The conversion of oridonin to spirolactone-type or enmein-type diterpenoid: Synthesis and biological evaluation of ent-6,7-seco-oridonin derivatives as novel potential anticancer agents-Reference-Cited by-同舟云学术

The conversion of oridonin to spirolactone-type or enmein-type diterpenoid: Synthesis and biological evaluation of ent-6,7-seco-oridonin derivatives as novel potential anticancer agents

Published:2012-06 Issue: Volume:52 Page:242-250
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Wang Lei,Li Dahong,Xu Shengtao,Cai Hao,Yao Hequan,Zhang Yihua,Jiang Jieyun,Xu Jinyi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference21 articles.

1. Natural products: An evolving role in future drug discovery

2. Occurrence, Biological Activities and Synthesis of Kaurane Diterpenes and their Glycosides

3. Recent Progress in the Development of Natural ent-Kaurane Diterpenoids with Anti-tumor Activity

4. Synthesis of rabdokunmin C analogues and their inhibitory effect on NF-κB activation

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