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    Oxyresveratrol

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      Oxyresveratrol

      SKU
      O0035

      Category: Phytochemicals

      Synonyms
      trans-2',3,4',5-Tetramethoxystilbene
      29700-22-9
      CAS-Number
      C14H12O4
      Molecular Formula
      244.2
      Molecular Weight

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Identity
      1H-NMR
      Appearance
      White to off-white powder

      Properties

      Solvents
      chloroform
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at -20°C.
      Long Term Storage
      -20°C
      Short Term Storage
      +4°C
      Shipping
      AMBIENT
      Transportation
      Not dangerous goods
      Signal word
      Warning
      GHS Symbol
      GHS07
      Precautionary statements
      P305 + P351 + P338
      Hazard statements
      H319
      Description
      Naturallly occuring analog of resveratrol. Potent antioxidant and free-radical scavenger. Shown to have neuroprotective activity against cerebral ischemia and against traumatic injury. Apoptosis inhibitor in transient cerebral ischemia. Inhibits viral DNA replication and late viral protein synthesis of African Swine fever virus. Has depigmenting effects by effectively inhibiting tyrosinase activity, which catalyzes the rate-limiting step in synthesizing melanin pigments. Has anti-inflammatory properties based on inhibition of iNOS expression through down-regulation of NF-kB binding activity and significant inhibition of COX-2 activity. Antihyperlipidemic agent.
      InChi
      InChI=1S/C14H12O4/c15-11-4-3-10(14(18)8-11)2-1-9-5-12(16)7-13(17)6-9/h1-8,15-18H/b2-1-
      References
      (1) Y.M. Kim, et al.: J. Biol. Chem. 277, 16340 (2002) , (2) P. Lorenz, et al.: Nitric Oxide 9, 64 (2003) , (3) K.-O. Chung, et al.: J. Pharm. Pharmacol. 55, 1695 (2003) , (4) S.A. Andrabi, et al.: Brain Res. 1017, 98 (2004) , (5) I. Galindo, et al.: Antiviral Res. 91, 57 (2011) , (6) M. Chatsumpun, et al.: Nat. Prod. Commun. 6, 41 (2011) , (7) J.T. Weber, et al.: Eur. J. Pharmacol. 680, 55 (2012) , (8) S.-P. Jo, et al.: Food Chem. Toxicol. 65, 213 (2014)
      InChi Key
      PDHAOJSHSJQANO-UPHRSURJSA-N
      Smiles
      OC1=CC(O)=C(C=CC2=CC(O)=CC(O)=C2)C=C1

      Naturallly occuring analog of resveratrol. Potent antioxidant and free-radical scavenger. Shown to have neuroprotective activity against cerebral ischemia and against traumatic injury. Apoptosis inhibitor in transient cerebral ischemia. Inhibits viral DNA replication and late viral protein synthesis of African Swine fever virus. Has depigmenting effects by effectively inhibiting tyrosinase activity, which catalyzes the rate-limiting step in synthesizing melanin pigments. Has anti-inflammatory properties based on inhibition of iNOS expression through down-regulation of NF-kB binding activity and significant inhibition of COX-2 activity. Antihyperlipidemic agent.

      SKU: O0035 Category: Phytochemicals
      • Additional information

      Additional information

      Synonyms

      trans-2',3,4',5-Tetramethoxystilbene

      Purity

      ≥98% (HPLC)

      Appearance

      White to off-white powder

      CAS-Number

      29700-22-9

      Molecular Formula

      C14H12O4

      Molecular Weight

      244.2

      Identity

      1H-NMR

      Solvents

      chloroform

      Smiles

      OC1=CC(O)=C(C=CC2=CC(O)=CC(O)=C2)C=C1

      InChi Key

      PDHAOJSHSJQANO-UPHRSURJSA-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.

      Hazard statements

      H319

      Precautionary statements

      P305 + P351 + P338

      GHS Symbol

      GHS07

      Signal word

      Warning

      Transportation

      Not dangerous goods

      References

      (1) Y.M. Kim, et al.: J. Biol. Chem. 277, 16340 (2002), (2) P. Lorenz, et al.: Nitric Oxide 9, 64 (2003), (3) K.-O. Chung, et al.: J. Pharm. Pharmacol. 55, 1695 (2003), (4) S.A. Andrabi, et al.: Brain Res. 1017, 98 (2004), (5) I. Galindo, et al.: Antiviral Res. 91, 57 (2011), (6) M. Chatsumpun, et al.: Nat. Prod. Commun. 6, 41 (2011), (7) J.T. Weber, et al.: Eur. J. Pharmacol. 680, 55 (2012), (8) S.-P. Jo, et al.: Food Chem. Toxicol. 65, 213 (2014)

      InChi

      InChI=1S/C14H12O4/c15-11-4-3-10(14(18)8-11)2-1-9-5-12(16)7-13(17)6-9/h1-8,15-18H/b2-1-

      Quantity

      100 mg, 1 g, Bulk

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