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Natural products that inhibit carbonic anhydrase
Sally-Ann Poulsen1, Rohan A Davis
1Eskitis Institute for Drug Discovery, Griffith University, Brisbane, QLD, Australia, s.poulsen@griffith.edu.au.
Abstract:
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 nature, demonstrating that natural product chemical space presents a rich source of potential alternate chemotypes for the discovery of novel drug-like carbonic anhydrase inhibitors.
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Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...

