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Myricetin

Myricetin Structure
CAS No.
529-44-2
Chemical Name:
Myricetin
Synonyms
MYRICETOL;bayberry bark extract;MYRICETIN 95%;CANNABISCETIN;3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one;MYRISETIN;MYRICETIN;NSC 407290;LDN 0014058;Myricetin>
CBNumber:
CB5142262
Molecular Formula:
C15H10O8
Molecular Weight:
318.24
MOL File:
529-44-2.mol
MSDS File:
SDS
Modify Date:
2024/7/25 20:04:51

Myricetin Properties

Melting point >300 °C(lit.)
Boiling point 377.41°C (rough estimate)
Density 1.4222 (rough estimate)
refractive index 1.4395 (estimate)
storage temp. 2-8°C
solubility ethanol: soluble10mg/mL, clear to very faintly turbid, yellow to very deep greenish-yellow
pka 6.30±0.40(Predicted)
form crystalline
color Yellowish Brown
Water Solubility Soluble in dimethyl sulfoxide,dimethyl formamide and ethanol. Insoluble in water.
Merck 14,6332
BRN 332331
Stability Hygroscopic
InChIKey IKMDFBPHZNJCSN-UHFFFAOYSA-N
LogP 1.206 (est)
CAS DataBase Reference 529-44-2(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Safety Statements  24/25
WGK Germany  3
RTECS  LK8646000
10
HS Code  29329990

Myricetin price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) M6760 Myricetin ≥96.0%, crystalline 529-44-2 10MG ₹7122.85 2022-06-14 Buy
Sigma-Aldrich(India) M6760 Myricetin ≥96.0%, crystalline 529-44-2 25MG ₹14104.98 2022-06-14 Buy
Sigma-Aldrich(India) 70050 Myricetin ≥96.0% (HPLC) 529-44-2 25MG ₹14353.95 2022-06-14 Buy
Sigma-Aldrich(India) 72576 Myricetin analytical standard 529-44-2 10MG ₹14635.4 2022-06-14 Buy
Sigma-Aldrich(India) 70050 Myricetin ≥96.0% (HPLC) 529-44-2 100MG ₹45573.25 2022-06-14 Buy
Product number Packaging Price Buy
M6760 10MG ₹7122.85 Buy
M6760 25MG ₹14104.98 Buy
70050 25MG ₹14353.95 Buy
72576 10MG ₹14635.4 Buy
70050 100MG ₹45573.25 Buy

Myricetin Chemical Properties,Uses,Production

Description

Myricetin[529-44-2] is a flavonoid compound found in many fruits and vegetables, including red wine, that acts as a powerful antioxidant. Myricetin inhibits TBARS formation with an IC50 value of 6.34 and at 20 μM, blocks oxLDL uptake by U937-derived macrophages, reducing CD36 expression. Myricetin demonstrates potent chemopreventative potential by binding JAK1/STAT3 to inhibit the neoplastic transformation of murine JB6 P+ cells and inhibiting MEK1 kinase activity.

Chemical Properties

The substance is a brown-yellow to brown-green crystalline powder. It can dissolve in methanol, ethanol, acetone, and ethyl acetate, and has a low solubility in water. It is not soluble in chloroform and petroleum ether. This compound is derived from the fruit of Myrica rubra (Lour.) Sieb. et Zucc. and belongs to the Populus family.

Uses

Myricetin is used as an antioxidant. It is a cell-permeable flavonoid used in inflammatory, diabetes, and cancer studies. It is effective in protecting neurons against oxidative stresses. Further, it inhibits yeast alfa-glucosidase,1 glyoxalase I in vitro and bovine milk xanthine oxidase.

Definition

ChEBI: Myricetin is a hexahydroxyflavone that is flavone substituted by hydroxy groups at positions 3, 3', 4', 5, 5' and 7. It has been isolated from the leaves of Myrica rubra and other plants. It has a role as a cyclooxygenase 1 inhibitor, an antineoplastic agent, an antioxidant, a plant metabolite, a food component, a hypoglycemic agent and a geroprotector. It is a hexahydroxyflavone and a 7-hydroxyflavonol. It is a conjugate acid of a myricetin(1-).

General Description

Myricetin is a novel flavanoid compound useful as chemotherapeutic, chemopreventive, and antiangiogenic agent. It also acts as an antioxidant, anti-inflammatory, and anti-cancer agent, and can inhibit the activity of reverse transcriptase.

Purification Methods

Myricetin (Cannabiscetin, 3,3',4',5,5',7-hexahydroxyflavone) [529-44-2] M 318.2, m > 3 0 0o, 357o(dec) (polyphenolic pKEst~8-11). Recrystallise myricetin from aqueous EtOH (m 357o dec, as monohydrate) or Me2CO (m 350o dec, with one mol of Me2CO) as yellow crystals. It is almost insoluble in CHCl3 and AcOH. The hexaacetate has m 213o. [Hergert J Org Chem 21 534 1956, Spada & Cameroni Gazzetta 86 965, 975 1956, Kalff & Robinson J Chem Soc 127 181 1925, Beilstein 18/5 V 670.]

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