Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50029802 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_123927 (CHEMBL729461) |
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IC50 | 800±n/a nM |
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Citation | Lebreton, L; Curet, O; Gueddari, S; Mazouz, F; Bernard, S; Burstein, C; Milcent, R Selective and potent monoamine oxidase type B inhibitors: 2-substituted 5-aryltetrazole derivatives. J Med Chem38:4786-92 (1996) [PubMed] |
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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_RAT | Amine oxidase (flavin-containing) B | Amine oxidase [flavin-containing] B | Maob | Monoamine Oxidase Type B (MAO-B) | Monoamine oxidase | Monoamine oxidase B (MAO-B) | Monoamine oxidase B (rMAO-B) | Monoamine oxidase type B (MAOB) | Monoamine oxidase-B (MAO-B) |
Type: | Enzyme |
Mol. Mass.: | 58469.65 |
Organism: | Rattus norvegicus (rat) |
Description: | P19643 |
Residue: | 520 |
Sequence: | MSNKCDVIVVGGGISGMAAAKLLHDCGLSVVVLEARDRVGGRTYTIRNKNVKYVDLGGSY
VGPTQNRILRLAKELGLETYKVNEVERLIHFVKGKSYAFRGPFPPVWNPITYLDYNNLWR
TMDEMGQEIPSDAPWKAPLAEEWDYMTMKELLDKICWTNSTKQIATLFVNLCVTAETHEV
SALWFLWYVKQCGGTTRIISTTNGGQERKFIGGSGQVSERIKDILGDRVKLERPVIHIDQ
TGENVVVKTLNHEIYEAKYVISAIPPVLGMKIHHSPPLPILRNQLITRVPLGSVIKCMVY
YKEPFWRKKDFCGTMVIEGEEAPIAYTLDDTKPDGSCAAIMGFILAHKARKLVRLTKEER
LRKLCELYAKVLNSQEALQPVHYEEKNWCEEQYSGGCYTAYFPPGILTQYGRVLRQPVGK
IFFAGTETASHWSGYMEGAVEAGERAAREILHAIGKIPEDEIWQPEPESVDVPARPITNT
FLERHLPSVPGLLKLLGLTTILSATALGFLAHKKGLFVRF
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BDBM50029802 |
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n/a |
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Name | BDBM50029802 |
Synonyms: | 2-{5-[4-(3-Methoxy-benzyloxy)-phenyl]-tetrazol-2-yl}-ethanol | CHEMBL144700 |
Type | Small organic molecule |
Emp. Form. | C17H18N4O3 |
Mol. Mass. | 326.3498 |
SMILES | COc1cccc(COc2ccc(cc2)-c2nnn(CCO)n2)c1 |
Structure |
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