Screening for caspase-3 inhibitors: A new class of potent small-molecule inhibitors of caspase-3

被引:17
|
作者
Okun, I
Malarchuk, S
Dubrovskaya, E
Khvat, A
Tkachenko, S
Kysil, V
Ilyin, A
Kravchenko, D
Prossnitz, ER
Sklar, L
Ivachtchenko, A
机构
[1] ChemDiv Inc, San Diego, CA 92121 USA
[2] Chem Divers Res Inst, Chimki 114401, Moscow Region, Russia
[3] Univ New Mexico, Albuquerque, NM 87131 USA
关键词
caspase-3; small molecules; inhibitors; apoptosis; structure-activity relationship;
D O I
10.1177/1087057105285048
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
From the authors' 650,000 compound collection, they have selected approximately 15,000 potential small-molecule protease inhibitors, which were subjected to high-through put screening against caspase-3. The screening yielded a series of hits that belong to II different scaffolds. Based on the structure of one of the hits, a new class of the small-molecule inhibitors with a double electrophilic warhead, 8-sulfonyl-pyrrolo[3,4-c]quinoline-1,3-diones (SPQ), was synthesized and tested in follow-up mechanistic and antiapoptosis assays. Mechanistic analysis of a representative Compound of this class, CD-001-0011, showed that the compound exhibited a high potency (IC50 = 130 nM), was reversible though noncompetitive, and had a broad selectivity profile to other caspases belonging to groups I to III. The compound was effective in preventing staurospoline-induced apoptosis in a few cell lines and retinoic acid-induced apoptosis in zebrafish.
引用
收藏
页码:277 / 285
页数:9
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