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_1464362 (CHEMBL3404821) |
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Kd | 66±n/a nM |
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Citation | Rojas, RJ; Edmondson, DE; Almos, T; Scott, R; Massari, ME Reversible and irreversible small molecule inhibitors of monoamine oxidase B (MAO-B) investigated by biophysical techniques. Bioorg Med Chem23:770-8 (2015) [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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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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