Lactams
beta-Lactams
Superinfection
Aminoglycosides
Cyclization
Randomized Controlled Trials as Topic
alpha-MSH
Heterocyclic Compounds, 1-Ring
Interleukin-1beta
Muramic Acids
Stereoisomerism
beta 2-Microglobulin
Molecular Structure
Amination
Cleome
Receptors, Melanocortin
Receptors, Adrenergic, beta
Integrin beta3
Imines
Streptothricins
Magnetic Resonance Spectroscopy
Transforming Growth Factor beta
Structure-Activity Relationship
Alkenes
Carboxylic Acids
Streptomyces
Amides
Drug Design
Bicyclo Compounds, Heterocyclic
Integrin alpha5beta1
Peptides, Cyclic
Integrin beta4
Chromatography, Paper
Integrin alpha6beta4
Integrin beta Chains
beta 2-Glycoprotein I
Aza Compounds
Models, Molecular
Integrin alpha4beta1
Indium Radioisotopes
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.
Beta-lactam
Beta-lactam antibiotics
Beta-lactam Ring Records
carboxyethyl)arginine beta-lactam-synthase
Lectka enantioselective beta-lactam synthesis
Piperacillin
Sulbactam
Ketene
Ertapenem
Flucloxacillin
Cephalosporin
Penem
Penicillin-binding proteins
QIAGEN Silicon Valley
Hermann Staudinger
MecA
M. J. Thirumalachar
Gerhard Domagk
Imine Diels-Alder reaction
Metabolism
Streptomyces cattleya
Streptomyces violaceus
Carfecillin
History of penicillin
Streptomyces clavuligerus
Latamoxef
Aztreonam
Streptomyces olivaceus
Penicillin
Peritonitis
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Beta-Lactams - Infectious Diseases - MSD Manual Professional Edition
Navigating Beta-Lactam Allergies | USF Health's IDPodcasts
Classification of antibiotics and beta-lactam compound. - Pharmacy Gyan
Give The Beta-Lactam Before the Vanc | BROWN MED-PEDS
Sensitivity of S. aureus to beta-lactam and glycopeptide. ("In vitro")
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Community-Acquired Pneumonia (CAP): Practice Essentials, Overview, Etiology of Community-Acquired Pneumonia
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Baker, Aidan: At The Fountain Of Thirst | Midheaven Mailorder
Data Source Search | CMLD-BU
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WTS database | WHO FCTC
Recalls, Market Withdrawals, & Safety Alerts | FDA
Lifeboat Foundation News Blog - Page 2
Escherichia coli (E coli) Infections Clinical Presentation: History, Physical, Causes
Piperacillin and Tazobactam Injection: MedlinePlus Drug Information
The Black Heart Procession :: Ink 19
Antibiotics6
- 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)
Antibiotic8
- 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)
Penicillin1
- Combination segment is further categorized into penicillin/beta lactamase inhibitors, cephalosporins/beta lactamase inhibitors, and carbapenems/beta lactamase inhibitors. (pharmiweb.com)
Required for bacterial1
- All beta-lactams bind to and inactivate enzymes required for bacterial cell wall synthesis. (msdmanuals.com)
Resistance3
- 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)
Cephalosporins1
- 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)
Allergies2
- 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)
Inhibitor3
- 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)
Allergy4
- 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)
Bacteria1
- 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)
Bacterial pathogens1
- 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)
Prevalence2
- 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)
Enzymes3
- 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)
Infection2
- 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)
Resistant2
Lactamase10
- 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)
Class1
- It groups beta-lactamases by class on the basis of molecular homology. (msdmanuals.com)
Patients6
- 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)
Antibiotic2
- 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)
Resistance3
- 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)
Penicillins1
- 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)
Antimicrobials2
- 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)
Metallo-beta-lactamase2
- 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)
Tetracyclines1
- The most commonly prescribed classes of antimicrobial agents used in veterinary medicine were tetracyclines followed by sulphonomides/trimethoprim and β-lactams. (thecattlesite.com)
Medication1
- This medication is a beta- blocker, prescribed for heart disease. (medindia.net)
Antimicrobial1
- The combination of tazobactam with piperacillin results in an antimicrobial agent with enhanced activity against most beta-lactamase-producing organisms. (nih.gov)
Drugs2
- [ 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)
Basis1
- It groups beta-lactamases by class on the basis of molecular homology. (msdmanuals.com)