Developments of isoCombretastatin A-4 derivatives as highly cytotoxic agents-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Developments of isoCombretastatin A-4 derivatives as highly cytotoxic agents

Published:2020-03 Issue: Volume:190 Page:112110
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Hamze Abdallah,Alami Mouad,Provot Olivier

Funder

CNRS

University Paris-Saclay

La Ligue Contre le Cancer

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference67 articles.

1. Antimitotic natural products combretastatin A-4 and combretastatin A-2: studies on the mechanism of their inhibition of the binding of colchicine to tubulin;Lin;Biochemistry,1989

2. Isolation and structure of the strong cell growth and tubulin inhibitor combretastatin A-4;Pettit;Experientia,1989

3. Differential cytotoxicity of combretastatins A1 and A4 in two daunorubicin-resistant P388 cell lines;Mc Gown;Canc. Chemother. Pharmacol.,1990

4. Combretastatin A-4, an agent that displays potent and selective toxicity toward tumor vasculature;Dark;Cancer Res.,1997

5. Antimitotic and cell growth inhibitory properties of combretastatin A-4-like ethers;Lawrence;Bioorg. Med. Chem. Lett,2001

Cited by 41 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Candida antarctica Lipase B mediated kinetic resolution: A sustainable method for chiral synthesis of antiproliferative β-lactams;European Journal of Medicinal Chemistry;2024-10

2. Design, synthesis, and bioevaluation of diarylpyrimidine derivatives as novel microtubule destabilizers;Frontiers in Chemistry;2024-07-25

3. Recent clinical trials and optical control as a potential strategy to develop microtubule-targeting drugs in colorectal cancer management;World Journal of Gastroenterology;2024-04-07

4. Controlling Reactivity and Selectivity in the Mizoroki–Heck Reaction: High Throughput Evaluation of 1,5-Diaza-3,7-diphosphacyclooctane Ligands;Journal of the American Chemical Society;2024-02-15

5. Design, synthesis, and bioevaluation of 1 h -pyrrolo[3,2- c ]pyridine derivatives as colchicine-binding site inhibitors with potent anticancer activities;Journal of Enzyme Inhibition and Medicinal Chemistry;2024-01-14

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3