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Myricetin

Catalog No. 70050 Name Sigma Aldrich
CAS Number 529-44-2 Website http://www.sigmaaldrich.com
M. F. C15H10O8 Telephone 1-800-521-8956
M. W. 318.2351 Fax
Purity ≥96.0% (HPLC) Email
Storage Chembase ID: 2116

SYNONYMS

IUPAC name
3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one
IUPAC Traditional name
myricetin
Synonyms
3,3′,4′,5,5′,7-Hexahydroxyflavone
Cannabiscetin

DATABASE IDS

PubChem SID 24886044
Beilstein Number 332331
CAS Number 529-44-2
MDL Number MFCD00006827
EC Number 208-463-2

PROPERTIES

Empirical Formula (Hill Notation) C15H10O8
Purity ≥96.0% (HPLC)
Gene Information human ... CYP1A2(1544)mouse ... Hexa(15211)rat ... Il4(287287), Tnf(24835)
Melting Point ≥300 °C
Melting Point >300 °C(lit.)
Solubility ethanol: soluble10 mg/mL, clear to very faintly turbid, yellow to very deep greenish-yellow
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Strongly inhibits yeast α-glucosidase,1 glyoxalase I in vitro,2 and bovine milk xanthine oxidase.3 Promotes complex formation between DNA and both topoisomerase I and II, an effect that may have implications in cancer chemotherapy.4
Description (简体中文)
Biochem/physiol Actions
Strongly inhibits yeast α-glucosidase,1 glyoxalase I in vitro,2 and bovine milk xanthine oxidase.3 Promotes complex formation between DNA and both topoisomerase I and II, an effect that may have implications in cancer chemotherapy.4

REFERENCES