Tamaoki T, Nakano H
Kyowa Hakko Co. Ltd., Tokyo Research Laboratories, Japan.
Biotechnology (N Y). 1990 Aug;8(8):732-5. doi: 10.1038/nbt0890-732.
Potent and specific inhibitors of protein kinase C have been found in streptomyces and fungi: Staurosporine, an alkaloid from Streptomyces sp., is the most potent inhibitor of protein kinases with an IC50 in the nanomolar range. UCN-01 (7-hydroxy staurosporine), isolated from Streptomyces sp., is a selective inhibitor of protein kinase C with antitumor activity. Calphostin, isolated from the fungus Cladosporium cladosporioides, specifically inhibits protein kinase C (IC50 = 0.05 microM) without inhibiting other protein kinases. Microbial metabolites appear to be a promising source of inhibitors that target signal transduction pathways of eukaryotes.
在链霉菌和真菌中发现了蛋白激酶C的强效特异性抑制剂:从链霉菌属中提取的生物碱星形孢菌素是蛋白激酶最有效的抑制剂,其半数抑制浓度(IC50)在纳摩尔范围内。从链霉菌属中分离出的UCN - 01(7 - 羟基星形孢菌素)是一种具有抗肿瘤活性的蛋白激酶C选择性抑制剂。从真菌枝孢霉中分离出的钙泊三醇能特异性抑制蛋白激酶C(IC50 = 0.05微摩尔),而不抑制其他蛋白激酶。微生物代谢产物似乎是靶向真核生物信号转导途径抑制剂的一个有前景的来源。