Carbonic anhydrases (CAs, EC 4.2.1.1) are widespread metalloenzymes in organisms in all life kingdoms, being involved in pH regulation, metabolic processes and many other physiological and pathological conditions. CA inhibitors and activators thus possess applications as pharmacological agents in the management of a range of diseases. Marine natural products have allowed the identification of some highly interesting CA inhibitors, among which are sulfonamides, phenols, polyamines, coumarins and several other miscellaneous inhibitors, which are reviewed here. Psammaplin C and some bromophenols were the most investigated classes of such marine-based inhibitors and have been used as lead molecules for developing interesting types of potent and...
Phenols are among the largest and most widely distributed groups of secondary metabolites within the...
An ihibition study of several carbonic anhydrase (CA, EC 4.2.1.1) isoforms with flavones and aminofl...
A series of benzamides incorporating 4-sulfamoyl moieties were obtained by reacting 4-sulfamoyl benz...
Natural products represent a straightforward source for molecular structures bearing a vast array of...
At least 14 different carbonic anhydrase (CA, EC 4.2.1.1) isoforms were isolated in higher vertebrat...
Coumarins constitute a relatively new class of inhibitors of the zinc enzyme carbonic anhydrase (CA,...
Inhibition of the newest isoform of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1), CA XV, wi...
Carbonic anhydrases (CAs; EC 4.2.1.1) are metalloenzymes present in all kingdoms of life, as they eq...
Here, we investigate 28 structurally new sulfonamides and their subsequent testing for enzyme inhibi...
Inhibition of specific carbonic anhydrase (CA) enzymes is a validated strategy for the development o...
Specific isoforms from the carbonic anhydrase (CA) family of zinc metalloenzymes have been associate...
Carbonic anhydrases (CAs) are metalloenzymes responsible for the reversible hydration of carbon diox...
Infections caused by pathogens resistant to the available antimicrobial treatments represent nowaday...
The inhibition of a newly cloned coral carbonic anhydrase (CA, EC 4.2.1.1) has been investigated wit...
The chemical diversity, binding specificity and propensity to interact with biological targets has i...
Phenols are among the largest and most widely distributed groups of secondary metabolites within the...
An ihibition study of several carbonic anhydrase (CA, EC 4.2.1.1) isoforms with flavones and aminofl...
A series of benzamides incorporating 4-sulfamoyl moieties were obtained by reacting 4-sulfamoyl benz...
Natural products represent a straightforward source for molecular structures bearing a vast array of...
At least 14 different carbonic anhydrase (CA, EC 4.2.1.1) isoforms were isolated in higher vertebrat...
Coumarins constitute a relatively new class of inhibitors of the zinc enzyme carbonic anhydrase (CA,...
Inhibition of the newest isoform of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1), CA XV, wi...
Carbonic anhydrases (CAs; EC 4.2.1.1) are metalloenzymes present in all kingdoms of life, as they eq...
Here, we investigate 28 structurally new sulfonamides and their subsequent testing for enzyme inhibi...
Inhibition of specific carbonic anhydrase (CA) enzymes is a validated strategy for the development o...
Specific isoforms from the carbonic anhydrase (CA) family of zinc metalloenzymes have been associate...
Carbonic anhydrases (CAs) are metalloenzymes responsible for the reversible hydration of carbon diox...
Infections caused by pathogens resistant to the available antimicrobial treatments represent nowaday...
The inhibition of a newly cloned coral carbonic anhydrase (CA, EC 4.2.1.1) has been investigated wit...
The chemical diversity, binding specificity and propensity to interact with biological targets has i...
Phenols are among the largest and most widely distributed groups of secondary metabolites within the...
An ihibition study of several carbonic anhydrase (CA, EC 4.2.1.1) isoforms with flavones and aminofl...
A series of benzamides incorporating 4-sulfamoyl moieties were obtained by reacting 4-sulfamoyl benz...