Ginsenoside Rs2CAS# 87733-66-2 |
| Cas No. | 87733-66-2 | SDF | File under preparation. |
| PubChem ID | 101596948.0 | Appearance | Powder |
| Formula | C55H92O23 | M.Wt | 1121.3 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | [(2R,3S,4S,5R,6S)-6-[(2R,3R,4S,5S,6R)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-methylhept-5-en-2-yl]-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate | ||
| SMILES | CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)COC(=O)C)O)O)O)C)C)O)C)OC7C(C(C(C(O7)COC8C(C(C(O8)CO)O)O)O)O)O)C | ||
| Standard InChIKey | XUBSZCIZVSPSMQ-HTVDCONZSA-N | ||
| Standard InChI | InChI=1S/C55H92O23/c1-24(2)11-10-15-55(9,78-49-45(69)41(65)39(63)31(75-49)23-71-47-43(67)37(61)29(21-57)72-47)26-12-17-54(8)35(26)27(59)19-33-52(6)16-14-34(51(4,5)32(52)13-18-53(33,54)7)76-50-46(42(66)36(60)28(20-56)73-50)77-48-44(68)40(64)38(62)30(74-48)22-70-25(3)58/h11,26-50,56-57,59-69H,10,12-23H2,1-9H3/t26-,27+,28+,29-,30+,31+,32-,33+,34-,35-,36+,37-,38+,39+,40-,41-,42-,43+,44+,45+,46+,47+,48-,49-,50-,52-,53+,54+,55-/m0/s1 | ||
| 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. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
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| About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
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| Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. | ||
Quality Control & MSDS
3D structure
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Number of papers citing our products
Ginsenoside Rs2 Dilution Calculator
Ginsenoside Rs2 Molarity Calculator
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Quinquenoside R1Catalog No.: BCX0684CAS No.: 85013-02-1 -
Pseudoginsenoside RC1Catalog No.: BCX1331CAS No.: 102805-32-3 -
Ginsenoside Rs1Catalog No.: BCX1097CAS No.: 87733-67-3 -
Ginsenoside Rb1Catalog No.: BCN1063CAS No.: 41753-43-9 -
Ginsenoside RcCatalog No.: BCN1072CAS No.: 11021-14-0 -
Malonylginsenoside Rb(1)Catalog No.: BCC9230CAS No.: 88140-34-5 -
Gypenoside XVIICatalog No.: BCN2339CAS No.: 80321-69-3 -
Notoginsenoside FeCatalog No.: BCN3852CAS No.: 88105-29-7 -
Notoginsenoside R4Catalog No.: BCN8834CAS No.: 87741-77-3 -
Ginsenoside Rb2Catalog No.: BCN1064CAS No.: 11021-13-9 -
Notoginsenoside FaCatalog No.: BCN3854CAS No.: 88100-04-3 -
Notoginsenoside FP2Catalog No.: BCN8692CAS No.: 1004988-75-3 -
Notoginsenoside SCatalog No.: BCN8371CAS No.: 575446-95-6 -
Notoginsenoside DCatalog No.: BCX1024CAS No.: 193895-50-0 -
Ginsenoside Rs3Catalog No.: BCN3716CAS No.: 194861-70-6 -
Ginsenoside Ra3Catalog No.: BCN0860CAS No.: 90985-77-6 -
Ginsenoside Ra2Catalog No.: BCN8555CAS No.: 83459-42-1 -
Notoginsenoside FcCatalog No.: BCN3853CAS No.: 88122-52-5 -
Ginsenoside Ra1Catalog No.: BCN8392CAS No.: 83459-41-0 -
StevenleafCatalog No.: BCN5978CAS No.: 80321-63-7 -
Ginsenoside Rd2Catalog No.: BCN8279CAS No.: 83480-64-2 -
Ginsenoside F2Catalog No.: BCN1245CAS No.: 62025-49-4 -
Vinaginsenoside R7Catalog No.: BCX1594CAS No.: 156009-83-5 -
Gypenoside LXXVCatalog No.: BCX0478CAS No.: 110261-98-8 -
20(R)-Ginsenoside Rg3Catalog No.: BCN5018CAS No.: 38243-03-7 -
