillin-resistant Staphylococcus aureus. (expasy.org)
  • The global emergence of carbapenemase-producing organisms is a public health emergency because these enzymes confer resistance to nearly all Beta-lactam drugs and are often associated with multidrug or pandrug resistance. (cdc.gov)
  • OXA beta-lactamases primarily hydrolyze narrow spectrum penicillins but certain OXA variants such as the plasmid encoded OXA 48 can hydrolyze carbapenems, even while leaving many cephalosporins active. (msdmanuals.com)
  • As shown in the previous report the most commonly prescribed classes of antimicrobial agents in humans were ß-lactams, followed by macrolides and tetracyclines, accounting for 90 per cent of antimicrobials prescribed. (thecattlesite.com)
  • Association of systemic antimicrobials with the expression of beta-lactamases in bacteria cultured from urological patients. (nih.gov)
  • 3 Screen for metallo-beta-lactamase production [Rasheed et al. (cdc.gov)
  • Worldwide dissemination of the Klebsiella pneumoniae , VIM, OXA, and New Delhi metallo-Beta-lactamase type carbapenemases among humans has been facilitated by intercontinental passenger travel, but the role of the global food trade in this dissemination has not been investigated. (cdc.gov)
  • The most commonly prescribed classes of antimicrobial agents used in veterinary medicine were tetracyclines followed by sulphonomides/trimethoprim and β-lactams. (thecattlesite.com)
  • This medication is a beta- blocker, prescribed for heart disease. (medindia.net)
  • The combination of tazobactam with piperacillin results in an antimicrobial agent with enhanced activity against most beta-lactamase-producing organisms. (nih.gov)
  • [ 4 ] The frequent incidence of drug hypersensitivity in the skin might be due to the readiness of skin CCR8 + , CD4 + , T cell receptor alpha-beta + T cells to be stimulated by drugs via the p-i mechanism. (medscape.com)
  • Although the organism was not extensively resistant, it was resistant to all Beta-lactam drugs tested, including ertapenem. (cdc.gov)
  • It groups beta-lactamases by class on the basis of molecular homology. (msdmanuals.com)