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TargetProtein-S-isoprenylcysteine O-methyltransferase
LigandBDBM50327705
Substrate/Competitorn/a
Meas. Tech.ChEMBL_664824 (CHEMBL1259548)
IC50 2500±n/a nM
Citation Go, MLLeow, JLGorla, SKSchüller, APWang, MCasey, PJ Amino derivatives of indole as potent inhibitors of isoprenylcysteine carboxyl methyltransferase. J Med Chem53:6838-50 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Protein-S-isoprenylcysteine O-methyltransferase
Name:Protein-S-isoprenylcysteine O-methyltransferase
Synonyms:ICMT | ICMT_HUMAN | Isoprenylcysteine carboxyl methyltransferase | PCCMT
Type:PROTEIN
Mol. Mass.:31943.26
Organism:Homo sapiens (Human)
Description:ChEMBL_956034
Residue:284
Sequence:
MAGCAARAPPGSEARLSLATFLLGASVLALPLLTRAGLQGRTGLALYVAGLNALLLLLYR
PPRYQIAIRACFLGFVFGCGTLLSFSQSSWSHFGWYMCSLSLFHYSEYLVTAVNNPKSLS
LDSFLLNHSLEYTVAALSSWLEFTLENIFWPELKQITWLSVTGLLMVVFGECLRKAAMFT
AGSNFNHVVQNEKSDTHTLVTSGVYAWFRHPSYVGWFYWSIGTQVMLCNPICGVSYALTV
WRFFRDRTEEEEISLIHFFGEEYLEYKKRVPTGLPFIKGVKVDL
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  Blast E-value cutoff:
BDBM50327705
n/a
NameBDBM50327705
Synonyms:2-(1-(3-(trifluoromethyl)benzyl)-5-m-tolyl-1H-indol-3-yl)acetamide | 2-(5-m-tolyl-1-(3-(trifluoromethyl)benzyl)-1H-indol-3-yl)acetamide | CHEMBL241264
TypeSmall organic molecule
Emp. Form.C25H21F3N2O
Mol. Mass.422.4422
SMILESCc1cccc(c1)-c1ccc2n(Cc3cccc(c3)C(F)(F)F)cc(CC(N)=O)c2c1
Structure
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