Ki Summary new BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetRibosyldihydronicotinamide dehydrogenase [quinone]
LigandBDBM50118456
Substrate/Competitorn/a
Meas. Tech.ChEMBL_104940
Ki 49±n/a nM
Citation Fukatsu KUchikawa OKawada MYamano TYamashita MKato KHirai KHinuma SMiyamoto MOhkawa S Synthesis of a novel series of benzocycloalkene derivatives as melatonin receptor agonists. J Med Chem 45:4212-21 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Ribosyldihydronicotinamide dehydrogenase [quinone]
Name:Ribosyldihydronicotinamide dehydrogenase [quinone]
Synonyms:Metallothionein-3 | 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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50118456
n/a
NameBDBM50118456
Synonyms:CHEMBL334645 | N-[2-(6-Methoxy-3H-inden-1-yl)-ethyl]-propionamide
TypeSmall organic molecule
Emp. Form.C15H19NO2
Mol. Mass.245.3169
SMILESCCC(=O)NCCC1=CCc2ccc(OC)cc12 |t:7|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: