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    Rutin

    Available from stock

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      Rutin

      SKU
      R0400

      Category: Phytochemicals

      Synonyms
      Rutoside, Phytomelin, Sophorin, Birutan, Eldrin, Birutan Forte, Rutin trihydrate, Globularicitrin, Violaquercitrin, Quercetin rutinoside
      153-18-4
      CAS-Number
      C27H30O16
      Molecular Formula
      610.52
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥95% (HPLC)
      Appearance
      Pale yellow powder
      Identity
      1H-NMR

      Properties

      Solvents
      Soluble in DMSO.
      Melting Point
      125 °C
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      RT
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at RT.
      Hazard statements
      H302
      Precautionary statements
      P264, P270, P301, P312, P330, P501
      GHS Symbol
      GHS07
      Signal word
      Warning
      Transportation
      Not dangerous goods
      Description
      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. Rutin ameliorates obesity through brown fat activation.
      Smiles
      O=C1C2=C(O)C=C(O)C=C2OC(C3=CC(O)=C(O)C=C3)=C1O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)O4
      InChi Key
      IKGXIBQEEMLURG-NVPNHPEKSA-N
      References
      (1) I.B. Afanas'ev, et al.; Biochem. Pharmacol. 38, 1763 (1989) , (2) R.P. Webster, et al.; Cancer Lett. 109, 185 (1996) , (3) E.A. Ostrakhovitch & I.B. Afanas'ev; Biochem. Pharmacol. 62, 743 (2001) , (4) N. Kamalakkannan & P.S. Prince; Basic Clin. Pharmacol. Toxicol. 98, 97 (2006) , (5) J.P. Lin, et al.; Leuk. Res. 33, 823 (2009) , (6) R. Lapa Fda, et al.; J. Pharm. Pharmacol. 63, 875 (2011) , (7) S.W. Wang, et al.; Neurotoxicology 33, 482 (2012) , (8) X. Yuan, et al.; FASEB J. 31, 333 (2016)
      InChi
      (1) S. Brandes, et al.: Chemistry 12, 6039 (2006) , (2) R. Gahlaut, et al.: Spectr. Acta Part A: Mol. Biomol. Spectr. 109, 164 (2013) , (3) F. Dogan, et al.: J. Poly,. Res. 22, 104 (2015)

      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. Rutin ameliorates obesity through brown fat activation.

      SKU: R0400 Category: Phytochemicals
      • Additional information

      Additional information

      Synonyms

      Rutoside, Phytomelin, Sophorin, Birutan, Eldrin, Birutan Forte, Rutin trihydrate, Globularicitrin, Violaquercitrin, Quercetin rutinoside

      Purity

      ≥95% (HPLC)

      Appearance

      Pale yellow powder

      CAS-Number

      153-18-4

      Molecular Formula

      C27H30O16

      Molecular Weight

      610.52

      Identity

      1H-NMR

      Solvents

      Soluble in DMSO.

      Melting Point

      125 °C

      Smiles

      O=C1C2=C(O)C=C(O)C=C2OC(C3=CC(O)=C(O)C=C3)=C1O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)O4

      InChi Key

      IKGXIBQEEMLURG-NVPNHPEKSA-N

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      RT

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at RT.

      Hazard statements

      H302

      Precautionary statements

      P264, P270, P301, P312, P330, P501

      GHS Symbol

      GHS07

      Signal word

      Warning

      Transportation

      Not dangerous goods

      References

      (1) I.B. Afanas'ev, et al.; Biochem. Pharmacol. 38, 1763 (1989), (2) R.P. Webster, et al.; Cancer Lett. 109, 185 (1996), (3) E.A. Ostrakhovitch & I.B. Afanas'ev; Biochem. Pharmacol. 62, 743 (2001), (4) N. Kamalakkannan & P.S. Prince; Basic Clin. Pharmacol. Toxicol. 98, 97 (2006), (5) J.P. Lin, et al.; Leuk. Res. 33, 823 (2009), (6) R. Lapa Fda, et al.; J. Pharm. Pharmacol. 63, 875 (2011), (7) S.W. Wang, et al.; Neurotoxicology 33, 482 (2012), (8) X. Yuan, et al.; FASEB J. 31, 333 (2016)

      InChi

      (1) S. Brandes, et al.: Chemistry 12, 6039 (2006), (2) R. Gahlaut, et al.: Spectr. Acta Part A: Mol. Biomol. Spectr. 109, 164 (2013), (3) F. Dogan, et al.: J. Poly,. Res. 22, 104 (2015)

      Quantity

      50 mg, Bulk

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