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Small-molecule caspase inhibitors
被引:7
|作者:
Zhenodarova, S. M.
[1
]
机构:
[1] Russian Acad Sci, Inst Theoret & Expt Biophys, Pushchino 142290, Moscow Region, Russia
基金:
英国经济与社会研究理事会;
英国医学研究理事会;
关键词:
SELECTIVE NONPEPTIDE INHIBITORS;
STRUCTURE-BASED DESIGN;
SULFONAMIDE ANALOGS;
ACYL DIPEPTIDES;
ALLOSTERIC SITE;
CELL-GROWTH;
POTENT;
DISCOVERY;
APOPTOSIS;
IDENTIFICATION;
D O I:
10.1070/RC2010v079n02ABEH004056
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
There view considers low-molecular weight inhibitors of caspases, cysteine proteases being key contributors to apoptosis (programmed cell death). The inhibitors with aspartic acid residues or various heterocyclic systems (both synthetic and natural) are covered. Their possible mechanisms of action are discussed. Data on inhibitor structure-activity relationship studies are systematically surveyed. The interactions of the non-peptide fragments of an inhibitor with the enzymes are examined. Examples of the use of some inhibitors for apoptosis suppression are provided. The bibliography includes 60 references.
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页码:119 / 143
页数:25
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