| Reaction Details |
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 | Report a problem with these data |
| Target | Peroxisome proliferator-activated receptor alpha |
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| Ligand | BDBM50266550 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_544081 (CHEMBL1019541) |
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| EC50 | 1±n/a nM |
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| Citation |  Yu, J; Tang, L; Yang, Y; Ji, R Synthesis and evaluation of a series of benzopyran derivatives as PPAR alpha/gamma agonists. Eur J Med Chem43:2428-35 (2008) [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 |
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| 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) |
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| Type: | Enzyme |
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| Mol. Mass.: | 52222.08 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Q07869 |
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| Residue: | 468 |
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| Sequence: | MVDTESPLCPLSPLEAGDLESPLSEEFLQEMGNIQEISQSIGEDSSGSFGFTEYQYLGSC
PGSDGSVITDTLSPASSPSSVTYPVVPGSVDESPSGALNIECRICGDKASGYHYGVHACE
GCKGFFRRTIRLKLVYDKCDRSCKIQKKNRNKCQYCRFHKCLSVGMSHNAIRFGRMPRSE
KAKLKAEILTCEHDIEDSETADLKSLAKRIYEAYLKNFNMNKVKARVILSGKASNNPPFV
IHDMETLCMAEKTLVAKLVANGIQNKEAEVRIFHCCQCTSVETVTELTEFAKAIPGFANL
DLNDQVTLLKYGVYEAIFAMLSSVMNKDGMLVAYGNGFITREFLKSLRKPFCDIMEPKFD
FAMKFNALELDDSDISLFVAAIICCGDRPGLLNVGHIEKMQEGIVHVLRLHLQSNHPDDI
FLFPKLLQKMADLRQLVTEHAQLVQIIKKTESDAALHPLLQEIYRDMY
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| BDBM50266550 |
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| n/a |
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| Name | BDBM50266550 |
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| Synonyms: | CHEMBL456912 | Methyl 7-(2-(5-methyl-2-p-tolyloxazol-4-yl)ethoxy)-2-oxo-2H-chromene-3-carboxylate |
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| Type | Small organic molecule |
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| Emp. Form. | C24H21NO6 |
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| Mol. Mass. | 419.4266 |
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| SMILES | COC(=O)c1cc2ccc(OCCc3nc(oc3C)-c3ccc(C)cc3)cc2oc1=O |
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| Structure | 
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