BDBM79917 (E)-2-cyano-N-(2-hydroxyphenyl)-3-(1-methyl-3-indolyl)-2-propenamide::(E)-2-cyano-N-(2-hydroxyphenyl)-3-(1-methylindol-3-yl)acrylamide::(E)-2-cyano-N-(2-hydroxyphenyl)-3-(1-methylindol-3-yl)prop-2-enamide::MLS001173404::SMR000539012::cid_729709

SMILES Cc1[nH]c(/C=C2C(=O)Nc3ccc(C(=O)N[C@H](C)c4ccccc4)cc32)c(C)c1C(=O)NCC(O)C1CCOC1

InChI Key InChIKey=IPLJETJUFOYRIU-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 79917   

TargetG protein-coupled receptor kinase 5(Human)
Purdue Research Foundation

US Patent
LigandChemical structure of BindingDB Monomer ID 79917BDBM79917(US20250388567, Compound 44)
Affinity DataIC50: 100nMAssay Description:Keywords: apoptosis, BH3 domain, Bcl2-A1, BIM, caspase, cancer Primary Collaborator: Todd Golub, Broad Institute, golub@broadinstitute.org Assay Over...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/6/2026
Entry Details
US Patent

TargetBeta-adrenergic receptor kinase 1(Bovine)
Purdue Research Foundation

US Patent
LigandChemical structure of BindingDB Monomer ID 79917BDBM79917(US20250388567, Compound 44)
Affinity DataIC50: 1.00E+4nMAssay Description:Keywords: apoptosis, BH3 domain, Bcl2-A1, BIM, caspase, cancer Primary Collaborator: Todd Golub, Broad Institute, golub@broadinstitute.org Assay Over...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/6/2026
Entry Details
US Patent