نتایج جستجو برای: competitive inhibitor

تعداد نتایج: 297248  

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 1995
G Erkel K Lorenzen T Anke R Velten A Gimenez W Steglich

In a search for new inhibitors of RNA-directed DNA-polymerases kuehneromycin A (1) was isolated from fermentations of a Tasmanian Kuehneromyces species. Its structure was elucidated by spectroscopic methods. Kuehneromycin A (1) is a non-competitive inhibitor of avian myeloblastosis virus (Ki 200 microM) and moloney murine leukemia virus (Ki 40 microM) reverse transcriptases. The second compound...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1972
I Yahara G M Edelman

The induction by anti-immunoglobulin of patch and cap formation on mouse lymphocytes was inhibited by the addition of concanavalin A. This effect was reversed by alpha-methyl-D-mannoside, a competitive inhibitor of the binding of concanavalin A. Concanavalin A prevented both patch and cap formation, in contrast to the metabolic inhibitor NaN(3), which prevented only cap formation. This suggests...

Journal: :Biochimica et biophysica acta 2010
Doriano Fabbro Paul W Manley Wolfgang Jahnke Janis Liebetanz Alexandra Szyttenholm Gabriele Fendrich Andre Strauss Jianming Zhang Nathanael S Gray Francisco Adrian Markus Warmuth Xavier Pelle Robert Grotzfeld Frederic Berst Andreas Marzinzik Sandra W Cowan-Jacob Pascal Furet Jürgen Mestan

The ATP-competitive inhibitors dasatinib and nilotinib, which bind to catalytically different conformations of the Abl kinase domain, have recently been approved for the treatment of imatinib-resistant CML. These two new drugs, albeit very efficient against most of the imatinib-resistant mutants of Bcr-Abl, fail to effectively suppress the Bcr-Abl activity of the T315I (or gatekeeper) mutation....

Journal: :The Journal of organic chemistry 2007
Yanlei Zhang Boris Illarionov Adelbert Bacher Markus Fischer Gunda I Georg Qi-Zhuang Ye David Vander Velde Phillip E Fanwick Yunlong Song Mark Cushman

Air oxidation of 1,3,6,8-tetrahydroxy-2,7-naphthyridine afforded 2,5,8,11-tetraaza-5,11-dihydro-4,10-dihydroxyperylene-1,3,6,7,9,12-hexaone. X-ray crystallography of the product revealed that it exists in the meso form in the solid state. The mechanism of product formation most likely involves oxidative phenolic coupling and oxidation. The product proved to be a competitive inhibitor of Schizos...

Journal: :The Journal of biological chemistry 1980
W R McClure

The mechanism of streptolydigin inhibition of RNA synthesis has been investigated with a combination of steady state kinetics and product analysis by employing the abortive initiation reaction of Escherichia coli RNA polymerase. The pattern of inhibition by streptolydigin on the poly[d(A-T)] . poly[d(A-T)]template (non-competitive versus AMP; competitive versus UTP) was consistent with one inhi...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه سیستان و بلوچستان - دانشکده مهندسی عمران 1391

one of the most commonly used techniques to reduce the corrosion rate of rebar in concrete is addition substances named corrosion inhibitors into the concrete. corrosion inhibitor is chemical compounds that were added to concrete to prevent corrosion of steel in concrete. sodium nitrate is a type of anodic inhibitors that this study investigatesthe effect of this inhibitor on the properties of ...

Journal: :Acta crystallographica. Section D, Biological crystallography 2005
P T Erskine L Coates R Newbold A A Brindley F Stauffer G D E Beaven R Gill A Coker S P Wood M J Warren P M Shoolingin-Jordan R Neier J B Cooper

The X-ray structure of the enzyme 5-aminolaevulinic acid dehydratase (ALAD) from yeast complexed with the competitive inhibitor 5-hydroxylaevulinic acid has been determined at a resolution of 1.9 A. The structure shows that the inhibitor is bound by a Schiff-base link to one of the invariant active-site lysine residues (Lys263). The inhibitor appears to bind in two well defined conformations an...

Journal: :Brain research 2008
Zeng-You Ye Yun-Gang Lu Hao Sun Xin-Ping Cheng Tian-Le Xu Jiang-Ning Zhou

Fluoxetine is a selective serotonin reuptake inhibitor widely used for treating depression. However, fluoxetine treatment may lead to seizures at higher doses, which underlying mechanism remains largely unknown. In this study, we examined the effects of fluoxetine on glycine receptor (GlyR) activity. Using the whole-cell patch-clamp recording method, we found that fluoxetine and its metabolite ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1978
G D Colello D M Hockenbery H B Bosmann S Fuchs K Folkers

Fractions of porcine cerebral cortex extract separated by molecular weight on a Sephadex G-75 column were tested for their activities and potencies to inhibit [3H]benzodiazepine binding to rat brain homogenates. The fractions spanned molecular weights from 500 to 100,000. A potent inhibitor (benzodiazepine-competitive factor I, BCF-I) was discovered in the fraction containing substances with mo...

Journal: :Biochemical and biophysical research communications 1991
N M Olken K M Rusche M K Richards M A Marletta

.N = O synthase catalyzes the oxidation of one of the two chemically equivalent guanido nitrogens of L-arginine to nitric oxide (.N = O). NG-Methyl-L-arginine has been previously characterized as a potent competitive inhibitor of both major types of .N = O synthases. Initial rate kinetics were performed with a spectrophotometric assay based on the oxidation of oxy- to methemoglobin by .N = O. N...

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