Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50278277 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1719682 (CHEMBL4134682) |
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IC50 | >100000±n/a nM |
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Citation | Duan, YC; Ma, YC; Qin, WP; Ding, LN; Zheng, YC; Zhu, YL; Zhai, XY; Yang, J; Ma, CY; Guan, YY Design and synthesis of tranylcypromine derivatives as novel LSD1/HDACs dual inhibitors for cancer treatment. Eur J Med Chem140:392-402 (2017) [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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BDBM50278277 |
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n/a |
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Name | BDBM50278277 |
Synonyms: | CHEMBL4169910 | US11352322, Compound 28 |
Type | Small organic molecule |
Emp. Form. | C17H18N2O2 |
Mol. Mass. | 282.337 |
SMILES | ONC(=O)c1ccc(CNC2CC2c2ccccc2)cc1 |
Structure |
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