Synthesis and bioactivity studies on new 4-(3-(4-Substitutedphenyl)-3a,4-dihydro-3H-indeno[1,2-c]pyrazol-2-yl) benzenesulfonamides-Reference-Cited by-同舟云学术

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Synthesis and bioactivity studies on new 4-(3-(4-Substitutedphenyl)-3a,4-dihydro-3H-indeno[1,2-c]pyrazol-2-yl) benzenesulfonamides

Published:2016-03-30 Issue:6 Volume:31 Page:1619-1624
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:

Gul Halise Inci¹,Tugrak Mehtap¹,Sakagami Hiroshi²,Taslimi Parham³,Gulcin Ilhami³⁴,Supuran Claudiu T.⁵

Affiliation:

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

2. Division of Pharmacology, Meikai University School of Dentistry, Sakado, Saitama, Japan,

3. Ataturk University, Faculty of Science, Department of Chemistry, Erzurum, Turkey,

4. College of Science, Department of Zoology, King Saud University, Riyadh, Saudi Arabia, and

5. Neurofarba Department and Laboratorio di Chimica Bioinorganica, Università degli Studi di Firenze, Sesto Fiorentino, Italy

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.3109/14756366.2016.1160077

Reference57 articles.

1. Molecular targets for breast cancer therapy and prevention

2. Carbonic anhydrase inhibitors: Synthesis, molecular docking, cytotoxic and inhibition of the human carbonic anhydrase isoforms I, II, IX, XII with novel benzenesulfonamides incorporating pyrrole, pyrrolopyrimidine and fused pyrrolopyrimidine moieties

3. Sulfonamides and their isosters as carbonic anhydrase inhibitors

4. Carbonic anhydrase inhibitors and their therapeutic potential

5. Sulfonamides and Sulfonylated Derivatives as Anticancer Agents

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