Reaction Details |
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Target | Peroxisome proliferator-activated receptor gamma |
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Ligand | BDBM50574985 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2123732 (CHEMBL4832965) |
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EC50 | 1323±n/a nM |
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Citation | Li, Z; Ren, Q; Zhou, Z; Cai, Z; Wang, B; Han, J; Zhang, L Discovery of the first-in-class dual PPAR?/? partial agonist for the treatment of metabolic syndrome. Eur J Med Chem225:0 (2021) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Peroxisome proliferator-activated receptor gamma |
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Name: | Peroxisome proliferator-activated receptor gamma |
Synonyms: | NR1C3 | Nuclear receptor subfamily 1 group C member 3 | PPAR-gamma | PPARG | PPARG_HUMAN | Peroxisome proliferator-activated receptor | Peroxisome proliferator-activated receptor gamma (PPAR gamma) | Peroxisome proliferator-activated receptor gamma (PPARG) | Peroxisome proliferator-activated receptor gamma (PPARĪ³) | Peroxisome proliferator-activated receptor gamma/Nuclear receptor corepressor 2 | peroxisome proliferator-activated receptor gamma isoform 2 |
Type: | Nuclear Receptor |
Mol. Mass.: | 57613.46 |
Organism: | Homo sapiens (Human) |
Description: | P37231 |
Residue: | 505 |
Sequence: | MGETLGDSPIDPESDSFTDTLSANISQEMTMVDTEMPFWPTNFGISSVDLSVMEDHSHSF
DIKPFTTVDFSSISTPHYEDIPFTRTDPVVADYKYDLKLQEYQSAIKVEPASPPYYSEKT
QLYNKPHEEPSNSLMAIECRVCGDKASGFHYGVHACEGCKGFFRRTIRLKLIYDRCDLNC
RIHKKSRNKCQYCRFQKCLAVGMSHNAIRFGRMPQAEKEKLLAEISSDIDQLNPESADLR
ALAKHLYDSYIKSFPLTKAKARAILTGKTTDKSPFVIYDMNSLMMGEDKIKFKHITPLQE
QSKEVAIRIFQGCQFRSVEAVQEITEYAKSIPGFVNLDLNDQVTLLKYGVHEIIYTMLAS
LMNKDGVLISEGQGFMTREFLKSLRKPFGDFMEPKFEFAVKFNALELDDSDLAIFIAVII
LSGDRPGLLNVKPIEDIQDNLLQALELQLKLNHPESSQLFAKLLQKMTDLRQIVTEHVQL
LQVIKKTETDMSLHPLLQEIYKDLY
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BDBM50574985 |
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n/a |
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Name | BDBM50574985 |
Synonyms: | CHEMBL4852747 |
Type | Small organic molecule |
Emp. Form. | C21H20O6 |
Mol. Mass. | 368.3799 |
SMILES | CCOc1ccc2C(=O)\C(Oc2c1)=C\c1cc(C)c(OCC(O)=O)c(C)c1 |
Structure |
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