메뉴 건너뛰기




Volumn 45, Issue 23, 2002, Pages 4950-4953

Discovery of the first nonpeptide agonist of the GPR14/Urotensin-II receptor: 3-(4-Chlorophenyl)-3-(2-(dimethylamino)ethyl)isochroman-1-one (AC-7954)

Author keywords

[No Author keywords available]

Indexed keywords

3 (4 CHLOROPHENYL) 3 [2 (DIMETHYLAMINO)ETHYL]ISOCHROMAN 1 ONE; AC 7954; G PROTEIN COUPLED RECEPTOR; ISOCHROMAN DERIVATIVE; NEUROPEPTIDE; UNCLASSIFIED DRUG; UROTENSIN II;

EID: 0037038316     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm025551+     Document Type: Article
Times cited : (61)

References (20)
  • 1
    • 0029102720 scopus 로고
    • Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors
    • Marchese, A.; Heiber, M.; Nguyen, T.; Heng, H. H.; Saldivia, V. R.; Cheng, R.; Murphy, P. M.; Tsui, L. C.; Shi, X.; Gregor, P.; et al. Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors. Genomics 1995, 29, 335-344.
    • (1995) Genomics , vol.29 , pp. 335-344
    • Marchese, A.1    Heiber, M.2    Nguyen, T.3    Heng, H.H.4    Saldivia, V.R.5    Cheng, R.6    Murphy, P.M.7    Tsui, L.C.8    Shi, X.9    Gregor, P.10
  • 5
    • 0034466374 scopus 로고    scopus 로고
    • Human urotensin-II, the most potent mammalian vasoconstrictor identified to date, as a therapeutic target for the management of cardiovascular disease
    • Douglas, S. A.; Ohlstein, E. H. Human urotensin-II, the most potent mammalian vasoconstrictor identified to date, as a therapeutic target for the management of cardiovascular disease. Trends Cardiovasc. Med. 2000, 10, 229-237.
    • (2000) Trends Cardiovasc. Med. , vol.10 , pp. 229-237
    • Douglas, S.A.1    Ohlstein, E.H.2
  • 7
    • 0033202995 scopus 로고    scopus 로고
    • Identification of the natural ligand of an orphan G-protein-coupled receptor involved in the regulation of vasoconstriction
    • Nothacker, H. P.; Wang, Z.; McNeill, AM.; Saito, Y.; Merten, S.; O'Dowd, B.; Duckles, S. P.; Civelli, O. Identification of the natural ligand of an orphan G-protein-coupled receptor involved in the regulation of vasoconstriction. Nat. Cell. Biol. 1999, 1, 383-385.
    • (1999) Nat. Cell. Biol. , vol.1 , pp. 383-385
    • Nothacker, H.P.1    Wang, Z.2    McNeill, A.M.3    Saito, Y.4    Merten, S.5    O'Dowd, B.6    Duckles, S.P.7    Civelli, O.8
  • 8
    • 0028986883 scopus 로고
    • High throughput assays of cloned adrenergic, muscarinic, neurokinin, and neurotrophin receptors in living mammalian cells
    • Messier, T. L.; Dorman, C. M.; Brauner-Osborne, H.; Eubanks, D.; Brann, M. R. High throughput assays of cloned adrenergic, muscarinic, neurokinin, and neurotrophin receptors in living mammalian cells. Pharmacol. Toxicol. 1995, 76, 308-311.
    • (1995) Pharmacol. Toxicol. , vol.76 , pp. 308-311
    • Messier, T.L.1    Dorman, C.M.2    Brauner-Osborne, H.3    Eubanks, D.4    Brann, M.R.5
  • 10
    • 0035289779 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 2001, 46, 3-26.
    • (2001) Adv. Drug Deliv. Rev. , vol.46 , pp. 3-26
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 11
    • 0001664595 scopus 로고
    • Metalation of N-methyl-o-toluamine with excess n-butyllithium. Condensations with ketones and aldehydes. Cyclizations
    • Vaulx, R. N.; Puterbaugh, W. H.; Hauser, C. R. Metalation of N-methyl-o-toluamine with excess n-butyllithium. Condensations with ketones and aldehydes. Cyclizations. J. Org. Chem. 1964, 29, 3514-3517.
