BDBM60216 4-chloranyl-N-[5-(3-methylphenyl)-1,3,4-oxadiazol-2-yl]benzamide::4-chloro-N-[5-(3-methylphenyl)-1,3,4-oxadiazol-2-yl]benzamide::4-chloro-N-[5-(m-tolyl)-1,3,4-oxadiazol-2-yl]benzamide::MLS000092396::SMR000027473::cid_691499
SMILES Cc1cccc(c1)-c1nnc(NC(=O)c2ccc(Cl)cc2)o1
InChI Key InChIKey=IWFWBYKOSXITDL-UHFFFAOYSA-N
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 60216
TargetKappa-type opioid receptor(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 5.54E+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
TargetC-C chemokine receptor type 6(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.93E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, CA...More data for this Ligand-Target Pair
TargetBeta-galactosidase(Escherichia coli)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 6.66E+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
