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Soyasapogenol C
Soyasapogenol C
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Soyasapogenol C
Price: $463 / 5mg
CAS No.: 595-14-2
Catalog No.: CFN91068
Molecular Formula: C30H48O2
Molecular Weight: 440.7 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The seeds of Glycine max.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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 / $463 / In-stock
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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.
Soyasapogenol C Description
Source: The seeds of Glycine max.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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

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 2.2691 mL 11.3456 mL 22.6912 mL 45.3823 mL 56.7279 mL
5 mM 0.4538 mL 2.2691 mL 4.5382 mL 9.0765 mL 11.3456 mL
10 mM 0.2269 mL 1.1346 mL 2.2691 mL 4.5382 mL 5.6728 mL
50 mM 0.0454 mL 0.2269 mL 0.4538 mL 0.9076 mL 1.1346 mL
100 mM 0.0227 mL 0.1135 mL 0.2269 mL 0.4538 mL 0.5673 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:
Pharmaceutical Biology, 2008, 22(1):1-10.
Lipids and Saponins of Phaseolus coccineus.[Reference: WebLink]
The lipids obtained from the roots, rhizomes and stems of Phaseolus coccineus were separated into saponifiable and unsaponifiable fractions.
METHODS AND RESULTS:
Analysis of the saponifiable fraction by gas-liquid chromatography (GLC) of the methyl esters showed the presence of a series of C8 to C18 saturated acids and C12 to C18 unsaturated acids. Oleic acid was the predominant fatty acid detected in the roots (22.3%) and rhizomes (34.4%). However, in the stems palmitic acid (30.0%) was the major component. Stearic acid, which was present in a fairly high concentration in the rhizomes, was not detected in either the roots or the stems. β-Bergamotane, 18α-oleanan-3-one and β-Sitosterol have been isolated from the roots, rhizomes and stems of unsaponifiable fraction. In all these three plant materials, the presence of saponins was also revealed. Two sapogenins were isolated from the roots and were identified as Soyasapogenol C and Ursa-12,15-diene-3,24-diol. Soyasapogenol C was also isolated from the rhizomes and the stems. In addition, soyasapogenol B was also isolated and identified in the stems.
CONCLUSIONS:
The compounds were identified by TLC, UV, IR, NMR and mass spectral methods. The sugar moieties associated with these sapogenins were identified as D-glucose, D-fructose, L(+)-arabinose, L(+)-rhamnose and D-galacturonic acid.
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Triptolide

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CAS No: 38748-32-2
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Caffeoyl alcohol

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