Irilona

Irilona
Nombre IUPAC
	9-hydroxy-7-(4-hydroxyphenyl)-[1,3]dioxolo[4,5-g]chromen-8-one
General
Fórmula estructural
Fórmula molecular	C16H10O6
Identificadores
Número CAS	41653-81-0
ChEBI	5970
ChEMBL	CHEMBL3527329
ChemSpider	4445092
PubChem	5281779
UNII	FB3FTT7LYK
KEGG	C10467
	SMILES C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=CC=C(C=C4)O)O
	InChI InChI=InChI=1S/C16H10O6/c17-9-3-1-8(2-4-9)10-6-20-11-5-12-16(22-7-21-12)15(19)13(11)14(10)18/h1-6,17,19H,7H2; Key: NUGRQNBDTZWXTP-UHFFFAOYSA-N
Propiedades físicas
Masa molar	298.24 g/mol g/mol
	Valores en el SI y en condiciones estándar; (25 ℃ y 1 atm), salvo que se indique lo contrario.
	[editar datos en Wikidata]

Irilona es una isoflavona, un tipo de flavonoide. Se puede encontrar en Trifolium pratense (trébol rojo),^[2] in Iris unguicularis^[3] y en Iris germanica.^[4]

Referencias

↑ Número CAS
↑ «The red clover isoflavone irilone is largely resistant to degradation by the human gut microbiota. Annett Braune, Ronald Maul, Nils Helge Schebb, Sabine E. Kulling and Michael Blaut, Molecular Nutrition & Food Research, 8 Dec 2009». Archivado desde el original el 5 de enero de 2013. Consultado el 21 de agosto de 2014.
↑ New and Known Constituents from Iris unguicularis and Their Antioxidant Activity. Atta-ur-Rahman, Sumaira Hareem, M. Iqbal Choudhary, Bilge Sener, Ahmed Abbaskhan, Hina Siddiqui, Shazia Anjum, Ilkay Orhan, Ilhan Gurbuz and Filiz Ayanoglu, HeteroCycles, 2010, Special issue, Vol 82, No. 1, pages 813-824, doi 10.3987/COM-10-S(E)6
↑ Lipase-catalyzed regioselective protection/deprotection of hydroxyl groups of the isoflavone irilone isolated from Iris germanica. Nighat Nazir, Surrinder Koul, Mushtaq Ahmad Qurishi, Subhash Chandra Taneja and Ghulam Nabi Qazi, Biocatalysis and Biotransformation, 2 December 2008, 1029-2446, Volume 27, Issue 2, Pages 118–123, INIST|21235726