Reaction Details |
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Target | Peroxisome proliferator-activated receptor gamma |
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Ligand | BDBM50320885 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_636347 (CHEMBL1169070) |
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Ki | 43600±n/a nM |
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Citation | Barros, CD; Amato, AA; de Oliveira, TB; Iannini, KB; Silva, AL; Silva, TG; Leite, ES; Hernandes, MZ; Alves de Lima, Mdo C; Galdino, SL; Neves, Fde A; Pitta, Ida R Synthesis and anti-inflammatory activity of new arylidene-thiazolidine-2,4-diones as PPARgamma ligands. Bioorg Med Chem18:3805-11 (2010) [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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BDBM50320885 |
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n/a |
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Name | BDBM50320885 |
Synonyms: | 5-Bipheny-4-ylmethylene-3-(3-chloro-benzyl)-thiazolidine-2,4-dione | CHEMBL1165451 |
Type | Small organic molecule |
Emp. Form. | C23H16ClNO2S |
Mol. Mass. | 405.897 |
SMILES | Clc1cccc(CN2C(=O)S\C(=C/c3ccc(cc3)-c3ccccc3)C2=O)c1 |
Structure |
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