Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50529578 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1908898 (CHEMBL4411256) |
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IC50 | >10000±n/a nM |
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Citation | Ernst, G; Akuma, D; Au, V; Buchler, IP; Byers, S; Carr, GV; Defays, S; de León, P; Demaude, T; DePasquale, M; Durieu, V; Huang, Y; Jigorel, E; Kimos, M; Kolobova, A; Montel, F; Moureau, F; Poslusney, M; Swinnen, D; Vandergeten, MC; Van Houtvin, N; Wei, H; White, N; Wood, M; Barrow, JC Synthesis and Evaluation of Bicyclic Hydroxypyridones as Inhibitors of Catechol ACS Med Chem Lett10:1573-1578 (2019) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Amine oxidase [flavin-containing] B |
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Name: | Amine oxidase [flavin-containing] B |
Synonyms: | AOFB_HUMAN | MAO-B | MAOB | Monoamine oxidase type B | Monoamine oxidase type B (MAO B) | Monoamine oxidase type B (MAO B) | Monoamine oxidase type B (MAOB) |
Type: | Protein |
Mol. Mass.: | 58768.76 |
Organism: | Homo sapiens (Human) |
Description: | P27338 |
Residue: | 520 |
Sequence: | MSNKCDVVVVGGGISGMAAAKLLHDSGLNVVVLEARDRVGGRTYTLRNQKVKYVDLGGSY
VGPTQNRILRLAKELGLETYKVNEVERLIHHVKGKSYPFRGPFPPVWNPITYLDHNNFWR
TMDDMGREIPSDAPWKAPLAEEWDNMTMKELLDKLCWTESAKQLATLFVNLCVTAETHEV
SALWFLWYVKQCGGTTRIISTTNGGQERKFVGGSGQVSERIMDLLGDRVKLERPVIYIDQ
TRENVLVETLNHEMYEAKYVISAIPPTLGMKIHFNPPLPMMRNQMITRVPLGSVIKCIVY
YKEPFWRKKDYCGTMIIDGEEAPVAYTLDDTKPEGNYAAIMGFILAHKARKLARLTKEER
LKKLCELYAKVLGSLEALEPVHYEEKNWCEEQYSGGCYTTYFPPGILTQYGRVLRQPVDR
IYFAGTETATHWSGYMEGAVEAGERAAREILHAMGKIPEDEIWQSEPESVDVPAQPITTT
FLERHLPSVPGLLRLIGLTTIFSATALGFLAHKRGLLVRV
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BDBM50529578 |
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n/a |
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Name | BDBM50529578 |
Synonyms: | CHEMBL4461693 |
Type | Small organic molecule |
Emp. Form. | C15H14Cl2N2O2 |
Mol. Mass. | 325.19 |
SMILES | Oc1cn2CCN(Cc3ccc(Cl)cc3Cl)Cc2cc1=O |
Structure |
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