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由一种海洋细菌产生的新型鞘氨醇激酶抑制剂B-535a、b和c;分类学、发酵、分离、理化性质及结构测定

B-535a, b and c, new sphingosine kinase inhibitors, produced by a marine bacterium; taxonomy, fermentation, isolation, physico-chemical properties and structure determination.

作者信息

Kono K, Tanaka M, Mizuno T, Kodama K, Ogita T, Kohama T

机构信息

Pharmacology and Molecular Biology Research Laboratories, Research Institute, Sankyo Co., Ltd., Shinagawa, Tokyo, Japan.

出版信息

J Antibiot (Tokyo). 2000 Aug;53(8):753-8. doi: 10.7164/antibiotics.53.753.

Abstract

In the course of our screening for inhibitors of sphingosine kinase, we found a series of active compounds in a culture broth of a novel marine bacterium, SANK 71896. The structures of the compounds, named B-5354a, b and c, were elucidated by a combination of spectroscopic analyses to be new esters of 4-amino-3-hydroxybenzoic acid with long-chain unsaturated alcohols. B-5354a, b and c inhibit sphingosine kinase activity with IC50 values of 21, 58 and 38 microm, respectively.

摘要

在筛选鞘氨醇激酶抑制剂的过程中,我们从一种新型海洋细菌SANK 71896的培养液中发现了一系列活性化合物。通过光谱分析相结合的方法阐明了这些名为B - 5354a、b和c的化合物的结构,它们是4 - 氨基 - 3 - 羟基苯甲酸与长链不饱和醇形成的新酯。B - 5354a、b和c抑制鞘氨醇激酶活性,IC50值分别为21、58和38微摩尔。

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