Molecule Details
InChIKeyJIVPVXMEBJLZRO-AWEZNQCLSA-N
Compound Name2-chloro-5-((1S)-1-hydroxy-3-oxo-2H-isoindol-1-yl)benzenesulfonamide
Canonical SMILESNS(=O)(=O)c1cc([C@@]2(O)NC(=O)c3ccccc32)ccc1Cl
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)8
Pfam Stratification Homologous
Avg pChEMBL7.34
SourceBindingDB
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB08046
Drug Name2-chloro-5-[(1S)-1-hydroxy-3-oxo-2H-isoindol-1-yl]benzenesulfonamide
CAS Number1441368-51-9
Groups experimental
ATC Codes nan
Descriptionnan

Cross-references: CHEMBL402262 ChemSpider: 599888 PDB: KLT PubChem:688424 PubChem:99444517 ZINC: ZINC000000057255
Target Activities (8)
Target Gene Organism Category Pfam pChEMBL Type Source
P43166 CA7 Homo sapiens Human PF00194 8.6 Ki BindingDB
O43570 CA12 Homo sapiens Human PF00194 8.3 Ki BindingDB
Q9Y2D0 CA5B Homo sapiens Human PF00194 8.1 Ki BindingDB
Q16790 CA9 Homo sapiens Human PF00194 7.6 Ki BindingDB
P00918 CA2 Homo sapiens Human PF00194 6.9 Ki BindingDB
P22748 CA4 Homo sapiens Human PF00194 6.7 Ki BindingDB
P00915 CA1 Homo sapiens Human PF00194 6.5 IC50 BindingDB
P35218 CA5A Homo sapiens Human PF00194 6.0 Ki BindingDB
DrugBank Target Actions (1)
Target Gene Target Name Action Type
P00918 CA2 Carbonic anhydrase 2 binder targets