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TargetAcyl-CoA:cholesterol acyltransferase
LigandBDBM50047599
Substrate/Competitorn/a
Meas. Tech.ChEMBL_28334 (CHEMBL645898)
IC50 230±n/a nM
Citation Kimura, TWatanabe, NMatsui, MHayashi, KTanaka, HOhtsuka, ISaeki, TKogushi, MKabayashi, HAkasaka, K Structure-activity relationship of a series of phenylureas linked to 4-phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity. 2. J Med Chem36:1641-53 (1993) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Acyl-CoA:cholesterol acyltransferase
Name:Acyl-CoA:cholesterol acyltransferase
Synonyms:ACAT
Type:n/a
Mol. Mass.:35405.31
Organism:Oryctolagus cuniculus
Description:n/a
Residue:305
Sequence:
PLFLKEVGSHFDDFVTNLIEKSASLDNGGCALTTFSILKEMKNNHRAKDLRAPPEQGKIF
VARRSLLDELFEVDHIRTIYHMFIALLILFILSTLVVDYIDEGRLVLEFNLLSYAFGKLP
TVVWTWWTMFLSTLSIPYFLFQHWANGYSKSSHPLMYSLFHGLLFMVFQLGILGFGPTYI
VLAYTLPPASRFIVILEQIRLIMKAHSFVRENVPRVLNSAKEKSSTVPIPTVNQYLYFLF
APTLIYRDSYPRTPTVRWGYVAMQFAQVFGCLFYVYYIFERLCAPLFRNIKQEPFSARVL
VLCIF
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50047599
n/a
NameBDBM50047599
Synonyms:1-{2-[3-(5-Methyl-4-phenyl-imidazol-1-yl)-propoxy]-6-methylsulfanyl-phenyl}-3-pentyl-urea | CHEMBL297553
TypeSmall organic molecule
Emp. Form.C26H34N4O2S
Mol. Mass.466.639
SMILESCCCCCNC(=O)Nc1c(OCCCn2cnc(c2C)-c2ccccc2)cccc1SC
Structure
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