- Axillarin
-
Axillarin 
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxychromen-4-oneOther namesDMQT
3,6-Dimethoxyquercetagetin
Quercetagetin 3,6-dimethyl ether
3',4',5,7-Tetrahydroxy-3,6-dimethoxyflavoneIdentifiers CAS number 5188-73-8 
=PubChem 5281603 ChemSpider 4444922 Jmol-3D images Image 1 - COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O
- InChI=1S/C17H14O8/c1-23-16-10(20)6-11-12(13(16)21)14(22)17(24-2)15(25-11)7-3-4-8(18)9(19)5-7/h3-6,18-21H,1-2H3
Key: KIGVXRGRNLQNNI-UHFFFAOYSA-N
InChI=1/C17H14O8/c1-23-16-10(20)6-11-12(13(16)21)14(22)17(24-2)15(25-11)7-3-4-8(18)9(19)5-7/h3-6,18-21H,1-2H3
Key: KIGVXRGRNLQNNI-UHFFFAOYAX
Properties Molecular formula C17H14O8 Molar mass 346.28 g/mol Exact mass 346.068867 u 
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Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references Axillarin is an O-methylated flavonol. It can be found in Pulicaria crispa, Filifolium sibiricum, Inula britannica[1], Wyethia bolanderi in Balsamorhiza macrophylla[2] and in Tanacetum vulgare [3]. It can also be synthetized[4].
Glycosides
Axillarin 7-O-β-D-glucoside can be found in Tagetes mendocina, a medicinal plant widely used in the Andean provinces of Argentina[5].
References
- ^ Acylated Flavonol Glycosides from the Flower of Inula britannica. Eun Jung Park, Youngleem Kim, and Jinwoong Kim, J. Nat. Prod., 2000, 63 (1), pp 34–36
- ^ Methylated flavonols from Wyethia bolanderi and Balsamorhiza macrophylla. Susan McCormick, Kathleen Robson and Bruce Bohm, Phytochemistry, Volume 24, Issue 9, 1985, Page 2133
- ^ Álvarez, Ángel L.; Habtemariam Solomon, Juan-Badaturuge Malindra, Jackson Caroline, and Parra Francisco. (2011). "In vitro anti HSV-1 and HSV-2 activity of Tanacetum vulgare extracts and isolated compounds: An approach to their mechanisms of action". Phytotherapy Research 25 (2): 296–301. doi:10.1002/ptr.3382.
- ^ The syntheses of axillarin and its related compounds. K. Fukui, M. Nakayama and T. Horie, Cellular and Molecular Life Sciences, Volume 24, Number 8 / august 1968, Pages 769-770
- ^ Free Radical Scavengers and Antioxidants from Tagetes mendocina. Guillermo Schmeda-Hirschmann, Alejandro Tapia, Cristina Theoduloz, Jaime Rodrıguez, Susana Lopez and Gabriela Egly Feresin.
Backbone Aglycones3-Hydroxyflavone (synthetic) and derivativesFlavonols AglyconesFisetin | Galangin | Gossypetin | Herbacetin | Kaempferol | Morin | Myricetin | Quercetagetin | QuercetinGlycosidesAstragalin | CTN-986 | Eupalin | Guaijaverin (quercetin 3-O-arabinoside) | Heliosin (Quercetin 3-digalactoside) | Hyperoside | Isoquercitin | Kaempferitrin | Myricetin 3-O-rutinoside | Myricitrin | Quercetin-3-sophorodide | Quercitrin | Rhodionin | Rhodiosin | Robinin | Rutin | SpiraeosideO-Methylated flavonols Aglycones5-O-methylmyricetin | Annulatin | Ayanin | Axillarin | Azaleatin | Brickellin | Centaureidin | Chrysosplenetin | Combretol | Ermanin | Eupatolitin | Eupalitin | Europetin | Isorhamnetin | Jaceidin | Kaempferide | Kumatakenin | Laricitrin | Natsudaidain | Ombuin | Pachypodol | Patuletin | Retusin | Mearnsetin | Rhamnazin | Rhamnetin | Santin | Spinacetin | Syringetin | TamarixetinGlycosidesAzalein | Centaurein | Eupatolin | Jacein | Patulitrin | Tamarixetin 7-rutinoside | XanthorhamninDerivative flavonols GlycosidesAmurensin | Icariin | Rutin SPyranoflavonols AglyconesKaranjachromeneFuranoflavonols AglyconesKaranjinGlycosidesPongamoside A, B and CSemisynthetic Glycosides
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