Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetCytochrome P450 2C9
LigandBDBM50435784
Substrate/Competitorn/a
Meas. Tech.ChEMBL_966356 (CHEMBL2396489)
IC50 750±n/a nM
Citation Gunzner-Toste, JZhao, GBauer, PBaumeister, TBuckmelter, AJCaligiuri, MClodfelter, KHFu, BHan, BHo, YCKley, NLiang, XLiederer, BMLin, JMukadam, SO'Brien, TOh, AReynolds, DJSharma, GSkelton, NSmith, CCSodhi, JWang, WWang, ZXiao, YYuen, PWZak, MZhang, LZheng, XBair, KWDragovich, PS Discovery of potent and efficacious urea-containing nicotinamide phosphoribosyltransferase (NAMPT) inhibitors with reduced CYP2C9 inhibition properties. Bioorg Med Chem Lett23:3531-8 (2013) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Cytochrome P450 2C9
Name:Cytochrome P450 2C9
Synonyms:(R)-limonene 6-monooxygenase | (S)-limonene 6-monooxygenase | CP2C9_HUMAN | CYP2C10 | CYP2C9 | CYPIIC9 | Cytochrome P450 2C9 (CYP2C9 ) | Cytochrome P450 2C9 (CYP2C9) | P-450MP | P450 MP-4/MP-8 | P450 PB-1 | S-mephenytoin 4-hydroxylase
Type:Enzyme
Mol. Mass.:55636.33
Organism:Homo sapiens (Human)
Description:P11712
Residue:490
Sequence:
MDSLVVLVLCLSCLLLLSLWRQSSGRGKLPPGPTPLPVIGNILQIGIKDISKSLTNLSKV
YGPVFTLYFGLKPIVVLHGYEAVKEALIDLGEEFSGRGIFPLAERANRGFGIVFSNGKKW
KEIRRFSLMTLRNFGMGKRSIEDRVQEEARCLVEELRKTKASPCDPTFILGCAPCNVICS
IIFHKRFDYKDQQFLNLMEKLNENIKILSSPWIQICNNFSPIIDYFPGTHNKLLKNVAFM
KSYILEKVKEHQESMDMNNPQDFIDCFLMKMEKEKHNQPSEFTIESLENTAVDLFGAGTE
TTSTTLRYALLLLLKHPEVTAKVQEEIERVIGRNRSPCMQDRSHMPYTDAVVHEVQRYID
LLPTSLPHAVTCDIKFRNYLIPKGTTILISLTSVLHDNKEFPNPEMFDPHHFLDEGGNFK
KSKYFMPFSAGKRICVGEALAGMELFLFLTSILQNFNLKSLVDPKNLDTTPVVNGFASVP
PFYQLCFIPV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50435784
n/a
NameBDBM50435784
Synonyms:CHEMBL2393190 | US11279687, Compound 134
TypeSmall organic molecule
Emp. Form.C19H24N4O4S
Mol. Mass.404.483
SMILESC[C@H]1CN(C[C@@H](C)O1)S(=O)(=O)c1ccc(NC(=O)NCc2cccnc2)cc1 |r|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: