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Chemical Structure
Chemical Structure
Chemical Structure

Altersolanol A [22268-16-2]

Research Use Only
AG-CN2-0436
AdipoGen Life Sciences
CAS Number22268-16-2
Product group Chemicals
Estimated Purity>97%
Molecular Weight336.3
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Altersolanol A
  • Delivery Days Customer
    10
  • CAS Number
    22268-16-2
  • Certification
    Research Use Only
  • Estimated Purity
    >97%
  • Molecular Formula
    C16H16O8
  • Molecular Weight
    336.3
  • Scientific Description
    Anticancer compound. Apoptosis inducer. Anti-angiogenic. Anti-inflammatory. Antibacterial. Phytotoxic. - Chemical. CAS: 22268-16-2. Formula: C16H16O8. MW: 336.3. Isolated from Alternaria sp. Anticancer compound. Apoptosis inducer. Anti-angiogenic. Anti-inflammatory. Antibacterial. Phytotoxic.
  • SMILES
    [H][C@@]12C=CC(=O)[C@@]1(C)[C@@H](O)[C@H]1[C@@H](C[C@H]2C)OC(=O)C1=C
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200

References

  • High-performance liquid chromatographic determination of macrosporin, altersolanol A, alterporriol A, B and C in fermentation of Alternaria porri (Ellis) Ciferri: R. Suemitsu, et al.; J. Chromatogr. 454, 406 (1988)
  • Mode of phytotoxic action of altersolanols: H. Haraguchi, et al.; Phytochemistry 43, 989 (1996)
  • Biologically active polyketide metabolites from an undetermined fungicolous hyphomycete resembling Cladosporium: U. Hoeller, et al.; J. Nat. Prod. 54, 876 (2002)
  • Secondary metabolite profiling of Alternaria dauci, A. porri, A. solani, and A. tomatophila: B. Andersen, et al.; Mycol. Res. 112, 241 (2008)
  • Anticancer effect of altersolanol A, a metabolite produced by the endophytic fungus Stemphylium globuliferum, mediated by its pro-apoptotic and anti-invasive potential via the inhibition of NF-kappaB activity: M.H. Teiten, et al.; Bioorg. Med. Chem. 21, 3850 (2013)
  • Antiangiogenetic effects of anthranoids from Alternaria sp. an endophytic fungus in a Thai medicinal plant Erythrina variegata: P. Pompeng, et al.; Phytomedicine 20, 918 (2013)