Rats, Inbred OLETF
Biological Science Disciplines
All of the divisions of the natural sciences dealing with the various aspects of the phenomena of life and vital processes. The concept includes anatomy and physiology, biochemistry and biophysics, and the biology of animals, plants, and microorganisms. It should be differentiated from BIOLOGY, one of its subdivisions, concerned specifically with the origin and life processes of living organisms.
A bibliographic database that includes MEDLINE as its primary subset. It is produced by the National Center for Biotechnology Information (NCBI), part of the NATIONAL LIBRARY OF MEDICINE. PubMed, which is searchable through NLM's Web site, also includes access to additional citations to selected life sciences journals not in MEDLINE, and links to other resources such as the full-text of articles at participating publishers' Web sites, NCBI's molecular biology databases, and PubMed Central.
Directories as Topic
Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)
Dictionaries as Topic
The soft tissue filling the cavities of bones. Bone marrow exists in two types, yellow and red. Yellow marrow is found in the large cavities of large bones and consists mostly of fat cells and a few primitive blood cells. Red marrow is a hematopoietic tissue and is the site of production of erythrocytes and granular leukocytes. Bone marrow is made up of a framework of connective tissue containing branching fibers with the frame being filled with marrow cells.
Coated Materials, Biocompatible
Neural Networks (Computer)
A computer architecture, implementable in either hardware or software, modeled after biological neural networks. Like the biological system in which the processing capability is a result of the interconnection strengths between arrays of nonlinear processing nodes, computerized neural networks, often called perceptrons or multilayer connectionist models, consist of neuron-like units. A homogeneous group of units makes up a layer. These networks are good at pattern recognition. They are adaptive, performing tasks by example, and thus are better for decision-making than are linear learning machines or cluster analysis. They do not require explicit programming.
Chromatography, Ion Exchange
Property, such as patents, trademarks, and copyright, that results from creative effort. The Patent and Copyright Clause (Art. 1, Sec. 8, cl. 8) of the United States Constitution provides for promoting the progress of science and useful arts by securing for limited times to authors and inventors, the exclusive right to their respective writings and discoveries. (From Black's Law Dictionary, 5th ed, p1014)
Introduction of a fluorine atom at C3 of 3-deazauridine shifts its antimetabolic activity from inhibition of CTP synthetase to inhibition of orotidylate decarboxylase, an early event in the de novo pyrimidine nucleotide biosynthesis pathway. (1/16)(+info)
Dual effects of pyrazofurin and 3-deazauridine upon pyrimidine and purine biosynthesis in mouse L1210 leukemia. (2/16)Pyrazofurin (NSC 143095) as the monophosphate derivative is a potent inhibitor of orotidine 5'-monophosphate (OMP) decarboxylase of the pyrimidine pathway and has been proposed to inhibit 5-aminoimidazole-4-carboxamide ribotide (AICAR) transformylase (EC 22.214.171.124) of the purine pathway (J. F. Worzalla, and M. J. Sweeney, Pyrazofurin inhibition of purine biosynthesis via 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranosyl 5'-monophosphate formyltransferase. Cancer Res., 40: 1482-1485, 1980). Measurement of levels of pyrimidine and purine intermediates in cultured mouse L1210 leukemia cells has shown that 25 microM pyrazofurin induces an 8-fold accumulation of OMP and large accumulations of intermediates proximal to the blockade with abrupt decreases in uridine and cytidine nucleotides. Considerable increases in the cellular concentrations of N-succino-AICAR (SAICAR), AICAR, 5-formamidoimidazole-4-carboxamide ribotide (FAICAR), IMP, XMP, and GMP at later times indicate that AICAR transformylase is not significantly inhibited in cultured cells; rather the purine pathway and the GMP branch are stimulated. However, addition of 25 microM 3-deazauridine (NSC 126849) to leukemia cells did result in inhibition of AICAR transformylase: AICAR and SAICAR accumulated, IMP disappeared and there was a large accumulation of guanosine nucleotides. Blockade of pyrimidine biosynthesis by derivatives of pyrazofurin or 3-deazauridine spares 5-phosphoribosyl-1-pyrophosphate and L-glutamine, elevated concentrations of which may stimulate initial reactions of purine biosynthesis and the reaction XMP----GMP. (+info)
Formation of 1-beta-D-arabinofuranosylcytosine diphosphate choline in cultured human leukemic RPMI 6410 cells. (3/16)When incubated with 1-beta-D-arabinofuranosylcytosine (ara-C), RPMI 6410 cells formed a hitherto unrecognized ara-C metabolite, 1-beta-D-arabinofuranosylcytosine diphosphate choline. This compound was characterized by (a) chromatographic behavior, (b) chemical and enzymatic hydrolysis, (c) phosphorus content, and (d) incorporation of [5-3H]ara-C and [methyl-14C]choline. Formation of 1-beta-D-arabinofuranosylcytosine diphosphate choline by RPMI 6410 cells was enhanced in the presence of 3-deazauridine (DU) and was preceded by that of 1-beta-D-arabinofuranosylcytosine triphosphate. The antiproliferative effects of ara-C and DU toward RPMI 6410 cells were potentiated when the agents were present together. The anabolism of ara-C during a 24-hr interval of culture was markedly enhanced by the presence of DU; cellular concentrations of 1-beta-D-arabinofuranosylcytosine triphosphate and 1-beta-D-arabinofuranosylcytosine diphosphate choline were 5- and 15-fold higher than those in the absence of DU. This enhancement appears to be the basis of the potentiation of cytotoxicity resulting from combination of the agents. Pretreatment of RPMI 6410 cells with DU resulted in enhanced rates of cellular uptake of ara-C. ara-C uptake under these circumstances was blocked by the inhibitor of nucleoside transport, nitrobenzylthioinosine. (+info)
Formation of 1-beta-D-arabinofuranosylcytosine diphosphate choline in neoplastic and normal cells. (4/16)1-beta-D-Arabinofuranosylcytosine diphosphate choline was formed from 1-beta-D-arabinofuranosylcytosine (ara-C) during incubation in vitro of peripheral myeloblasts from patients with acute myelogenous leukemia and cultured cells (nonleukemic human lymphocytes, mouse lymphoma L5178Y, and HeLa); as well, 1-beta-D-arabinofuranosylcytosine diphosphate choline was formed in vivo in mouse leukemia L1210 cells and mouse liver. 3-Deazauridine enhanced the anabolism of ara-C in nonleukemic lymphocytes in vitro and leukemia L1210 cells in vivo but did not influence ara-C anabolism in the other cell types. In acute myelogenous leukemia myeloblasts incubated in vitro with ara-C, concentrations of 1-beta-D-arabinofuranosylcytosine 5'-triphosphate were maximal after 8 hr of incubation and formation of the latter preceded that of 1-beta-D-arabinofuranosylcytosine diphosphate choline. (+info)
