Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50307369 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_610656 (CHEMBL1071676) |
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Ki | 2230±n/a nM |
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Citation | Lühr, S; Vilches-Herrera, M; Fierro, A; Ramsay, RR; Edmondson, DE; Reyes-Parada, M; Cassels, BK; Iturriaga-Vásquez, P 2-Arylthiomorpholine derivatives as potent and selective monoamine oxidase B inhibitors. Bioorg Med Chem18:1388-95 (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_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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BDBM50307369 |
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n/a |
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Name | BDBM50307369 |
Synonyms: | (+/-)-2-Phenylthiomorpholine | CHEMBL608438 |
Type | Small organic molecule |
Emp. Form. | C10H13NS |
Mol. Mass. | 179.282 |
SMILES | C1CSC(CN1)c1ccccc1 |
Structure |
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