Substance

ID:351751

Names and Identifiers
IUPAC Traditional name
isorhamnetin
IUPAC name
3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-chromen-4-one
Synonyms
3′-Methoxy-3,4′,5,7-tetrahydroxyflavoneIsorhamnetin
Registration numbers
Beilstein Number
CAS Number
EC Number
MDL Number
PubChem SID
Properties
Safety Information
MSDS Link
Personal Protective Equipment
Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
Safety Statements
36/37
German water hazard class
3
GHS Hazard statements
H351
GHS Signal Word
Warning
GHS Pictograms
GHS08
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
GHS Precautionary statements
P281
Risk Statements
40
European Hazard Symbols
Harmful Harmful (Xn)
RTECS
LK9275450
Product Information
Empirical Formula (Hill Notation)
C16H12O7
Purity
≥95.0% (HPLC)
Molecule Details
Biochem/physiol Actions
Isorhamnetin inhibits adipogenesis by interfering with differentiation of adipose stem cells, by a mechanism involving stabilization of β-catenin and up-regulating the Wnt signaling pathway.1
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 17794.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Protocols & Applications
Ginkgo (Ginkgo biloba) Plant Profile: bioactives, mechanism of action, references
Molecular Spectra
No Data Available
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References
No Data Available
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