BDBM67315 4-(4-bromophenyl)-2-hydrazino-6-phenylpyrimidine::MLS001001220::SMR000496265::[4-(4-bromophenyl)-6-phenyl-2-pyrimidinyl]hydrazine::[4-(4-bromophenyl)-6-phenyl-pyrimidin-2-yl]diazane::[4-(4-bromophenyl)-6-phenyl-pyrimidin-2-yl]hydrazine::[4-(4-bromophenyl)-6-phenylpyrimidin-2-yl]hydrazine::cid_780302

SMILES NNc1nc(cc(n1)-c1ccc(Br)cc1)-c1ccccc1

InChI Key InChIKey=HRTJDFZRPAYGEZ-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 = 67315   

TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM67315(4-(4-bromophenyl)-2-hydrazino-6-phenylpyrimidine |...)
Affinity DataIC50:  2.09E+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
In DepthDetails PCBioAssay
TargetApelin receptor(Homo sapiens (Human))
Sanford-Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM67315(4-(4-bromophenyl)-2-hydrazino-6-phenylpyrimidine |...)
Affinity DataIC50: >4.00E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford- Sanford-Burnham Medical Research Institute(SBMRI, San...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay