Title : Benzimidazole design, synthesis, and docking to build selective carbonic anhydrase VA inhibitors.

Pub. Date : 2018 Feb 1

PMID : 29305297






1 Functional Relationships(s)
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1 A series of chloro-substituted benzenesulfonamides bearing a heterocyclic tail, together with molecular docking, was used to build inhibitors that explore substituent influence on the binding affinity to the CA VA isoform. chloro-substituted benzenesulfonamides carbonic anhydrase 5A Homo sapiens