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Rutin hydrate_Molecular_structure_CAS_207671-50-9)
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Rutin hydrate

Catalog No. R5143 Name Sigma Aldrich
CAS Number 207671-50-9 Website http://www.sigmaaldrich.com
M. F. C27H36O19 Telephone 1-800-521-8956
M. W. 664.56334 Fax
Purity ≥94% (HPLC) Email
Storage Chembase ID: 155100

SYNONYMS

Title
芦丁 水合物
IUPAC name
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-4H-chromen-4-one trihydrate
IUPAC Traditional name
troxerutin trihydrate
Synonyms
Quercetin-3-rutinoside hydrate
Vitamin P 水合物
Vitamin P hydrate
Quercetin-3-rutinoside 水合物

DATABASE IDS

MDL Number MFCD00149490
Beilstein Number 75455
EC Number 205-814-1
CAS Number 207671-50-9
PubChem SID 24899379

PROPERTIES

Empirical Formula (Hill Notation) C27H30O16 · xH2O
Purity ≥94% (HPLC)
Apperance yellow to green powder
Melting Point 195 °C (dec.)(lit.)
Solubility pyridine: soluble50 mg/mL
Solubility DMSO: soluble
Solubility aqueous base: soluble
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
Risk Statements 22
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
A polyphenolic flavonoid that acts as an antioxidant and NO scavenger. It can attenuate peroxide production in glial cells by acting as a free radical scavenger and protect renal cells from oxidative injury. Inclusion of rutin in the diet of rats significantly reduced the appearance of single-strand breaks in nuclear DNA caused by hepatocarcinogens aflatoxin B1 and N-nitrosodimethylamine. This protection from DNA damage was found to be due to a reduction in the induction of repair enzymes polymerase, DNA polymerase β and DNA ligase. Since DNA damage and inefficient repair are thought to initiate the process of carcinogenesis, effects of rutin on these functions suggests a protective role of this flavonoid against carcinogenesis induced by chemical carcinogens.
Protocols & Applications
Ginkgo (Ginkgo biloba) Plant Profile: bioactives, mechanism of action, references
Description (简体中文)
Biochem/physiol Actions
A polyphenolic flavonoid that acts as an antioxidant and NO scavenger. It can attenuate peroxide production in glial cells by acting as a free radical scavenger and protect renal cells from oxidative injury. Inclusion of rutin in the diet of rats significantly reduced the appearance of single-strand breaks in nuclear DNA caused by hepatocarcinogens aflatoxin B1 and N-nitrosodimethylamine. This protection from DNA damage was found to be due to a reduction in the induction of repair enzymes polymerase, DNA polymerase β and DNA ligase. Since DNA damage and inefficient repair are thought to initiate the process of carcinogenesis, effects of rutin on these functions suggests a protective role of this flavonoid against carcinogenesis induced by chemical carcinogens.
Protocols & Applications
Ginkgo (Ginkgo biloba) Plant Profile: bioactives, mechanism of action, references

REFERENCES