Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50341156 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_740468 (CHEMBL1764623) |
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Ki | 4.21±n/a nM |
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Citation | Mishra, N; Sasmal, D Development of selective and reversible pyrazoline based MAO-B inhibitors: virtual screening, synthesis and biological evaluation. Bioorg Med Chem Lett21:1969-73 (2011) [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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BDBM50341156 |
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n/a |
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Name | BDBM50341156 |
Synonyms: | 3-(anthracen-9-yl)-5-phenyl-4,5-dihydro-1H-pyrazole | CHEMBL1760717 |
Type | Small organic molecule |
Emp. Form. | C23H18N2 |
Mol. Mass. | 322.4024 |
SMILES | C1C(N=NC1c1c2ccccc2cc2ccccc12)c1ccccc1 |c:2| |
Structure |
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