245523-67-5
Chemical Structure
7α,24(S)-Dihydroxycholesterol
Synonym(s): (3β,7α,24S)-Cholest-5-ene-3,7,24-triol
- CAS No.: 245523-67-5
- Formula:C27H46O3
- Molecular Weight:418.65
IUPAC Name: (3S,7S,8S,9S,10R,13R,14S,17R)-17-((2R,5S)-5-hydroxy-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol
InChIKey: ZNCHPOYZMVVJCK-LIZWOPGQSA-N
SMILES: C[C@@]12[C@](CC[C@]2([H])[C@H](C)CC[C@H](O)C(C)C)([H])[C@@]3([H])[C@@](CC1)([H])[C@@]4(C(C[C@H](CC4)O)=C[C@H]3O)C
Biological Activity: 7α,24(S)-Dihydroxycholesterol ((3β,7α,24S)-Cholest-5-ene-3,7,24-triol) serves as a ligand for liver X receptor (LXR), binding specifically to the ligand binding domains of both LXRα and LXRβ. This compound is synthetically produced from E-α,β-enone, utilizing Arsonium ylide and J-tert-butyldimethylsilyloxy-bisnor-5-cholenaldehyde as starting materials, followed by a series of transformations to yield 7α,24(S)-dihydroxycholesterol.
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7α,24(S)-Dihydroxycholesterol | 7α,24(S)-Dihydroxycholesterol ((3β,7α,24S)-Cholest-5-ene-3,7,24-triol) serves as a ligand for liver X receptor (LXR), binding specifically to the ligand binding domains of both LXRα and LXRβ. This compound is synthetically produced from E-α,β-enone, utilizing Arsonium ylide and J-tert-butyldimethylsilyloxy-bisnor-5-cholenaldehyde as starting materials, followed by a series of transformations to yield 7α,24(S)-dihydroxycholesterol. | |||||||||||||||||||||
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