Synthesis of 4-(thiazol-2-ylamino)-benzenesulfonamides with carbonic anhydrase I, II and IX inhibitory activity and cytotoxic effects against breast cancer cell lines-Reference-Cited by-同舟云学术

Synthesis of 4-(thiazol-2-ylamino)-benzenesulfonamides with carbonic anhydrase I, II and IX inhibitory activity and cytotoxic effects against breast cancer cell lines

Published:2016-07 Issue:13 Volume:24 Page:3043-3051
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Abdel Gawad Nagwa M.,Amin Noha H.,Elsaadi Mohammed T.,Mohamed Fatma M.M.,Angeli Andrea,De Luca Viviana,Capasso Clemente,Supuran Claudiu T.^ORCID

Publisher

Elsevier BV

Subject

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

Reference85 articles.

1. Overcoming Hypoxia-Mediated Tumor Progression: Combinatorial Approaches Targeting pH Regulation, Angiogenesis and Immune Dysfunction

2. Hallmarks of Cancer: The Next Generation

3. Inhibition of carbonic anhydrase IX as a novel anticancer mechanism

4. Protein tyrosine kinase inhibitors as anticancer agents

5. Polypharmacology of sulfonamides: pazopanib, a multitargeted receptor tyrosine kinase inhibitor in clinical use, potently inhibits several mammalian carbonic anhydrases

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