Synthesis and biological evaluation of cis-restrained carbocyclic combretastatin A-4 analogs: Influence of the ring size and saturation on cytotoxic properties-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of cis-restrained carbocyclic combretastatin A-4 analogs: Influence of the ring size and saturation on cytotoxic properties

Published:2019-10 Issue:19 Volume:27 Page:115032
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Nowikow Christina,Fuerst Rita,Kauderer Maria,Dank Christian,Schmid Walther,Hajduch Marian,Rehulka Jiri,Gurska Sona,Mokshyna Olena,Polishchuk Pavel,Zupkó István,Dzubak Petr,Rinner Uwe

Funder

Technology Agency of the Czech Republic

Ministry of Health of the Czech Republic

Palacky University

Czech Ministry of Education, Youth and Sports

European Regional Development Fund

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference58 articles.

1. Plants used against cancer. A survey;Hartwell;Lloydia,1967

2. Antineoplastic agents. 145. Isolation and structure of the strong cell-growth and tubulin inhibitor combretastatin-a-4;Pettit;Experientia,1989

3. Antineoplastic agents. 291. Isolation and synthesis of combretastatins a-4, a-5, and a-6;Pettit;J Med Chem,1995

4. Antineoplastic agents. 113. Synthesis of natural (−)-combretastatin;Pettit;J Org Chem,1985

5. Antineoplastic agents. 122. Constituents of combretum-caffrum;Pettit;J Nat Prod,1987

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