BDBM57750 2-[1-(3-Hydroxy-phenyl)-meth-(E)-ylidene]-5,6-diphenyl-imidazo[2,1-b]thiazol-3-one::MLS000587039::SMR000211124::acetic acid;2-(3-hydroxybenzylidene)-5,6-diphenyl-imidazo[2,1-b]thiazol-3-one::acetic acid;2-[(3-hydroxyphenyl)methylidene]-5,6-diphenyl-3-imidazo[2,1-b]thiazolone::acetic acid;2-[(3-hydroxyphenyl)methylidene]-5,6-diphenylimidazo[2,1-b][1,3]thiazol-3-one::cid_16187201::ethanoic acid;2-[(3-hydroxyphenyl)methylidene]-5,6-diphenyl-imidazo[2,1-b][1,3]thiazol-3-one
SMILES Oc1cccc(C=c2sc3nc(c(-c4ccccc4)n3c2=O)-c2ccccc2)c1
InChI Key InChIKey=REHFCQCKUSKXCO-UHFFFAOYSA-N
Data 2 EC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 57750
TargetNeurotensin receptor type 1(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataEC50: 2.72E+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
Affinity DataEC50: 4.22E+3nMAssay Description:Keywords: Group A streptococcus, GAS, streptokinase, expression, virulence, inhibition, dose response, EC50 Assay Overview: The goal of this assa...More data for this Ligand-Target Pair