Reaction Details |
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Target | Oxysterols receptor LXR-alpha [197-447] |
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Ligand | BDBM26075 |
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Substrate/Competitor | BDBM19993 |
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Meas. Tech. | LXR Binding Assay and hLXR Reporter Assay |
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IC50 | 465±n/a nM |
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EC50 | 15830±n/a nM |
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Citation | Wrobel, J; Steffan†, R; Bowen, SM; Magolda, R; Matelan†, E; Unwalla†, R; Basso, M; Clerin, V; Gardell, SJ; Nambi, P; Quinet, E; Reminick, JI; Vlasuk, GP; Wang, S; Feingold, I; Huselton, C; Bonn, T Indazole-Based Liver X Receptor (LXR) Modulators with Maintained Atherosclerotic Lesion Reduction Activity but Diminished Stimulation of Hepatic Triglyceride Synthesis J Med Chem51:7161-8 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Oxysterols receptor LXR-alpha [197-447] |
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Name: | Oxysterols receptor LXR-alpha [197-447] |
Synonyms: | LXRA | Liver X Receptor alpha (LXR-alpha) | NR1H3 | NR1H3_HUMAN | Nuclear orphan receptor LXR-alpha | Nuclear receptor subfamily 1 group H member 3 | Oxysterols receptor LXR-alpha |
Type: | Receptor |
Mol. Mass.: | 28986.41 |
Organism: | Homo sapiens (Human) |
Description: | LXR alpha ligand binding domain (amino acid residues 197-447) with an N-terminal biotinylation tag expressed in E.coli, was used for the binding assays. |
Residue: | 251 |
Sequence: | SSPPQILPQLSPEQLGMIEKLVAAQQQCNRRSFSDRLRVTPWPMAPDPHSREARQQRFAH
FTELAIVSVQEIVDFAKQLPGFLQLSREDQIALLKTSAIEVMLLETSRRYNPGSESITFL
KDFSYNREDFAKAGLQVEFINPIFEFSRAMNELQLNDAEFALLIAISIFSADRPNVQDQL
QVERLQHTYVEALHAYVSIHHPHDRLMFPRMLMKLVSLRTLSSVHSEQVFALRLQDKKLP
PLLSEIWDVHE
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BDBM26075 |
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BDBM19993 |
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Name | BDBM26075 |
Synonyms: | 2-benzyl-3-aryl-7-trifluoromethylindazole, 21 | 3-(4-chlorophenyl)-7-(trifluoromethyl)-2-{[2-(trifluoromethyl)phenyl]methyl}-2H-indazole |
Type | Small organic molecule |
Emp. Form. | C22H13ClF6N2 |
Mol. Mass. | 454.795 |
SMILES | FC(F)(F)c1ccccc1Cn1nc2c(cccc2c1-c1ccc(Cl)cc1)C(F)(F)F |
Structure |
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