Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50029816 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2284159 |
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IC50 | 30±n/a nM |
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Citation | Tripathi, AC; Upadhyay, S; Paliwal, S; Saraf, SK Privileged scaffolds as MAO inhibitors: Retrospect and prospects. Eur J Med Chem145:445-497 (2018) [PubMed] |
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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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BDBM50029816 |
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n/a |
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Name | BDBM50029816 |
Synonyms: | 5-Chloro-pyridine-2-carboxylic acid (2-amino-ethyl)-amide | CHEMBL279390 | Lazabemide | Ro-19-6327 |
Type | Small organic molecule |
Emp. Form. | C8H10ClN3O |
Mol. Mass. | 199.638 |
SMILES | NCCNC(=O)c1ccc(Cl)cn1 |
Structure |
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