BDBM79882 4-oxidanylidene-4-[2-(2-phenyl-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)hydrazinyl]-N-prop-2-enyl-butanamide::4-oxo-4-[(2-phenyl-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)hydrazo]-N-prop-2-enylbutanamide::4-oxo-4-[2-(2-phenyl-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)hydrazinyl]-N-prop-2-enylbutanamide::MLS000731308::N-allyl-4-keto-4-[N'-(2-phenyl-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)hydrazino]butyramide::N-allyl-4-oxo-4-[2-(2-phenyl[1,2,4]triazolo[1,5-c]quinazolin-5-yl)hydrazino]butanamide::SMR000309583::cid_16195424

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

InChI Key InChIKey=FZABWBNTZZNJOC-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 79882   

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

US Patent
LigandChemical structure of BindingDB Monomer ID 79882BDBM79882(US20250388567, Compound 18)
Affinity DataIC50: 550nMAssay 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 79882BDBM79882(US20250388567, Compound 18)
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