AbstractChitin is an essential structural component of the fungal cell wall. Chitinases are thought to be important for fungal cell wall remodelling, and inhibition of these enzymes has been proposed as a potential strategy for development of novel anti-fungals. The fungal pathogen Aspergillus fumigatus possesses two distinct multi-gene chitinase families. Here we explore acetazolamide as a chemical scaffold for the inhibition of an A. fumigatus ‘plant-type’ chitinase. A co-crystal structure of AfChiA1 with acetazolamide was used to guide synthesis and screening of acetazolamide analogues that yielded SAR in agreement with these structural data. Although acetazolamide and its analogues are weak inhibitors of the enzyme, they have a high lig...
Inhibition of glycosylhydrolases by peptides mimicking carbohydrates opens a new field in antifungal...
Chitinases belong to family 18 glycosyl hydrolases that can hydrolyze chitin by cleaving beta-1,4-gl...
Our research group has been involved for a long time in the development of macrocyclic amidinoureas ...
Chitin is an essential structural component of the fungal cell wall. Chitinases are thought to be im...
AbstractA limited therapeutic arsenal against increasing clinical disease due to Aspergillus spp. ne...
SummaryChitinases hydrolyse the β(1,4)-glycosidic bonds of chitin, an essential fungal cell wall com...
Chitinases hydrolyse the ß(1,4)-glycosidic bonds of chitin, an essential fungal cell wall component....
SummaryNatural products are often large, synthetically intractable molecules, yet frequently offer s...
Chitinases represent an alternative therapeutic target for opportunistic invasive mycosis since they...
Natural products are often large, synthetically intractable molecules, yet frequently offer surprisi...
Chitinases play important roles in pathogen invasion, arthropod molting, plant defense, and human in...
Chitinase proteins are expressed in most of reigns, from fungi to mammals. This kind of proteins can...
A limited therapeutic arsenal against increasing clinical disease due to Aspergillus spp. necessitat...
Abstract Phytopathogenic fungi secrete chitin deacetylase (CDA) to escape the host’s immunological d...
In the last ten years, we identified and developed a new therapeutic class of antifungal agents, the...
Inhibition of glycosylhydrolases by peptides mimicking carbohydrates opens a new field in antifungal...
Chitinases belong to family 18 glycosyl hydrolases that can hydrolyze chitin by cleaving beta-1,4-gl...
Our research group has been involved for a long time in the development of macrocyclic amidinoureas ...
Chitin is an essential structural component of the fungal cell wall. Chitinases are thought to be im...
AbstractA limited therapeutic arsenal against increasing clinical disease due to Aspergillus spp. ne...
SummaryChitinases hydrolyse the β(1,4)-glycosidic bonds of chitin, an essential fungal cell wall com...
Chitinases hydrolyse the ß(1,4)-glycosidic bonds of chitin, an essential fungal cell wall component....
SummaryNatural products are often large, synthetically intractable molecules, yet frequently offer s...
Chitinases represent an alternative therapeutic target for opportunistic invasive mycosis since they...
Natural products are often large, synthetically intractable molecules, yet frequently offer surprisi...
Chitinases play important roles in pathogen invasion, arthropod molting, plant defense, and human in...
Chitinase proteins are expressed in most of reigns, from fungi to mammals. This kind of proteins can...
A limited therapeutic arsenal against increasing clinical disease due to Aspergillus spp. necessitat...
Abstract Phytopathogenic fungi secrete chitin deacetylase (CDA) to escape the host’s immunological d...
In the last ten years, we identified and developed a new therapeutic class of antifungal agents, the...
Inhibition of glycosylhydrolases by peptides mimicking carbohydrates opens a new field in antifungal...
Chitinases belong to family 18 glycosyl hydrolases that can hydrolyze chitin by cleaving beta-1,4-gl...
Our research group has been involved for a long time in the development of macrocyclic amidinoureas ...