(20S)-Protopanaxatriol

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Names

[ Name ]:
(20S)-Protopanaxatriol

[Synonym ]:
PROTOPANAXTRIOL
20(S)-APPT,g-PPT
Gonane-3,6,12-triol, 17-[(1S)-1-hydroxy-1,5-dimethyl-4-hexen-1-yl]-4,4,10,14-tetramethyl-, (3β,6α,12β,14β,17β)-
(3β,6α,12β,14β)-4,4,14-Trimethyl-18-norcholest-24-ene-3,6,12,20-tetrol
20S-Protopanaxatriol
Protopanaxatriol, 20S-
(20S)-Protopanaxatriol

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
588.8±50.0 °C at 760 mmHg

[ Molecular Formula ]:
C₃₀H₅₂O₄

[ Molecular Weight ]:
476.73

[ Flash Point ]:
242.9±24.7 °C

[ PSA ]:
80.92000

[ LogP ]:
5.41

[ Vapour Pressure ]:
0.0±3.7 mmHg at 25°C

[ Index of Refraction ]:
1.541

[ Storage condition ]:
-20°C

Safety Information

[ RIDADR ]:
NONH for all modes of transport

Articles

Dual functions of ginsenosides in protecting human endothelial cells against influenza H9N2-induced inflammation and apoptosis.

J. Ethnopharmacol. 137 , 1542-1546, (2011)

Panax ginseng is a precious traditional Chinese herbal medicine which has been utilized as herbal tonic for improving immunity. The active component, ginsenosides have been shown to possess various ph...

Cytochrome P450 CYP716A53v2 catalyzes the formation of protopanaxatriol from protopanaxadiol during ginsenoside biosynthesis in Panax ginseng.

Plant Cell Physiol. 53 , 1535-1545, (2012)

Ginseng (Panax ginseng C.A. Meyer) is one of the most popular medicinal herbs, and the root of this plant contains pharmacologically active components, called ginsenosides. Ginsenosides, a class of te...

The in vitro structure-related anti-cancer activity of ginsenosides and their derivatives.

Molecules 16(12) , 10619-30, (2011)

Panax ginseng has long been used in Asia as a herbal medicine for the prevention and treatment of various diseases, including cancer. The current study evaluated the cytotoxic potency against a variet...

(20S)-protopanaxatriol
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