Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM15579 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1811203 (CHEMBL4310663) |
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IC50 | 71±n/a nM |
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Citation | Duan, Y; Qin, W; Suo, F; Zhai, X; Guan, Y; Wang, X; Zheng, Y; Liu, H Design, synthesis and in vitro evaluation of stilbene derivatives as novel LSD1 inhibitors for AML therapy. Bioorg Med Chem26:6000-6014 (2018) [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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BDBM15579 |
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n/a |
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Name | BDBM15579 |
Synonyms: | CHEMBL972 | DEPRENYL | L-Deprenyl | N-methyl-N-[(2R)-1-phenylpropan-2-yl]prop-2-yn-1-amine | SLG | Selegiline | US8633208, Deprenyl | US9469653, Selegiline | methyl[(2R)-1-phenylpropan-2-yl]prop-2-yn-1-ylamine |
Type | Small organic molecule |
Emp. Form. | C13H17N |
Mol. Mass. | 187.2808 |
SMILES | C[C@H](Cc1ccccc1)N(C)CC#C |r| |
Structure |
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