Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetRibosyldihydronicotinamide dehydrogenase [quinone]
LigandBDBM50118451
Substrate/Competitorn/a
Meas. Tech.ChEMBL_104940 (CHEMBL714719)
Ki 1770±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 Chem45:4212-21 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Ribosyldihydronicotinamide dehydrogenase [quinone]
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50118451
n/a
NameBDBM50118451
Synonyms:2,2,2-Trifluoro-N-[2-(6-methoxy-2-phenyl-indan-1-yl)-ethyl]-acetamide | CHEMBL134544
TypeSmall organic molecule
Emp. Form.C20H20F3NO2
Mol. Mass.363.3735
SMILESCOc1ccc2CC(C(CCNC(=O)C(F)(F)F)c2c1)c1ccccc1
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: