BDBM33659 MLS000535054::N-[(1-ethyl-5-oxo-3-phenyl-2-thioxo-4-imidazolidinylidene)methyl]-N-phenylacetamide::N-[(Z)-(1-ethyl-5-keto-3-phenyl-2-thioxo-imidazolidin-4-ylidene)methyl]-N-phenyl-acetamide::N-[(Z)-(1-ethyl-5-oxidanylidene-3-phenyl-2-sulfanylidene-imidazolidin-4-ylidene)methyl]-N-phenyl-ethanamide::N-[(Z)-(1-ethyl-5-oxo-3-phenyl-2-sulfanylidene-4-imidazolidinylidene)methyl]-N-phenylacetamide::N-[(Z)-(1-ethyl-5-oxo-3-phenyl-2-sulfanylideneimidazolidin-4-ylidene)methyl]-N-phenylacetamide::SMR000142491::cid_2177873
SMILES CCN1C(=S)N(\C(=C/N(C(C)=O)c2ccccc2)C1=O)c1ccccc1
InChI Key InChIKey=NATNSCSPRLIHAB-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 33659
Affinity DataIC50: 5.00E+4nMpH: 7.5 T: 2°CAssay Description:HTS was performed using 217,350 compounds of the MLSCN library individually plated into 10ul 1536 compound plates at a concentration of 2.5 mM each, ...More data for this Ligand-Target Pair
Affinity DataIC50: 5.00E+4nMAssay Description:Molecular Library Screening Center Network (MLSCN) Penn Center for Molecular Discovery (PCMD) Assay Provider: Scott L. Diamond, University of Pennsy...More data for this Ligand-Target Pair
TargetNeurotensin receptor type 1(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataEC50: 1.80E+4nMAssay 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
