Reaction Details | |||
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Target | Oxysterols receptor LXR-beta | ||
Ligand | BDBM50172188 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_321167 (CHEMBL882896) | ||
IC50 | 100±n/a nM | ||
Citation | Liu, W; Chen, S; Dropinski, J; Colwell, L; Robins, M; Szymonifka, M; Hayes, N; Sharma, N; MacNaul, K; Hernandez, M; Burton, C; Sparrow, CP; Menke, JG; Singh, SB Design, synthesis, and structure-activity relationship of podocarpic acid amides as liver X receptor agonists for potential treatment of atherosclerosis. Bioorg Med Chem Lett15:4574-8 (2005) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Oxysterols receptor LXR-beta | |||
Name: | Oxysterols receptor LXR-beta | ||
Synonyms: | LXRB | Liver X receptor beta (NR1H2) | Liver X, LXR beta | NER | NR1H2 | NR1H2_HUMAN | Nuclear receptor NER | UNR | Ubiquitously-expressed nuclear receptor | ||
Type: | Enzyme Catalytic Domain | ||
Mol. Mass.: | 50978.79 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P55055 | ||
Residue: | 460 | ||
Sequence: |
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BDBM50172188 | |||
n/a | |||
Name | BDBM50172188 | ||
Synonyms: | (4S,4aR)-6-Hydroxy-4a-methyl-1-(S)-methyl-1,2,3,4,4a,9,10,10a-octahydro-phenanthrene-1-carboxylic acid adamantan-2-ylamide | CHEMBL194409 | ||
Type | Small organic molecule | ||
Emp. Form. | C27H37NO2 | ||
Mol. Mass. | 407.5882 | ||
SMILES | C[C@@]1(CCC[C@@]2(C)[C@H]1CCc1ccc(O)cc21)C(=O)NC1C2CC3CC(C2)CC1C3 |wU:1.19,7.8,5.5,wD:1.0,TLB:19:20:23.22.29:25.26.27,19:20:27:23.29.24,22:23:20.21.26:27,THB:24:23:20:25.26.27,24:25:20:23.22.29,22:21:27:23.29.24,(4.72,-6.63,;3.97,-5.3,;2.62,-4.51,;2.64,-2.96,;4,-2.2,;5.32,-2.99,;5.3,-1.45,;5.3,-4.53,;6.63,-5.3,;7.99,-4.53,;7.98,-2.99,;9.32,-2.22,;9.32,-.68,;7.98,.09,;7.96,1.63,;6.65,-.68,;6.65,-2.22,;2.88,-6.37,;1.38,-5.98,;2.97,-7.91,;1.69,-8.76,;.15,-8.73,;-.65,-10.04,;.1,-11.39,;.08,-12.93,;1.17,-11.86,;.5,-10.23,;2.67,-11.49,;2.43,-10.1,;1.64,-11.42,)| | ||
Structure |