    • (1964) J. Org. Chem. , vol.29 , pp. 3514-3517
    • Vaulx, R.N.1    Puterbaugh, W.H.2    Hauser, C.R.3
  • 12
    • 0037171726 scopus 로고    scopus 로고
    • Identification of nonpeptidic urotensin II receptor antagonists by virtual screening based on a pharmacophore model derived from structure-activity relationships and nuclear magnetic resonance studies on urotensin II
    • Flohr, S.; Kurz, M.; Kostenis, E.; Brkovich, A.; Fournier, A.; Klabunde, T. Identification of nonpeptidic urotensin II receptor antagonists by virtual screening based on a pharmacophore model derived from structure-activity relationships and nuclear magnetic resonance studies on urotensin II. J. Med. Chem. 2002, 45, 1799-1805.
    • (2002) J. Med. Chem. , vol.45 , pp. 1799-1805
    • Flohr, S.1    Kurz, M.2    Kostenis, E.3    Brkovich, A.4    Fournier, A.5    Klabunde, T.6
  • 13
    • 0033986943 scopus 로고    scopus 로고
    • Therapeutic and chemical developments of cholecystokinin receptor ligands
    • de Tullio, P.; Delarge, J.; Pirotte, B. Therapeutic and chemical developments of cholecystokinin receptor ligands. Expert Opin. Investig. Drugs 2000, 9, 129-146.
    • (2000) Expert Opin. Investig. Drugs , vol.9 , pp. 129-146
    • De Tullio, P.1    Delarge, J.2    Pirotte, B.3
  • 14
    • 0032726682 scopus 로고    scopus 로고
    • FR190997, a novel bradykinin B2 agonist, expresses longer action than bradykinin in paw edema formation and hypotensive response
    • Ueno, A.; Naraba, H.; Kojima, F.; Morita, E.; Oh-ishi, S. FR190997, a novel bradykinin B2 agonist, expresses longer action than bradykinin in paw edema formation and hypotensive response. Immunopharmacology 1999, 45, 89-93.
    • (1999) Immunopharmacology , vol.45 , pp. 89-93
    • Ueno, A.1    Naraba, H.2    Kojima, F.3    Morita, E.4    Oh-ishi, S.5
  • 15
  • 18
    • 0023145815 scopus 로고
    • Contraction of major artery segments of rat by fish neuropeptide urotensin II
    • Itoh, H.; Itoh, Y.; Rivier, J.; Lederis, K. Contraction of major artery segments of rat by fish neuropeptide urotensin II. Am. J. Physiol. 1987, 252 (2 Pt 2), R361-R366.
    • (1987) Am. J. Physiol. , vol.252 , Issue.2 PART 2
    • Itoh, H.1    Itoh, Y.2    Rivier, J.3    Lederis, K.4
  • 19
    • 0028208429 scopus 로고
    • NMR and dynamical simulated annealing studies on the solution conformation of urotensin II
    • Bhaskaran, R.; Arunkumar, A. I.; Yu C. NMR and dynamical simulated annealing studies on the solution conformation of urotensin II. Biochim. Biophys. Acta 1994, 1199, 115-122.
    • (1994) Biochim. Biophys. Acta , vol.1199 , pp. 115-122
    • Bhaskaran, R.1    Arunkumar, A.I.2    Yu, C.3
  • 20
    • 0011091026 scopus 로고    scopus 로고
    • note
    • Structures related to 1 have been patented for compounds that elicited hypotension, hypertension, or diuresis. A U. S. patent involving related compounds from Houlihan, W. J, and Nadelson, J. in 1975 (US 3880885) relates diuretic and antihypertensive activity. The biological responses observed with these compounds may have been related to modulation of the UII receptor. Hence, the present study suggests a molecular mechanism for these earlier pharmacological observations.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.