1790089-97-2

LXRα agonist 1 Chemical Structure
1790089-97-2

Chemical Structure

LXRα agonist 1

  • CAS No.: 1790089-97-2
  • Formula:C28H27N3O2
  • Molecular Weight:437.53

InChIKey: XNAXGNVKNMAHSV-UHFFFAOYSA-N

SMILES: O=C(C(C1=CC=CC=C1)=C2NC3=CC=C(N4CCCCC4)C=C3)N(CC5=CC=CC=C5)C2=O

Biological Activity: LXRα agonist 1 is a selective LXRα agonist, with EC50 values of 42 nM and 266 nM against purified LXRα and LXRβ, respectively. LXRα agonist 1 acts as a lipotoxicity inducer, triggering the production of toxic saturated fatty acids in tumor cells, and induces lipotoxicity-mediated cancer cell death when combined with the Raf inhibitor Sorafenib (HY-10201). LXRα agonist 1 can be used in the research of hepatocellular carcinoma[1].

Cat. No. Nom du produit Pureté Description Pricing
HY-173393
LXRα agonist 1 LXRα agonist 1 is a selective LXRα agonist, with EC50 values of 42 nM and 266 nM against purified LXRα and LXRβ, respectively. LXRα agonist 1 acts as a lipotoxicity inducer, triggering the production of toxic saturated fatty acids in tumor cells, and induces lipotoxicity-mediated cancer cell death when combined with the Raf inhibitor Sorafenib (HY-10201). LXRα agonist 1 can be used in the research of hepatocellular carcinoma.
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