Sakuranetin structure
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Common Name | Sakuranetin | ||
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CAS Number | 2957-21-3 | Molecular Weight | 286.28 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | 555.9±50.0 °C at 760 mmHg | |
Molecular Formula | C16H14O5 | Melting Point | 153-154ºC | |
MSDS | Chinese USA | Flash Point | 212.4±23.6 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of SakuranetinSakuranetin is a rice flavonoid phytoalexin, shows strong antifungal activity[1]. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury[2]. |
Name | Sakuranetin |
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Synonym | More Synonyms |
Description | Sakuranetin is a rice flavonoid phytoalexin, shows strong antifungal activity[1]. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury[2]. |
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Related Catalog | |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 555.9±50.0 °C at 760 mmHg |
Melting Point | 153-154ºC |
Molecular Formula | C16H14O5 |
Molecular Weight | 286.28 |
Flash Point | 212.4±23.6 °C |
Exact Mass | 286.084137 |
PSA | 75.99000 |
LogP | 3.37 |
Vapour Pressure | 0.0±1.6 mmHg at 25°C |
Index of Refraction | 1.638 |
Storage condition | 2-8℃ |
A nicotinic receptor-mediated anti-inflammatory effect of the flavonoid rhamnetin in BV2 microglia.
Fitoterapia 98 , 11-21, (2014) The alpha7 nicotinic acetylcholine receptor (nAChR) is a potential target in neuroinflammation. Screening a plant extract library identified Solidago nemoralis as containing methyl-quercetin derivativ... |
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In vitro antileishmanial and antitrypanosomal activities of flavanones from Baccharis retusa DC. (Asteraceae).
Exp. Parasitol. 130(2) , 141-5, (2012) Leishmaniasis and Chagas' are parasitic protozoan diseases that affect the poorest population in the world, causing a high mortality and morbidity. As a result of highly toxic and long-term treatments... |
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Isoprenylated flavonoid and adipogenesis-promoting constituents of Dodonaea viscosa.
J. Nat. Prod. 75(4) , 699-706, (2012) Ten new isoprenylated flavonol derivatives, dodoviscins A-J (1-10), and seven known compounds (11-17) were isolated from the aerial parts of Dodonaea viscosa. Compounds 1, 2, 4, 5, 7-9, 5,7,4'-trihydr... |
5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one |
4',5-Dihydroxy-7-methoxyflavanone |
(S)-(-)-4',5-dihydroxy-7-methoxyflavanone |
4',5-DIHYDROXY-7-METHOXYFLAVONE |
4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-, (2S)- |
Naringenin 7-O-methyl ether |
5,4'-dihydroxy-7-methoxyflavanone |
(2S)-sakuranetin |
7-O-Methylnaringenin |
naringenin 7-methylether |
(S)-(-)-4',5-Dihydroxy-7-methoxy-flavanone |
(2S)-5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydro-4H-chromen-4-one |
Sakuranetin |
Naringenin 7-methyl ether |
EINECS 220-980-5 |