Reaction Details |
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Target | Protein-S-isoprenylcysteine O-methyltransferase |
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Ligand | BDBM50327726 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_664824 (CHEMBL1259548) |
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IC50 | 76000±n/a nM |
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Citation | Go, ML; Leow, JL; Gorla, SK; Schüller, AP; Wang, M; Casey, PJ Amino derivatives of indole as potent inhibitors of isoprenylcysteine carboxyl methyltransferase. J Med Chem53:6838-50 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Protein-S-isoprenylcysteine O-methyltransferase |
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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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BDBM50327726 |
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n/a |
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Name | BDBM50327726 |
Synonyms: | CHEMBL1257397 | methyl 2-(1-octyl-5-m-tolyl-1H-indol-3-yl)acetate |
Type | Small organic molecule |
Emp. Form. | C26H33NO2 |
Mol. Mass. | 391.5457 |
SMILES | CCCCCCCCn1cc(CC(=O)OC)c2cc(ccc12)-c1cccc(C)c1 |
Structure |
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