Exploring new structural features of the 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzenesulphonamide scaffold for the inhibition of human carbonic anhydrases
A library of 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzene-1-sulphonamides (EMAC8002a–m) was designed and synthesised to evaluate the effect of substituents in the positions 3 and 4 of the dihydrothiazole ring on the inhibitory potency and selectivity toward human carbonic anhy...
Main Authors: | Simona Distinto, Rita Meleddu, Francesco Ortuso, Filippo Cottiglia, Serenella Deplano, Lisa Sequeira, Claudia Melis, Benedetta Fois, Andrea Angeli, Clemente Capasso, Rossella Angius, Stefano Alcaro, Claudiu T. Supuran, Elias Maccioni |
---|---|
Format: | Article |
Language: | English |
Published: |
Taylor & Francis Group
2019-01-01
|
Series: | Journal of Enzyme Inhibition and Medicinal Chemistry |
Subjects: | |
Online Access: | http://dx.doi.org/10.1080/14756366.2019.1654470 |
Similar Items
-
Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors
by: Claudia Melis, et al.
Published: (2017-01-01) -
Novel thiazolone-benzenesulphonamide inhibitors of human and bacterial carbonic anhydrases
by: Morteza Abdoli, et al.
Published: (2023-12-01) -
Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives
by: Rita Meleddu, et al.
Published: (2021-01-01) -
Synthesis and Anticancer Activity of Novel Thiazole-5-Carboxamide Derivatives
by: Wen-Xi Cai, et al.
Published: (2016-01-01) -
N-(2-Phenoxy-4-(3-phenoxyprop-1-ynyl)phenyl)methane Sulfonamide
by: Shylaprasad Durgadas, et al.
Published: (2012-03-01)