Reaction Details |
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Target | Cytochrome P450 1A2 |
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Ligand | BDBM50462746 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1776483 (CHEMBL4233475) |
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IC50 | 350±n/a nM |
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Citation | Engers, DW; Bollinger, SR; Engers, JL; Panarese, JD; Breiner, MM; Gregro, A; Blobaum, AL; Bronson, JJ; Wu, YJ; Macor, JE; Rodriguez, AL; Zamorano, R; Conn, PJ; Lindsley, CW; Niswender, CM; Hopkins, CR Discovery and characterization of N-(1,3-dialkyl-1H-indazol-6-yl)-1H-pyrazolo[4,3-b]pyridin-3-amine scaffold as mGlu Bioorg Med Chem Lett28:2641-2646 (2018) [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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BDBM50462746 |
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n/a |
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Name | BDBM50462746 |
Synonyms: | CHEMBL4239430 |
Type | Small organic molecule |
Emp. Form. | C17H16N6 |
Mol. Mass. | 304.3491 |
SMILES | Cn1nc(C2CC2)c2ccc(Nc3n[nH]c4cccnc34)cc12 |
Structure |
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