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(20R)-Ginsenoside Rh1

(20R)-Ginsenoside Rh1

Catalog No. BCN3700
Size Price Stock
20mg $198 In stock
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Quality Control of (20R)-Ginsenoside Rh1

Chemical structure

(20R)-Ginsenoside Rh1

(20R)-Ginsenoside Rh1 Dilution Calculator

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Chemical Properties of (20R)-Ginsenoside Rh1

Cas No. 80952-71-2 SDF Download SDF
Chemical Name (2R,3R,4S,5S,6R)-2-[[(6R,8R,10R,12S,14S)-3,12-dihydroxy-17-[(2R)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES CC(C)=CCC[C@@](C)(O)C1CC[C@@]2(C)C1[C@@H](O)CC3[C@@]4(C)CCC(O)C(C)(C)C4[C@@H](C[C@@]23C)O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O
Standard InChI InChI=1S/C36H62O9/c1-19(2)10-9-13-36(8,43)20-11-15-34(6)26(20)21(38)16-24-33(5)14-12-25(39)32(3,4)30(33)22(17-35(24,34)7)44-31-29(42)28(41)27(40)23(18-37)45-31/h10,20-31,37-43H,9,11-18H2,1-8H3/t20?,21-,22+,23+,24?,25?,26?,27+,28-,29+,30?,31+,33+,34-,35+,36+/m0/s1
Type of Compound Triterpenoids Appearance Powder
Formula C36H62O9 M.Wt 638.9
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other courier with RT , or blue ice upon request.

Preparing Stock Solutions of (20R)-Ginsenoside Rh1

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.5652 mL 7.826 mL 15.6519 mL 31.3038 mL 39.1298 mL
5 mM 0.313 mL 1.5652 mL 3.1304 mL 6.2608 mL 7.826 mL
10 mM 0.1565 mL 0.7826 mL 1.5652 mL 3.1304 mL 3.913 mL
50 mM 0.0313 mL 0.1565 mL 0.313 mL 0.6261 mL 0.7826 mL
100 mM 0.0157 mL 0.0783 mL 0.1565 mL 0.313 mL 0.3913 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

Preparation of (20R)-Ginsenoside Rh1

This product is isolated and purified from the roots of Panax ginseng C. A. Mey.

References on (20R)-Ginsenoside Rh1

Chemical constituents from processed rhizomes of Panax notoginseng.[Pubmed: 24558875]

On the basis of physicochemical properties and spectral data analysis, their structures were identified to be 6'-O-Acetylginsenoside Rh1 (1), ginsenoside RK3 (2), ginsenoside Rh4 (3), 20S-ginsenoside Rg3 (4), ginsenoside Rk1 (5), 20R-ginsenoside Rg3 (6), ginsenoside Rg5 (7), ginsenoside F2 (8), 20S-ginsenoside Rh1 (9), (20R)-Ginsenoside Rh1 (10), gypenoside X VII (11), notoginsenoside Fa, (12), ginsenoside Ra3 (13), ginsenoside Rg1 (14), ginsenoside Re (15), notoginsenoside R2 (16), ginsenoside Rg2 (17), notoginsenoside R1 (18), ginsenoside Rd (19), ginsenoside Rb1 (20), notoginsenoside D (21), notoginsenoside R4 (22) and ginsenoside Rb2 (23), respectively.

Pharmacological Study on Panax ginseng C.A. MEYER V. : Effects of Red Ginseng on the Experimental Disseminated Intravascular Coagulation (4). On Ginsenoside-Rg3, Rh1 and Rh2[Reference: WebLink]

20S, 20R ginsenoside-Rg3, 20S, 20R ginsenoside-Rh1 and ginsenoside-Rh2 isolated from Red Ginseng were investigated for their effect on blood platelet aggregation and thrombin-induced conversion of fibrinogen to fibrin in vitro. 20S, 20R ginsenoside-Rg3 inhibited collagen- and ADP-induced blood platelet aggregation. 20S ginsenoside-Rg3, 20S, 20R ginsenoside-Rh1 inhibited the thrombin-induced conversion of fibrinogen to fibrin.


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