Synthesis, cytotoxicities, and carbonic anhydrase inhibition potential of 6-(3-aryl-2-propenoyl)-2(3H)-benzoxazolones-Reference-Cited by-同舟云学术

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Synthesis, cytotoxicities, and carbonic anhydrase inhibition potential of 6-(3-aryl-2-propenoyl)-2(3H)-benzoxazolones

Published:2019-01-01 Issue:1 Volume:34 Page:1722-1729
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Bilginer Sinan¹,Gul Halise Inci¹^ORCID,Erdal Feyza Sena¹,Sakagami Hiroshi²,Levent Serkan³,Gulcin Ilhami⁴,Supuran Claudiu T.⁵^ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey;

2. School of Dentistry, Meikai University Research Institute of Odontology (M-RIO), Meikai University, Sakado, Japan;

3. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Anadolu University, Eskisehir, Turkey;

4. Department of Chemistry, Faculty of Science, Ataturk University, Erzurum, Turkey;

5. Neurofarba Department, University Firenze, Florence, Italy

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14756366.2019.1670657

Reference61 articles.

1. Ferlay J, Colombet M, Soerjomataram I, et al. Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods. Int J Cancer 2019;144:1941–1953.

2. Dual or multi-targeting inhibitors: The next generation anticancer agents

3. Cytotoxic activity of 4′-hydroxychalcone derivatives against Jurkat cells and their effects on mammalian DNA topoisomerase I

4. Antimicrobial Evaluation of Some Styryl Ketone Derivatives and Related Thiol Adducts

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