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1.
Proinflammatory role of vasopressin through V1b receptors in hapten-induced experimental colitis in rodents: implication in IBD.
Am J Physiol Gastrointest Liver Physiol
; 299(6): G1298-307, 2010 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-20864658
2.
Differential Virtual Screening (DVS) with Active and Inactive Molecular Models for Finding and Profiling GPCR Modulators: Case of the CCK1 Receptor.
Mol Inform
; 30(4): 345-58, 2011 Apr 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-27466951
3.
Biological characterization of rodent and human vasopressin V1b receptors using SSR-149415, a nonpeptide V1b receptor ligand.
Am J Physiol Regul Integr Comp Physiol
; 293(2): R938-49, 2007 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-17522130
4.
In vitro and in vivo pharmacological characterization of ethyl-4-[trans-4-[((2S)-2-hydroxy-3-[4-hydroxy-3[(methylsulfonyl)amino]-phenoxy]propyl) amino]cyclohexyl]benzoate hydrochloride (SAR150640), a new potent and selective human beta3-adrenoceptor agonist for the treatment of preterm labor.
J Pharmacol Exp Ther
; 321(3): 1118-26, 2007 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-17351104
5.
Pancreatic vasopressin V1b receptors: characterization in In-R1-G9 cells and localization in human pancreas.
Am J Physiol Endocrinol Metab
; 285(3): E566-76, 2003 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-12736162
6.
Anxiolytic- and antidepressant-like effects of the non-peptide vasopressin V1b receptor antagonist, SSR149415, suggest an innovative approach for the treatment of stress-related disorders.
Proc Natl Acad Sci U S A
; 99(9): 6370-5, 2002 Apr 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-11959912
7.
Structure and stereochemistry of the active metabolite of clopidogrel.
Drug Metab Dispos
; 30(11): 1288-95, 2002 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-12386137
8.
Biochemical and pharmacological activities of SSR 146977, a new potent nonpeptide tachykinin NK3 receptor antagonist.
Can J Physiol Pharmacol
; 80(5): 482-8, 2002 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-12056557
9.
Characterization of (2S,4R)-1-[5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-N,N-dimethyl-2-pyrrolidine carboxamide (SSR149415), a selective and orally active vasopressin V1b receptor antagonist.
J Pharmacol Exp Ther
; 300(3): 1122-30, 2002 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-11861823
10.
SSR240600 [(R)-2-(1-[2-[4-[2-[3,5-bis(trifluoromethyl)phenyl]acetyl]-2-(3,4-dichlorophenyl)-2-morpholinyl]ethyl]- 4-piperidinyl)-2-methylpropanamide], a centrally active nonpeptide antagonist of the tachykinin neurokinin-1 receptor: I. biochemical and pharmacological characterization.
J Pharmacol Exp Ther
; 303(3): 1171-9, 2002 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-12438541
11.
4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1,3-thiazol-2-amine hydrochloride (SSR125543A): a potent and selective corticotrophin-releasing factor(1) receptor antagonist. I. Biochemical and pharmacological characterization.
J Pharmacol Exp Ther
; 301(1): 322-32, 2002 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-11907190
12.
SSR126768A (4-chloro-3-[(3R)-(+)-5-chloro-1-(2,4-dimethoxybenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl]-N-ethyl-N-(3-pyridylmethyl)-benzamide, hydrochloride): a new selective and orally active oxytocin receptor antagonist for the prevention of preterm labor.
J Pharmacol Exp Ther
; 309(1): 414-24, 2004 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-14722330
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