CAS 7755-01-3|(20R)-Protopanaxdiol

Introduction：Basic information about CAS 7755-01-3|(20R)-Protopanaxdiol, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. (20R)-Protopanaxdiol BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Articles37
6. Synonyms

Common Name	(20R)-Protopanaxdiol
CAS Number	7755-01-3	Molecular Weight	460.73200
Density	1.036 g/cm3	Boiling Point	559.5ºC at 760 mmHg
Molecular Formula	C₃₀H₅₂O₃	Melting Point	/
MSDS	ChineseUSA	Flash Point	226.1ºC

Names

Name	(20R)-protopanaxadiol
Synonym	More Synonyms

(20R)-Protopanaxdiol BiologicalActivity

Description	(20R)-Protopanaxadiol is a triterpenoid saponin metabolite of 20(R)-ginsenoside Rg3 in black ginseng. (20R)-Protopanaxadiol exhibits anti-tumor activity and cytotoxicity, and potently inhibits the growth of Helicobacter pylori[1][2][3].
Related Catalog	Research Areas >>CancerResearch Areas >>InfectionSignaling Pathways >>Others >>Others
References	[1]. Liu L, et al. Enzymatic preparation of 20(S, R)-protopanaxadiol by transformation of 20(S, R)-Rg3 from black ginseng. Phytochemistry. 2010 Sep;71(13):1514-20. [2]. Bae EA, et al. Metabolism of 20(S)- and 20(R)-ginsenoside Rg3 by human intestinal bacteria and its relation to in vitro biological activities. Biol Pharm Bull. 2002 Jan;25(1):58-63. [3]. Hasegawa H, et al. Inhibitory effect of some triterpenoid saponins on glucose transport in tumor cells and its application to in vitro cytotoxic and antiviral activities. Planta Med. 1994 Jun;60(3):240-3.

Description

(20R)-Protopanaxadiol is a triterpenoid saponin metabolite of 20(R)-ginsenoside Rg3 in black ginseng. (20R)-Protopanaxadiol exhibits anti-tumor activity and cytotoxicity, and potently inhibits the growth of Helicobacter pylori[1][2][3].

Related Catalog

Research Areas >>CancerResearch Areas >>InfectionSignaling Pathways >>Others >>Others

References

[1]. Liu L, et al. Enzymatic preparation of 20(S, R)-protopanaxadiol by transformation of 20(S, R)-Rg3 from black ginseng. Phytochemistry. 2010 Sep;71(13):1514-20.

[2]. Bae EA, et al. Metabolism of 20(S)- and 20(R)-ginsenoside Rg3 by human intestinal bacteria and its relation to in vitro biological activities. Biol Pharm Bull. 2002 Jan;25(1):58-63.

[3]. Hasegawa H, et al. Inhibitory effect of some triterpenoid saponins on glucose transport in tumor cells and its application to in vitro cytotoxic and antiviral activities. Planta Med. 1994 Jun;60(3):240-3.

Chemical & Physical Properties

Density	1.036 g/cm3
Boiling Point	559.5ºC at 760 mmHg
Molecular Formula	C₃₀H₅₂O₃
Molecular Weight	460.73200
Flash Point	226.1ºC
Exact Mass	460.39200
PSA	60.69000
LogP	6.50060
Index of Refraction	1.528
InChIKey	PYXFVCFISTUSOO-VUFVRDRTSA-N
SMILES	CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3CCC12C
Storage condition	2-8°C

Safety Information

RIDADR	NONH for all modes of transport

Articles37

An integrated high resolution mass spectrometric data acquisition method for rapid screening of saponins in Panax notoginseng (Sanqi).

J. Pharm. Biomed. Anal. 109 , 184-91, (2015)

The aim of this study was to develop a convenient method without pretreatments for nontarget discovery of interested compounds. The segment and exposure strategy, coupled with two mass spectrometer da...

Integrated evaluation of malonyl ginsenosides, amino acids and polysaccharides in fresh and processed ginseng.

J. Pharm. Biomed. Anal. 107 , 89-97, (2015)

Many analytical methods have been developed to characterize ginsenosides in ginseng. Relatively less attention has been paid to the malonyl ginsenosides, amino acids and polysaccharides in various pro...

TRAIL pathway is associated with inhibition of colon cancer by protopanaxadiol.

J. Pharmacol. Sci. 127(1) , 83-91, (2015)

Among important components of American ginseng, protopanaxadiol (PPD) showed more active anticancer potential than other triterpenoid saponins. In this study, we determined the in vivo effects of PPD ...

Synonyms

Protopanaxadiol

20R-Betulafolienetriol

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