Reaction Details | |||
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Target | Amine oxidase [flavin-containing] B | ||
Ligand | BDBM254554 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Fluorescence-Based (Inhibitor)-Screening Assay | ||
pH | 7.5±n/a | ||
Temperature | 310.15±n/a K | ||
Ki | 20000±n/a nM | ||
Comments | extracted | ||
Citation | Ortega Muñoz, A; Fyfe, MC; Martinell Pedemonte, M; Estiarte Martínez, M; Valls Vidal, N; Kurz, G; Castro Palomino Laria, JC (Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors US Patent US9469597 Publication Date 10/18/2016 | ||
More Info.: | Get all data from this article, Assay Method | ||
Amine oxidase [flavin-containing] B | |||
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: |
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BDBM254554 | |||
n/a | |||
Name | BDBM254554 | ||
Synonyms: | US10214477, Example 13 | US9469597, 13 | US9670136, 13 N-(4-(((trans)-2-(6-(3-(trifluoromethyl)phenyl)pyridin-3-yl)cyclopropyl)amino)cyclohexyl)acetamide | ||
Type | Small organic molecule | ||
Emp. Form. | C23H26F3N3O | ||
Mol. Mass. | 417.4672 | ||
SMILES | CC(=O)NC1CCC(CC1)N[C@H]1C[C@@H]1c1ccc(nc1)-c1cccc(c1)C(F)(F)F |r,wU:13.15,wD:11.11,(9.54,5.39,;8.21,4.62,;8.21,3.08,;6.87,5.39,;5.54,4.62,;5.54,3.08,;4.21,2.31,;2.87,3.08,;2.87,4.62,;4.21,5.39,;1.54,2.31,;.21,3.08,;-.56,4.41,;-1.33,3.08,;-2.67,2.31,;-4,3.08,;-5.33,2.31,;-5.33,.77,;-4,,;-2.67,.77,;-6.67,,;-8,.77,;-9.34,,;-9.34,-1.54,;-8,-2.37,;-6.67,-1.54,;-8,-3.91,;-8,-5.45,;-9.54,-3.91,;-6.46,-3.91,)| | ||
Structure |