Discovery of O 6 -benzyl glaziovianin A, a potent cytotoxic substance and a potent inhibitor of α,β-tubulin polymerization-Reference-Cited by-同舟云学术

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Discovery of O 6 -benzyl glaziovianin A, a potent cytotoxic substance and a potent inhibitor of α,β-tubulin polymerization

Published:2016-11 Issue:21 Volume:24 Page:5639-5645
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Hayakawa Ichiro,Shioda Shuya,Chinen Takumi,Hatanaka Taisei,Ebisu Haruna,Sakakura Akira,Usui Takeo,Kigoshi Hideo

Funder

Grants-in-Aid for Scientific Research

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

Elsevier BV

Subject

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

Reference19 articles.

1. Tubulin-Interactive Natural Products as Anticancer Agents

2. Localization of the colchicine-binding site of tubulin.

3. Structural basis for the regulation of tubulin by vinblastine

4. Characterization of the Taxol Binding Site on the Microtubule

5. Glaziovianin A, a new isoflavone, from the leaves of Ateleia glazioviana and its cytotoxic activity against human cancer cells

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1. Perplexing Polyphenolics: The Isolations, Syntheses, Reappraisals, and Bioactivities of Flavonoids, Isoflavonoids, and Neoflavonoids from 2016 to 2022;Life;2023-03-09

2. Development of Gatastatin G2, a γ-Tubulin-specific Inhibitor;Journal of Synthetic Organic Chemistry, Japan;2022-06-01

3. Iron-catalyzed arene C−H hydroxylation;Science;2021-10

4. In silico mechanistic model of microtubule assembly inhibition by selective chromone derivatives;Journal of Molecular Structure;2021-10

5. Tubulin Inhibitors Binding to Colchicine-Site: A Review from 2015 to 2019;Current Medicinal Chemistry;2020-11-26

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