BindingDB logo
myBDB logout

BDBM50151520 3-{4-(3-chlorophenyl)-5-[4-cyanophenyl(1-methyl-1H-5-imidazolyl)methoxymethyl]-2-oxo-1,2-dihydro-1-pyridinylmethyl}benzonitrile::CHEMBL365269

SMILES: Cn1cncc1C(OCc1cn(Cc2cccc(c2)C#N)c(=O)cc1-c1cccc(Cl)c1)c1ccc(cc1)C#N

InChI Key: InChIKey=XLADCPZMAAXJBZ-UHFFFAOYSA-N

Data: 1 IC50  1 EC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50151520   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha


(Mus musculus)
BDBM50151520
PNG
(3-{4-(3-chlorophenyl)-5-[4-cyanophenyl(1-methyl-1H...)
Show SMILES Cn1cncc1C(OCc1cn(Cc2cccc(c2)C#N)c(=O)cc1-c1cccc(Cl)c1)c1ccc(cc1)C#N
Show InChI InChI=1S/C32H24ClN5O2/c1-37-21-36-17-30(37)32(25-10-8-22(15-34)9-11-25)40-20-27-19-38(18-24-5-2-4-23(12-24)16-35)31(39)14-29(27)26-6-3-7-28(33)13-26/h2-14,17,19,21,32H,18,20H2,1H3
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 9n/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Factor Xa


Bioorg Med Chem Lett 14: 4603-6 (2004)


Article DOI: 10.1016/j.bmcl.2004.07.004
BindingDB Entry DOI: 10.7270/Q27080WG
More data for this
Ligand-Target Pair
Geranylgeranyl transferase type-1 subunit beta/Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha


(Bos taurus (bovine))
BDBM50151520
PNG
(3-{4-(3-chlorophenyl)-5-[4-cyanophenyl(1-methyl-1H...)
Show SMILES Cn1cncc1C(OCc1cn(Cc2cccc(c2)C#N)c(=O)cc1-c1cccc(Cl)c1)c1ccc(cc1)C#N
Show InChI InChI=1S/C32H24ClN5O2/c1-37-21-36-17-30(37)32(25-10-8-22(15-34)9-11-25)40-20-27-19-38(18-24-5-2-4-23(12-24)16-35)31(39)14-29(27)26-6-3-7-28(33)13-26/h2-14,17,19,21,32H,18,20H2,1H3
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.90E+3n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Transcriptional repression in HepG2 cells expressing human glucocorticoid receptor


Bioorg Med Chem Lett 14: 4603-6 (2004)


Article DOI: 10.1016/j.bmcl.2004.07.004
BindingDB Entry DOI: 10.7270/Q27080WG
More data for this
Ligand-Target Pair