Cyclophilin inhibition by a (Z)-alkene cis-proline mimic

被引:29
作者
Hart, SA [1 ]
Etzkorn, FA [1 ]
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22901 USA
关键词
D O I
10.1021/jo990409a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:2998 / 2999
页数:2
相关论文
共 45 条
[41]  
Wiederrecht Greg, 1994, Perspectives in Drug Discovery and Design, V2, P57, DOI 10.1007/BF02171737
[42]   Sequence-specific and phosphorylation-dependent proline isomerization: A potential mitotic regulatory mechanism [J].
Yaffe, MB ;
Schutkowski, M ;
Shen, MH ;
Zhou, XZ ;
Stukenberg, PT ;
Rahfeld, JU ;
Xu, J ;
Kuang, J ;
Kirschner, MW ;
Fischer, G ;
Cantley, LC ;
Lu, KP .
SCIENCE, 1997, 278 (5345) :1957-1960
[43]   A COMPOSITE FKBP12-FK506 SURFACE THAT CONTACTS CALCINEURIN [J].
YANG, D ;
ROSEN, MK ;
SCHREIBER, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (02) :819-820
[44]   THE STEREOSELECTIVE SYNTHESIS OF (E)-ALKENE DIPEPTIDE ISOSTERES [J].
YONG, YF ;
LIPTON, MA .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1993, 3 (12) :2879-2882
[45]   ACTIVE-SITE MUTANTS OF HUMAN CYCLOPHILIN-A SEPARATE PEPTIDYL-PROLYL ISOMERASE ACTIVITY FROM CYCLOSPORINE-A BINDING AND CALCINEURIN INHIBITION [J].
ZYDOWSKY, LD ;
ETZKORN, FA ;
CHANG, HY ;
FERGUSON, SB ;
STOLZ, LA ;
HO, SI ;
WALSH, CT .
PROTEIN SCIENCE, 1992, 1 (09) :1092-1099