Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50536257 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1933261 (CHEMBL4478913) |
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IC50 | 65000±n/a nM |
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Citation | Di Pietro, O; Alencar, N; Esteban, G; Viayna, E; Sza?aj, N; Vázquez, J; Juárez-Jiménez, J; Sola, I; Pérez, B; Solé, M; Unzeta, M; Muñoz-Torrero, D; Luque, FJ Design, synthesis and biological evaluation of N-methyl-N-[(1,2,3-triazol-4-yl)alkyl]propargylamines as novel monoamine oxidase B inhibitors. Bioorg Med Chem24:4835-4854 (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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BDBM50536257 |
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n/a |
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Name | BDBM50536257 |
Synonyms: | CHEMBL4577856 |
Type | Small organic molecule |
Emp. Form. | C15H18N4 |
Mol. Mass. | 254.3302 |
SMILES | CN(CC#C)Cc1cccc(Cc2cn(C)nn2)c1 |
Structure |
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