Quercetin 3-O-neohesperidoside

Quercetin 3-O-neohesperidoside
Product Name Quercetin 3-O-neohesperidoside
CAS No.: 32453-36-4
Catalog No.: CFN91148
Molecular Formula: C27H30O16
Molecular Weight: 610.5 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The herbs of Callicarpa bodinieri
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price: $338/5mg
Quercetin 3-O-neohesperidoside shows anti-atherosclerosis, and antiplatelet aggregation activities.
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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.
  • Pharmacological Reports31 May 2017
  • Pharmacogn Mag.2015 Jul-Sep.
  • J Ethnopharmacol. 2017 Jul 12;
  • Phytomedicine.2018 Jan 1;
  • Oncotarget. 2017 Nov 14;
  • Nat Prod Sci.2016 Jun;22(2)
  • Front Pharmacol. 2016 Nov 30
  • Sci Rep. 2017 Apr 11;
  • Mol Cell2017 Nov 16;
  • J. Acta Agr. Scandinavica17 Apr 2017
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    Zhongguo Zhong Yao Za Zhi. 2015 Aug;40(16):3187-93.
    Study on antiplatelet and antithrombin activitives and effective components variation of Puhuang-Wulingzhi before and after compatibility.[Pubmed: 26790290]
    The changes of bioactive constituents were analyzed for Puhuang-Wulingzhi before and after compatibility and the antiplatelet and antithrombin activitives were evaluated in order to elucidate the scientific and reasonable of Puhuang-Wulingzhi compatibility.
    METHODS AND RESULTS:
    UPLC-QTOF-MA-Markerlynx, principal component analysis (PCA) and orthogonal partial least-squares discriminant analysis were used for data analysis and tracking changes of chemical composition during the decocting process. In vitro platelet aggregation induced by ADP, thrombin time(TT) and prothrombin time (PT) were investigated for Puhuang-Wulingzhi before and after compatibility. The results showed that significant differences were found between the mixed decoction and codecoction of Wulingzhi and Puhuang. Five compounds changed obviously were identified as typhaneoside, naringenin, isorhamnetin-3-O-ruinoside, Quercetin 3-O-neohesperidoside, kaempferol-3-O-neohesperidoside.
    CONCLUSIONS:
    The codecoction, comparing with the single decoction, was more significant in antiplatelet aggregation and could prolong thrombin time. In the same crude drug dose, the thrombin time (TT) elongation were greater. These data could provide references for elucidation of bioactive components for this herb pair.
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    METHODS AND RESULTS:
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