The chemical diversity, binding specificity and propensity to interact with biological targets has inspired many researchers to utilize natural products as molecular probes. Almost all reported carbonic anhydrase inhibitors comprise a zinc binding group in their structure of which the primary sulfonamide moiety (-SO2NH2) is the foremost example and to a lesser extent the primary sulfamate (-O-SO2NH2) and sulfamide (-NH-SO2NH2) groups. Natural products that comprise these zinc binding groups in their structure are however rare and relatively few natural products have been explored as a source for novel carbonic anhydrase inhibitors. This chapter will highlight the recent and growing interest in carbonic anhydrase inhibitors sourced from natu...
A large library of saccharin and acesulfame derivatives has been synthesised and evaluated against f...
A novel class of effective CAIs has been identified, starting from a very weak carbonic anhydrase in...
Small libraries of N-substituted saccharin and N-/O-substituted acesulfame derivatives were synthesi...
A new series of compounds containing a sulfamide moiety as zinc-binding group (ZBG) has been synthes...
A set of compounds incorporating carbon-based zinc-binding groups (ZBGs), of the type PhX (X = COOH,...
Carbonic Anhydrases (CAs) are pharmaceutically relevant targets for the treatment of several disease...
A series of potent inhibitors of human carbonic anhydrase (CA) isoforms I and II has been prepared v...
Here we report the synthesis of natural products (NPs) 5′-O-sulfamoyl adenosine 1 and 5′-O-sulfamoyl...
So far, the design of human carbonic anhydrase (CA) inhibitors has been easily driven by the introdu...
A series of compounds incorporating both sulfonamide and sulfamide as zinc-binding groups (ZBGs) are...
Specific isoforms from the carbonic anhydrase (CA) family of zinc metalloenzymes have been associate...
A small library of phosphorylated sulfamates (N-(O-alkylsulfamoyl)-phosphoramidic acids) incorporati...
Being the primary sulfonamide among the most efficient zinc binding group (ZBG) to design inhibitors...
Herein we report the synthesis of a new series of aromatic sulfamates investigated for the inhibitio...
At least 14 different carbonic anhydrase (CA, EC 4.2.1.1) isoforms were isolated in higher vertebrat...
A large library of saccharin and acesulfame derivatives has been synthesised and evaluated against f...
A novel class of effective CAIs has been identified, starting from a very weak carbonic anhydrase in...
Small libraries of N-substituted saccharin and N-/O-substituted acesulfame derivatives were synthesi...
A new series of compounds containing a sulfamide moiety as zinc-binding group (ZBG) has been synthes...
A set of compounds incorporating carbon-based zinc-binding groups (ZBGs), of the type PhX (X = COOH,...
Carbonic Anhydrases (CAs) are pharmaceutically relevant targets for the treatment of several disease...
A series of potent inhibitors of human carbonic anhydrase (CA) isoforms I and II has been prepared v...
Here we report the synthesis of natural products (NPs) 5′-O-sulfamoyl adenosine 1 and 5′-O-sulfamoyl...
So far, the design of human carbonic anhydrase (CA) inhibitors has been easily driven by the introdu...
A series of compounds incorporating both sulfonamide and sulfamide as zinc-binding groups (ZBGs) are...
Specific isoforms from the carbonic anhydrase (CA) family of zinc metalloenzymes have been associate...
A small library of phosphorylated sulfamates (N-(O-alkylsulfamoyl)-phosphoramidic acids) incorporati...
Being the primary sulfonamide among the most efficient zinc binding group (ZBG) to design inhibitors...
Herein we report the synthesis of a new series of aromatic sulfamates investigated for the inhibitio...
At least 14 different carbonic anhydrase (CA, EC 4.2.1.1) isoforms were isolated in higher vertebrat...
A large library of saccharin and acesulfame derivatives has been synthesised and evaluated against f...
A novel class of effective CAIs has been identified, starting from a very weak carbonic anhydrase in...
Small libraries of N-substituted saccharin and N-/O-substituted acesulfame derivatives were synthesi...