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Suavissimoside F1

CAS# 95645-51-5

Suavissimoside F1

Catalog No. BCN6361----Order now to get a substantial discount!

Product Name & Size Price Stock
Suavissimoside F1:5mg $308 In stock
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Quality Control of Suavissimoside F1

Quality Control & MSDS

Number of papers citing our products

Chemical structure

Suavissimoside F1

3D structure

Chemical Properties of Suavissimoside F1

Cas No. 95645-51-5 SDF Download SDF
PubChem ID 21626352 Appearance Powder
Formula C36H56O12 M.Wt 680.8
Type of Compound Triterpenoids Storage Desiccate at -20°C
Synonyms Suavissimoside R1
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,12,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carboxylic acid
SMILES CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O
Standard InChIKey YXSQSVWHKZZWDD-FPLSKCGGSA-N
Standard InChI InChI=1S/C36H56O12/c1-17-9-12-36(30(45)48-28-25(41)24(40)23(39)20(16-37)47-28)14-13-32(3)18(26(36)35(17,6)46)7-8-21-31(2)15-19(38)27(42)34(5,29(43)44)22(31)10-11-33(21,32)4/h7,17,19-28,37-42,46H,8-16H2,1-6H3,(H,43,44)/t17-,19-,20-,21-,22-,23-,24+,25-,26-,27+,28+,31-,32-,33-,34+,35-,36+/m1/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.
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.
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.

Source of Suavissimoside F1

The herbs of Sanguisorba officinalis

Protocol of Suavissimoside F1

Structure Identification
Phytochemistry (Oxford), 1985, 24(1):115-118.

Triterpenoids and glycosides from Geum japonicum.[Reference: WebLink]


METHODS AND RESULTS:
Two new glucosides and two known ester glucosides have been isolated from Geum japonicum. The two new glucosides were isolated by formation of their acetates and were identified as glucosides of 2-isopropyl-5-methylhydroquinone by chemical and spectral studies.
CONCLUSIONS:
The two known ester glucosides were identified as niga-ichigoside F1 and Suavissimoside F1 by direct comparison with authentic samples. 2α,19α-Dihydroxyursolic acid and the known glycoside, gein, were also isolated from the same plant, in addition to a mixture of 2α-hydroxyursolic acid and 2α-hydroxyoleanolic acid.

Suavissimoside F1 Dilution Calculator

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Suavissimoside F1 Molarity Calculator

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Preparing Stock Solutions of Suavissimoside F1

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.4689 mL 7.3443 mL 14.6886 mL 29.3772 mL 36.7215 mL
5 mM 0.2938 mL 1.4689 mL 2.9377 mL 5.8754 mL 7.3443 mL
10 mM 0.1469 mL 0.7344 mL 1.4689 mL 2.9377 mL 3.6722 mL
50 mM 0.0294 mL 0.1469 mL 0.2938 mL 0.5875 mL 0.7344 mL
100 mM 0.0147 mL 0.0734 mL 0.1469 mL 0.2938 mL 0.3672 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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Description

Suavissimoside R1, isolated from the roots of Rubus parvifollus, possesses potent neuroprotective activity and has the potential to treat anti-Parkinson's disease drug.

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