Effects of pyrimidine antagonists on sialic acid regeneration in HL-60 cells. (5/16)Because alterations in cell membrane sialoglycoconjugates can affect the behavior of neoplastic cells, we investigated the effects of in vitro treatment with antimetabolites used in cancer therapy on the expression of membrane sialic acid in cultured HL-60 leukemic cells. In these studies, cells were incubated with Vibrio cholerae neuraminidase to remove surface sialic acid. Reappearance of membrane sialic acid during drug treatment was followed (a) by measuring changes in radioactive surface labeling of viable cells with sodium metaperiodate-sodium[3H]-borohydride, (b) by measuring the decline in accessible surface galactosyl receptor sites which occurred coincident with membrane sialic acid replacement, and (c) by measuring the incorporation of [3H]glucosamine into membrane-associated neuraminidase-labile sialic acid. We were especially interested in learning whether drugs that affect intracellular pools of cytidine triphosphate (CTP), an important nucleotide intermediate in sialylation reactions, could inhibit regeneration of membrane sialic acid. 3-Deazauridine, a competitive inhibitor of CTP synthetase, depleted CTP pools and curtailed surface membrane resialylation with little or no effect on synthesis of de novo sialic acid from precursor sugars. The addition of cytidine restored CTP pools and sialic acid regeneration. Acivicin, a glutamine antagonist, also depleted CTP pools and curtailed surface membrane resialylation. In addition, it retarded de novo synthesis of sialic acid. The addition of cytidine restored intracellular CTP pools and sialic acid regeneration. However, both cytidine and guanosine were required to restore sialic acid synthesis from precursor sugars. 1-beta-D-Arabinofuranosylcytosine, a competitive inhibitor of sialic acid synthetase and of sialyltransferase, inhibited both de novo sialic acid synthesis and membrane resialylation. Only the latter effect was reversed by the addition of exogenous cytidine. Hydroxyurea, an agent shown previously to inhibit glycoconjugate production in hamster fibroblasts, curtailed membrane resialylation and de novo synthesis of sialic acid without depleting CTP pools. Doxorubicin, at levels that caused marked arrest of cell proliferation, had no effect on sialic acid synthesis or expression on the membrane surface. These data suggest that antimetabolites, apart from their cytotoxic effects or effects on cellular growth, may directly inhibit the expression of membrane sialic acid.(ABSTRACT TRUNCATED AT 400 WORDS) (+info)
Drug sequence-dependent toxicity and small bowel mucosal injury in mice treated with low doses of 3-deazauridine and 1-beta-D-arabinofuranosylcytosine. (6/16)The toxicity to mice of combinations of 1-beta-D-arabinofuranosylcytosine and 3-deazauridine was investigated. The drugs were administered daily i.p. on Days 1 to 5, each drug at 10 mg/kg body weight; these dosages are small fractions of the dosages at which 10% of the treated animals died when either drug was administered alone on the foregoing schedule. This drug combination was severely toxic when 3-deazauridine was administered 2 to 8 hr prior to 1-beta-D-arabinofuranosylcytosine; most mice treated in this way died within 3 days of the last treatment. Histological examination showed that severe damage to the small bowel mucosa resulted from treatment with the drugs in the above, lethal sequence. In contrast, treatments with this drug combination at the same dosages were tolerated when the two agents were administered simultaneously or when 1-beta-D-arabinofuranosylcytosine preceded 3-deazauridine. Under the latter conditions, small bowel mucosal injury was much less severe. Female mice were more sensitive to the toxic treatment regimen than were male mice and were protected against the latter when either the 3-deazauridine or the 1-beta-D-arabinofuranosylcytosine component was preceded by treatment with nitrobenzylthioinosine (100 mg/kg), a potent inhibitor of nucleoside transport. (+info)
Synergistic action of 5-aza-2'-deoxycytidine and 3-deazauridine on L1210 leukemic cells and EMT6 tumor cells. (7/16)The biochemical and biological effects of the combination of 5-aza-2'-deoxycytidine (5-aza-dCyd) and 3-deazauridine (3-DU) on L1210 leukemic cells and EMT6 tumor cells were investigated. The cytotoxic action of 5-aza-dCyd and 3-DU on both L1210 and EMT6 cells in vitro was synergistic when these agents were used in combination. The combination of 5-aza-dCyd and 3-DU produced a greater inhibition of in vitro growth of L1210 and EMT6 cells than did either agent alone. The in vivo antineoplastic activity of this combination was synergistic with respect to the increased survival time of BALB/c x DBA/2 F1 mice with L1210 leukemia. 3-DU, an agent that reduces the intracellular pool size of cytosine nucleotides, stimulated the incorporation of [3H]-5-aza-dCyd into DNA of both L1210 and EMT6 cells, suggesting that the synergistic action of this combination is related to the increased incorporation of 5-aza-dCyd in the presence of 3-DU. (+info)
Penetration of 3-deazauridine into human brain, intracerebral tumor, and cerebrospinal fluid. (8/16)The antitumor agent 3-deazauridine (DAU) was administered rapidly to four patients before surgical removal of intracerebral tumor. Tumor, adjacent brain tissue, and temporalis muscle were assayed for DAU by high-pressure liquid chromatography. DAU penetrated comparably into tumor, brain, and muscle; in one patient, tissue concentrations were higher than concurrent plasma concentrations. The active metabolite 3-deazauridine 5'-triphosphate was quantitated in one tumor sample and greatly exceeded its Ki for cytidine 5'-triphosphate synthetase. DAU was also present in autopsy brain specimens from two patients treated shortly antemortem. Cerebrospinal fluid concentrations were 22.1 and 59.0%, respectively, of concurrent plasma concentrations during continuous infusion of DAU in two patients. Cerebrospinal fluid concentration was 3.1 microgram/ml 2 hr after a 30-min infusion of 1.5 g of drug per sq m and fell to 1.9 microgram/ml at 16 hr. Thus, DAU is capable of penetrating into intracerebral tumor, brain, and cerebrospinal fluid and is worthy of investigation in the treatment of intracerebral and meningeal neoplasms. (+info)
Effect of Uridine on Response of 5-Azacytidine-resistant Human Leukemic Cells to Inhibitors of de Novo Pyrimidine Synthesis<...
TY - JOUR. T1 - Effect of Uridine on Response of 5-Azacytidine-resistant Human Leukemic Cells to Inhibitors of de Novo Pyrimidine Synthesis. AU - Grant, S.. AU - Bhalla, K.. AU - Gleyzer, M.. PY - 1984/12/1. Y1 - 1984/12/1. N2 - A uridine-cytidine kinase-deficient human promyelocytic leukemic subline (HL-60-5-aza-Cyd) has been isolated which is highly resistant to the antileukemic agent 5-azacytidine. Resistant cells exposed to 10-5 M 5-azacytidine for 2 hr exhibit a marked reduction in both the total intracellular accumulation of 5-azacytidine (11.9 versus 156.0 pmol/106 cells) as well as its incorporation into RNA (3.1 versus 43.4 pmol/μg D-ribose) compared to the parent line. These biochemical changes are associated with nearly a 100-fold decrease in sensitivity to the growth inhibitory effects of 5-azacytidine (concentration of drug associated with a 50% reduction in cell growth, 3.5 x 10-5 versus 5.0 x 10-7 M). 5-Azacytidine-resistant cells exhibit cross-resistance to 3-deazauridine, ...
Antimetabolic agent - definition of Antimetabolic agent by The Free Dictionary
Define Antimetabolic agent. Antimetabolic agent synonyms, Antimetabolic agent pronunciation, Antimetabolic agent translation, English dictionary definition of Antimetabolic agent. n. A substance that closely resembles an essential metabolite and therefore inhibits physiological reactions involving that metabolite. an′ti·met′a·bol′ic...
Antimetabolic agent synonyms, Antimetabolic agent antonyms - FreeThesaurus.com
Synonyms for Antimetabolic agent in Free Thesaurus. Antonyms for Antimetabolic agent. 9 words related to antimetabolite: antineoplastic, antineoplastic drug, cancer drug, fluorouracil, mercaptopurine, Purinethol, amethopterin, methotrexate.... What are synonyms for Antimetabolic agent?
