Molecule Details
InChIKeyWEXGHQDVDVWOIU-UHFFFAOYSA-N
Compound Name4-(((4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino)methyl)phenyl sulfamate
Canonical SMILESN#Cc1ccc(N(Cc2ccc(OS(N)(=O)=O)cc2)n2cnnc2)cc1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Cross-Family
Avg pChEMBL7.07
SourceBindingDB;ChEMBL
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB04601
Drug Name4-[(4-O-SULFAMOYLBENZYL)(4-CYANOPHENYL)AMINO]-4H-[1,2,4]-TRIAZOLE
CAS Numbernan
Groups experimental
ATC Codes nan
Descriptionnan

Cross-references: BindingDB: 10017 CHEMBL430879 ChemSpider: 3571980 PDB: 4TZ PubChem:4369413 PubChem:46507413 ZINC: ZINC000001550080
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P00918 CA2 Homo sapiens Human PF00194 7.6 IC50 BindingDB
P11511 CYP19A1 Homo sapiens Human PF00067 7.0 IC50 ChEMBL;BindingDB
P08842 STS Homo sapiens Human PF00884 PF14707 6.6 IC50 ChEMBL;BindingDB
DrugBank Target Actions (1)
Target Gene Target Name Action Type
P00918 CA2 Carbonic anhydrase 2 binder targets