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Chemical Structure
Chemical Structure
Chemical Structure

Viridiol [23820-80-6]

Research Use Only
AG-CN2-0126
AdipoGen Life Sciences
CAS Number23820-80-6
Product group Chemicals
Estimated Purity>95%
Molecular Weight354.4
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Viridiol
  • Delivery Days Customer
    10
  • CAS Number
    23820-80-6
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Hazard Information
    Warning
  • Molecular Formula
    C20H18O6
  • Molecular Weight
    354.4
  • Scientific Description
    Chemical. CAS: 23820-80-6. Formula: C20H18O6. MW: 354.4. Isolated from Trichoderma sp. Steroidal antibiotic. Belongs to the Viridin family, including Wortmannin (Prod. No. AG-CN2-0023 http://www.adipogen.com/ag-cn2-0023/wortmannin.html ). Antifungal. Phytotoxin. Shows necrotic activity on plants. Phosphatidylinositol 3-kinase (PI3K) inhibitor. - Steroidal antibiotic. Belongs to the Viridin family, including Wortmannin (Prod. No. AG-CN2-0023 http://www.adipogen.com/ag-cn2-0023/wortmannin.html ). Antifungal. Phytotoxin. Shows necrotic activity on plants. Phosphatidylinositol 3-kinase (PI3K) inhibitor.
  • SMILES
    CO[C@@H]1[C@H](O)C2=COC3=C2[C@](C)([C@@H]1O)C1=CC=C2C(=O)CCC2=C1C3=O
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200

References

  • Viridiol, a steroid-like product from Trichoderma viride: J.S. Moffatt, et al.; J. Chem. Soc. D, 1969, 839a (1969)
  • Conversion of viridin to viridiol by viridin-producing fungi: R.W. Jones & J.G. Hancock; Can. J. Microbiol. 33, 963 (1987)
  • The biosynthesis of the steroid, viridiol, by Gliocladium deliquescens: R. James, et al.; Phytochemistry 27, 387 (1988)
  • Plant Growth Response to the Phytotoxin Viridiol Produced by the Fungus Gliocladium virens: R.W. Jones, et al.; Weed Sci. 36, 683 (1988)
  • Isolation, identification and necrotic activity of viridiol from Chalara fraxinea, the fungus responsible for dieback of ash: P.F. Andersson, et al.; Forest Pathol. 40, 43 (2010)
  • Asterogynins: secondary metabolites from a Costa Rican endophytic fungus: S. Cao, et al.; Org. Lett. 12, 4661 (2010)