Reaction Details |
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Target | 3-hydroxyanthranilate 3,4-dioxygenase |
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Ligand | BDBM50446510 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1287917 (CHEMBL3112336) |
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IC50 | 1100±n/a nM |
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Citation | Vallerini, GP; Amori, L; Beato, C; Tararina, M; Wang, XD; Schwarcz, R; Costantino, G 2-Aminonicotinic acid 1-oxides are chemically stable inhibitors of quinolinic acid synthesis in the mammalian brain: a step toward new antiexcitotoxic agents. J Med Chem56:9482-95 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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3-hydroxyanthranilate 3,4-dioxygenase |
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Name: | 3-hydroxyanthranilate 3,4-dioxygenase |
Synonyms: | 3-HAO | 3-hydroxyanthranilate oxygenase | 3-hydroxyanthranilic acid dioxygenase | 3HAO_HUMAN | HAAO | HAD |
Type: | PROTEIN |
Mol. Mass.: | 32552.73 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_108017 |
Residue: | 286 |
Sequence: | MERRLGVRAWVKENRGSFQPPVCNKLMHQEQLKVMFIGGPNTRKDYHIEEGEEVFYQLEG
DMVLRVLEQGKHRDVVIRQGEIFLLPARVPHSPQRFANTVGLVVERRRLETELDGLRYYV
GDTMDVLFEKWFYCKDLGTQLAPIIQEFFSSEQYRTGKPIPDQLLKEPPFPLSTRSIMEP
MSLDAWLDSHHRELQAGTPLSLFGDTYETQVIAYGQGSSEGLRQNVDVWLWQLEGSSVVT
MGGRRLSLAPDDSLLVLAGTSYAWERTQGSVALSVTQDPACKKPLG
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BDBM50446510 |
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n/a |
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Name | BDBM50446510 |
Synonyms: | CHEMBL3110069 |
Type | Small organic molecule |
Emp. Form. | C7H8N2O3 |
Mol. Mass. | 168.15 |
SMILES | Cc1ccc(C(O)=O)c(N)[n+]1[O-] |
Structure |
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