Reaction Details |
| Report a problem with these data |
Target | Peroxisome proliferator-activated receptor gamma |
---|
Ligand | BDBM50290272 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEBML_154360 |
---|
Ki | >10000±n/a nM |
---|
Citation | Tomkinson, NC; Sefler, AM; Plunket, KD; Blanchard, SG; Parks, DJ; Willson, TM Solid-phase synthesis of hybrid thiazolidinedione-fatty acid PPARγ ligands Bioorg Med Chem Lett7:2491-2496 (1997) Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Peroxisome proliferator-activated receptor gamma |
---|
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
|
|
|
BDBM50290272 |
---|
n/a |
---|
Name | BDBM50290272 |
Synonyms: | (E)-Pent-3-enoic acid {2-[4-(2,4-dioxo-thiazolidin-5-ylmethyl)-phenoxy]-ethyl}-amide | CHEMBL79557 |
Type | Small organic molecule |
Emp. Form. | C17H20N2O4S |
Mol. Mass. | 348.417 |
SMILES | C\C=C\CC(=O)NCCOc1ccc(Cc2sc(=O)[nH]c2O)cc1 |
Structure |
|