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Notoginsenoside ST4

CAS# 155683-02-6

Notoginsenoside ST4

Catalog No. BCX1063----Order now to get a substantial discount!

Product Name & Size Price Stock
Notoginsenoside ST4: 5mg Please Inquire In Stock
Notoginsenoside ST4: 10mg Please Inquire In Stock
Notoginsenoside ST4: 20mg Please Inquire Please Inquire
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Quality Control of Notoginsenoside ST4

Number of papers citing our products

Chemical structure

Notoginsenoside ST4

Chemical Properties of Notoginsenoside ST4

Cas No. 155683-02-6 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C47H80O17 M.Wt 917.14
Type of Compound Triterpenoids Storage Desiccate at -20°C
Synonyms Notoginsenoside ST-4
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.
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 Notoginsenoside ST4

Panax notoginseng

Notoginsenoside ST4 Dilution Calculator

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Notoginsenoside ST4 Molarity Calculator

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Preparing Stock Solutions of Notoginsenoside ST4

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.0903 mL 5.4517 mL 10.9035 mL 21.8069 mL 27.2587 mL
5 mM 0.2181 mL 1.0903 mL 2.1807 mL 4.3614 mL 5.4517 mL
10 mM 0.109 mL 0.5452 mL 1.0903 mL 2.1807 mL 2.7259 mL
50 mM 0.0218 mL 0.109 mL 0.2181 mL 0.4361 mL 0.5452 mL
100 mM 0.0109 mL 0.0545 mL 0.109 mL 0.2181 mL 0.2726 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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References on Notoginsenoside ST4

Chemical transformation and target preparation of saponins in stems and leaves of Panax notoginseng.[Pubmed:29983608]

J Ginseng Res. 2018 Jul;42(3):270-276.

BACKGROUND: Notoginsenoside Ft1 is a promising potential candidate for cardiovascular and cancer disease therapy owing to its positive pharmacological activities. However, the yield of Ft1 is ultralow utilizing reported methods. Herein, an acid hydrolyzing strategy was implemented in the acquirement of rare notoginsenoside Ft1. METHODS: Chemical profiles were identified by ultraperformance liquid chromatography coupled with quadruple-time-of-flight and electrospray ionization mass spectrometry (UPLC-Q/TOF-ESI-MS). The acid hydrolyzing dynamic changes of chemical compositions and the possible transformation pathways of saponins were monitored by ultrahigh-performance LC coupled with tandem MS (UHPLC-MS/MS). RESULTS AND CONCLUSION: Notoginsenoside Ft1 was epimerized from Notoginsenoside ST4, which was generated through cleaving the carbohydrate side chains at C-20 of notoginsenosides Fa and Fc, and vina-ginsenoside R7, and further converted to other compounds via hydroxylation at C-25 or hydrolysis of the carbohydrate side chains at C-3 under the acid conditions. High temperature contributed to the hydroxylation reaction at C-25 and 25% acetic acid concentration was conducive to the preparation of notoginsenoside Ft1. C-20 epimers of notoginsenoside Ft1 and ST4 were successfully separated utilizing solvent method of acetic acid solution. The theoretical preparation yield rate of notoginsenoside Ft1 was about 1.8%, which would be beneficial to further study on its bioactivities and clinical application.

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