Chemodex

Myricetin

CHF 54.00
In stock
CDX-M0504-M02525 mgCHF 54.00
CDX-M0504-M100100 mgCHF 135.00
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Product Details
Synonyms 3,3',4',5,5',7-Hexahydroxyflavone; Cannabiscetin; Myricetol; NSC 407290
Product Type Chemical
Properties
Formula

C15H10O8

MW 318.24
CAS 529-44-2
RTECS LK8646000
Source/Host Chemicals Plant
Purity Chemicals ≥98% (HPLC)
Appearance Yellow powder.
Solubility Soluble in DMSO (10mg/ml), DMF (10mg/ml) or ethanol (2mg/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 IKMDFBPHZNJCSN-UHFFFAOYSA-N
Smiles OC1=C2C(OC(C3=CC(O)=C(O)C(O)=C3)=C(O)C2=O)=CC(O)=C1
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.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

Myricetin is a naturally occurring flavonol with powerful antioxidant property. It also exhibits a wide range of additional effects that include, anticancer, antidiabetic, neuroprotective and anti-inflammatory activities. It is also used as a preserving agent to extend the shelf life of foods containing oils and fats, based on it's ability to protect lipids against oxidation. Myricetin has been shown to suppress cancer cell invasion and metastasis, to induce cell cycle arrest and apoptosis of cancer cells and to inhibit their proliferation. Myricetin inhibits NLRP3 inflammasome activation via reduction of ROS-dependent ubiquitination of ASC and promotion of ROS-independent NLRP3 ubiquitination.

Product References

(1) K.C. Ong & H.E. Khoo; Gen. Pharmacol. 29, 121 (1997) (Review) | (2) K.P. Devi, et al.; Life Sci. 142, 19 (2015) (Review) | (3) D.K. Semwal, et al.; Nutrients 8, 90 (2016) (Review) | (4) M. Jiang, et al.; Biomed. Pharmacother. 120, 109506 (2019) (Review) | (5) H. Chen, et al.; Toxicol. Appl. Pharmacol. 365, 19 (2019)

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