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BDBM14438 2-quinolone analog 2d::N-{[4-(3-chlorophenyl)-1-methyl-2-oxo-1,2-dihydroquinolin-6-yl]({1-[(4-cyanophenyl)methyl]-1H-imidazol-5-yl})methyl}formamide

SMILES: Cn1c2ccc(cc2c(cc1=O)-c1cccc(Cl)c1)C(NC=O)c1cncn1Cc1ccc(cc1)C#N

InChI Key: InChIKey=JHZVNQFWHURWJH-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 14438   
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
Geranylgeranyl Transferase (GGTase-I)


(Bos taurus (bovine))
BDBM14438
PNG
(2-quinolone analog 2d | N-{[4-(3-chlorophenyl)-1-m...)
Show SMILES Cn1c2ccc(cc2c(cc1=O)-c1cccc(Cl)c1)C(NC=O)c1cncn1Cc1ccc(cc1)C#N
Show InChI InChI=1S/C29H22ClN5O2/c1-34-26-10-9-22(12-25(26)24(13-28(34)37)21-3-2-4-23(30)11-21)29(33-18-36)27-15-32-17-35(27)16-20-7-5-19(14-31)6-8-20/h2-13,15,17-18,29H,16H2,1H3,(H,33,36)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



Abbott Laboratories



Assay Description
The in vitro activity of compounds inhibiting GGTase-1 was determined by measuring the transfer of [3H]-geranylgeranylpyrophosphate to substrate Ha-R...


Bioorg Med Chem Lett 15: 2033-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.02.062
BindingDB Entry DOI: 10.7270/Q23J3B61
More data for this
Ligand-Target Pair
Protein Farnesyltransferase (PFT)


(Bos taurus (bovine))
BDBM14438
PNG
(2-quinolone analog 2d | N-{[4-(3-chlorophenyl)-1-m...)
Show SMILES Cn1c2ccc(cc2c(cc1=O)-c1cccc(Cl)c1)C(NC=O)c1cncn1Cc1ccc(cc1)C#N
Show InChI InChI=1S/C29H22ClN5O2/c1-34-26-10-9-22(12-25(26)24(13-28(34)37)21-3-2-4-23(30)11-21)29(33-18-36)27-15-32-17-35(27)16-20-7-5-19(14-31)6-8-20/h2-13,15,17-18,29H,16H2,1H3,(H,33,36)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.10n/an/an/an/a7.537



Abbott Laboratories



Assay Description
The in vitro activity of compounds inhibiting FTase was determined by measuring the transfer of [3H]-FPP to substrate Ha-Ras-CVLS. The incorporated r...


Bioorg Med Chem Lett 15: 2033-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.02.062
BindingDB Entry DOI: 10.7270/Q23J3B61
More data for this
Ligand-Target Pair