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CAS 62218-13-7: α-Viniferin

Formula:C42H30O9
InChI:InChI=1S/C42H30O9/c43-22-7-1-19(2-8-22)40-37-28-13-25(46)17-32-35(28)39(42(50-32)21-5-11-24(45)12-6-21)30-15-27(48)18-33-36(30)38(29-14-26(47)16-31(49-40)34(29)37)41(51-33)20-3-9-23(44)10-4-20/h1-18,37-48H/t37-,38-,39+,40+,41+,42-/m0/s1
InChI key:InChIKey=KUTVNHOAKHJJFL-MHZVOPJQSA-N
SMILES:OC=1C=C2[C@]3(C=4C([C@@]5(C=6C([C@]7(C2=C(O[C@@H]7C8=CC=C(O)C=C8)C1)[H])=CC(O)=CC6O[C@H]5C9=CC=C(O)C=C9)[H])=CC(O)=CC4O[C@@H]3C%10=CC=C(O)C=C%10)[H]
Synonyms:
  • (+)-.alpha.-Viniferin
  • (+)-a-Viniferin
  • (2R,2aR,7R,7aR,12S,12aS)-2,7,12-Tris(4-hydroxyphenyl)-2,2a,7,7a,12,12a-hexahydrobis[1]benzofuro[3',4':4,5,6
  • 3'',4'':7,8,9]Cyclonona[1,2,3-Cd][1]Benzofuran-4,9,14-Triol
  • 3'',4'':7,8,9]cyclonona[1,2,3-cd]benzofuran-4,9,14-triol, 2,2a,7,7a,12,12a-hexahydro-2,7,12-tris(4-hydroxyphenyl)-, (2R,2aR,7R,7aR,12S,12aS)-
  • Bisbenzofuro[3',4':4,5,6
  • Cyclonona[1,2,3-cd:4,5,6-c'd′:7,8,9-c′′d′′]trisbenzofuran-4,9,14-triol, 2,2a,7,7a,12,12a-hexahydro-2,7,12-tris(4-hydroxyphenyl)-, (2R*,2aR*,7R*,7aR*,12S*,12aS*)-(+)-
  • Cyclonona[1,2,3-cd:4,5,6-c'd′:7,8,9-c′′d′′]trisbenzofuran-4,9,14-triol, 2,2a,7,7a,12,12a-hexahydro-2,7,12-tris(4-hydroxyphenyl)-, (2R,2aR,7R,7aR,12S,12aS)-rel-(+)-
  • rel-(+)-(2R,2aR,7R,7aR,12S,12aS)-2,2a,7,7a,12,12a-Hexahydro-2,7,12-tris(4-hydroxyphenyl)cyclonona[1,2,3-cd:4,5,6-c'd′:7,8,9-c′′d′′]trisbenzofuran-4,9,14-triol
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Found 4 products.
  • α-Viniferin

    CAS:
    α-Viniferin known as 2-arylbenzofuran flavonoids, that are inhibitors of prostaglandin H2 synthetase. α-Viniferin has anti-Alzheimer's disease, anti-tuberculosis, anti-tumor, anti-inflammation, anti-diabetes and other pharmacological activitie
    Formula:C42H30O9
    Purity:98%
    Color and Shape:Solid
    Molecular weight:678.68

    Ref: TM-TN1378

    1mg
    137.00€
    5mg
    329.00€
    10mg
    560.00€
    25mg
    879.00€
  • ±-Viniferin

    CAS:
    ±-Viniferin is a stilbenoid compound, which is a type of oligomer derived from the natural phytoalexin resveratrol. It is sourced mainly from grapevines, particularly in the bark, roots, and leaves of Vitis vinifera. Its biosynthesis occurs as a defense response mechanism in plants when under stress from pathogens or environmental conditions. The mode of action of ±-Viniferin involves its ability to scavenger free radicals and inhibit inflammatory pathways. It exerts its effects through modulation of various signaling molecules and enzymes involved in oxidative stress and inflammation. This action is imparted by its structural configuration, which allows it to interact effectively with biological pathways. Utilized predominantly in research, ±-Viniferin is explored for its potential therapeutic benefits, particularly in its antioxidant and anti-inflammatory capacities. It holds promise in the development of treatments for oxidative stress-related conditions such as neurodegenerative diseases, cardiovascular issues, and various inflammatory disorders. Furthermore, its role in plant defense mechanisms highlights its potential applications in agriculture for enhancing disease resistance in crops.
    Formula:C42H30O9
    Purity:Min. 95%
    Molecular weight:678.7 g/mol

    Ref: 3D-MCA21813

    10mg
    786.00€
    25mg
    1,208.00€
    50mg
    1,933.00€
  • α-Viniferin

    CAS:
    Formula:C42H30O9
    Purity:95%~99%
    Color and Shape:Powder
    Molecular weight:678.693

    Ref: BP-SBP00225

    ne
    To inquire
  • α-viniferin

    CAS:
    Formula:C42H30O9
    Purity:95%
    Color and Shape:Solid
    Molecular weight:678.6822

    Ref: IN-DA00EGTE

    5mg
    To inquire