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Design, synthesis, anti-proliferative evaluation, docking, and MD simulations studies of new thiazol...

Design, synthesis, anti-proliferative evaluation, docking, and MD simulations studies of new thiazol...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2717290495

Design, synthesis, anti-proliferative evaluation, docking, and MD simulations studies of new thiazolidine-2,4-diones targeting VEGFR-2 and apoptosis pathway

About this item

Full title

Design, synthesis, anti-proliferative evaluation, docking, and MD simulations studies of new thiazolidine-2,4-diones targeting VEGFR-2 and apoptosis pathway

Publisher

San Francisco: Public Library of Science

Journal title

PloS one, 2022-09, Vol.17 (9), p.e0272362

Language

English

Formats

Publication information

Publisher

San Francisco: Public Library of Science

More information

Scope and Contents

Contents

We report herein, the design and synthesis of thiazolidine-2,4-diones derivatives as new inhibitors for VEGFR-2. The designed members were assessed for their
in vitro
anticancer activity against four cancer cell lines; A549, Caco-2, HepG-2 and MDA-MB-231. Compound
14a
showed the most potent effects against Caco-2, and HepG-2 cell lines...

Alternative Titles

Full title

Design, synthesis, anti-proliferative evaluation, docking, and MD simulations studies of new thiazolidine-2,4-diones targeting VEGFR-2 and apoptosis pathway

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_2717290495

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2717290495

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0272362

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