Reaction Details |
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Target | Peroxisome proliferator-activated receptor alpha |
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Ligand | BDBM50531655 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1920580 (CHEMBL4423425) |
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EC50 | >10000±n/a nM |
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Citation | Li, Z; Chen, Y; Zhou, Z; Deng, L; Xu, Y; Hu, L; Liu, B; Zhang, L Discovery of first-in-class thiazole-based dual FFA1/PPAR? agonists as potential anti-diabetic agents. Eur J Med Chem164:352-365 (2019) [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 | 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
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BDBM50531655 |
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n/a |
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Name | BDBM50531655 |
Synonyms: | CHEMBL4579901 |
Type | Small organic molecule |
Emp. Form. | C22H18F3NO4S |
Mol. Mass. | 449.443 |
SMILES | Cc1nc(sc1COc1ccc2[C@H](CC(O)=O)COc2c1)-c1ccc(cc1)C(F)(F)F |r| |
Structure |
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