Zobrazeno 1 - 6
of 6
pro vyhledávání: '"T D, Meek"'
Autor:
M J, Bossard, T A, Tomaszek, M A, Levy, C F, Ijames, M J, Huddleston, J, Briand, S, Thompson, S, Halpert, D F, Veber, S A, Carr, T D, Meek, D G, Tew
Publikováno v:
Biochemistry. 38(48)
The nature of the inhibition of thiol proteases by a new class of mechanism-based inhibitors, 1,5-diacylcarbohydrazides, is described. These potent, time-dependent, active-site spanning inhibitors include compounds that are selective for cathepsin K,
Publikováno v:
Medicinal research reviews. 17(1)
With the advent of the first generation of both selective and nonselective endothelin antagonists being a relatively recent event, the manifold therapeutic potentials of these compounds are only now being explored clinically. Undoubtedly, numerous cl
Autor:
S K, Thompson, K H, Murthy, B, Zhao, E, Winborne, D W, Green, S M, Fisher, R L, DesJarlais, T A, Tomaszek, T D, Meek, J G, Gleason
Publikováno v:
Journal of medicinal chemistry. 37(19)
The rational design and synthesis of a highly potent inhibitor of HIV-1 protease have been accomplished. The inhibitor, SB 206343, is based on a model derived from the structure of the MVT-101/HIV-1 protease complex and contains a 4(5)-acylimidazole
Publikováno v:
Methods in enzymology. 241
Despite the current plethora of structural data of HIV-1 protease and the availability of potent inhibitors, whose structures are based in part on the presumed mechanism of action of this enzyme, our actual understanding of its chemical mechanism has
Publikováno v:
Biochemistry. 21(9)
Autor:
T D, Meek
Publikováno v:
Texas medicine. 66(7)