Reaction Details |
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Target | Amine oxidase [flavin-containing] A |
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Ligand | BDBM50272865 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_661995 (CHEMBL1251643) |
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IC50 | 4813±n/a nM |
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Citation | Chimenti, F; Secci, D; Bolasco, A; Chimenti, P; Granese, A; Carradori, S; Maccioni, E; Cardia, MC; Yáñez, M; Orallo, F; Alcaro, S; Ortuso, F; Cirilli, R; Ferretti, R; Distinto, S; Kirchmair, J; Langer, T Synthesis, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitors. Bioorg Med Chem18:5063-70 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Amine oxidase [flavin-containing] A |
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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: | MENQEKASIAGHMFDVVVIGGGISGLSAAKLLTEYGVSVLVLEARDRVGGRTYTIRNEHV
DYVDVGGAYVGPTQNRILRLSKELGIETYKVNVSERLVQYVKGKTYPFRGAFPPVWNPIA
YLDYNNLWRTIDNMGKEIPTDAPWEAQHADKWDKMTMKELIDKICWTKTARRFAYLFVNI
NVTSEPHEVSALWFLWYVKQCGGTTRIFSVTNGGQERKFVGGSGQVSERIMDLLGDQVKL
NHPVTHVDQSSDNIIIETLNHEHYECKYVINAIPPTLTAKIHFRPELPAERNQLIQRLPM
GAVIKCMMYYKEAFWKKKDYCGCMIIEDEDAPISITLDDTKPDGSLPAIMGFILARKADR
LAKLHKEIRKKKICELYAKVLGSQEALHPVHYEEKNWCEEQYSGGCYTAYFPPGIMTQYG
RVIRQPVGRIFFAGTETATKWSGYMEGAVEAGERAAREVLNGLGKVTEKDIWVQEPESKD
VPAVEITHTFWERNLPSVSGLLKIIGFSTSVTALGFVLYKYKLLPRS
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BDBM50272865 |
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n/a |
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Name | BDBM50272865 |
Synonyms: | 1-(4-(2,4-difluorophenyl)thiazol-2-yl)-2-((S)-2-methylcyclohexylidene)hydrazine | CHEMBL1242992 | CHEMBL497675 |
Type | Small organic molecule |
Emp. Form. | C16H17F2N3S |
Mol. Mass. | 321.388 |
SMILES | C[C@H]1CCCCC1=NNc1nc(cs1)-c1ccc(F)cc1F |r,w:7.8| |
Structure |
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