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单环甾醇A和B,来自韩国海绵Monanchora sp.的具有生物活性的双环[4.3.1]甾体

Monanchosterols A and B, bioactive bicyclo[4.3.1]steroids from a Korean sponge Monanchora sp.

作者信息

Wang Weihong, Lee Tae Gu, Patil Rahul S, Mun Bora, Yang Inho, Kim Hiyoung, Hahn Dongyup, Won Dong Hwan, Lee Jihye, Lee Yehee, Choi Hyukjae, Nam Sang-Jip, Kang Heonjoong

机构信息

‡College of Pharmacy, Yeungnam University, 214-1 Dae-dong, Gyeongsan, 712-749, Korea.

§Department of Chemistry and Nano Science, Global Top 5 Program, Ewha Womans University, Seoul, 120-750, Korea.

出版信息

J Nat Prod. 2015 Mar 27;78(3):368-73. doi: 10.1021/np500760v. Epub 2014 Dec 2.

Abstract

Chemical investigation of a Korean marine sponge, Monanchora sp., led to the isolation of three new steroids (1-3). Compounds 1 and 2, designated as monanchosterols A and B, respectively, represent the first examples of steroids possessing the bicyclo[4.3.1] A/B ring system from a natural source. Compounds 1-3 were investigated for their anti-inflammatory activity by evaluating their inhibitory effects on the mRNA expression of IL-6, TNF-α, and COX-2 in the LPS-stimulated murine RAW264.7 macrophage cells. Compounds 2 and 3 exhibited significant inhibitory effects on the mRNA expression of IL-6 without notable cytotoxicity to the cells in a dose-dependent manner.

摘要

对韩国海洋海绵Monanchora sp.进行化学研究,从中分离出三种新的甾体化合物(1 - 3)。化合物1和2分别被命名为莫南胆固醇A和B,它们是天然来源中具有双环[4.3.1] A/B环系统的甾体化合物的首个实例。通过评估化合物1 - 3对脂多糖刺激的小鼠RAW264.7巨噬细胞中IL - 6、TNF - α和COX - 2的mRNA表达的抑制作用,研究了它们的抗炎活性。化合物2和3对IL - 6的mRNA表达表现出显著的抑制作用,且对细胞无明显细胞毒性,呈剂量依赖性。

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