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Merck

70050

Sigma-Aldrich

Myricetin

≥96.0% (HPLC)

Synonym(e):

3,3′,4′,5,5′,7-Hexahydroxy-flavon, Cannabiscetin, Myricetol

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About This Item

Empirische Formel (Hill-System):
C15H10O8
CAS-Nummer:
Molekulargewicht:
318.24
Beilstein:
332331
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352202
PubChem Substanz-ID:
NACRES:
NA.77

Qualitätsniveau

Assay

≥96.0% (HPLC)

Form

powder

mp (Schmelzpunkt)

≥300 °C
>300 °C (lit.)

Löslichkeit

ethanol: 10 mg/mL, clear to very faintly turbid, yellow to very deep greenish-yellow

Anwendung(en)

metabolomics
vitamins, nutraceuticals, and natural products

SMILES String

Oc1cc(O)c2C(=O)C(O)=C(Oc2c1)c3cc(O)c(O)c(O)c3

InChI

1S/C15H10O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,16-20,22H

InChIKey

IKMDFBPHZNJCSN-UHFFFAOYSA-N

Angaben zum Gen

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Allgemeine Beschreibung

Myricetin (MYR) is a natural polyhydroxyflavonol compound, first isolated from the bark of Morella rubra (Myrica rubra) tree.

Anwendung

Myricetin has been used:
  • to study its preventive effect as an antioxidant on noise-induced hearing loss (NIHL) in rats
  • as a flavonoid compound to test antiviral activity of Bourbon virus (BRBV) and in inhibition of RNA-dependent RNA polymerase (RdRP)
  • to study its effect as a treatment on biofilms of Streptococcus mutans and Candida albicans
  • as a reference standard for the quantification of phenolic compounds from Juniperus species

Biochem./physiol. Wirkung

Myricetin exerts anti-oxidant effects, and anti-inflammatory effects by regulating multiple signal pathways. It also displays anti-diabetic and hepatoprotective effects. Myricetin strongly inhibits yeast α-glucosidase, glyoxalase I in vitro, and bovine milk xanthine oxidase. It also promotes complex formation between DNA and both topoisomerase I and II, an effect that may have implications in cancer chemotherapy. Myricetin also has various nutraceuticals values and therapeutic effects.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Xiaominting Song et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 134, 111017-111017 (2020-12-19)
Myricetin(MYR) is a flavonoid compound widely found in many natural plants including bayberry. So far, MYR has been proven to have multiple biological functions and it is a natural compound with promising research and development prospects. This review comprehensively retrieved
M. Iio, et al.
Agricultural and Biological Chemistry, 48, 1559-1559 (1984)
M. Iio et al.
Agricultural and Biological Chemistry, 49, 2173-2173 (1985)
Deepak Kumar Semwal et al.
Nutrients, 8(2), 90-90 (2016-02-20)
Myricetin is a common plant-derived flavonoid and is well recognised for its nutraceuticals value. It is one of the key ingredients of various foods and beverages. The compound exhibits a wide range of activities that include strong anti-oxidant, anticancer, antidiabetic
R.B. Brandt et al.
International Journal of Quantum Chemistry, 11, 195-195 (1984)

Artikel

Antioxidants protect biological systems from oxidative damage produced by oxygen-containing free radicals and from redoxactive transition metal ions such as iron, copper, and cadmium.

Protokolle

Protocol for HPLC Analysis of Flavonoids on Ascentis® RP-Amide

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