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Sanleng acid

CAS# 163860-24-0

Sanleng acid

2D Structure

Catalog No. BCX2155----Order now to get a substantial discount!

Product Name & Size Price Stock
Sanleng acid: 5mg $308 In Stock
Sanleng acid: 10mg Please Inquire In Stock
Sanleng acid: 20mg Please Inquire Please Inquire
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Quality Control of Sanleng acid

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Sanleng acid

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Chemical Properties of Sanleng acid

Cas No. 163860-24-0 SDF File under preparation.
PubChem ID N/A Appearance Powder
Formula C18H34O5 M.Wt 330.5
Type of Compound Miscellaneous 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.

Source of Sanleng acid

The rhizomes of Sparganium stoloniferum

Sanleng acid Dilution Calculator

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Sanleng acid Molarity Calculator

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Preparing Stock Solutions of Sanleng acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.0257 mL 15.1286 mL 30.2572 mL 60.5144 mL 75.643 mL
5 mM 0.6051 mL 3.0257 mL 6.0514 mL 12.1029 mL 15.1286 mL
10 mM 0.3026 mL 1.5129 mL 3.0257 mL 6.0514 mL 7.5643 mL
50 mM 0.0605 mL 0.3026 mL 0.6051 mL 1.2103 mL 1.5129 mL
100 mM 0.0303 mL 0.1513 mL 0.3026 mL 0.6051 mL 0.7564 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 Sanleng acid

Study of the active ingredients and mechanism of Sparganii rhizoma in gastric cancer based on HPLC-Q-TOF-MS/MS and network pharmacology.[Pubmed:33479376]

Sci Rep. 2021 Jan 21;11(1):1905.

Sparganii rhizoma (SL) has potential therapeutic effects on gastric cancer (GC), but its main active ingredients and possible anticancer mechanism are still unclear. In this study, we used HPLC-Q-TOF-MS/MS to comprehensively analyse the chemical components of the aqueous extract of SL. On this basis, a network pharmacology method incorporating target prediction, gene function annotation, and molecular docking was performed to analyse the identified compounds, thereby determining the main active ingredients and hub genes of SL in the treatment of GC. Finally, the mRNA and protein expression levels of the hub genes of GC patients were further analysed by the Oncomine, GEPIA, and HPA databases. A total of 41 compounds were identified from the aqueous extract of SL. Through network analysis, we identified seven main active ingredients and ten hub genes: acacetin, Sanleng acid, ferulic acid, methyl 3,6-dihydroxy-2-[(2-hydroxyphenyl) ethynyl]benzoate, caffeic acid, adenine nucleoside, azelaic acid and PIK3R1, PIK3CA, SRC, MAPK1, AKT1, HSP90AA1, HRAS, STAT3, FYN, and RHOA. The results indicated that SL might play a role in GC treatment by controlling the PI3K-Akt and other signalling pathways to regulate biological processes such as proliferation, apoptosis, migration, and angiogenesis in tumour cells. In conclusion, this study used HPLC-Q-TOF-MS/MS combined with a network pharmacology approach to provide an essential reference for identifying the chemical components of SL and its mechanism of action in the treatment of GC.

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