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    Hyperoside

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      Hyperoside

      SKU
      H0298

      Category: Phytochemicals

      Synonyms
      3,3',4',5,7-Pentahydroxyflavone 3-D-galactoside , Hyperin , Quercetin 3-D-galactoside , NSC 407304
      482-36-0
      CAS-Number
      C21H20O12
      Molecular Formula
      464.38
      Molecular Weight

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

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Appearance
      Yellow powder
      Identity
      1H-NMR

      Properties

      Solvents
      DMSO (10 mg/ml), DMF (10 mg/ml)
      Melting Point
      220-230° C
      Refractive Index
      1.80 (Predicted)
      Density
      ~1.9 g/cm3
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      Long Term Storage
      -20°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at -20°C.
      Transportation
      Not dangerous goods
      Description
      Hyperoside is a 3-O-galactoside of quercetin that can be found in a wide range of plants. It shows diverse biological activities, including antioxidant, anti-inflammatory, neuroprotective, antihypoglycemic and antiadipogenic, antibacterial and anticancer properties. It has powerful antioxidant action through its ability to scavenge free radicals. It inhibits the NF-&kappa,B signaling pathway. Hyperoside selectively interrupted NLRC4 and AIM2 inflammasome activation but did not alter cytokine expression. The quorum sensing-inhibiting effect of hyperoside may lead to a reduction in biofilm formation in P. aeruginosa. Honokiol exerts broad-range anticancer activity, such as induction of apoptosis and autophagy and inhibition of cell proliferation. Hyperoside has a beneficial effect on the prevention and treatment of obesity.
      Smiles
      O=C1C2=C(O)C=C(O)C=C2OC(C3=CC=C(O)C(O)=C3)=C1O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O
      InChi Key
      OVSQVDMCBVZWGM-DTGCRPNFSA-N
      References
      (1) M.J. Piao, et al., Biochim. Biophys. Acta 1780, 1448 (2008) , (2) S.J. Kim, et al., Am. J. Chin. Med. 39, 171 (2011) , (3) K.W. Zeng, et al., Eur. J. Pharmacol. 672, 45 (2011) , (4) N. Zhang, et al., PLoS One 9, e98973 (2014) , (5) S.K. Ku, et al., Inflammation 38, 784 (2015) , (6) T. Fu, et al., Acta Pharmacol. Sin. 37, 505 (2016) , (7) P. Lu, Biomed. Pharmacother. 82, 216 (2016) , (8) H. Ahn & G.S. Lee, Phytomedicine 24, 77 (2017) , (9) Y. Sun, et al., Exp. Ther. Med. 14, 1647 (2017) , (10) Y. Zhang, et al., Int. J. Mol. Med. 41, 77 (2018) , (11) M. Berkoz, Acta Endocrinol. 15, 165 (2019)
      InChi
      InChI=1S/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-27,29-30H,6H2/t13-,15+,17+,18-,21+/m1/s1

      Hyperoside is a 3-O-galactoside of quercetin that can be found in a wide range of plants. It shows diverse biological activities, including antioxidant, anti-inflammatory, neuroprotective, antihypoglycemic and antiadipogenic, antibacterial and anticancer properties. It has powerful antioxidant action through its ability to scavenge free radicals. It inhibits the NF-&kappa,B signaling pathway. Hyperoside selectively interrupted NLRC4 and AIM2 inflammasome activation but did not alter cytokine expression. The quorum sensing-inhibiting effect of hyperoside may lead to a reduction in biofilm formation in P. aeruginosa. Honokiol exerts broad-range anticancer activity, such as induction of apoptosis and autophagy and inhibition of cell proliferation. Hyperoside has a beneficial effect on the prevention and treatment of obesity.

      SKU: H0298 Category: Phytochemicals
      • Additional information

      Additional information

      Synonyms

      3,3',4',5,7-Pentahydroxyflavone 3-D-galactoside, Hyperin, Quercetin 3-D-galactoside, NSC 407304

      Purity

      ≥98% (HPLC)

      Appearance

      Yellow powder

      CAS-Number

      482-36-0

      Molecular Formula

      C21H20O12

      Molecular Weight

      464.38

      Identity

      1H-NMR

      Solvents

      DMSO (10 mg/ml), DMF (10 mg/ml)

      Melting Point

      220-230° C

      Refractive Index

      1.80 (Predicted)

      Density

      ~1.9 g/cm3

      Smiles

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

      InChi Key

      OVSQVDMCBVZWGM-DTGCRPNFSA-N

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      Long Term Storage

      -20°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at -20°C.

      Transportation

      Not dangerous goods

      References

      (1) M.J. Piao, et al., Biochim. Biophys. Acta 1780, 1448 (2008), (2) S.J. Kim, et al., Am. J. Chin. Med. 39, 171 (2011), (3) K.W. Zeng, et al., Eur. J. Pharmacol. 672, 45 (2011), (4) N. Zhang, et al., PLoS One 9, e98973 (2014), (5) S.K. Ku, et al., Inflammation 38, 784 (2015), (6) T. Fu, et al., Acta Pharmacol. Sin. 37, 505 (2016), (7) P. Lu, Biomed. Pharmacother. 82, 216 (2016), (8) H. Ahn & G.S. Lee, Phytomedicine 24, 77 (2017), (9) Y. Sun, et al., Exp. Ther. Med. 14, 1647 (2017), (10) Y. Zhang, et al., Int. J. Mol. Med. 41, 77 (2018), (11) M. Berkoz, Acta Endocrinol. 15, 165 (2019)

      InChi

      InChI=1S/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-27,29-30H,6H2/t13-,15+,17+,18-,21+/m1/s1

      Quantity

      25 mg, Bulk

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