Salirepin

Salirepin
Product Name Salirepin
CAS No.: 26652-12-0
Catalog No.: CFN98314
Molecular Formula: C13H18O8
Molecular Weight: 302.3 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Targets: NO
Source: The herbs of Idesia polycarpa
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Salirepin has anti-inflammatory activity, it can significantly inhibit lipopolysaccharide- induced nitric oxide production in BV2 microglia.
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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

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.
  • Food Science.2023, 4(20):268-282.
  • Jour. of Stored Pro & Postharvest Res.2016, 7(3):32-36
  • Phytochemistry.2024, 222:114102.
  • Int J Mol Sci.2021, 22(21):11836.
  • Food Research International2023, 113792.
  • J Bone Miner Res.2017, 32(12):2415-2430
  • Environ Toxicol.2023, 23929.
  • Food Chem X.2024, 24:101909.
  • Sci Rep.2020, 10:4495(2020)
  • J Pharm Pharmacol.2022, rgac033.
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    Two new phenolic glycosides characterized as idesin salicylate (1) and 2-hydroxyphenol-1-O-beta-D-glucopyranosyl-(6-->1)- alpha-L-rhamnopyranoside (2) were isolated with four known compounds, idescarpin (3), idesin (4), 1-hydroxy-6-oxocyclohex-2-enecarboxylic acid methyl ester (5) and Salirepin (6), from the fruits of IDESIA POLYCARPA.
    CONCLUSIONS:
    All six compounds significantly inhibited lipopolysaccharide-induced nitric oxide production in BV2 microglia at concentrations from 1 microM to 100 microM.
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