Ginsenoside Rg3Catalog No.: BCN1068CAS No.: 14197-60-5 -
Vinaginsenoside R4Catalog No.: BCN8659CAS No.: 156009-80-2 -
Vinaginsenoside R3Catalog No.: BCN8550CAS No.: 156012-92-9
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 0.8918 mL | 4.4591 mL | 8.9182 mL | 17.8364 mL | 22.2955 mL |
| 5 mM | 0.1784 mL | 0.8918 mL | 1.7836 mL | 3.5673 mL | 4.4591 mL |
| 10 mM | 0.0892 mL | 0.4459 mL | 0.8918 mL | 1.7836 mL | 2.2296 mL |
| 50 mM | 0.0178 mL | 0.0892 mL | 0.1784 mL | 0.3567 mL | 0.4459 mL |
| 100 mM | 0.0089 mL | 0.0446 mL | 0.0892 mL | 0.1784 mL | 0.223 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. | |||||
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[Chemical constituents of leaves of Panax japonicus var. major].[Pubmed:25095375]
Zhongguo Zhong Yao Za Zhi. 2014 May;39(9):1635-8.
Seven compounds were isolated from the leaves of Panax japonicus var. major by chromatographic methods including silica gel, Sephadex LH-20, ODS and semi-preparative HPLC. Their structures were elucidated by their physical and chemical properties and spectral data analysis as 5, 7-dihydroxy-8-methoxyl flavone (1), Ginsenoside Rs2 (2), quinquenoside R1 (3), ginsenoside Rs1 (4), notoginsenoside Fe (5), ginsenoside Rd2 (6) and gypenosiden IX (7). Among them, compound 1 was obtained from the Panax genus for the first time, and compounds 2-7 were isolated from this plant for the first time.
[Chemical constituents from roots and rhizomes of Panax ginseng cultivated in Jilin province].[Pubmed:24380303]
Zhongguo Zhong Yao Za Zhi. 2013 Sep;38(17):2807-17.
The chemical constituents of the roots and rhizomes of Panax ginseng were systematically investigated by various column chromatographic methods including Amberlite XAD-4 macroporous adsorptive resins and silica gel as well as high-performance liquid chromatography, and their chemical structures were identified by physico-chemical properties and spectral analyses. Twenty-eight compounds were isolated from the 70% ethanolic-aqueous extract and identified as koryoginsenoside R1 (1), ginsenoside Rg1 (2), ginsenoside Rf (3), notoginsenoside R2 (4), ginsenoside Rg2 (5), notoginsenoside Fe (6), ginsenjilinol (7), ginsenoside Re5 (8), noto-ginsenoside N (9), notoginsenoside R1 (10), ginsenoside Re2 (11), ginsenoside Re1 (12), ginsenoside Re (13), Ginsenoside Rs2 (14), ginsenoside Ro methyl ester (15), ginsenoside Rd (16), ginsenoside Re3 (17), ginsenoside Re4 (18), 20-gluco-ginsenoside Rf (19), ginsenoside Ro (20), ginsenoside Rc (21), quinquenoside-R1 (22), ginsenoside Ra2 (23), ginsenoside Rb1 (24), ginsenoside Ra1 (25), ginsenoside Ra3 (26), ginsenoside Rb2 (27), and notoginsenoside R4 (28). All isolated compounds are 20 (S) -protopanaxadiol or protopanaxatriol type triterpenoid saponins. Compound 1 was isolated from the roots and rhizomes of P. ginseng cultivated in Jilin province for the first time and compound 6 was isolated from the roots and rhizomes of P. ginseng for the first time. The 1H-NMR data of compounds 6, 14 and 19 were assigned for the first time.
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