Literature DB >> 20949916

Structure and cytotoxicity of diterpenoids from Isodon eriocalyx.

Xiao-Nian Li1, Jian-Xin Pu, Xue Du, Li-Guang Lou, Li-Mei Li, Sheng-Xiong Huang, Bo Zhao, Mei Zhang, Fei He, Xiao Luo, Wei-Lie Xiao, Han-Dong Sun.   

Abstract

A new ent-atisanoid, eriocatisin A (1), six new ent-abietanoids, eriocasins B-E (2-4, 7), 3-acetyleriocasin C (5), and 3β-acetoxyeriocasin D (6), and seven new ent-kauranoids, maoesins A-F (8, 10-14) and 3α-acetoxy-maoesin A (9), together with 21 known compounds, were isolated from the aerial parts of Isodon eriocalyx. The structures of 1-14 were determined by spectroscopic data interpretation. All compounds isolated were evaluated for their in vitro growth inhibitory activity against the HT-29, BEL-7402, and SK-OV-3 human cancer cell lines. Compounds 17, 18, and 20 showed inhibitory effects for all three tumor cell lines used, with IC(50) values in the range 2.1-7.3 μM.

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Year:  2010        PMID: 20949916     DOI: 10.1021/np1004328

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  3 in total

Review 1.  Discovery and development of natural product oridonin-inspired anticancer agents.

Authors:  Ye Ding; Chunyong Ding; Na Ye; Zhiqing Liu; Eric A Wold; Haiying Chen; Christopher Wild; Qiang Shen; Jia Zhou
Journal:  Eur J Med Chem       Date:  2016-06-13       Impact factor: 6.514

Review 2.  Bioactive Natural Spirolactone-Type 6,7-seco-ent-Kaurane Diterpenoids and Synthetic Derivatives.

Authors:  Haonan Li; Runwei Jiao; Jiahui Mu; Shengtao Xu; Xu Li; Xianhua Wang; Zhanlin Li; Jinyi Xu; Huiming Hua; Dahong Li
Journal:  Molecules       Date:  2018-11-08       Impact factor: 4.411

3.  A database-driven approach identifies additional diterpene synthase activities in the mint family (Lamiaceae).

Authors:  Sean R Johnson; Wajid Waheed Bhat; Jacob Bibik; Aiko Turmo; Britta Hamberger; Björn Hamberger
Journal:  J Biol Chem       Date:  2018-11-29       Impact factor: 5.157

  3 in total

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