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Target
Peroxisome proliferator-activated receptor alpha
Ligand
BDBM50248411
Substrate
n/a
Meas. Tech.
ChEMBL_566252 (CHEMBL953555)
IC50
>50000±n/a nM
Citation
 Zhang, H; Ryono, DE; Devasthale, P; Wang, W; O'Malley, K; Farrelly, D; Gu, L; Harrity, T; Cap, M; Chu, C; Locke, K; Zhang, L; Lippy, J; Kunselman, L; Morgan, N; Flynn, N; Moore, L; Hosagrahara, V; Zhang, L; Kadiyala, P; Xu, C; Doweyko, AM; Bell, A; Chang, C; Muckelbauer, J; Zahler, R; Hariharan, N; Cheng, PT Design, synthesis and structure-activity relationships of azole acids as novel, potent dual PPAR alpha/gamma agonists. Bioorg Med Chem Lett 19:1451-6 (2009) [PubMed]  Article 
Target
Name:
Peroxisome proliferator-activated receptor alpha
Synonyms:
NR1C1 | Nuclear receptor subfamily 1 group C member 1 | PPAR | PPAR alpha/gamma | PPAR-alpha | PPARA | PPARA_HUMAN | Peroxisome Proliferator-Activated Receptor alpha | Peroxisome proliferator-activated receptor | Peroxisome proliferator-activated receptor alpha (PPAR alpha)
Type:
Enzyme
Mol. Mass.:
52222.08
Organism:
Homo sapiens (Human)
Description:
Q07869
Residue:
468
Sequence:
MVDTESPLCPLSPLEAGDLESPLSEEFLQEMGNIQEISQSIGEDSSGSFGFTEYQYLGSCPGSDGSVITDTLSPASSPSSVTYPVVPGSVDESPSGALNIECRICGDKASGYHYGVHACEGCKGFFRRTIRLKLVYDKCDRSCKIQKKNRNKCQYCRFHKCLSVGMSHNAIRFGRMPRSEKAKLKAEILTCEHDIEDSETADLKSLAKRIYEAYLKNFNMNKVKARVILSGKASNNPPFVIHDMETLCMAEKTLVAKLVANGIQNKEAEVRIFHCCQCTSVETVTELTEFAKAIPGFANLDLNDQVTLLKYGVYEAIFAMLSSVMNKDGMLVAYGNGFITREFLKSLRKPFCDIMEPKFDFAMKFNALELDDSDISLFVAAIICCGDRPGLLNVGHIEKMQEGIVHVLRLHLQSNHPDDIFLFPKLLQKMADLRQLVTEHAQLVQIIKKTESDAALHPLLQEIYRDMY
  
Inhibitor
Name:
BDBM50248411
Synonyms:
5-(4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)phenyl)-2-phenyl-2H-1,2,3-triazole-4-carboxylic acid | CHEMBL489506
Type:
Small organic molecule
Emp. Form.:
C27H22N4O4
Mol. Mass.:
466.488
SMILES:
Cc1oc(nc1CCOc1ccc(cc1)-c1nn(nc1C(O)=O)-c1ccccc1)-c1ccccc1
Structure:
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