Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50261968 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_514664 (CHEMBL975558) |
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IC50 | 230000±n/a nM |
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Citation | Hruschka, S; Rosen, TC; Yoshida, S; Kirk, KL; Fröhlich, R; Wibbeling, B; Haufe, G Fluorinated phenylcyclopropylamines. Part 5: Effects of electron-withdrawing or -donating aryl substituents on the inhibition of monoamine oxidases A and B by 2-aryl-2-fluoro-cyclopropylamines. Bioorg Med Chem16:7148-66 (2008) [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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BDBM50261968 |
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n/a |
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Name | BDBM50261968 |
Synonyms: | CHEMBL468855 | trans-2-Fluoro-2-(3,4-dimethoxyphenyl)cyclopropylamine |
Type | Small organic molecule |
Emp. Form. | C11H14FNO2 |
Mol. Mass. | 211.2328 |
SMILES | COc1ccc(cc1OC)[C@@]1(F)C[C@@H]1N |r| |
Structure |
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