2. Natural Products
  3. Plants Phenylpropanoids
  4. Putranjivaceae Lignans
  5. Drypetes littoralis (C. B. Rob.) Merr.
  6. 479-20-9

479-20-9

Atranorin Chemical Structure

479-20-9

Chemical Structure

  • Atranorin
  • CAS No: 479-20-9
    Formula: C19H18O8
    Molecular Weight: 374.34
  • IUPAC Name: 3-hydroxy-4-(methoxycarbonyl)-2,5-dimethylphenyl 3-formyl-2,4-dihydroxy-6-methylbenzoate
  • InChIKey: YLOYKYXNDHOHHT-UHFFFAOYSA-N
  • SMILES: O=C(OC1=CC(C)=C(C(OC)=O)C(O)=C1C)C2=C(C)C=C(O)C(C=O)=C2O

Biological Activity: Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2].

Cat. No. Product Name Purity Description
HY-N2907 Atranorin 99.68% Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity.
HY-N2907R Atranorin (Standard) ≥98% Atranorin (Standard) is the analytical standard of Atranorin. This product is intended for research and analytical applications. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity.

References

[1]. Studzinska-Sroka E, et al. Atranorin - An Interesting Lichen Secondary Metabolite. Mini Rev Med Chem. 2017;17(17):1633-1645. [Content Brief]
[2]. Zhou R, et al. The lichen secondary metabolite atranorin suppresses lung cancer cell motility and tumorigenesis. Sci Rep. 2017 Aug 15;7(1):8136. [Content Brief]

Keywords:

AtranorinAtranorin (Standard)