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首页> 外文期刊>Journal of biomolecular screening: The official journal of the Society for Biomolecular Screening >Screening for caspase-3 inhibitors: A new class of potent small-molecule inhibitors of caspase-3
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Screening for caspase-3 inhibitors: A new class of potent small-molecule inhibitors of caspase-3

机译:筛选caspase-3抑制剂:一类新型的caspase-3强力小分子抑制剂

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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.
机译:从作者的650,000种化合物中,他们选择了大约15,000种潜在的小分子蛋白酶抑制剂,并对它们进行了针对caspase-3的高通量筛选。筛选产生了一系列属于II个不同支架的命中。根据其中一个命中物的结构,合成了具有双亲电子战斗部的新型小分子抑制剂8-磺酰基-吡咯并[3,4-c]喹啉-1,3-二酮(SPQ)并在后续的机制和抗凋亡试验中进行了测试。对此类代表性化合物CD-001-0011的机理分析表明,该化合物表现出较高的效价(IC50 = 130 nM),可逆但不具有竞争性,并且对属于I至I类的其他胱天蛋白酶具有广泛的选择性三,该化合物可有效预防星形孢菌素诱导的一些细胞系凋亡和视黄酸诱导的斑马鱼凋亡。

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