Reaction Details |
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Target | Cytochrome P450 1A2 |
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Ligand | BDBM50183183 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_354702 (CHEMBL853122) |
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IC50 | >50000±n/a nM |
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Citation | Hall, A; Bit, RA; Brown, SH; Chaignot, HM; Chessell, IP; Coleman, T; Giblin, GM; Hurst, DN; Kilford, IR; Lewell, XQ; Michel, AD; Mohamed, S; Naylor, A; Novelli, R; Skinner, L; Spalding, DJ; Tang, SP; Wilson, RJ Discovery of novel biaryl heterocyclic EP1 receptor antagonists. Bioorg Med Chem Lett16:2666-71 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cytochrome P450 1A2 |
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Name: | Cytochrome P450 1A2 |
Synonyms: | CP1A2_HUMAN | CYP1A2 | CYPIA2 | Cholesterol 25-hydroxylase | Cytochrome P(3)450 | Cytochrome P450 1A | Cytochrome P450 1A2 (CYP1A2) | Cytochrome P450 4 | Cytochrome P450-P3 |
Type: | Enzyme |
Mol. Mass.: | 58423.38 |
Organism: | Homo sapiens (Human) |
Description: | P05177 |
Residue: | 516 |
Sequence: | MALSQSVPFSATELLLASAIFCLVFWVLKGLRPRVPKGLKSPPEPWGWPLLGHVLTLGKN
PHLALSRMSQRYGDVLQIRIGSTPVLVLSRLDTIRQALVRQGDDFKGRPDLYTSTLITDG
QSLTFSTDSGPVWAARRRLAQNALNTFSIASDPASSSSCYLEEHVSKEAKALISRLQELM
AGPGHFDPYNQVVVSVANVIGAMCFGQHFPESSDEMLSLVKNTHEFVETASSGNPLDFFP
ILRYLPNPALQRFKAFNQRFLWFLQKTVQEHYQDFDKNSVRDITGALFKHSKKGPRASGN
LIPQEKIVNLVNDIFGAGFDTVTTAISWSLMYLVTKPEIQRKIQKELDTVIGRERRPRLS
DRPQLPYLEAFILETFRHSSFLPFTIPHSTTRDTTLNGFYIPKKCCVFVNQWQVNHDPEL
WEDPSEFRPERFLTADGTAINKPLSEKMMLFGMGKRRCIGEVLAKWEIFLFLAILLQQLE
FSVPPGVKVDLTPIYGLTMKHARCEHVQARLRFSIN
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BDBM50183183 |
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n/a |
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Name | BDBM50183183 |
Synonyms: | 3-(3-(2-(benzyloxy)-5-chlorophenyl)pyridin-2-yl)benzoic acid | CHEMBL206096 |
Type | Small organic molecule |
Emp. Form. | C25H18ClNO3 |
Mol. Mass. | 415.868 |
SMILES | OC(=O)c1cccc(c1)-c1ncccc1-c1cc(Cl)ccc1OCc1ccccc1 |
Structure |
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