| Identification | Back Directory | [Name]
eupatilin | [CAS]
22368-21-4 | [Synonyms]
eupatilin
NSC 122413
Eupatilin, BR
Eupatilin 22368-21-4
5,7-Dihydroxy-3',4',6-trimethoxyflavone
2-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-6-methoxychromen-4-one
2-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-6-methoxy-4H-chromen-4-one
2-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-6-methoxy-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 2-(3,4-diMethoxyphenyl)-5,7-dihydroxy-6-Methoxy-
Eupatilin
2-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-6-methoxychromen-4-one
2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxy-4H-chromen-4-one (EUPATILIN) | [Molecular Formula]
C18H16O7 | [MDL Number]
MFCD13194819 | [MOL File]
22368-21-4.mol | [Molecular Weight]
344.31 |
| Chemical Properties | Back Directory | [Melting point ]
236-238 °C | [Boiling point ]
583.6±50.0 °C(Predicted) | [density ]
1.387±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Store in freezer, under -20°C | [solubility ]
Acetonitrile (Slightly), DMSO (Slightly), Methanol (Slightly, Heated) | [form ]
Solid | [pka]
6.47±0.40(Predicted) | [color ]
Pale Beige | [Stability:]
Hygroscopic |
| Hazard Information | Back Directory | [Uses]
Eupatilin maintains anticoagulant and antiplatelet activity isolated from the Artemisia princeps Pampanini flower. | [Definition]
ChEBI: A trimethoxyflavone with flavone substituted by hydroxy groups at C-5 and C-7 and methoxy groups at C-6, C-3' and C-4' respectively. Isolated from Citrus reticulata and Salvia tomentosa, it exhibits anti-inflammatory, anti-ulcer a
d antineoplastic activities. | [storage]
+4°C |
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