Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50113851 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_585481 (CHEMBL1059215) |
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IC50 | 20000±n/a nM |
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Citation | Boppana, K; Dubey, PK; Jagarlapudi, SA; Vadivelan, S; Rambabu, G Knowledge based identification of MAO-B selective inhibitors using pharmacophore and structure based virtual screening models. Eur J Med Chem44:3584-90 (2009) [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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BDBM50113851 |
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n/a |
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Name | BDBM50113851 |
Synonyms: | (+/-)-Tranylcypromine | 2-PCPA | 2-Phenyl-cyclopropylamine | 2-phenylcyclopropanamine | CHEMBL313833 | TRANYLCYPROMINE | Tranylcypromine,(+) | Tranylcypromine,(-) | US8609708, 6 Tranyl- cypromine | US8609708, 6 Tranylcypromine |
Type | Small organic molecule |
Emp. Form. | C9H11N |
Mol. Mass. | 133.1903 |
SMILES | NC1CC1c1ccccc1 |
Structure |
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