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Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Cholesteryl ester transfer protein' and Ligand = 'BDBM50070315'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cholesteryl ester transfer protein


(Homo sapiens (Human))
BDBM50070315
PNG
((3S,9S)-9-Benzyl-3-isobutyl-6-methyl-13-(1-methyl-...)
Show SMILES CCCCC(C)C1CC(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)O1
Show InChI InChI=1S/C27H41N3O5/c1-6-7-11-18(4)23-16-24(31)29-21(15-20-12-9-8-10-13-20)26(33)28-19(5)25(32)30-22(14-17(2)3)27(34)35-23/h8-10,12-13,17-19,21-23H,6-7,11,14-16H2,1-5H3,(H,28,33)(H,29,31)(H,30,32)/t18?,19-,21-,22-,23?/m0/s1
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n/an/a 300n/an/an/an/an/an/a



Schering Plough Research Institute

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibitory activity against cholesteryl ester transfer protein


Bioorg Med Chem Lett 8: 1277-80 (1999)


BindingDB Entry DOI: 10.7270/Q25X282F
More data for this
Ligand-Target Pair
Cholesteryl ester transfer protein


(Homo sapiens (Human))
BDBM50070315
PNG
((3S,9S)-9-Benzyl-3-isobutyl-6-methyl-13-(1-methyl-...)
Show SMILES CCCCC(C)C1CC(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)O1
Show InChI InChI=1S/C27H41N3O5/c1-6-7-11-18(4)23-16-24(31)29-21(15-20-12-9-8-10-13-20)26(33)28-19(5)25(32)30-22(14-17(2)3)27(34)35-23/h8-10,12-13,17-19,21-23H,6-7,11,14-16H2,1-5H3,(H,28,33)(H,29,31)(H,30,32)/t18?,19-,21-,22-,23?/m0/s1
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n/an/a 4.00E+4n/an/an/an/an/an/a



Schering Plough Research Institute

Curated by ChEMBL


Assay Description
Tested for inhibition of substrate hydrolysis in the presence of porcine kidney esterase at a concentration of 45 nM


Bioorg Med Chem Lett 8: 1277-80 (1999)


BindingDB Entry DOI: 10.7270/Q25X282F
More data for this
Ligand-Target Pair
Cholesteryl ester transfer protein


(Homo sapiens (Human))
BDBM50070315
PNG
((3S,9S)-9-Benzyl-3-isobutyl-6-methyl-13-(1-methyl-...)
Show SMILES CCCCC(C)C1CC(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)O1
Show InChI InChI=1S/C27H41N3O5/c1-6-7-11-18(4)23-16-24(31)29-21(15-20-12-9-8-10-13-20)26(33)28-19(5)25(32)30-22(14-17(2)3)27(34)35-23/h8-10,12-13,17-19,21-23H,6-7,11,14-16H2,1-5H3,(H,28,33)(H,29,31)(H,30,32)/t18?,19-,21-,22-,23?/m0/s1
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n/an/a 5.00E+4n/an/an/an/an/an/a



Schering Plough Research Institute

Curated by ChEMBL


Assay Description
pA2 value towards endothelin receptor A was determined as functional ETA antagonism


Bioorg Med Chem Lett 8: 1277-80 (1999)


BindingDB Entry DOI: 10.7270/Q25X282F
More data for this
Ligand-Target Pair