Reaction Details | |||
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Target | Amine oxidase [flavin-containing] A | ||
Ligand | BDBM254556 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Monoamine Oxidase Assays | ||
Ki | 20500±n/a nM | ||
Citation | Ortega Muñoz, A; Fyfe, MC; Martinell Pedemonte, M; Estiarte Martinez, M; Valls Vidal, N; Kurz, G; Castro Palomino Laria, JC (Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors US Patent US9670136 Publication Date 6/6/2017 | ||
More Info.: | Get all data from this article, Assay Method | ||
Amine oxidase [flavin-containing] A | |||
Name: | Amine oxidase [flavin-containing] A | ||
Synonyms: | AOFA_HUMAN | Amine oxidase (flavin-containing) A | MAO-A | MAOA | Monoamine oxidase | Monoamine oxidase type A | Monoamine oxidase type A (MAO A) | Monoamine oxidase type A (MAO A) | Monoamine oxidase type A (MAOA) | ||
Type: | Protein | ||
Mol. Mass.: | 59689.53 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P21397 | ||
Residue: | 527 | ||
Sequence: |
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BDBM254556 | |||
n/a | |||
Name | BDBM254556 | ||
Synonyms: | US10214477, Example 15 | US9469597, 15 | US9670136, 15 (R)-1-(4-(((trans)-2-phenylcyclopropyl)amino)cyclohexyl)pyrrolidin-3-amine trihydrochloride | ||
Type | Small organic molecule | ||
Emp. Form. | C19H29N3 | ||
Mol. Mass. | 299.4537 | ||
SMILES | N[C@@H]1CCN(C1)C1CCC(CC1)N[C@H]1C[C@@H]1c1ccccc1 |r,wU:15.18,wD:13.14,1.0,(7.15,4.37,;6.38,3.04,;7.29,1.79,;6.38,.54,;4.92,1.02,;4.92,2.56,;3.59,.25,;3.59,-1.29,;2.25,-2.06,;.92,-1.29,;.92,.25,;2.25,1.02,;-.41,-2.06,;-1.75,-1.29,;-2.52,.04,;-3.29,-1.29,;-4.62,-2.06,;-4.62,-3.6,;-5.96,-4.37,;-7.29,-3.6,;-7.29,-2.06,;-5.96,-1.29,)| | ||
Structure |