化学
葡萄孢霉素
链霉菌
立体化学
噻唑
弗氏链霉菌
突变体
细胞毒性
拉伤
吲哚试验
放线菌
组合化学
激酶
蛋白激酶C
生物化学
体外
基因
细菌
生物
遗传学
解剖
作者
Peng Fu,Yibin Zhuang,Yi Wang,Peipei Liu,Xin Qi,Kang-bo Gu,Daojing Zhang,Weiming Zhu
出处
期刊:Organic Letters
[American Chemical Society]
日期:2012-12-10
卷期号:14 (24): 6194-6197
被引量:46
摘要
Fradcarbazoles A–C (1–3), three new indolocarbazoles, were isolated from a mutant strain of the marine-derived actinomycete Streptomyces fradiae 007M135. Their structures were established by spectroscopic analysis, quantum chemical calculation, CD spectra, and chemical transformation. Fradcarbazole A (1) possessed a unique skeleton consisting of a staurosporine core, a thiazole ring, and an indole fragment. Compounds 1–3 displayed significant cytotoxicity against HL-60, K562, A-549, and BEL-7402 cell lines and inhibitory effects on the kinase PKC-α with IC50 values of 0.001–4.58 μM.
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