NCAM1 monoclonal antibody, clone MEM-188 (FITC) - (MAB5003) - Products - Abnova
Mouse monoclonal antibody raised against native NCAM1. Native purified NCAM1 from KG-1 human acute myelogenous leukemia cell line. (MAB5003) - Products - Abnova
PRESS RELEASE: ANDRITZ to supply new pickling and galvanizing line and acid regeneration plant with ECOmode to Prosperity Tieh,...
=------------------------------------------------------------------------------- Corporate news transmitted by euro adhoc with the aim of a Europe-wide distribution. The issuer is responsible... | June 14, 2021
Starvation and antimetabolic therapy promote cytokine release and recruitment of immune cells | PNAS
Nutrient limitation occurs during physiological tissue growth or as a consequence of various pathological events, such as wounds or vascular occlusions that lead to transient ischemia. To recover, ischemic tissues employ mechanisms that promote wound healing and the restoration of the nutrient flux. These mechanisms include angiogenesis and inflammation, which have been classically attributed to hypoxia or to necrotic inflammatory signals, respectively. We show here that nutrient deprivation could be, by itself, a powerful signal to induce inflammation as part of a normal wound-healing response as pathogens and sterile injuries trigger similar events which include the recruitment of the innate immune system. It is possible that nutrient deprivation followed by the ISR is one of the many signals that the body uses to detect infections as pathogens also deprive nutrients from the site of infection. In fact, the kinase PKR, that detects viral dsRNA, is one of the kinases that activate the ISR ...
Vita-Peptide Eye Gel - D A P H N E
Youth EssentiA Vita-Peptide Eye Gel is a new scientifically advanced formulation which intelligently combines a highly specialized system of essential vitamins (A,C & E), antioxidants, peptides, and a new hyaluronic acid regeneration technology, Optim-Hyal™. This light weight eye gel assists in restoring the benefi
Youth EssentiA Vita-Peptide Eye Gel 10ml - Noosa Skin Studio
This youth enhancing Vita-Peptide Eye Gel contains essential vitamins & antioxidants as well as specially selected peptides plus hyaluronic acid regeneration technology. It assists in reducing the visible signs of ageing, promoting a youthful luminous, smooth and plumped appearance. BENEFITS FOR YOUR SKIN Contains
Buy Renor (Norfloxacin) Online
Buy Renor Online! Renor is a white to pale yellow crystalline powder with a molecular weight of 319.34 and a melting point of about 221°C. Renor, a fluoroquinolone, differs from non-fluorinated quinolones by having a fluorine atom at the 6 position and a piperazine moiety at the 7 position.
Therapeutic Efficacy of 3 BP
This is a third-party research done by a grant from YuFoundation for Tom Seyfried to research Dr. Young Kos 3 Bromopyruvate antimetabolic drug used in cancers. The important outcome is when 3 BP was injected into the primary cancer site, the metastatic rate was impressively low. Therefore, spread of the cancers may be hindered with this molecule. Please read more in section under grants and scientific information.. ...
Steel Pickling - HCl Process Facilities and Hydrochloric Acid Regeneration Plants: National Emission Standards for Hazardous...
This rule sets national emission standards for hazardous air pollutants (NESHAP) for hydrochloric acid (HCI) process steel pickling facilities and hydrochloric acid regeneration plants pursuant to section 112 of the Clean Air Act (Act).. Pickling is a process in which an acid solution is used to remove oxide scale from steel strip, rod, wire, tubing, and discreet shapes. Oxide scale forms on the surface of the steel when steel cools from a molten state. The steel pickling facilities that are affected by this rule use a solution of hydrochloric acid (HCl) to remove the oxide scale.. This process emits HCI, a hazardous air pollutant (HAP). Chronic exposure to HCl has been reported to cause gastritis, chronic bronchitis, dermatitis, and photosensitization. Acute inhalation exposure to HCl may cause hoarseness, inflammation and ulceration of the respiratory tract, chest pain, and pulmonary edema. Hydrochloric acid regeneration plants also emit chlorine (Cl2), which is also a HAP. Acute exposure to ...
ANDRITZ METALS supplies complete lines for the production and further processing of cold-rolled strip from carbon steel, stainless steel and non-ferrous metals, as well as industrial furnaces. In plants for production of stainless steel strip, acid regeneration, electrolytic galvanizing and push pickling lines we lead the world market.
CDP-Choline Caps | 250 mg 60 vegetarian capsules | Gray Zone Fitness
CDP-choline stands for cytidine-5Í-diphosphate choline. This unique form of choline readily passes through the blood-brain barrier (BBB) directly into the brain tissue. Once past the blood-brain barrier, CDP-choline activates the synthesis of critical components in cell membranes, enhances cerebral energy metabolism and increases levels of various neurotransmitters.. Supplement ...
Cytidine diphosphate choline definition | Drugs.com
Definition of cytidine diphosphate choline. Provided by Stedmans medical dictionary and Drugs.com. Includes medical terms and definitions.
Items where Subject is model organism - CSHL Scientific Digital Repository
Baker, Lindsey A., Tiriac, Hervé, Clevers, Hans, Tuveson, David A. (April 2016) Modeling Pancreatic Cancer with Organoids. Trends in Cancer, 2 (4). pp. 176-190. ISSN 2405-8033 Bapiro, T. E., Frese, K. K., Courtin, A., Bramhall, J. L., Madhu, B., Cook, N., Neesse, A., Griffiths, J. R., Tuveson, D. A., Jodrell, D. I., Richards, F. M. (May 2014) Gemcitabine diphosphate choline is a major metabolite linked to the Kennedy pathway in pancreatic cancer models in vivo. British Journal of Cancer, 111 (2). pp. 318-325. ISSN 0007-0920 Bergerson, R. J., Collier, L. S., Sarver, A. L., Been, R. A., Lugthart, S., Diers, M. D., Zuber, J., Rappaport, A. R., Nixon, M. J., Silverstein, K. A. T., Fan, D. H., Lamblin, A. F. J., Wolff, L., Kersey, J. H., Delwel, R., Lowe, S. W., OSullivan, M. G., Kogan, S. C., Adams, D. J., Largaespada, D. A. (May 2012) An insertional mutagenesis screen identifies genes that cooperate with Mll-AF9 in a murine leukemogenesis model. Blood, 119 (19). pp. 4512-4523. ISSN 0006-4971 Boj, ...
Antitumor activity of the novel melphalan containing tripeptide J3 (L-prolyl-melphalanyl-p-L-fluorophenylalanine ethyl ester) :...
Oligopeptides can be used to carry cytotoxic agents in cancer chemotherapy, using tumour-associated proteins as the molecular target for selectivity. During the seventies and eighties Peptichemio, a cocktail of six alkylating oligopeptides carrying m-L-sarcolysin, was investigated in a wide variety of human malignancies. Positive clinical results were suggested to result from rapid and effective DNA-crosslinking following uptake in neoplastic cells, but also from antimetabolic properties of the drug. Although m-L-sarcolysin never reached widespread clinical use, the well established para-isomer melphalan still, after nearly fifty years, has a place in cancer chemotherapy.. The present study was undertaken to synthesise the melphalan containing analogue of the tripeptide P2 (L-prolyl-m-L-sarcolysyl-p-L-fluorophenylalanine ethyl ester, the main contributor to Peptichemios activity) and similar compounds, preferably dipeptides. The new compounds compared favourably with melphalan, m-L-sarcolysin ...
Chapter 5 Test Flashcards
In the compound sodium flouride, NaF, the sodium atom loses one electron and the fluorine atom gains one electron to form ions that have electron configurations similar to _____. ...
