Reaction Details |
| Report a problem with these data |
Target | Peroxisome proliferator-activated receptor alpha |
---|
Ligand | BDBM50312453 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_620646 (CHEMBL1114854) |
---|
EC50 | >10000±n/a nM |
---|
Citation | Epple, R; Cow, C; Xie, Y; Azimioara, M; Russo, R; Wang, X; Wityak, J; Karanewsky, DS; Tuntland, T; Nguyêñ-Trân, VT; Cuc Ngo, C; Huang, D; Saez, E; Spalding, T; Gerken, A; Iskandar, M; Seidel, HM; Tian, SS Novel bisaryl substituted thiazoles and oxazoles as highly potent and selective peroxisome proliferator-activated receptor delta agonists. J Med Chem53:77-105 (2010) [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 | 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: | MVDTESPLCPLSPLEAGDLESPLSEEFLQEMGNIQEISQSIGEDSSGSFGFTEYQYLGSC
PGSDGSVITDTLSPASSPSSVTYPVVPGSVDESPSGALNIECRICGDKASGYHYGVHACE
GCKGFFRRTIRLKLVYDKCDRSCKIQKKNRNKCQYCRFHKCLSVGMSHNAIRFGRMPRSE
KAKLKAEILTCEHDIEDSETADLKSLAKRIYEAYLKNFNMNKVKARVILSGKASNNPPFV
IHDMETLCMAEKTLVAKLVANGIQNKEAEVRIFHCCQCTSVETVTELTEFAKAIPGFANL
DLNDQVTLLKYGVYEAIFAMLSSVMNKDGMLVAYGNGFITREFLKSLRKPFCDIMEPKFD
FAMKFNALELDDSDISLFVAAIICCGDRPGLLNVGHIEKMQEGIVHVLRLHLQSNHPDDI
FLFPKLLQKMADLRQLVTEHAQLVQIIKKTESDAALHPLLQEIYRDMY
|
|
|
BDBM50312453 |
---|
n/a |
---|
Name | BDBM50312453 |
Synonyms: | 2-(4-(4,5-Bis(4-methoxyphenyl)thiazol-2-ylthio)-3-chlorophenyl)acetic Acid | CHEMBL1081044 |
Type | Small organic molecule |
Emp. Form. | C25H20ClNO5S2 |
Mol. Mass. | 514.013 |
SMILES | COc1ccc(cc1)-c1nc(Sc2ccc(OCC(O)=O)cc2Cl)sc1-c1ccc(OC)cc1 |
Structure |
|