Reaction Details |
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Target | Peroxisome proliferator-activated receptor alpha |
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Ligand | BDBM28699 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_153485 (CHEMBL761650) |
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EC50 | 51000±n/a nM |
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Citation | Willson, TM; Cobb, JE; Cowan, DJ; Wiethe, RW; Correa, ID; Prakash, SR; Beck, KD; Moore, LB; Kliewer, SA; Lehmann, JM The structure-activity relationship between peroxisome proliferator-activated receptor gamma agonism and the antihyperglycemic activity of thiazolidinediones. J Med Chem39:665-8 (1996) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Peroxisome proliferator-activated receptor alpha |
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Name: | Peroxisome proliferator-activated receptor alpha |
Synonyms: | Nr1c1 | Nuclear receptor subfamily 1 group C member 1 | PPAR-alpha | PPARA_MOUSE | Peroxisome Proliferator-Activated Receptor alpha | Ppar | Ppara |
Type: | PROTEIN |
Mol. Mass.: | 52343.28 |
Organism: | Mus musculus |
Description: | ChEMBL_572395 |
Residue: | 468 |
Sequence: | MVDTESPICPLSPLEADDLESPLSEEFLQEMGNIQEISQSIGEESSGSFGFADYQYLGSC
PGSEGSVITDTLSPASSPSSVSCPVIPASTDESPGSALNIECRICGDKASGYHYGVHACE
GCKGFFRRTIRLKLVYDKCDRSCKIQKKNRNKCQYCRFHKCLSVGMSHNAIRFGRMPRSE
KAKLKAEILTCEHDLKDSETADLKSLGKRIHEAYLKNFNMNKVKARVILAGKTSNNPPFV
IHDMETLCMAEKTLVAKMVANGVEDKEAEVRFFHCCQCMSVETVTELTEFAKAIPGFANL
DLNDQVTLLKYGVYEAIFTMLSSLMNKDGMLIAYGNGFITREFLKNLRKPFCDIMEPKFD
FAMKFNALELDDSDISLFVAAIICCGDRPGLLNIGYIEKLQEGIVHVLKLHLQSNHPDDT
FLFPKLLQKMVDLRQLVTEHAQLVQVIKKTESDAALHPLLQEIYRDMY
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BDBM28699 |
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n/a |
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Name | BDBM28699 |
Synonyms: | 2-(4-chlorophenoxy)-2-methylpropanoic acid | CHEMBL683 | Clofibrate | Clofibrinic acid | clofibric acid |
Type | Small organic molecule |
Emp. Form. | C10H11ClO3 |
Mol. Mass. | 214.646 |
SMILES | CC(C)(Oc1ccc(Cl)cc1)C(O)=O |
Structure |
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