Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50249871 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_619728 (CHEMBL1111192) |
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IC50 | 32810±n/a nM |
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Citation | Chimenti, F; Carradori, S; Secci, D; Bolasco, A; Bizzarri, B; Chimenti, P; Granese, A; Yáñez, M; Orallo, F Synthesis and inhibitory activity against human monoamine oxidase of N1-thiocarbamoyl-3,5-di(hetero)aryl-4,5-dihydro-(1H)-pyrazole derivatives. Eur J Med Chem45:800-4 (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] 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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BDBM50249871 |
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n/a |
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Name | BDBM50249871 |
Synonyms: | 3-phenyl-5-p-tolyl-4,5-dihydro-1H-pyrazole-1-carbothioamide | Amino[5-(4-methylphenyl)-3-phenyl(2-pyrazolinyl)]methane-1-thione | CHEMBL489743 |
Type | Small organic molecule |
Emp. Form. | C17H17N3S |
Mol. Mass. | 295.402 |
SMILES | Cc1ccc(cc1)C1CC(=NN1C(N)=S)c1ccccc1 |c:10| |
Structure |
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