BDBM80034 MLS001180103::N-[(p-toluoylamino)thiocarbamoyl]benzamide::N-[[(4-methylbenzoyl)amino]carbamothioyl]benzamide::N-[[(4-methylphenyl)carbonylamino]carbamothioyl]benzamide::N-[[[(4-methylphenyl)-oxomethyl]hydrazo]-sulfanylidenemethyl]benzamide::N-{[2-(4-methylbenzoyl)hydrazino]carbothioyl}benzamide::SMR000477082::cid_1788711

SMILES Cc1ccc(cc1)C(=O)NNC(=S)NC(=O)c1ccccc1

InChI Key InChIKey=FMEMNCREVJAVHG-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 80034   

TargetC-C chemokine receptor type 6(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM80034(MLS001180103 | N-[(p-toluoylamino)thiocarbamoyl]be...)
Affinity DataIC50:  3.02E+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
In DepthDetails PCBioAssay
TargetBeta-galactosidase(Escherichia coli)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM80034(MLS001180103 | N-[(p-toluoylamino)thiocarbamoyl]be...)
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
In DepthDetails PCBioAssay