PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
29305297-3	2018	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	12-50	carbonic anhydrase 5A	Homo sapiens	208-213