Molecule Details
InChIKeyKWEFZSZCLBHIEQ-YYADALCUSA-N
Compound Name(1E)-5-(1-piperidin-4-yl-3-pyridin-4-yl-1H-pyrazol-4-yl)-2,3-dihydro-1H-inden-1-one oxime
Canonical SMILESO/N=C1\CCc2cc(-c3cn(C4CCNCC4)nc3-c3ccncc3)ccc21
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Cross-Family
Avg pChEMBL8.87
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB08553
Drug Name(1E)-5-(1-piperidin-4-yl-3-pyridin-4-yl-1H-pyrazol-4-yl)-2,3-dihydro-1H-inden-1-one oxime
CAS Numbernan
Groups experimental
ATC Codes nan
Description(1E)-5-(1-piperidin-4-yl-3-pyridin-4-yl-1h-pyrazol-4-yl)-2,3-dihydro-1h-inden-1-one oxime is a solid. This compound belongs to the phenylpyrazoles. These are compounds containing a phenylpyrazole skeleton, which consists of a pyrazole bound to a phenyl group. It targets the protein serine/threonine-...

Cross-references: BindingDB: 50006650 CHEMBL526479 ChemSpider: 9828390 PDB: SM5 PubChem:11653652 PubChem:99445024 ZINC: ZINC000039110119
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P15056 BRAF Homo sapiens Human PF00130 PF07714 PF02196 10.5 IC50 ChEMBL;BindingDB
P27361 MAPK3 Homo sapiens Human PF00069 8.1 IC50 ChEMBL
P28482 MAPK1 Homo sapiens Human PF00069 8.1 IC50 ChEMBL
DrugBank Target Actions (1)
Target Gene Target Name Action Type
P15056 BRAF Serine/threonine-protein kinase B-raf binder targets