We are greatly indebted to The Scientific and Technological Research Council of Turkey (TUBITAK, Grant no. TBAG-109T241) and Ataturk University (BAP2012/152) for their financial support of this study for (YA, AA, SG)
A series of sulfamates were synthesized using as lead compound SLC-0111, a sulfonamide carbonic anhy...
AbstractCarbonic Anhydrases (CAs; EC 4.2.1.1) are zinc metalloenzymes which play a pivotal role both...
Herein we report on a new series of hydrazidoureidobenzensulfonamides investigated as inhibitors of ...
WOS: 000467327900002PubMed ID: 30811749Human carbonic anhydrase I and II isoenzymes (hCA I and II) a...
N-protected amino acids (Gly, Ala and Phe protected with Boc and Z groups) were reacted with sulfona...
A series of new thienyl-substituted pyrazoline benzenesulfonamides were synthesized and their carbon...
A set of sulfamides and sulfamates were synthesized and tested against several isoforms of carbonic ...
The inhibition of two human cytosolic carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I, II and human ...
A series of new compounds was obtained by reaction of aromatic/heterocyclic sulfonamides incorporati...
Background Thiophene(s) are an important group in therapeutic applications, and sulfonamides are the...
Inhibition of Carbonic Anhydrases (CAs) has been clinically exploited for many decades for a variety...
Carbonic anhydrases (CAs, EC 4.2.1.1) catalyze the fundamental reaction of CO2 hydration in all livi...
A series of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesu...
This study was financed by Turkish Republic Prime Ministry State Planning Organization (DPT), (Proje...
Here we report a small library of hydrazinocarbonyl-ureido and thioureido benzenesulfonamide derivat...
A series of sulfamates were synthesized using as lead compound SLC-0111, a sulfonamide carbonic anhy...
AbstractCarbonic Anhydrases (CAs; EC 4.2.1.1) are zinc metalloenzymes which play a pivotal role both...
Herein we report on a new series of hydrazidoureidobenzensulfonamides investigated as inhibitors of ...
WOS: 000467327900002PubMed ID: 30811749Human carbonic anhydrase I and II isoenzymes (hCA I and II) a...
N-protected amino acids (Gly, Ala and Phe protected with Boc and Z groups) were reacted with sulfona...
A series of new thienyl-substituted pyrazoline benzenesulfonamides were synthesized and their carbon...
A set of sulfamides and sulfamates were synthesized and tested against several isoforms of carbonic ...
The inhibition of two human cytosolic carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I, II and human ...
A series of new compounds was obtained by reaction of aromatic/heterocyclic sulfonamides incorporati...
Background Thiophene(s) are an important group in therapeutic applications, and sulfonamides are the...
Inhibition of Carbonic Anhydrases (CAs) has been clinically exploited for many decades for a variety...
Carbonic anhydrases (CAs, EC 4.2.1.1) catalyze the fundamental reaction of CO2 hydration in all livi...
A series of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesu...
This study was financed by Turkish Republic Prime Ministry State Planning Organization (DPT), (Proje...
Here we report a small library of hydrazinocarbonyl-ureido and thioureido benzenesulfonamide derivat...
A series of sulfamates were synthesized using as lead compound SLC-0111, a sulfonamide carbonic anhy...
AbstractCarbonic Anhydrases (CAs; EC 4.2.1.1) are zinc metalloenzymes which play a pivotal role both...
Herein we report on a new series of hydrazidoureidobenzensulfonamides investigated as inhibitors of ...
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