Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50272865 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_509965 (CHEMBL1005558) |
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IC50 | 36.06±n/a nM |
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Citation | Chimenti, F; Maccioni, E; Secci, D; Bolasco, A; Chimenti, P; Granese, A; Carradori, S; Alcaro, S; Ortuso, F; Yáñez, M; Orallo, F; Cirilli, R; Ferretti, R; La Torre, F Synthesis, stereochemical identification, and selective inhibitory activity against human monoamine oxidase-B of 2-methylcyclohexylidene-(4-arylthiazol-2-yl)hydrazones. J Med Chem51:4874-80 (2008) [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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BDBM50272865 |
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n/a |
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Name | BDBM50272865 |
Synonyms: | 1-(4-(2,4-difluorophenyl)thiazol-2-yl)-2-((S)-2-methylcyclohexylidene)hydrazine | CHEMBL1242992 | CHEMBL497675 |
Type | Small organic molecule |
Emp. Form. | C16H17F2N3S |
Mol. Mass. | 321.388 |
SMILES | C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1F |r,w:7.8| |
Structure |
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