Synthesis and antitumor activity of a series of lactone-opened camptothecin derivatives-Reference-Cited by-同舟云学术

Synthesis and antitumor activity of a series of lactone-opened camptothecin derivatives

Published:2017-10-24 Issue:1 Volume:21 Page:51-61
ISSN:1028-6020
Container-title:Journal of Asian Natural Products Research
language:en
Short-container-title:Journal of Asian Natural Products Research

Author:

Zheng Chao¹,Li Ming-Zong²,You Tian-Pa²,Tang Wei-Ping³,Lou Li-Guang³

Affiliation:

1. Key Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Collaborative Innovation Center of Tropical Biological Resources, Hainan Normal University, Haikou 571158, China

2. Department of Chemistry, University of Science & Technology of China, Hefei 230026, China

3. Shanghai Institute of Materia Medica, Chinese Academy of Science, Shanghai 201203, China

Funder

National Natural Science Foundation of China

Hainan Province Natural Science Foundation of Innovative Research Team Project

Program for Innovative Research Team in University

Publisher

Informa UK Limited

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,General Medicine,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10286020.2017.1392941

Reference16 articles.

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

2. Synthesis and Antitumor Activity of 20(S)-Camptothecin Derivatives: Carbamate-Linked, Water-Soluble Derivatives of 7-Ethyl-10-hydroxycamptothecin.

3. Synthesis of water-soluble (aminoalkyl)camptothecin analogs: inhibition of topoisomerase I and antitumor activity

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