3D-QSAR study of 20 (S)-camptothecin analogs-Reference-Cited by-同舟云学术

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3D-QSAR study of 20 (S)-camptothecin analogs

Published:2007-02 Issue:2 Volume:28 Page:307-314
ISSN:1671-4083
Container-title:Acta Pharmacologica Sinica
language:en
Short-container-title:Acta Pharmacologica Sinica

Author:

LU Ai-jun,ZHANG Zhen-shan,ZHENG Ming-yue,ZOU Han-jun,LUO Xiao-min,JIANG Hua-liang

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,General Medicine

Reference23 articles.

1. Comparison of Topoisomerase I Inhibition, DNA Damage, and Cytotoxicity of Camptothecin Derivatives Presently in Clinical Trials

2. Topoisomerase I inhibitors and other new cytotoxic drugs

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

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2. QSAR studies of quinoline alkaloids camptothecin derivatives for prediction anticancer activity using linear and nonlinear methods;International Journal of Quantum Chemistry;2024-01-04

3. Plant Cell Biofactories as In Vitro Production Platforms of the Anticancer Drug Camptothecin;Exploring Plant Cells for the Production of Compounds of Interest;2021

4. Anticancer activity, topoisomerase I inhibition, DNA ‘light switch’ behavior and molecular docking of two ruthenium complexes containing phenazine ring;Journal of Biomolecular Structure and Dynamics;2020-07-28

5. CamptothecaSpecies;Secondary Metabolites of Medicinal Plants;2020-03-27

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