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Suavissimoside F1
Suavissimoside F1
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Suavissimoside F1
Price: $298 / 5mg
CAS No.: 95645-51-5
Catalog No.: CFN91067
Molecular Formula: C36H56O12
Molecular Weight: 680.8 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The herbs of Sanguisorba officinalis
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / $387.4 / In-stock
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Product Use Citation
Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Reference standards.
Suavissimoside F1 Description
Source: The herbs of Sanguisorba officinalis
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals
More...

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
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 need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
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.
CFN98465Ziyuglycoside II35286-59-0604.8 C35H56O8
CFN90993Ilexoside D109008-27-7766.97C41H66O13
CFN92273Ilexside I83725-19-3472.7C41H66O13
CFN90994Ilexoside K109008-26-6929.10C47H76O18
CFN97328Pomolic acid 28-O-beta-D-glucopyranosyl ester83725-24-0634.9 C36H58O9
CFN89311Kaji-ichigoside F195298-47-8650.85C36H58O10
CFN89097Rosamultin88515-58-6650.85C36H58O10
CFN91060Niga-ichigoside F195262-48-9666.9C36H58O11
CFN91067Suavissimoside F195645-51-5680.8C36H56O12
CFN98464Ziyuglycoside I35286-58-9767.0 C41H66O13
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