Overview

  • Product name

    Ledol, Antifungal agent
  • Description

    Antifungal agent. Putative anti-inflammatory and antinociceptive agent.
  • Biological description

    Antifungal agent. Putative anti-inflammatory and antinociceptive agent. May show expectorant, anti-inflammatory, antitussive and antinociceptive effects in vivo. Orally active.
  • Purity

    > 95%
  • CAS Number

    577-27-5
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    (1aR,4R,4aS,7R,7aS,7bS)-1,1,4,7-Tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol
  • Molecular weight

    222.37
  • Molecular formula

    C15H26O
  • PubChem identifier

    92812
  • Storage instructions

    Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in ethanol and in DMSO
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    C[C@@H]1CC[C@H]2[C@@H]1[C@H]3[C@H](C3(C)C)CC[C@@]2(C)O
  • Source

    Ledum palustre

  • Research areas

References

This product has been referenced in:

  • Baananou S  et al. Supercritical CO2 extract and essential oil of aerial part of Ledum palustre L. - Chemical composition and anti-inflammatory activity. Nat Prod Res :1-7 (2014). Read more (PubMed: 25427723) »
  • Pinheiro BG  et al. Chemical composition, antinociceptive and anti-inflammatory effects in rodents of the essential oil of Peperomia serpens (Sw.) Loud. J Ethnopharmacol 138:479-86 (2011). Read more (PubMed: 21971207) »
  • Kaplan MA  et al. The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study. Phytochemistry 55:749-53 (2000). Read more (PubMed: 11190391) »
See 1 Publication for this product

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