Chemodex

Hyperoside

CHF 272.00
In stock
CDX-H0298-M02525 mgCHF 272.00
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Product Details
Synonyms 3,3',4',5,7-Pentahydroxyflavone 3-D-galactoside; Hyperin; Quercetin 3-D-galactoside; NSC 407304
Product Type Chemical
Properties
Formula

C21H20O12

MW 464.38
CAS 482-36-0
RTECS DJ3009200
Source/Host Chemicals Plant
Purity Chemicals ≥98% (HPLC)
Appearance Yellow powder.
Solubility Soluble in DMSO (10mg/ml) or DMF (10mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key OVSQVDMCBVZWGM-DTGCRPNFSA-N
Smiles O=C1C2=C(O)C=C(O)C=C2OC(C3=CC=C(O)C(O)=C3)=C1O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
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Product Specification Sheet
Datasheet Download PDF
Description

Hyperoside is a 3-O-galactoside of quercetin that can be found in a wide range of plants. It shows diverse biological activities, including antioxidant, anti-inflammatory, neuroprotective, antihypoglycemic and antiadipogenic, antibacterial and anticancer properties. It has powerful antioxidant action through its ability to scavenge free radicals. It inhibits the NF-κB signaling pathway. Hyperoside selectively interrupted NLRC4 and AIM2 inflammasome activation but did not alter cytokine expression. The quorum sensing-inhibiting effect of hyperoside may lead to a reduction in biofilm formation in P. aeruginosa. Honokiol exerts broad-range anticancer activity, such as induction of apoptosis and autophagy and inhibition of cell proliferation. Hyperoside has a beneficial effect on the prevention and treatment of obesity.

Product References

(1) M.J. Piao, et al.; Biochim. Biophys. Acta 1780, 1448 (2008) | (2) S.J. Kim, et al.; Am. J. Chin. Med. 39, 171 (2011) | (3) K.W. Zeng, et al.; Eur. J. Pharmacol. 672, 45 (2011) | (4) N. Zhang, et al.; PLoS One 9, e98973 (2014) | (5) S.K. Ku, et al.; Inflammation 38, 784 (2015) | (6) T. Fu, et al.; Acta Pharmacol. Sin. 37, 505 (2016) | (7) P. Lu; Biomed. Pharmacother. 82, 216 (2016) | (8) H. Ahn & G.S. Lee; Phytomedicine 24, 77 (2017) | (9) Y. Sun, et al.; Exp. Ther. Med. 14, 1647 (2017) | (10) Y. Zhang, et al.; Int. J. Mol. Med. 41, 77 (2018) | (11) M. Berkoz; Acta Endocrinol. 15, 165 (2019)

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