Reaction Details |
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Target | Ribosyldihydronicotinamide dehydrogenase [quinone] |
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Ligand | BDBM50112205 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_104942 (CHEMBL713109) |
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Ki | 1000±n/a nM |
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Citation | Leclerc, V; Yous, S; Delagrange, P; Boutin, JA; Renard, P; Lesieur, D Synthesis of nitroindole derivatives with high affinity and selectivity for melatoninergic binding sites MT(3). J Med Chem45:1853-9 (2002) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Ribosyldihydronicotinamide dehydrogenase [quinone] |
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Name: | Ribosyldihydronicotinamide dehydrogenase [quinone] |
Synonyms: | Metallothionein-3 | NMOR2 | NQO2 | NQO2_HUMAN | NRH dehydrogenase [quinone] 2 | NRH:quinone oxidoreductase 2 | QR2 | Quinone reductase 2 | Quinone reductase 2 (NQO2) | Ribosyldihydronicotinamide dehydrogenase [quinone] |
Type: | Protein |
Mol. Mass.: | 25917.25 |
Organism: | Homo sapiens (Human) |
Description: | P16083 |
Residue: | 231 |
Sequence: | MAGKKVLIVYAHQEPKSFNGSLKNVAVDELSRQGCTVTVSDLYAMNLEPRATDKDITGTL
SNPEVFNYGVETHEAYKQRSLASDITDEQKKVREADLVIFQFPLYWFSVPAILKGWMDRV
LCQGFAFDIPGFYDSGLLQGKLALLSVTTGGTAEMYTKTGVNGDSRYFLWPLQHGTLHFC
GFKVLAPQISFAPEIASEEERKGMVAAWSQRLQTIWKEEPIPCTAHWHFGQ
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BDBM50112205 |
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n/a |
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Name | BDBM50112205 |
Synonyms: | CHEMBL298335 | N-[2-(5-Methoxy-6-nitro-1H-indol-3-yl)-ethyl]-acetamide |
Type | Small organic molecule |
Emp. Form. | C13H15N3O4 |
Mol. Mass. | 277.2759 |
SMILES | COc1cc2c(CCNC(C)=O)c[nH]c2cc1[N+]([O-])=O |
Structure |
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