Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50168969 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_302416 (CHEMBL828820) |
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Ki | 42000±n/a nM |
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Citation | Di Santo, R; Costi, R; Roux, A; Artico, M; Befani, O; Meninno, T; Agostinelli, E; Palmegiani, P; Turini, P; Cirilli, R; Ferretti, R; Gallinella, B; La Torre, F Design, synthesis, and biological activities of pyrrolylethanoneamine derivatives, a novel class of monoamine oxidases inhibitors. J Med Chem48:4220-3 (2005) [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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BDBM50168969 |
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n/a |
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Name | BDBM50168969 |
Synonyms: | 2-Amino-1-(1-methyl-1H-pyrrol-2-yl)-2-phenyl-ethanone | CHEMBL361891 |
Type | Small organic molecule |
Emp. Form. | C13H14N2O |
Mol. Mass. | 214.2631 |
SMILES | Cn1cccc1C(=O)C(N)c1ccccc1 |
Structure |
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