| Identification | Back Directory | [Name]
Eupatoriochromene | [CAS]
19013-03-7 | [Synonyms]
Demethylencecalin
Eupatoriochromene
Des-O-methylencecalin
1-(7-hydroxy-2,2-dimethylchromen-6-yl)ethanone
6-Acetyl-7-hydroxy-2,2-dimethyl-2H-1-benzopyran
1-(2,2-Dimethyl-7-hydroxy-α-chromene-6-yl)ethanone
Methyl(2,2-dimethyl-7-hydroxy-2H-1-benzopyran-6-yl) ketone
Ethanone,1-(7-hydroxy-2,2-dimethyl-2H-1- benzopyran-6-yl)- | [Molecular Formula]
C13H14O3 | [MDL Number]
MFCD00597242 | [MOL File]
19013-03-7.mol | [Molecular Weight]
218.25 |
| Chemical Properties | Back Directory | [Melting point ]
80 °C | [Boiling point ]
366.7±42.0 °C(Predicted) | [density ]
1.154±0.06 g/cm3(Predicted) | [form ]
Off-white to yellowish solid. | [pka]
9.92±0.40(Predicted) | [LogP]
4.150 (est) |
| Hazard Information | Back Directory | [Uses]
Eupatoriochromene is a chromene and has inhibitory activity against xanthine oxidase (XO)[1][2]. | [Definition]
ChEBI: Eupatoriochromene is a 1-benzopyran. | [References]
[1] G B Merrill?. Eupatoriochromene and encecalin, plant growth regulators from yellow starthistle (Centaurea solstitialis L.). J Chem Ecol.?1989 Jul;15(7):2073-87. DOI:10.3389/fnut.2021.737157
[2] Xin-Sheng Liu, et al. Chemical Compounds, Antioxidant Activities, and Inhibitory Activities Against Xanthine Oxidase of the Essential Oils From the Three Varieties of Sunflower ( Helianthus annuus L.) Receptacles. Front Nutr. 2021 Nov 19;8:737157. DOI:10.3389/fnut.2021.737157 |
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