Reaction Details |
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Target | Amine oxidase [flavin-containing] B |
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Ligand | BDBM50087800 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1453699 (CHEMBL3364101) |
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IC50 | 1250±n/a nM |
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Citation | Tzvetkov, NT; Hinz, S; Küppers, P; Gastreich, M; Müller, CE Indazole- and indole-5-carboxamides: selective and reversible monoamine oxidase B inhibitors with subnanomolar potency. J Med Chem57:6679-703 (2014) [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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BDBM50087800 |
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n/a |
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Name | BDBM50087800 |
Synonyms: | (5-Benzyloxy-1H-indol-2-ylmethyl)-prop-2-ynyl-amine | CHEMBL45069 |
Type | Small organic molecule |
Emp. Form. | C19H18N2O |
Mol. Mass. | 290.359 |
SMILES | C#CCNCc1cc2cc(OCc3ccccc3)ccc2[nH]1 |
Structure |
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