Reaction Details |
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Target | Cytochrome c oxidase subunit 1 |
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Ligand | BDBM50229774 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_530100 (CHEMBL967598) |
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IC50 | 157200±n/a nM |
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Citation | Erdélyi, P; Fodor, T; Varga, AK; Czugler, M; Gere, A; Fischer, J Chemical and biological investigation of N-hydroxy-valdecoxib: An active metabolite of valdecoxib. Bioorg Med Chem16:5322-30 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cytochrome c oxidase subunit 1 |
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Name: | Cytochrome c oxidase subunit 1 |
Synonyms: | COI | COX1_SHEEP | COXI | MT-CO1 | MTCO1 |
Type: | PROTEIN |
Mol. Mass.: | 57042.19 |
Organism: | Ovis aries |
Description: | ChEMBL_662814 |
Residue: | 514 |
Sequence: | MFINRWLFSTNHKDIGTLYLLFGAWAGMVGTALSLLIRAELGQPGTLLGDDQIYNVIVTA
HAFVMIFFMVMPIMIGGFGNWLVPLMIGAPDMAFPRMNNMSFWLLPPSFLLLLASSMVEA
GAGTGWTVYPPLAGNLAHAGASVDLTIFSLHLAGVSSILGAINFITTIINMKPPAMSQYQ
TPLFVWSVLITAVLLLLSLPVLAAGITMLLTDRNLNTTFFDPAGGGDPILYQHLFWFFGH
PEVYILILPGFGMISHIVTYYSGKKEPFGYMGMVWAMMSIGFLGFIVWAHHMFTVGMDVD
TRAYFTSATMIIAIPTGVKVFSWLATLHGGNIKWSPAMMWALGFIFLFTVGGLTGIVLAN
SSLDIVLHDTYYVVAHFHYVLSMGAVFAIMGGFVHWFPLFSGYTLNDTWAKIHFAIMFVG
VNMTFFPQHFLGLSGMPRRYSDYPDAYTMWNTISSMGSFISLTAVMLMIFIIWEAFASKR
EVLTVDLTTTNLEWLNGCPPPYHTFEEPTYVNLK
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BDBM50229774 |
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n/a |
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Name | BDBM50229774 |
Synonyms: | CHEMBL254418 | N-Hydroxy-4-(5-methyl-3-phenylisoxazol-4-yl)benzenesulfonamide monohydrate | N-hydroxy-4-(5-methyl-3-phenylisoxazol-4-yl)benzenesulfonamide hydrate |
Type | Small organic molecule |
Emp. Form. | C16H14N2O4S |
Mol. Mass. | 330.358 |
SMILES | Cc1onc(c1-c1ccc(cc1)S(=O)(=O)NO)-c1ccccc1 |
Structure |
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