甲氧基万寿菊素

Axillarin
	IUPAC名; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4H-1-benzopyran-4-one
别名	2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4H-chromen-4-one; DMQT; 3,6-Dimethoxyquercetagetin; Quercetagetin 3,6-dimethyl ether; 3',4',5,7-Tetrahydroxy-3,6-dimethoxyflavone;
识别
CAS号	5188-73-8
PubChem	5281603
ChemSpider	4444922
SMILES	COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O;
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;
InChIKey	KIGVXRGRNLQNNI-UHFFFAOYAX
ChEBI	2941
性质
化学式	C17H14O8
摩尔质量	346.29 g·mol−1
密度	1.659 g/mL
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

甲氧基万寿菊素（英語：Axillarin，也称为5,7,3',4'-四羟基-3,6-二甲氧基黄酮，3′,4′,5,7-Tetrahydroxy-3,6-dimethoxyflavone，或栎草亭-3,6-二甲醚，Quercetagetin 3,6-dimethyl ether）是一种天然的栎草亭衍生O-甲基化黄酮，分子式C₁₇H₁₄O₈，存在于线叶菊（Filifolium sibiricum）^[1]、菊蒿（Tanacetum vulgare）^[2]等植物中，能人工合成^[3]。

参考文献

^ Jung Park, Eun; Kim, Youngleem; Kim, Jinwoong. Acylated Flavonol Glycosides from the Flower ofInula britannica. Journal of Natural Products. 2000, 63 (1): 34–36. PMID 10650074. doi:10.1021/np990271r.
^ Álvarez, Ángel L.; Habtemariam Solomon; Juan-Badaturuge Malindra; Jackson Caroline; Parra Francisco. 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 (Submitted manuscript). 2011, 25 (2): 296–301. PMID 21171142. S2CID 9011931. doi:10.1002/ptr.3382.
^ Fukui, K.; Nakayama, M.; Horie, T. The syntheses of axillarin and its related compounds. Experientia. 1968, 24 (8): 769–770. S2CID 33789154. doi:10.1007/BF02144856.

[1] Jung Park, Eun; Kim, Youngleem; Kim, Jinwoong. Acylated Flavonol Glycosides from the Flower ofInula britannica. Journal of Natural Products. 2000, 63 (1): 34–36. PMID 10650074. doi:10.1021/np990271r.

[Parral-2] Álvarez, Ángel L.; Habtemariam Solomon; Juan-Badaturuge Malindra; Jackson Caroline; Parra Francisco. 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 (Submitted manuscript). 2011, 25 (2): 296–301. PMID 21171142. S2CID 9011931. doi:10.1002/ptr.3382.

[3] Fukui, K.; Nakayama, M.; Horie, T. The syntheses of axillarin and its related compounds. Experientia. 1968, 24 (8): 769–770. S2CID 33789154. doi:10.1007/BF02144856.

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