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Marstenacisside F1

CAS# 2902666-68-4

Marstenacisside F1

Catalog No. BCX1869----Order now to get a substantial discount!

Product Name & Size Price Stock
Marstenacisside F1: 5mg Please Inquire In Stock
Marstenacisside F1: 10mg Please Inquire In Stock
Marstenacisside F1: 20mg Please Inquire Please Inquire
Marstenacisside F1: 50mg Please Inquire Please Inquire
Marstenacisside F1: 100mg Please Inquire Please Inquire
Marstenacisside F1: 200mg Please Inquire Please Inquire
Marstenacisside F1: 500mg Please Inquire Please Inquire
Marstenacisside F1: 1000mg Please Inquire Please Inquire

Quality Control of Marstenacisside F1

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Chemical structure

Marstenacisside F1

Chemical Properties of Marstenacisside F1

Cas No. 2902666-68-4 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C47H66O14 M.Wt 855.02
Type of Compound Other Steroids Storage Desiccate at -20°C
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.

Marstenacisside F1 Dilution Calculator

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Marstenacisside F1 Molarity Calculator

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Preparing Stock Solutions of Marstenacisside F1

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.1696 mL 5.8478 mL 11.6956 mL 23.3913 mL 29.2391 mL
5 mM 0.2339 mL 1.1696 mL 2.3391 mL 4.6783 mL 5.8478 mL
10 mM 0.117 mL 0.5848 mL 1.1696 mL 2.3391 mL 2.9239 mL
50 mM 0.0234 mL 0.117 mL 0.2339 mL 0.4678 mL 0.5848 mL
100 mM 0.0117 mL 0.0585 mL 0.117 mL 0.2339 mL 0.2924 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 Marstenacisside F1

Polyoxypregnane Glycosides from Root of Marsdenia tenacissima and Inhibited Nitric Oxide Levels in LPS Stimulated RAW 264.7 Cells.[Pubmed:36677943]

Molecules. 2023 Jan 16;28(2):886.

Six new polyoxypregnane glycosides, Marstenacisside F1-F3 (1-3), G1-G2 (4-5) and H1 (6), as well as 3-O-beta-D-glucopyranosyl-(1-->4)-6-deoxy-3-O-methyl-beta-D-allopyranosyl-(1-->4)-beta-D-oleandropyranosyl-11alpha,12beta-di-O-benzoyl-tenacigenin B (7), were isolated from the roots of Marsdenia tenacissima. Their structures were established by an extensive interpretation of their 1D and 2D NMR and HRESIMS data. Compounds 1-7 were tenacigenin B derivatives with an oligosaccharide chain at C-3. This was the first time that compound 7 had been isolated from the title plant and its 1H and 13C NMR data were reported. Compounds 4 and 5 were the first examples of C21 steroid glycoside bearing unique beta-glucopyranosyl-(1-->4)-beta-glucopyranose sugar moiety. All the isolated compounds were evaluated for anti-inflammatory activity by inhibiting nitric oxide (NO) production in the lipopolysaccharide-induced RAW 264.7 cells. The results showed that Marstenacisside F1 and F2 exhibited significant NO inhibitory activity with an inhibition rate of 48.19 +/- 4.14% and 70.33 +/- 5.39%, respectively, at 40 muM, approximately equal to the positive control (L-NMMA, 68.03 +/- 0.72%).

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