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溴代和碘代含海绵衍生化合物的物理和生物活性性质研究,这些化合物具有氧苯乙胺核心。

Investigation of the Physical and Bioactive Properties of Bromo- and Iodo-Containing Sponge-Derived Compounds Possessing an Oxyphenylethanamine Core.

机构信息

Department of Chemistry and Biochemistry, University of California , Santa Cruz, California 95064, United States.

Department of Microbiology and Environmental Toxicology, University of California , Santa Cruz, California 95064, United States.

出版信息

J Nat Prod. 2017 Dec 22;80(12):3255-3266. doi: 10.1021/acs.jnatprod.7b00694. Epub 2017 Nov 16.

Abstract

This research set out to identify compounds from marine sponges that can act as bacterial virulence blockers. Extracts from a total of 80 sponges collected from throughout Indonesia were screened in a high-throughput NF-κB-based screen that identifies compounds capable of inhibiting the bacterial type III secretion system (T3SS) in Yersinia pseudotuberculosis. An extract that was shown to inhibit T3SS-driven NF-κB expression was obtained from an Iotrochota cf. iota sponge and was the source of seven new bromo- and iodo-containing compounds, all of which contain a 2-(4-oxyphenyl)ethan-1-amine core. Five were determined to be new compounds and named enisorines A-E (1-5). The remaining two were determined to be new hemibastadinol analogues named (+)-1-O-methylhemibastadinol 2 (6) and (+)-1-O-methylhemibastadinol 4 (7). All seven compounds inhibited T3SS-dependent YopE secretion and did not affect the growth or metabolic activity of Y. pseudotuberculosis. The most potent inhibitors of T3SS activity were enisorine C (3), enisorine E (5), and (+)-1-O-methylhemibastadinol 2 (6), all of which inhibited YopE secretion by >50% at 30 μM.

摘要

本研究旨在从海绵中鉴定出能抑制细菌毒力的化合物。从印度尼西亚各地采集的总共 80 种海绵的提取物在高通量 NF-κB 基础筛选中进行了筛选,该筛选可识别出能抑制假结核耶尔森氏菌(Yersinia pseudotuberculosis)III 型分泌系统(T3SS)的化合物。从 Iotrochota cf. iota 海绵中提取的一种提取物被证明能抑制 T3SS 驱动的 NF-κB 表达,它是七种新的含溴和碘的化合物的来源,这些化合物都含有 2-(4-氧代苯基)乙-1-胺核心。其中 5 种被确定为新化合物,分别命名为 enisorines A-E(1-5)。其余两种被确定为新的半巴卡丁醇类似物,分别命名为(+)-1-O-甲基半巴卡丁醇 2(6)和(+)-1-O-甲基半巴卡丁醇 4(7)。这七种化合物均抑制 T3SS 依赖性 YopE 分泌,且不影响假结核耶尔森氏菌的生长或代谢活性。对 T3SS 活性抑制作用最强的化合物是 enisorine C(3)、ensenrine E(5)和(+)-1-O-甲基半巴卡丁醇 2(6),它们在 30 μM 时均能抑制 YopE 分泌超过 50%。

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