Senescence Effects of Angelica sinensis Polysaccharides on Human Acute Myelogenous Leukemia Stem and Progenitor Cells ...
Senescence Effects of Angelica sinensis Polysaccharides on Human Acute Myelogenous Leukemia Stem and Progenitor Cells Angelica sinensis polysaccharide;leukemia stem/progenitor cells;senescence;telomerase;telomere; Leukemia stem cells (LSCs) play important roles in leukemia initiation, progression and relapse, and thus represent a critical target for therapeutic intervention. Hence, it is extremely urgent to explore new therapeutic strategies directly targeting LSCs for acute myelogenous leukemia (AML) therapy. We show here that Angelica sinensis polysaccharide (ASP), a major active component in Dong quai (Chinese Angelica sinensis), effectively inhibited human AML $CD34^+CD38^-$ cell proliferation in vitro culture in a dose-dependent manner while sparing normal hematopoietic stem and progenitor cells at physiologically achievable concentrations. Furthermore, ASP exerted cytotoxic effects on AML K562 cells, especially LSC-enriched $CD34^+CD38^-$ cells. Colony formation assays further showed that ASP
NioCorp Completes Acid Regeneration Pilot Plant for Elk Creek Project Feasibility Study
NioCorp $NB $NIOBF $BR3 #Niobium #Scandium #ElkCreek. About NioCorp. NioCorp is developing a superalloy materials project in Southeast Nebraska that will produce Niobium, Scandium, and Titanium. Niobium is used to produce superalloys as well as High Strength, Low Alloy (HSLA) steel, which is a lighter, stronger steel used in automotive, structural, and pipeline applications. Scandium is a superalloy material that can be combined with Aluminum to make alloys with increased strength and improved corrosion resistance. Scandium also is a critical component of advanced solid oxide fuel cells. Titanium is used in various superalloys and is a key component of pigments used in paper, paint and plastics and is also used for aerospace applications, armor and medical implants.. Cautionary Note Regarding Forward-Looking Statements Neither TSX nor its Regulation Services Provider (as that term is defined in the policies of the TSX) accepts responsibility for the adequacy or accuracy of this document. ...
Water Repellent Additive for Immersion Resist - Patent application
0123] On the other hand, a monomer having fluorine at its ester moiety is an acrylic acid ester or methacrylic acid ester having a unit where the ester moiety is a perfluoroalkyl group or a fluoroalkyl group serving as a flurine-containing group or a unit having both a cyclic structure and a fluorine atom at a-position, the cyclic structure being a fluorine-containing benzene ring, fluorine-containing cyclopentane ring, fluorine-containing cyclohexane ring or fluorine-containing cycloheptane ring or the like in which substitution with a fluorine atom, trifluoromethyl group, hexafluoroisopropyl hydroxyl group or the like has been made. It is also possible to use an acrylic acid or methacrylic acid ester having a fluorine-containing t-butyl ester group at ester moiety. It is also possible to use monomers in which these fluorine-containing functional groups are used in combination with a fluorine-containing alkyl group of a-position. Of such units, as particularly typical ones are exemplarily ...
For regeneration of pickling acids in your steel mill, the PYROMARS (mixed acid regeneration) plant from ANDRITZ METALS is an efficient and effective solution. The high recovery rates of 99% hydrofluoric acid, 80% nitric acid, and 99% metals need no further comment.
Ask Norm Lieberman: 2012
Norm Lieberman has been a process engineer for 50 years. His first employment was with AMOCO Oil as a process design engineer. He worked at Texas City as an operating superintendent of alkylation, sulfuric acid regeneration, and mercaptan extraction. Norm has designed: • Sulfur Plants • Amine Regenerators • Delayed Cokers • Crude Units • Vacuum Towers Hes the author of several well known troubleshooting books: • A Working Guide to Process Equipment • Process Design for Reliable Operations • Troubleshooting Natural Gas Processing • Troubleshooting Process Operations • Troubleshooting Process Plant Control • Process Engineering for a Small Planet • Process Equipment Malfunctions • Troubleshooting Vacuum Systems • My Race Against Death He has instructed 820 process troubleshooting seminars, attended by over 19,000 engineers and experienced operators since 1983. Mr. Lieberman is still actively involved in field troubleshooting and instructing process seminars. In 2015, ...
Citicoline - Cometa Wellness Center
60 Vegetarian capsules Optimize Your Brain Function * Enhances memory in the elderly * Supports balanced mood and cognitive function * Promotes phospholipid balance in the brain and enhances neurotransmitter production * Clinically shown to aid in recovery from traumatic brain injury Citicoline is cytidine diphosphate choline, or CDP-choline, a nutrient that has been shown to support memory in patients with age-associated memory impairment, and brain cell recovery from injuries such as stroke or concussion. Citicoline also increases the production of key neurotransmitters, including acetylcholine, norepinephrine, dopamine, and serotonin, all of which are essential for mood balance and memory. Additionally, it supports nerves in the eye, and studies administering Citicoline to patients with lazy-eye and other vision disorders have noted beneficial results. The main component of Citicoline is its cytidine group, which is what Citicoline delivers to
A radioimmunoassay for 1-beta-d-arabinofuranosylcytosine. by T Okabayashi, S Mihara et al.
Okabayashi, T; Mihara, S; Repke, D B.; and Moffatt, J G., A radioimmunoassay for 1-beta-d-arabinofuranosylcytosine. (1977). Subject Strain Bibliography 1977. 1646 ...
Berry Pseudorotation in Phosphorus Pentafluoride - Wolfram Demonstrations Project
The molecule has the configuration of a trigonal bipyramid as predicted by the VSEPR model Two of the fluorine atoms designated as axial are aligned with the phosphorus atom with PF bond distances of 158 Aring The remaining three fluorine atoms designated as equatorial are arranged in an equilateral triangle with PF bond distances of 153 Aring Even though there exist two geometrically inequivalent
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Bună sara! Ne-am mutat la casâ nouâ șî am zâs câ ar fi ghini sâ vă cinstesc oleacă! Am pentru voi o sacoșâ cu dulșiuri șî niști bieri. Aș fi vrut sâ vă dau o tavâ cu poale-n brâu șî Continue reading Bre, dam premii pi digeaba!→. ...
Colorado Tick Fever | Quick Medical Diagnosis & Treatment Pediatrics | AccessPediatrics | McGraw-Hill Medical
Colorado Tick Fever. In: Hay, Jr WW, Levin MJ, Deterding RR, Abzug MJ. Hay, Jr W.W., Levin M.J., Deterding R.R., Abzug M.J. Eds. William W. Hay, Jr, et al.eds. Quick Medical Diagnosis & Treatment Pediatrics New York, NY: McGraw-Hill; . http://accesspediatrics.mhmedical.com/content.aspx?bookid=2196§ionid=166956538. Accessed January 20, 2018 ...
Tissue distribution and intracerebral tumor penetration of 2,5-diaziridinyl-3,6-biscarboethoxyamino-1,4-benzoquinone (AZO, NSC...
TY - CHAP. T1 - Tissue distribution and intracerebral tumor penetration of 2,5-diaziridinyl-3,6-biscarboethoxyamino-1,4-benzoquinone (AZO, NSC 182986) in man. AU - Savaraj, Niramol. AU - Lu, K.. AU - Stewart, D.. PY - 1981/1/1. Y1 - 1981/1/1. UR - http://www.scopus.com/inward/record.url?scp=17544399898&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=17544399898&partnerID=8YFLogxK. M3 - Chapter. AN - SCOPUS:17544399898. VL - Vol. 22. BT - Proceedings of the American Association for Cancer Research. ER - ...
