BDBM61111 5,7-dimethoxy-8-[3-oxidanylidene-3-pyrrolidin-1-yl-1-(3,4,5-trimethoxyphenyl)propyl]-4-phenyl-chromen-2-one::5,7-dimethoxy-8-[3-oxo-3-(1-pyrrolidinyl)-1-(3,4,5-trimethoxyphenyl)propyl]-4-phenyl-1-benzopyran-2-one::5,7-dimethoxy-8-[3-oxo-3-pyrrolidin-1-yl-1-(3,4,5-trimethoxyphenyl)propyl]-4-phenylchromen-2-one::8-[3-keto-3-pyrrolidino-1-(3,4,5-trimethoxyphenyl)propyl]-5,7-dimethoxy-4-phenyl-coumarin::MLS000879490::SMR000465536::cid_16746465
SMILES COc1cc(cc(OC)c1OC)C(CC(=O)N1CCCC1)c1c(OC)cc(OC)c2c(cc(=O)oc12)-c1ccccc1
InChI Key InChIKey=DUJFBAAKSXBINP-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 61111
Affinity DataKi: 1.10E+3nMAssay Description:Inhibition of ELAV1 (unknown origin)-ARE sequence of Mushashi1 transcript complex formation after 2 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
Affinity DataKi: 7.30E+3nMAssay Description:Inhibition of ELAV1 RRM1/RRM2 domains (unknown origin) interaction with ARE sequence of Mushashi1 transcript after 2 hrs by AlphaLISA methodMore data for this Ligand-Target Pair
TargetG-protein coupled receptor 55(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataEC50: 6.57E+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
Affinity DataIC50: 1.76E+4nMAssay Description:Inhibition of ELAV1 RRM1/RRM2 domains (unknown origin) interaction with ARE sequence of Mushashi1 transcript after 2 hrs by AlphaLISA methodMore data for this Ligand-Target Pair
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of ELAV1 (unknown origin)-ARE sequence of Mushashi1 transcript complex formation after 2 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair