Epanorin

Epanorin
Names
IUPAC name
(1R,2R,13S,15R,16R,23R)-7,9,21-triazahexacyclo[11.9.1.11,15.02,7.09,23.016,21]tetracosane
Other names
CHEBI:144243
Identifiers
3D model (JSmol)
ChEBI
  • InChI=1S/C25H25NO6/c1-15(2)14-18(24(29)31-3)26-23(28)20(17-12-8-5-9-13-17)22-21(27)19(25(30)32-22)16-10-6-4-7-11-16/h4-13,15,18,27H,14H2,1-3H3,(H,26,28)/b22-20-/t18-/m0/s1
    Key: IBSRGCBHIASQMQ-BKBKCADHSA-N
  • CC(C)C[C@@H](C(=O)OC)NC(=O)C(=C1C(=C(C(=O)O1)C2=CC=CC=C2)O)C3=CC=CC=C3
Properties
C25H25NO6
Molar mass 435.476 g·mol−1
Melting point 162–163 °C (324–325 °F; 435–436 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Epanorin is a lichen secondary metabolite with the molecular formula C25H25NO6.[2] Epanorin inhibits the proliferation of MCF-7 cancer cells.[2]

References

  1. ^ "Epanorin,18463-10-0 - LookChemical.com". www.lookchemical.com.
  2. ^ a b Palacios-Moreno, Juan; Rubio, Cecilia; Quilhot, Wanda; Cavieres, M. Fernanda; de la Peña, Eduardo; Quiñones, Natalia V.; Díaz, Hugo; Carrión, Flavio; Henríquez-Roldán, Carlos F.; Weinstein-Oppenheimer, Caroline R. (December 2019). "Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cells". Biological Research. 52 (1): 55. doi:10.1186/s40659-019-0261-4. PMC 6786276. PMID 31601259.

Further reading

  • Issues in Life Sciences: Botany and Plant Biology Research: 2011 Edition. ScholarlyEditions. 9 January 2012. ISBN 978-1-4649-6343-8.
  • Der Stoffwechsel Sekundärer Pflanzenstoffe / The Metabolism of Secondary Plant Products. Springer Science & Business Media. 11 November 2013. p. 572. ISBN 978-3-662-26784-4.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.