Synthesis of pro-apoptotic indapamide derivatives as anticancer agents-Reference-Cited by-同舟云学术

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Synthesis of pro-apoptotic indapamide derivatives as anticancer agents

Published:2015-02-16 Issue:6 Volume:30 Page:967-980
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:

Yılmaz Özgür¹,Özbaş Turan Suna²,Akbuğa Jülide²,Tiber Pınar Mega³,Orun Oya³,Supuran Claudiu T.⁴,Küçükgüzel Ş. Güniz⁵

Affiliation:

1. TUBITAK Marmara Research Center, Materials Institute Gebze, Kocaeli, Turkey,

2. Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Marmara University, Haydarpaşa, İstanbul, Turkey,

3. Department of Biophysics, School of Medicine, Marmara University, Haydarpaşa, İstanbul, Turkey,

4. Laboratorio di Chimica Bioinorganica, Università degli Studi di Firenze, Sesto Fiorentino (Firenze), Italy, and

5. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Marmara University, Haydarpaşa, İstanbul, Turkey

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.3109/14756366.2014.1001756

Reference37 articles.

1. Structure-based drug discovery of carbonic anhydrase inhibitors

2. Diuretics: From Classical Carbonic Anhydrase Inhibitors to Novel Applications of the Sulfonamides

3. Anticancer and Antiviral Sulfonamides

4. Carbonic anhydrases: from biomedical applications of the inhibitors and activators to biotechnological use for CO2 capture

5. 3-Phenyl-1H-Indole-5-Sulfonamides: Structure-Based Drug Design of a Promising Class of Carbonic Anhydrase Inhibitors

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1. Development of Thiazolidinones as Fungal Carbonic Anhydrase Inhibitors;International Journal of Molecular Sciences;2020-04-22

2. Inhibitory activity against carbonic anhydrase IX and XII as a candidate selection criterion in the development of new anticancer agents;Journal of Enzyme Inhibition and Medicinal Chemistry;2020-01-01

3. Design, synthesis, molecular modeling, in vivo studies and anticancer evaluation of quinazolin-4(3H)-one derivatives as potential VEGFR-2 inhibitors and apoptosis inducers;Bioorganic Chemistry;2020-01

4. Design, synthesis, molecular docking, and anticancer activity of benzoxazole derivatives as VEGFR‐2 inhibitors;Archiv der Pharmazie;2019-08-25

5. Discovery of thiazolin-4-one-based aromatic sulfamates as a new class of carbonic anhydrase isoforms I, II, IV, and IX inhibitors;Bioorganic Chemistry;2018-04

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