نتایج جستجو برای: high affinity receptor

تعداد نتایج: 2600326  

Journal: :The Journal of pharmacology and experimental therapeutics 2001
B R Rorabaugh M A Scofield D D Smith W B Jeffries P W Abel

Calcitonin gene-related peptide (CGRP) receptors are classified into CGRP subtype 1 (CGRP(1)) and CGRP subtype 2 (CGRP(2)) based on the affinity of the antagonist, human alpha (halpha)-CGRP(8-37). halpha-CGRP(8-37) antagonizes CGRP(1) receptor-mediated responses with high affinity (K(B) < 100 nM) and antagonizes CGRP(2) receptor-mediated responses with low affinity (K(B) > 1 microM). CGRP(2) re...

Journal: :iranian journal of pharmaceutical research 0
fatemeh ahmadi department of radiopharmacy, school of pharmacy, tehran university of medical sciences sara dabirian department of pharmaceutical chemistry, school of pharmacy, shahid behesti university of medical sciences mehrdad faizi department of pharmacology and toxicology, school of pharmacy, shahid beheshti university of medical sciences sayyed abbas tabatabai department of pharmaceutical chemistry, school of pharmacy, shahid behesti university of medical sciences davood beiki research center for nuclear medicine, tehran university of medical sciences soraya shahhosseini department of pharmaceutical chemistry, school of pharmacy, shahid beheshti university of medical sciences

to obtain drugs which are more selective at benzodiazepine (bzd) receptors, design and synthesis of functionally selective ligands for bzd receptors is the current strategy of our pharmaceutical chemistry department. the affinity of newly synthesized ligands is assessed by radioligand receptor binding assays. based on our previous studies, 2-phenyl-5-oxo-7-methyl-1,3,4-oxadiazolo[a,2,3]-pyrimid...

2012
Jonathan Simonin Sanjeev Kumar V. Vernekar Andrew J. Thompson J. Daniel Hothersall Christopher N. Connolly Sarah C.R. Lummis Martin Lochner

The synthesis, photophysical and biological characterization of a small library of fluorescent 5-HT(3) receptor ligands is described. Several of these novel granisetron conjugates have high quantum yields and show high affinity for the human 5-HT(3)AR.

Journal: :Cardiovascular research 1995
J A Schetz P A Anderson

UNLABELLED Apamin is a potent blocker of calcium-activated small conductance potassium (SK) channels in neurons, liver, skeletal muscle and ileum smooth muscle, but not in cardiac muscle. Cardiac muscle is devoid of SK channels; however, in isolated, single ventricular myocytes apamin is an extremely potent blocker of the L-type calcium current, and the anti-arrhythmic drug quinidine reverses a...

1998
Stefan Kraft Jörg H. M. Weßendorf Daniel Hanau Thomas Bieber

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Guillaume Stewart-Jones Andreas Wadle Anja Hombach Eugene Shenderov Gerhard Held Eliane Fischer Sascha Kleber Natko Nuber Frank Stenner-Liewen Stefan Bauer Andrew McMichael Alexander Knuth Hinrich Abken Andreas A Hombach Vincenzo Cerundolo E Yvonne Jones Christoph Renner

T-cell interaction with a target cell is a key event in the adaptive immune response and primarily driven by T-cell receptor (TCR) recognition of peptide-MHC (pMHC) complexes. TCR avidity for a given pMHC is determined by number of MHC molecules, availability of coreceptors, and TCR affinity for MHC or peptide, respectively, with peptide recognition being the most important factor to confer tar...

Journal: :iranian journal of medical sciences 0
fan chen department of biochemistry and molecular biology, life sciences school of hubei university, wuhan, china si-chong chen evolution and ecology research centre, school of biological, earth and environmental sciences, the university of new south wales, sydney, australia jing zhou clinical laboratory, wuhan tuberculosis dispensary, wuhan health bureau, wuhan, china zhi-de chen department of biochemistry and molecular biology, life sciences school of hubei university, wuhan, china fang chen department of biochemistry and molecular biology, school of basic medical science, wuhan university, wuhan, china

hepatitis c virus (hcv) encodes two envelope glycoproteins, e1 and e2. our previous work selected a specific aptamer ze2, which could bind to e2 with high affinity, with a great potential for developing new molecular probes as an early diagnostic reagents or therapeutic drugs targeting hcv. in this study, the binding sites between e2 and aptamer ze2 were further explored. e2 was truncated to 15...

Journal: :American Journal of Physiology-gastrointestinal and Liver Physiology 2021

The hepatic bile acid transporter NTCP is a high-affinity receptor for hepatitis B and D viruses. This study shows that TLC rapidly accumulates in NTCP-expressing hepatoma cells mediates long-lasting trans-inhibition of NTCP’s function via an intracellularly accessible domain, without substantially affecting its membrane expression. domain promising novel target site pharmacological long-acting...

Journal: :Cell 1998
Scott C. Garman Jean-Pierre Kinet Theodore S. Jardetzky

Allergic responses result from the activation of mast cells by the human high-affinity IgE receptor. IgE-mediated allergic reactions may develop to a variety of environmental compounds, but the initiation of a response requires the binding of IgE to its high-affinity receptor. We have solved the X-ray crystal structure of the antibody-binding domains of the human IgE receptor at 2.4 A resolutio...

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