Reaction Details |
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Target | D-amino-acid oxidase |
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Ligand | BDBM50605570 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2252172 (CHEMBL5166382) |
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IC50 | 3300±n/a nM |
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Citation | Tang, H; Jensen, K; Houang, E; McRobb, FM; Bhat, S; Svensson, M; Bochevarov, A; Day, T; Dahlgren, MK; Bell, JA; Frye, L; Skene, RJ; Lewis, JH; Osborne, JD; Tierney, JP; Gordon, JA; Palomero, MA; Gallati, C; Chapman, RSL; Jones, DR; Hirst, KL; Sephton, M; Chauhan, A; Sharpe, A; Tardia, P; Dechaux, EA; Taylor, A; Waddell, RD; Valentine, A; Janssens, HB; Aziz, O; Bloomfield, DE; Ladha, S; Fraser, IJ; Ellard, JM Discovery of a Novel Class of d-Amino Acid Oxidase Inhibitors Using the Schrödinger Computational Platform. J Med Chem65:6775-6802 (2022) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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D-amino-acid oxidase |
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Name: | D-amino-acid oxidase |
Synonyms: | D-amino-acid oxidase (DAAO) | DAAO | DAMOX | DAO | OXDA_HUMAN |
Type: | Homodimer |
Mol. Mass.: | 39476.06 |
Organism: | Homo sapiens (Human) |
Description: | P14920 |
Residue: | 347 |
Sequence: | MRVVVIGAGVIGLSTALCIHERYHSVLQPLDIKVYADRFTPLTTTDVAAGLWQPYLSDPN
NPQEADWSQQTFDYLLSHVHSPNAENLGLFLISGYNLFHEAIPDPSWKDTVLGFRKLTPR
ELDMFPDYGYGWFHTSLILEGKNYLQWLTERLTERGVKFFQRKVESFEEVAREGADVIVN
CTGVWAGALQRDPLLQPGRGQIMKVDAPWMKHFILTHDPERGIYNSPYIIPGTQTVTLGG
IFQLGNWSELNNIQDHNTIWEGCCRLEPTLKNARIIGERTGFRPVRPQIRLEREQLRTGP
SNTEVIHNYGHGGYGLTIHWGCALEAAKLFGRILEEKKLSRMPPSHL
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BDBM50605570 |
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n/a |
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Name | BDBM50605570 |
Synonyms: | CHEMBL5191030 |
Type | Small organic molecule |
Emp. Form. | C11H9ClN2O2 |
Mol. Mass. | 236.654 |
SMILES | Clc1ccc(Cc2c[nH]c(=O)c(=O)[nH]2)cc1 |
Structure |
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