Design of potent and selective cathepsin K inhibitors which span the active site.

被引：0

作者：

Thompson, SK

Halbert, SM

Michaud, E

Bossard, MJ

Tomaszek, TA

Levy, MA

Meek, TD

Zhao, B

Smith, WW

Janson, CA

McQueney, MS

AbdelMeguid, SS

Briand, J

Sarkar, SK

Huddleston, MJ

Ijames, CF

Carr, SA

DesJarlais, RL

Shu, A

Garnes, K

Heys, JR

Zembryki, D

LeeRykaczewski, LV

James, IE

Lark, M

Bradbeer, JN

Drake, FH

Gowen, M

Veber, DF

机构：

[1] SMITHKLINE BEECHAM PHARMACEUT,DEPT MED CHEM,KING OF PRUSSIA,PA 19406

[2] SMITHKLINE BEECHAM PHARMACEUT,DEPT MOL RECOGNIT,KING OF PRUSSIA,PA 19406

[3] SMITHKLINE BEECHAM PHARMACEUT,DEPT MACROMOL SCI,KING OF PRUSSIA,PA 19406

[4] SMITHKLINE BEECHAM PHARMACEUT,DEPT PHYS & STRUCT CHEM,KING OF PRUSSIA,PA 19406

[5] SMITHKLINE BEECHAM PHARMACEUT,DEPT RADIOCHEM,KING OF PRUSSIA,PA 19406

[6] SMITHKLINE BEECHAM PHARMACEUT,DEPT CELLULAR BIOCHEM,KING OF PRUSSIA,PA 19406

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1997年 / 214卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：279 / MEDI

页数：1