R5143

Rutin hydrate

≥94% (HPLC), powder

• Synonyme(s) : Quercetin-3-rutinoside hydrate, Vitamin P hydrate
• Formule empirique (notation de Hill): C₂₇H₃₀O₁₆ · xH₂O
• Numéro CAS: 207671-50-9
• Poids moléculaire : 610.52 (anhydrous basis)
• Numéro Beilstein : 75455
• Numéro CE : 205-814-1
• Numéro MDL: MFCD01319140
• Code UNSPSC : 12352201
• ID de substance PubChem : 24899379
• Nomenclature NACRES : NA.25

Propriétés

• Niveau de qualité: 200
• Pureté: ≥94% (HPLC)
• Forme: powder
• Couleur: yellow to green
• Pf: 195 °C (dec.) (lit.)
• Solubilité: pyridine: 50 mg/mL; DMSO: soluble; aqueous base: soluble
• Application(s): metabolomics; vitamins, nutraceuticals, and natural products
• Chaîne SMILES: [H]O[H].O[C@H]1[C@H](OC[C@H]([C@H]2O)O[C@@H](OC(C3=O)=C(C4=CC=C(O)C(O)=C4)OC5=C3C(O)=CC(O)=C5)[C@H](O)[C@H]2O)O[C@H]([C@@H]([C@H]1O)O)C
• InChI: 1S/C27H30O16.H2O/c1-8-17(32)20(35)22(37)26(40-8)39-7-15-18(33)21(36)23(38)27(42-15)43-25-19(34)16-13(31)5-10(28)6-14(16)41-24(25)9-2-3-11(29)12(30)4-9;/h2-6,8,15,17-18,20-23,26-33,35-38H,7H2,1H3;1H2/t8-,15+,17-,18+,20+,21-,22+,23+,26+,27-;/m0./s1
• Clé InChI: PGHSKTKIQIBATG-ZAAWVBGYSA-N

Description

Description générale

Rutin hydrate has radioprotective and antiplatelet activity. Rutin reduces hepatic and blood cholesterol levels.

Application

Rutin hydrate has been used:

• as an inhibitory compound against Skeletonema costatum
• to analyze the phenolic component and antioxidant activity of nettle
• to assess the flavonoid content in Propolis

Actions biochimiques/physiologiques

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-nitrosodiumethylamine. 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.

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: dust mask type N95 (US), Eyeshields, Gloves