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TargetPeroxisome proliferator-activated receptor alpha
LigandBDBM50371235
Substrate/Competitorn/a
Meas. Tech.ChEMBL_459972 (CHEMBL943100)
EC50>10000±n/a nM
Citation Matthews, JMChen, XCryan, EHlasta, DJRybczynski, PJStrauss, KTang, YXu, JZYang, MZhou, LDemarest, KT Design and synthesis of indane-ureido-thioisobutyric acids: A novel class of PPARalpha agonists. Bioorg Med Chem Lett17:6773-8 (2008) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Peroxisome proliferator-activated receptor alpha
Name:Peroxisome proliferator-activated receptor alpha
Synonyms:Nr1c1 | Nuclear receptor subfamily 1 group C member 1 | PPAR-alpha | PPARA_RAT | Peroxisome Proliferator-Activated Receptor alpha | Ppar | Ppara
Type:PROTEIN
Mol. Mass.:52374.28
Organism:Rattus norvegicus
Description:ChEMBL_834194
Residue:468
Sequence:
MVDTESPICPLSPLEADDLESPLSEEFLQEMGNIQEISQSLGEESSGSFSFADYQYLGSC
PGSEGSVITDTLSPASSPSSVSCPAVPTSTDESPGNALNIECRICGDKASGYHYGVHACE
GCKGFFRRTIRLKLAYDKCDRSCKIQKKNRNKCQYCRFHKCLSVGMSHNAIRFGRMPRSE
KAKLKAEILTCEHDLKDSETADLKSLAKRIHEAYLKNFNMNKVKARVILAGKTSNNPPFV
IHDMETLCMAEKTLVAKMVANGVENKEAEVRFFHCCQCMSVETVTELTEFAKAIPGFANL
DLNDQVTLLKYGVYEAIFTMLSSLMNKDGMLIAYGNGFITREFLKNLRKPFCDIMEPKFD
FAMKFNALELDDSDISLFVAAIICCGDRPGLLNIGYIEKLQEGIVHVLKLHLQSNHPDDT
FLFPKLLQKMVDLRQLVTEHAQLVQVIKKTESDAALHPLLQEIYRDMY
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  Blast E-value cutoff:
BDBM50371235
n/a
NameBDBM50371235
Synonyms:CIPROFIBRATE
TypeSmall organic molecule
Emp. Form.C13H14Cl2O3
Mol. Mass.289.154
SMILESCC(C)(Oc1ccc(cc1)C1CC1(Cl)Cl)C(O)=O
Structure
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