Dendritic cells derived in vitro from acute myelogenous leukemia cells stimulate autologous, antileukemic T-cell responses<...
TY - JOUR. T1 - Dendritic cells derived in vitro from acute myelogenous leukemia cells stimulate autologous, antileukemic T-cell responses. AU - Choudhury, A.. AU - Liang, J. C.. AU - Thomas, E. K.. AU - Flores-Romo, L.. AU - Xie, O. S.. AU - Agusala, K.. AU - Sutaria, S.. AU - Sinha, I.. AU - Champlin, R. E.. AU - Claxton, D. F.. N1 - Copyright: Copyright 2020 Elsevier B.V., All rights reserved.. PY - 1999/2/1. Y1 - 1999/2/1. N2 - We have previously reported that leukemic dendritic cells (DC) can be generated ex vivo from myelomonocytic precursors in chronic myelogenous leukemia. In this study we report the generation of DC from acute mye1ogenous leukemia (AML) cells and their potent ability to stimulate leukemia-specific cytolytic activity in autologous lymphocytes. DC were generated in vitro using granulocyte-macrophage colony-stimulating factor+interleukin-4 in combination with either tumor necrosis factor-α or CD40 ligand (CD40L). Cells from 19 AML patients with a variety of chromosomal ...
Salvage Pathway Of Purine Nucleotide Biosynthesis
This chapter discusses the de novo pathway of pyrimidine nucleotide biosynthesis. Animals do not have a dietary requirement for pyrimidines, and many microorgan
Fluoride Action Network | New Way To Prepare Fluorinated Pharmaceuticals
A team of MIT chemists has devised a new way to add fluorine to a variety of compounds used in many drugs and agricultural chemicals, an advance that could offer more flexibility and potential cost-savings in designing new drugs.. Drug developers commonly add fluorine atoms to drugs, such as the cholesterol-lowering rosuvastatin, to keep the body from breaking them down too quickly. Many of these drugs contain aromatic rings - a type of six-carbon ring - and attaching a fluorine atom to the rings can be a difficult, expensive process.. Its hard to add fluorine at a late stage, once you have a complete molecule already put together, because traditional methods can be quite harsh with respect to temperature or other factors, says Stephen L. Buchwald, the Camille Dreyfus Professor of Chemistry at MIT.. In their new technique, Buchwald and his colleagues used a palladium catalyst to attach a fluorine atom to aromatic compounds. The technique could be used in the design and testing of new drugs, ...
IUCr) Tris(hy-dr-oxy-meth-yl)methanaminium tri-fluoro-acetate
Recently much attention has been devoted to crystals containing organic ions and inorganic ions due to the possibility of tuning their special structural features and their potential ferroelectrics properties (Fu et al., 2011; Zhang et al., 2010.).. The compound (C4H12O3N)+(C2F3O2)- has an asymmetric unit that consists of one tris(hydroxymethyl)methanaminium cation and one trifluoroacetate anion (Fig 1). N-H···O and O-H···O hydrogen bonds form a complex three-dimensional network, (Fig 2). The trifluoromethyl group is quite mobile, but examination of a difference map in the plane of the fluorine atoms does show that the fluorine atoms exist as three distinct atoms.. For structure of the related tris(hydroxymethyl)methanaminium hydrogenhalides seen (Rudman et al., 1983).. ...
2-Fluoroamphetamine - Wikipedia
2-Fluoroamphetamine (2-FA) is a stimulant drug from the amphetamine family which has been sold as a designer drug. 2-Fluoroamphetamine differs from 3- and 4-fluoroamphetamine in the position of the fluorine atom on the aromatic ring, making them positional isomers of one another. The replacement of a hydrogen atom with a fluorine atom in certain compounds to facilitate passage through the blood-brain barrier, as is desirable in central nervous system pharmaceutical agents, is a common practice due to the corresponding increase in lipophilicity granted by the substitute. ...
Dioxygen difluoride : Wikis (The Full Wiki)
The bonding within dioxygen difluoride has been the subject of considerable speculation over the years, particularly because of the very short O-O distance and the long O-F distances. Bridgeman has proposed a scheme which essentially has an O-O triple bond and an O-F single bond that is destabilised and lengthened by repulsion between the lone pairs on the fluorine atoms and the π-orbitals of the O-O bond. Repulsion involving the fluorine lone pairs is also responsible for the long and weak covalent bonding in the fluorine molecule.. ...
Colorado tick fever virus ATCC ® VR-1233CAF™
Colorado tick fever virus ATCC ® VR-1233CAF™ Designation: Colorado tick fever control ascitic fluid [V-506-401-562] Application:
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TY - JOUR. T1 - Delivery of herpesvirus and adenovirus to nude rat intracerebral tumors after osmotic blood-brain barrier disruption. AU - Nilaver, Gajanan. AU - Muldoon, Leslie L.. AU - Kroll, Robert A.. AU - Pagel, Michael A.. AU - Breakefield, Xandra O.. AU - Davidson, Beverly L.. AU - Neuwelt, Edward A.. N1 - Copyright: Copyright 2007 Elsevier B.V., All rights reserved.. PY - 1995/10/10. Y1 - 1995/10/10. N2 - The delivery of viral vectors to the brain for treatment of intracerebral tumors is most commonly accomplished by stereotaxic inoculation directly into the tumor. However, the small volume of distribution by inoculation may limit the efficacy of vital therapy of large or disseminated tumors. We have investigated mechanisms to increase vector delivery to intracerebral xenografts of human LX-1 small-cell lung carcinoma tumors in the nude rat. The distribution of Escherichia coli lacZ transgene expression from primary viral infection was assessed after delivery of recombinant virus by ...
Effects of Selective Checkpoint Kinase 1 Inhibition on Cytarabine Cytotoxicity in Acute Myelogenous Leukemia Cells In Vitro |...
Results of the present study show for the first time that Chk1 undergoes activating phosphorylation in marrow blasts in vivo during cytarabine-containing induction therapy. Building on this result, we also show in human AML cell lines that the selective Chk1 inhibitor SCH 900776 abrogates cytarabine-induced S-phase arrest, increases cytarabine-induced apoptosis, and enhances the effects of cytarabine on colony formation. Likewise, SCH 900776 increases the effects of cytarabine in a majority of primary AML isolates but not normal myeloid progenitors in vitro. This sensitization was observed at SCH 900776 concentrations far below the approximate 5 μmol/L SCH 900776 peak levels observed at the maximum tolerated dose in solid tumor patients. These observations have potentially important implications for current efforts to enhance the efficacy of cytarabine-containing AML regimens.. Previous results have shown that cytarabine activates the ATR/Chk1 checkpoint in tissue culture cell lines in vitro ...
http://www.wisegeek.com/what-is-nucleotide-biosynthesis.htm Nucleotide biosynthesis is the process whereby nucleotides are created or synthesized. This process
Definition of anabolism - What it is, Meaning and Concept - I want to know everything - 2020
The idea of anabolism refers to a series of metabolism processes that involve the synthesis of different complex molecules through other molecules of greater simplicity. Anabolism, in this way, consists in the synthesis of certain biomolecules from molecules that, in comparison, are simpler.
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Colorado Tick Fever - Lyme Disease Association
Colorado tick fever (CTF) is a disease caused by an RNA virus, Colorado tick fever virus (CTFV). Symptoms, which are often non-specific, begin 3 to 5 days after the bite with an abrupt onset of fever and any of these: headaches, chills, malaise, photophobia, myalgias, nausea, vomiting, diarrhea and abdominal pain. In 5 to 15% of cases a rash occurs. Neurologic complications may also occur. 50% of patients have single recurrence of fever (saddleback fever).. IFA titers for diagnosis. PCR (Polymerase Chain Reaction) is the test most often used to diagnose the disease. CTF is transmitted by Dermacentor andersoni (Rocky Mt. wood tick) which causes illness from the Western Black Hills to the West Coast in the USA. Some cases of transmission through blood transfusion have been reported. Treatment consists of supportive care.. ©LDA. 2014. 2015. This web site provides practical and useful information on the subject matters covered. It is distributed with the understanding that LDA is not engaged in ...
Serologic Diagnosis of Colorado Tick Fever | The American Journal of Tropical Medicine and Hygiene
Abstract Isolation of the virus, the most reliable means of diagnosing Colorado tick fever, is not always practicable. The standard complement-fixation test, using a mouse-brain-derived antigen, may not detect significant rises in antibody titer during the usual 2- or 3-week observation period. Complement-fixation (CF) tests, with antigens derived from infected mouse brains and from an established line of hamster-kidney cells, were compared with a neutralization (plaque-reduction) test and an indirect fluorescent-antibody (IFA) staining test for usefulness in the serologic diagnosis of 34 cases of Colorado tick fever. The cell-culture antigen was as reliable as the mouse-brain antigen, and its preparation was simpler. The CF-antibody titers and the neutralizing-antibody titers tended to be lower and slower to appear than the IFA titers. The IFA method was simple, rapid, and accurate. The IFA titers frequently appeared earlier after onset of illness and reached higher levels than did the CF titers.
Colorado Tick Fever | Atlanta Outpatient Surgery Center
Learn more about Colorado Tick Fever at Atlanta Outpatient Surgery Center DefinitionCausesRisk FactorsSymptomsDiagnosisTreatmentPreventionrevision ...
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In a new paper, Partha Bera and colleagues at NASAs Ames Research Center and Purdue University put these gases under the microscope to find out exactly why they are such powerful heat trappers. They focus on CFCs, HFCs and PFCs - all chemicals containing fluorine or chlorine - that are used in medicine, fridges, and as solvents, among other things. By probing the molecular structure of these compounds, they have found that molecules containing several fluorine atoms are especially strong greenhouse gases, for two reasons. First, unlike many other atmospheric molecules, they can absorb radiation that makes it through our atmosphere from space. Second, they absorb the radiation (and trap the heat) very efficiently, because of the nature of the fluorine bonds inside them. (In technical terms, fluorine atoms create a larger separation of electric charge within the molecule, and this helps the molecular bonds absorb electromagnetic radiation more effectively.) HFCs and other fluorine-based gases ...
Mediterranean Tick Fever: Specialist
Another name for Mediterranean Tick Fever is Boutonneuse Fever. Physicians from the following specialties evaluate and treat boutonneuse fever: * Infectious ...
Bianca Charity Blog: Fausto - ADOPTED!
When Fausto was found, he was running desoriented in the middle of the road among the cars, very thin and covered with wounds that did not seem to be healing. We took him to the vet who did the snap blood tests and it resulted that he had a tick fever and a suspicion of leshmaniasis. When a dog has a tick fever, the leshmaniasis test is very often inconclusive - neither positive nor negative but suspected. The tick fever influences the results so it is advisable to cure the tick fever first and then repeat the leshmaniasis test. So we did ...
Fluorocarbon polymer | chemical compound | Britannica
Fluorocarbon polymer, any of a number of organic polymers whose large, multiple-unit molecules consist of a chain of carbon atoms to which fluorine atoms are appended. Owing to the presence of the highly polar fluorine atoms, which form extremely strong bonds with the carbon chain and resist
Backreaction: Rösers equation, again
I am not sure whether (1) the dopant fluorine atoms group pairwise at iron atoms and (2) if the decorated iron atoms indeed form a superlattice. However, this may be checked experimentally. But then, (3), if there is a superlattice, it is not clear to me why it should be ordered in the way claimed in the paper, with a pattern stacking five unit cells on top of each other for COFFA, for example. There can be many ways to arrange unit cells to form a superlattice with the right supercell volume. This is more obvious in the case of LOFFA, where the supercell comprises 18 unit cells, and there seems to be no a priori reason to select a superstructure which has 6 unit cells stacked on top of each other ...
Reaction of methanol with perfluorotetracyclobuta-1,3,5,7-cyclooctatetraene | UBC Chemistry
Perfluorotetracyclobuteno-1,3,5,7-cyclooctatetraene (PCOT) is a planar and centrosymmetric molecule which possesses an extraordinary electron affinity due to the planarity of the eight pi-electron system and the cumulative electron-withdrawing effects of the 16 fluorine atoms. An improved method for the synthesis of PCOT and the product resulting from the spontaneous reaction of PCOT with excess alcohol is reported. Crystal structures of the methyl (1) and ethyl (2) derivatives are described.. ...
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I suppose you think Im going to do something cute like put The End here. You would be wrong to think that, even though I did just put The End. There I did it again. What I intended to show is the pattern on the top of the abdomen. The spider ID books normally make some type of reference to this pattern, so it pays to make note of it. I actually got a lot of shots like this. The spider kept running from me and I had a tough time getting it to stay still long enough to get a full body shot ...
List of MeSH codes (D13)
3' untranslated regions MeSH D13.444.735.790.878.885 - 5' untranslated regions MeSH D13.444.735.828 - rna, viral MeSH D13.570. ... 3' untranslated regions MeSH D13.444.735.544.875.885 - 5' untranslated regions MeSH D13.444.735.615 - rna, neoplasm MeSH ... 3-thiotriphosphate) MeSH D13.695.667.454.504.400 - guanylyl imidodiphosphate MeSH D13.695.667.454.525 - 5'-guanylic acid MeSH ... 3-thiotriphosphate) MeSH D13.695.827.426.504.400 - guanylyl imidodiphosphate MeSH D13.695.827.426.525 - 5'-guanylic acid MeSH ...
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Ctps cytidine 5'-triphosphate synthase [Mus musculus (house mouse)] - Gene - NCBI
Introduction of a fluorine atom at C3 of 3-deazauridine shifts its antimetabolic activity from inhibition of CTP synthetase to ... Introduction of a fluorine atom at C3 of 3-deazauridine shifts its antimetabolic activity from inhibition of CTP synthetase to ... Title: Introduction of a fluorine atom at C3 of 3-deazauridine shifts its antimetabolic activity from inhibition of CTP ...
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List of MeSH codes (D13) - Wikipedia
3 untranslated regions MeSH D13.444.735.790.878.885 - 5 untranslated regions MeSH D13.444.735.828 - rna, viral MeSH D13.570. ... 3 untranslated regions MeSH D13.444.735.544.875.885 - 5 untranslated regions MeSH D13.444.735.615 - rna, neoplasm MeSH ... 3-thiotriphosphate) MeSH D13.695.667.454.504.400 - guanylyl imidodiphosphate MeSH D13.695.667.454.525 - 5-guanylic acid MeSH ... 3-thiotriphosphate) MeSH D13.695.827.426.504.400 - guanylyl imidodiphosphate MeSH D13.695.827.426.525 - 5-guanylic acid MeSH ...
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3-DAU pretreatment for 2 hours increases inhibitory activity of Ara-C 35 fold. The in vivo studies using ATS-mouse xenografts ... Two chemotherapeutic combinations, 2′-deoxycoformycin (DCF) plus 8-azaadenosine (8-Aza-Ado) or formycin and 3-deazauridine (3- ... 3). Fiber dosimetry and biologic markers of response will be compared following intrapleural injection and inhalation of ... 3) To determine whether asbestos-activated macrophages stimulate invasion of preneoplastic and neoplastic mesothelial cells; 4 ...
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2.A.41.2.3. Pyrimidine-preferring nucleoside:Na+ symporter, CNT1 (Na+/nucleoside = 2)(transports uridine, gemcitabine and 5- ... 2.A.41.1.3. The purine nucleoside uptake transporter NupG (YxjA) (Johansen et al., 2003) ... Solute carrier family 28 member 3 (Concentrative Na+-nucleoside cotransporter 3) (CNT 3) (hCNT3). This protein is distinct from ... Broadly selective nucleoside:Na+ cotransporter, hfCNT (transports uridine, thymidine, inosine, 3-azido-3deoxythymidine, 23 ...
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3.. Herbst KD, Corder MP, Justice GR: Successful Therapy with Methotrexate of a Multicentric Mixed Lymphoma of the Central ... Stewart DJ, Benvenuto JA, Leavens M, Hall SW, Benjamin RS, Plunkett W, McCredie KD, Burgess MA, Loo TL: Penetration of 3- ... Deazauridine into Human Brain, Intracerebral Tumor, and Cerebrospinal Fluid. Cancer Research 39: 4119-4122, 1979PubMedGoogle ... The other 5 patients all had rapid marked shrinkage of tumor, but 3 developed progression or appearance of meningeal disease. ...
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2004;20(3):109-112. [PubMed].  Martin RE, Henry RI, Abbey JL, Clements JD, Kirk K. Genome Biol. 2005;6(3) art. no.-R26. [ ... 2004;3(2):245-254. [PMC free article] [PubMed].  De Koning HP, Al-Salabi MI, Cohen AM, Coombs GH, Wastling JM. Int. J. ... 1996;3(10):881-887. [PubMed].  Heroux A, White EL, Ross LJ, Kuzin AP, Borhani DW. Structure. 2000;8(12):1309-1318. [PubMed ... 2002;13(3):167-172. [PubMed].  Rubin H, Salem JS, Li LS, Yang FD, Mama S, Wang ZM, Fisher A, Hamann CS, Cooperman BS. Proc ...
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Steric hindrance at the 3-position and positive charge at the 5-position of the pyrimidine ring were favorable for transport. ... Two hCNT3 pharmacophore models revealed the minimal features required for hCNT3 transport as two hydrogen bond acceptors at 3′- ... and 3-deazauridine (506 ± 30 nA, 50.8 ± 9.90 μM). K0.5 and Imax for substrate were dependent on membrane potential (both ... of the human concentrative nucleoside transporter 3 (hCNT3) expressed in Xenopus laevis oocytes by measuring substrate-induced ...
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Effect of Uridine on Response of 5-Azacytidine-resistant Human Leukemic Cells to Inhibitors of de Novo Pyrimidine Synthesis<...
5-Azacytidine-resistant cells exhibit cross-resistance to 3-deazauridine, 6-azauridine, and 5-fluorouridine, but not to 1-β-D- ... 5-Azacytidine-resistant cells exhibit cross-resistance to 3-deazauridine, 6-azauridine, and 5-fluorouridine, but not to 1-β-D- ... 5-Azacytidine-resistant cells exhibit cross-resistance to 3-deazauridine, 6-azauridine, and 5-fluorouridine, but not to 1-β-D- ... 5-Azacytidine-resistant cells exhibit cross-resistance to 3-deazauridine, 6-azauridine, and 5-fluorouridine, but not to 1-β-D- ...
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ethyl-β-carboline-3-carboxylate Antagonists Prostaglandins PGE1, PGE2, PGI2 Anticonvulsants hydantoins such as phenytoin, ... cytarabine), 3-deazaguanine, dihydro-5-azacytidine, tiazofurin, sangivamycin, Ara-A (vitarabine), 6-MMPR, PCNU, FENU, HENU, ... 24 (3): 356-363.. *Haspel, H. C., Stephenson, K. N., Davies-Hill, T., El-Barbary, A., Lobo, J. F., Croxen, R. L., Mougrabi, W ... Berl) 147(3):217-249 (1999).. *Wang et al., "Conjugation patterns of endogenous plasma catecholamines in human and rat," J. Lab ...
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Yi-Dong Hong1,2,*, Jian Zhang3,*, Ming Zhuang1,*, Wei Li4, Puy-Uan Wu5, Ru-Tian Li5, Nan Hu1, Bao-Xiang Bian1, Zi-Yan Song1 and ... Figure 3: MKN45 (A) and MKN28 (B) cells were treated with Rhodamine-B-loaded NPs and TNPs, respectively. Fluorescent signals ... 3. Ebert MP, Tänzer M, Balluff B, Burgermeister E, Kretzschmar AK, Hughes DJ, Tetzner R, Lofton-Day C, Rosenberg R, Reinacher- ... 2013; 5:3.. 22. Lirk P, Berger R, Hollmann MW, Fiegl H. Lidocaine time- and dose-dependently demethylates deoxyribonucleic acid ...
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The addition of soluble STC-1 to MDA-MB-231 cultures resulted in the activation of the phosphoinositide 3-kinase (PI3K)/Akt ... Intracisternal administration of mesulergine (0.03, 0.3 and 3 mg/kg) did not produce any change in blood pressure. One well- ... vinacea, while the three hydroxyl groups (OH-3, -4, and -6) are necessary for the activity of the A. ... Negative ion fast atom bombardment and collision-induced dissociation mass spectrometry of the 2-, 3-, 4- and 6-deoxy ...
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Protein names and data: S28A3_HUMAN, Full=Solute carrier family 28 member 3, Full=Concentrative Na(+)-nucleoside cotransporter ... CNT 3;Short=hCNT3; Length: 691 a.a., Mass: 76930 Da, fasta formatted sequence Function: Sodium-dependent, pyrimidine- and ... Also able to transport gemcitabine, 3-azido-3-deoxythymidine (AZT), ribavirin and 3-deazauridine. Cellular location: Membrane ...
US7638158B2 - Drug release from antithrombogenic multi-layer coated stent - Google Patents
... deazauridine, dexrazoxane, dianhydrogalactitol, diaziquone, dibromodulcitol, didemnin B, diethyldithiocarbamate, ... 3(. a), magnified 2000 times.. FIG. 4. shows three stent surfaces after they have undergone a whole blood test; Stent A is the ... 3(. a) and 3(b), respectively.. EXAMPLE 5. Blood Compatibility of the Multi-Layer Coated Stent-Whole Blood Test. Three ... 3(. a) is an SEM image of a stent surface coated by a spray-coating method, magnified 50 times. ...
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The early response (1 to 3 h) of the macrophage cell line ANA-1 to H-Candida results in enhanced tumor necrosis factor (TNF) ... The aim of this study was to report on the outcomes of complex displaced 3- and 4-part fractures of the proximal humerus ... The uridine analog 3-deazauridine has been given to 19 patients in a phase I and pharmacokinetic study. ... while those in the FGFR-3 gene may cause isolated unicoronal synostosis. An anatomical substrate for integration among ...
