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Ginsenoside Ro

Catalog No. T3915 CAS 34367-04-9

Synonyms: Polysciasaponin P3, Prostaglandin Receptor, Calcium Channel, Polysciasaponin P-3, Polysciasaponin P 3, Inhibitor, Ca2+ channels, Ginsenoside Ro, Chikusetsusaponin5, Chikusetsusaponin-5, Chikusetsusaponin V, Chikusetsusaponin 5, Ca channels, inhibit

GinsenosideRo exhibits a Ca2+-antagonistic antiplatelet effect.

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Ginsenoside Ro, CAS 34367-04-9

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Purity: 98%

Biological Description

Chemical Properties

Storage & Solubility Information

Description	GinsenosideRo exhibits a Ca2+-antagonistic antiplatelet effect.
Targets&IC50	Ca2+-antagonistic:155 μM

Synonyms	Polysciasaponin P3, Prostaglandin Receptor, Calcium Channel, Polysciasaponin P-3, Polysciasaponin P 3, Inhibitor, Ca2+ channels, Ginsenoside Ro, Chikusetsusaponin5, Chikusetsusaponin-5, Chikusetsusaponin V, Chikusetsusaponin 5, Ca channels, inhibit
Molecular Weight	957.117
Formula	C48H76O19
CAS No.	34367-04-9

Storage

Powder: -20°C for 3 years

In solvent: -80°C for 2 years

Solubility Information

DMSO: 10 mM

( < 1 mg/ml refers to the product slightly soluble or insoluble )

Citations

References and Literature

1. Kang HJ, et al. Antioxidative properties of ginsenoside Ro against UV-B-induced oxidative stress in human dermal fibroblasts. Biosci Biotechnol Biochem. 2015 Jul 27:1-4. 2. Zhang XH, et al. Ginsenoside Ro suppresses interleukin-1β-induced apoptosis and inflammation in rat chondrocytes by inhibiting NF-κB. Chin J Nat Med. 2015 Apr;13(4):283-9. 3. Murata K, et al. Effects of ginseng rhizome and ginsenoside Ro on testosterone 5α-reductase and hair re-growth in testosterone-treated mice. Phytother Res. 2012 Jan;26(1):48-53. 4. Matsuda H, et al. Anti-hepatitic activity of ginsenoside Ro. Planta Med. 1991 Dec;57(6):523-6. 6. Jung-HaeShin, et al. Inhibitory effects of thromboxane A2 generation by ginsenoside Ro due to attenuation of cytosolic phospholipase A2 phosphorylation and arachidonic acid release. J Ginseng Res. 9 Jan 2018. 7. Jiang Z, et al. The traditional Chinese medicine Achyranthes bidentata and our de novo conception of its metastatic chemoprevention: from phytochemistry to pharmacology. Sci Rep. 2017 Jun 20;7(1):3888.

Related compound libraries

This product is contained In the following compound libraries：

Terpene Natural Product Library GPCR Compound Library Anti-Cancer Metabolism Compound Library Traditional Chinese Medicine Monomer Library Tibetan medicine Compound Library Endocrinology-Hormone Compound Library Lipid Metabolism Compound Library Inhibitor Library Natural Product Library for HTS Anti-Metabolism Disease Compound Library

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