Zobrazeno 1 - 6
of 6
pro vyhledávání: '"G J, Zingaro"'
Autor:
W T, Ashton, S M, Hutchins, W J, Greenlee, G A, Doss, R S, Chang, V J, Lotti, K A, Faust, T B, Chen, G J, Zingaro, S D, Kivlighn
Publikováno v:
Journal of Medicinal Chemistry. 36:3595-3605
Two series of potential angiotensin II antagonists derived from carboxyl-functionalized "diazole" heterocycles have been prepared and evaluated. Initially, a limited investigation of 4-arylimidazole-5-carboxylates led to 2-n-butyl-4-(2-chlorophenyl)-
Autor:
S D, Kivlighn, G J, Zingaro, R A, Gabel, T P, Broten, R S, Chang, D L, Ondeyka, N B, Mantlo, R E, Gibson, W J, Greenlee, P K, Siegl
Publikováno v:
European journal of pharmacology. 294(2-3)
L-163,017 (6-[benzoylamino]-7-methyl-2-propyl-3-[[2'-(N-(3-methyl-1-butoxy) carbonylaminosulfonyl)[1,1']-biphenyl-4-yl]methyl]-3H-imidazo[4,5- b]pyridine) is a potent, orally active, nonpeptide angiotensin II receptor antagonist. Conscious rats and d
Autor:
D L, Williams, K L, Murphy, N A, Nolan, J A, O'Brien, D J, Pettibone, S D, Kivlighn, S M, Krause, E V, Lis, G J, Zingaro, R A, Gabel
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 275(3)
L-754,142, (-)-N-(4-iso-propylbenzenesulfonyl)-alpha-(4-carboxyl-2-n-propy lphenoxy)-3,4- methylenedioxyphenylacetamide, is a potent nonpeptidyl endothelin antagonist (e.g., Ki: cloned human ETA = 0.062 nM: cloned human ETB = 2.25 nM), with high spec
Autor:
S. D. Kivlighn, W. R. Huckle, G. J. Zingaro, R. A. Rivero, V. J. Lotti, R. S. Chang, T. W. Schorn, N. Kevin, R. G. Johnson, W. J. Greenlee, al. et
Publikováno v:
The American journal of physiology. 268(3 Pt 2)
L-162,313 (5,7-dimethyl-2-ethyl-3-[[4-[2(n- butyloxycarbonylsulfonamido)-5-isobutyl-3-thienyl]phenyl]methyl]- imadazo[4,5-b]pyridine) is a nonpeptide that mimics the biological actions of angiotensin II (ANG II). The intravenous administration of L-1
Autor:
S D, Kivlighn, G J, Zingaro, R A, Gabel, T P, Broten, T W, Schorn, L W, Schaffer, E M, Naylor, P K, Chakravarty, A A, Patchett, W J, Greenlee
Publikováno v:
American journal of hypertension. 8(1)
MK-996, N-(4'-(5,7-dimethyl-2-ethyl-3H-imidazo[4,5-b]pyridin-3-yl- methyl)1,1'-biphenyl-2-yl)-sulfonylbenzamide, is a potent, orally active, highly selective, nonpeptide angiotensin II (AII) receptor antagonist. MK-996 prevents the pressor response t
Autor:
P K, Chakravarty, E M, Naylor, A, Chen, R S, Chang, T B, Chen, K A, Faust, V J, Lotti, S D, Kivlighn, R A, Gable, G J, Zingaro
Publikováno v:
Journal of medicinal chemistry. 37(24)