BDBM52732 1,5-diketo-2,4-dihydropyrrolo[1,2-a]quinazoline-3-carboxylic acid ethyl ester::1,5-dioxo-2,4-dihydropyrrolo[1,2-a]quinazoline-3-carboxylic acid ethyl ester::MLS001005827::SMR000349054::cid_5680364::ethyl 1,5-bis(oxidanylidene)-2,4-dihydropyrrolo[1,2-a]quinazoline-3-carboxylate::ethyl 1,5-dioxo-2,4-dihydropyrrolo[1,2-a]quinazoline-3-carboxylate
SMILES CCOC(=O)C1=C2NC(=O)c3ccccc3N2C(=O)C1
InChI Key InChIKey=GPSSHZBXZDTIGY-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 52732
Affinity DataEC50: 3.88E+4nMAssay Description:Broad Institute: MLPCN maternal gene expression Project ID: 2024 Keywords: Zinc finger, C. elegans, maternal gene expression, RNA-protein interac...More data for this Ligand-Target Pair
Affinity DataEC50: 8.90E+4nMAssay Description:Broad Institute: MLPCN maternal gene expression Project ID: 2024 Keywords: Zinc finger, C. elegans, maternal gene expression, RNA-protein interac...More data for this Ligand-Target Pair
Affinity DataIC50: 8.35E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford- Sanford-Burnham Medical Research Institute(SBMRI, San...More data for this Ligand-Target Pair
TargetType-1 angiotensin II receptor(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 9.25E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...More data for this Ligand-Target Pair