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Patent US20020155424 - Device for monitoring cells - Google Patents
... deazauridine, anguidine, PALA, aphidicolin, L-alanosine, maytansine, DQ-1, camptothecin, cremophor EL, homoharringtonine, ... Table 3 lists the results at 0, 1, 2, 3, and 4 hours after addition of organisms. TABLE 3. ... One hundred and fifty microliters of a suspension of E. coli (ATCC #11775) was added to the wells to yield about 3 107 CFU/ml. ... 3, 1993, which issued as U.S. Pat. No. 5,567,598 on Oct. 22, 1996, and which is continuation of U.S. Ser. No. 07/687,359, filed ...
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3. To construct databases (chemical libraries) that allow efficacious handling of the data generated and extraction of ... We perform first-rate pre-clinical (7 Tesla Bruker) and clinical (3 Tesla Siemens) research using structural and functional MRI ... This invention concerns new family of C3-arylated-3-deazauridine with potent anti-HSV activities and negligible cytotoxicity ... The laboratory is equipped with 3 high resolution gamma spectrometry detectors, 1 Nal gamma spectrometry detector for measuring ...
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1995;22:3-10.Google Scholar. *. Oettle H, Post S, Neuhaus P, Gellert K, Langrehr J, Ridwelski K, Schramm H, Fahlke J, Zuelke C ... 3). Previously, Flores et al. described that p53 requires TAp73 and/or TAp63 for DNA damage-induced cell death, whereas TAp73 ... Meijer A, Kruyt FA, van der Zee AG, Hollema H, Le P, ten Hoor KA, Groothuis GM, Quax WJ, de Vries EG, de Jong S. Nutlin-3 ... 3 RUNX2 prohibits pro-apoptotic TAp63 in p53-mutated pancreatic cancer cells. RUNX2 collaborates with mutant p53 to inhibitpro- ...
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Biologija 3:10-12. * Semėnaitė, R., R. Gasparavičiūtė, R. Duran, S. Precigou, L. Marcinkevičienė, I. Bachmatova, and R. Meškys. ... Biologija 3:13-15. * Ger, M., V. Tunaitis, and M. Valius. 2003. Elucidation of the complex formation between Nck-α, RasGTPase ... Biologija 3:53-55. * Klausa, V., L. Piešinienė, J. Staniulis, and R. Nivinskas. 2003. Abundance of T4-type bacteriophages in ... Biologija 3:3-6. * Piešinienė, L., A. Zajančkauskaitė, L. Truncaitė, and R. Nivinskas. 2003. Analysis of sequence-specific ...
- Introduction of a fluorine atom at C3 of 3-deazauridine shifts its antimetabolic activity from inhibition of CTP synthetase to inhibition of orotidylate decarboxylase, an early event in the de novo pyrimidine nucleotide biosynthesis pathway. (nih.gov)
- The IMP dehydrogenase inhibitor mycophenolic acid antagonizes the CTP synthetase inhibitor 3-deazauridine in MOLT-3 human leukemia cells: a central role for phosphoribosyl pyrophosphate. (storysteel.tk)
- Also probably transports gemcitabine, 3'-azido-3'-deoxythymidine (AZT), ribavirin and 3-deazauridine. (tcdb.org)
- We measured the I max and K 0.5 for substrate at -50 mV for the nucleoside analog drugs gemcitabine (638 ± 58 nA, 59.7 ± 17.5 μM), ribavirin (546 ± 37 nA, 61.0 ± 13.2 μM), AZT (420 ± 4 nA, 310 ± 9 μM), and 3-deazauridine (506 ± 30 nA, 50.8 ± 9.90 μM). (aspetjournals.org)
- 3-deazauridine inhibits cytidine synthase, thereby reducing intracellular levels of cytidine and deoxycytidine and disrupting DNA and RNA synthesis. (healthmatics.info)
- Solute carrier family 28 member 3 (Concentrative Na + -nucleoside cotransporter 3) (CNT 3) (hCNT3). (tcdb.org)
- We characterized the electrophysiology, kinetics, and quantitative structure-activity relationship (QSAR) of the human concentrative nucleoside transporter 3 (hCNT3) expressed in Xenopus laevis oocytes by measuring substrate-induced inward currents using a two-microelectrode voltage-clamp system. (aspetjournals.org)
- Two statistically significant QSAR models identified electrostatic interaction as the major force in hCNT3 transport and attributed a critical role to the 3′-hydroxyl position of hCNT3 substrates. (aspetjournals.org)
- Two hCNT3 pharmacophore models revealed the minimal features required for hCNT3 transport as two hydrogen bond acceptors at 3′-OH and 5′-O and the hydrophobic center occupied by the base ring. (aspetjournals.org)
- Negative ion fast atom bombardment and collision-induced dissociation mass spectrometry of the 2-, 3-, 4- and 6-deoxy derivatives from methyl beta-D-galactopyranoside and related compounds. (statescale.cf)
- Purine and uridine nucleoside drug analogues including cordycepin (3'-deoxyadenosine) are substrates. (tcdb.org)
- We perform first-rate pre-clinical (7 Tesla Bruker) and clinical (3 Tesla Siemens) research using structural and functional MRI, resonance spectroscopy, molecular imaging, image processing among other MR techniques. (transbio-sudoe.eu)
- Coadministration of 50 μM uridine prevented depletion of pyrimidine nucleoside triphosphates and inhibition of colony formation of HL-60 cells exposed to 3 mM N-(phosphonacetyl)-L-aspartate) or 5 x 10 -6 M pyrazofurin but was not capable of protecting HL-60-5-azacytidine under the same conditions. (houstonmethodist.org)
- Analog of uridine lacking a ring-nitrogen in the 3-position. (healthmatics.info)
- A synthetic analogue of nucleoside uridine lacking a ring nitrogen in the 3-position. (healthmatics.info)
- Often after 3-5 years of treatment patients reportedly develop complex dose-related unpredictable response fluctuations leading to a progressive decrease in therapeutic efficacy and also possible onset of serious side effects such as abnormal involuntary movements, end-of-dose deterioration and abrupt near instantaneous on-off changes in patient disability. (justia.com)
- For instance, hypermethylation of the transcription factor AP-2 epsilon (TFAP2E) affects the therapeutic efficacy of 5-FU based chemotherapy in colorectal cancer [ 3 ] and GC [ 4 ]. (oncotarget.com)
- 2003. Synthesis of 1-(9-alkyl-9H-carbazol-3-yl)-4-carboxy-2-pyrrolidinones. (vu.lt)
- 3. The device of claim 1, which provides sustained release of the therapeutically active form of A for a period of at least 24 hours, and, over the period of release, the concentration of the prodrug eluting from polymer is less than 10% of the concentration of the therapeutically active form of A. 4. (freepatentsonline.com)
- For AML 3 cells, the com bination of five AZA CdR, GSK 126, and TSA showed a similar synergistic interaction in a colony assay because the triple blend that contained DZNep. (bossforum.net)
- The hypermethylation decreases TFAP2E expression and consequently increases expression of its downstream target dickkopf homolog 4 protein (DKK4), which is related to 5-FU resistance [ 3 , 4 ]. (oncotarget.com)
- vinacea, while the three hydroxyl groups (OH-3, -4, and -6) are necessary for the activity of the A. (statescale.cf)
- The other 5 patients all had rapid marked shrinkage of tumor, but 3 developed progression or appearance of meningeal disease. (springer.com)
- All 3 patients developed further neurophychiatric manifestations of SLE, leading to death in 1. (storysteel.tk)
- The racemic form (DL-threo-3,4-dihydroxyphenylserine) has also been used, and has been investigated in the treatment of orthostatic hypotension. (healthmatics.info)