Synthesis and Biological Evaluation of Novel Homocamptothecins Conjugating with Dihydropyrimidine Derivatives as Potent Topoisomerase I Inhibitors-Reference-Cited by-同舟云学术

Synthesis and Biological Evaluation of Novel Homocamptothecins Conjugating with Dihydropyrimidine Derivatives as Potent Topoisomerase I Inhibitors

Published:2011-09-29 Issue:11 Volume:344 Page:726-734
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:en
Short-container-title:Arch. Pharm. Pharm. Med. Chem.

Author:

Zhu Lingjian,Cheng Pengfei,Lei Ning,Yao Jianzhong,Sheng Chunquan,Zhuang Chunlin,Guo Wei,Liu Wenfeng,Zhang Yongqiang,Dong Guoqiang,Wang Shengzhang,Miao Zhenyuan,Zhang Wannian

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Reference29 articles.

1. Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata1,2

2. Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I.

3. Camptothecins

4. BN 80245: An E-ring modified camptothecin with potent antiproliferative and topoisomerase I inhibitory activities

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