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
CAS Number	18463-10-0 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:144243;
PubChem CID	101710315;
	InChI 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;
	SMILES 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
Chemical formula	C25H25NO6
Molar mass	435.476 g·mol−1
Melting point	162–163 °C (324–325 °F; 435–436 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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

References[edit]

^ "Epanorin,18463-10-0 - LookChemical.com". www.lookchemical.com.
^ ^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.

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.

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