Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50049692 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_124230 (CHEMBL733984) |
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IC50 | 10000±n/a nM |
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Citation | Harfenist, M; Heuser, DJ; Joyner, CT; Batchelor, JF; White, HL Selective inhibitors of monoamine oxidase. 3. Structure-activity relationship of tricyclics bearing imidazoline, oxadiazole, or tetrazole groups. J Med Chem39:1857-63 (1996) [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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BDBM50049692 |
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n/a |
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Name | BDBM50049692 |
Synonyms: | 2-Phenoxathiin-2-yl-4,5-dihydro-1H-imidazole | CHEMBL301625 |
Type | Small organic molecule |
Emp. Form. | C15H12N2OS |
Mol. Mass. | 268.334 |
SMILES | C1CN=C(N1)c1ccc2Oc3ccccc3Sc2c1 |c:2| |
Structure |
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