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ProductsBack/Ophiobolin A [4611-05-6]
Chemical Structure
Chemical Structure
Chemical Structure

Ophiobolin A [4611-05-6]

Research Use Only
AG-CN2-0431
AdipoGen Life Sciences
CAS Number4611-05-6
DownloadMSDS
Product group Chemicals
Estimated Purity>95%
Molecular Weight400.6
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Ophiobolin A [4611-05-6]
  • Delivery Days Customer
    10
  • ADR Class
    6.1
  • CAS Number
    4611-05-6
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Hazard Information
    Danger,Excepted quantity
  • Molecular Formula
    C25H36O4
  • Molecular Weight
    400.6
  • Scientific Description
    Cell permeable, irreversible calmodulin antagonist. Acts by covalently binding to a lysine-rich inhibitory site. Inhibits by blocking the activation of the Ca2+/calmodulin-dependent phosphodiesterase [1-3, 5, 6, 9]. Herbicidal mycotoxin [7]. Phytotoxic, antifungal, antibacterial and nematocidal compound [4, 6, 10]. Anticancer compound. Shown to induce paraptosis-like cell death [11, 12]. Shown to inhibit P-glycoprotein-mediated transport [8]. Disruptor of intracellular sulfhydryl proteostasis, leading to ER stress and dilation. - Chemical. CAS: 4611-05-6. Formula: C25H36O4. MW: 400.6. Isolated from Bipolaris leersia. Cell permeable, irreversible calmodulin antagonist. Acts by covalently binding to a lysine-rich inhibitory site. Inhibits by blocking the activation of the Ca2+/calmodulin-dependent phosphodiesterase. Herbicidal mycotoxin. Phytotoxic, antifungal, antibacterial and nematocidal compound. Anticancer compound. Shown to induce paraptosis-like cell death. Shown to inhibit P-glycoprotein-mediated transport.
  • SMILES
    [H]C(=O)C1=C[C@]2([H])[C@](C)(CC[C@@]22O[C@H](C[C@@H]2C)C=C(C)C)C[C@@]2([H])[C@]1([H])C(=O)C[C@@]2(C)O
  • Storage Instruction
    -20°C,2°C to 8°C
  • UN Number
    UN 3462
  • UNSPSC
    12352200

References

  • Ophiobolin A. A natural product inhibitor of calmodulin: P.C. Leung, et al.; J. Biol. Chem. 259, 2742 (1984)
  • Role of Calmodulin Inhibition in the Mode of Action of Ophiobolin A: P.C. Leung, et al.; Plant Physiol. 77, 303 (1985)
  • Characterization of the interaction of ophiobolin A and calmodulin: P.C. Leung, et al.; Int. J. Biochem. 20, 1351 (1988)
  • Microbial metabolites of ophiobolin A and antimicrobial evaluation of ophiobolins: E. Li, et al.; J. Nat. Prod. 58, 74 (1995)
  • Identification of the binding and inhibition sites in the calmodulin molecule for ophiobolin A by site-directed mutagenesis: T. Kong Au & P. Chow Leung; Plant Physiol. 118, 965 (1998)
  • The biology of ophiobolins: T.K. Au, et al.; Life Sci. 67, 733 (2000) (Review)
  • Herbicidal potential of ophiobolins produced by Drechslera gigantea: A. Evidente, et al.; J. Agric. Food Chem. 54, 1779 (2006)
  • Inhibition of P-glycoprotein-mediated transport by terpenoids contained in herbal medicines and natural products: N. Yoshida, et al.; Food Chem. Toxicol. 44, 2033 (2006)
  • Calcium depletion and calmodulin inhibition affect the import of nuclear-encoded proteins into plant mitochondria: S. Kuhn, et al.; Plant J. 58, 694 (2009)
  • Effect of the sesterterpene-type metabolites, ophiobolins A and B, on zygomycetes fungi: K. Krizsan, et al.; FEMS Microbiol. Lett. 313, 135 (2010)