Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50148941 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1557703 (CHEMBL3772921) |
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IC50 | 204±n/a nM |
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Citation | Distinto, S; Meleddu, R; Yanez, M; Cirilli, R; Bianco, G; Sanna, ML; Arridu, A; Cossu, P; Cottiglia, F; Faggi, C; Ortuso, F; Alcaro, S; Maccioni, E Drug design, synthesis, in vitro and in silico evaluation of selective monoaminoxidase B inhibitors based on 3-acetyl-2-dichlorophenyl-5-aryl-2,3-dihydro-1,3,4-oxadiazole chemical scaffold. Eur J Med Chem108:542-52 (2016) [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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BDBM50148941 |
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n/a |
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Name | BDBM50148941 |
Synonyms: | CHEMBL3771328 |
Type | Small organic molecule |
Emp. Form. | C16H11Cl3N2O2 |
Mol. Mass. | 369.63 |
SMILES | CC(=O)N1N=C(O[C@@H]1c1ccc(Cl)c(Cl)c1)c1ccc(Cl)cc1 |r,c:4| |
Structure |
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