Reaction Details |
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Target | Cytochrome P450 2C8 |
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Ligand | BDBM50336507 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_738491 (CHEMBL1743392) |
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Ki | 170000±n/a nM |
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Citation | Fontana, E; Dansette, PM; Poli, SM Cytochrome p450 enzymes mechanism based inhibitors: common sub-structures and reactivity. Curr Drug Metab6:413-54 (2005) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Cytochrome P450 2C8 |
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Name: | Cytochrome P450 2C8 |
Synonyms: | CP2C8_HUMAN | CYP2C8 | CYPIIC8 | Cytochrome P450 2C8 (CYP2C8) | P450 IIC2 | P450 MP-12/MP-20 | P450 form 1 | S-mephenytoin 4-hydroxylase |
Type: | Protein |
Mol. Mass.: | 55839.23 |
Organism: | Homo sapiens (Human) |
Description: | P10632 |
Residue: | 490 |
Sequence: | MEPFVVLVLCLSFMLLFSLWRQSCRRRKLPPGPTPLPIIGNMLQIDVKDICKSFTNFSKV
YGPVFTVYFGMNPIVVFHGYEAVKEALIDNGEEFSGRGNSPISQRITKGLGIISSNGKRW
KEIRRFSLTTLRNFGMGKRSIEDRVQEEAHCLVEELRKTKASPCDPTFILGCAPCNVICS
VVFQKRFDYKDQNFLTLMKRFNENFRILNSPWIQVCNNFPLLIDCFPGTHNKVLKNVALT
RSYIREKVKEHQASLDVNNPRDFIDCFLIKMEQEKDNQKSEFNIENLVGTVADLFVAGTE
TTSTTLRYGLLLLLKHPEVTAKVQEEIDHVIGRHRSPCMQDRSHMPYTDAVVHEIQRYSD
LVPTGVPHAVTTDTKFRNYLIPKGTTIMALLTSVLHDDKEFPNPNIFDPGHFLDKNGNFK
KSDYFMPFSAGKRICAGEGLARMELFLFLTTILQNFNLKSVDDLKNLNTTAVTKGIVSLP
PSYQICFIPV
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BDBM50336507 |
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n/a |
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Name | BDBM50336507 |
Synonyms: | 4-pyridinecarbohydrazide(Isoniazid) | CHEMBL64 | Dow-isoniazid | Hyzyd | INH | ISONICOTINIC ACID HYDRAZIDE(ISONIAZIDE) | Isoniazid (INH) | Isonicotinic acid hydrazide (Isoniazid) | Isonicotinic acid hydrazide(Isoniazid) | Isonicotinylhydrazine | Laniazid | Nydrazid | Rimifon | Stanozide | isoniazid | isonicotinamide | isonicotinhydrazide | isonicotinohydrazide | isonicotinyl hydrazide | pyridine-4-carbohydrazide |
Type | Small organic molecule |
Emp. Form. | C6H7N3O |
Mol. Mass. | 137.1393 |
SMILES | NNC(=O)c1ccncc1 |
Structure |
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