2. Natural Products
  3. Disease Research Fields Plants Microorganisms Endogenous metabolite Terpenoids
  4. Other Diseases Polyporaceae other families Human Gut Microbiota Metabolites Triterpenes
  5. 110241-19-5

110241-19-5

Ganoderic acid N Chemical Structure

110241-19-5

Chemical Structure

  • Ganoderic acid N
  • CAS No: 110241-19-5
    Formula: C30H42O8
    Molecular Weight: 530.65
  • IUPAC Name: 6-hydroxy-6-((5R,7S,10S,13R,14R,17S)-7-hydroxy-4,4,10,13,14-pentamethyl-3,11,15-trioxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methyl-4-oxoheptanoic acid
  • InChIKey: XXHBQOHASACCAP-QNYQZGHFSA-N
  • SMILES: O=C1CC[C@]2([C@]([H])(C1(C)C)C[C@@H](C([C@@](C)([C@@]3(C4)C)C(C[C@@H]3C(O)(C)CC(CC(C)C(O)=O)=O)=O)=C2C4=O)O)C

Biological Activity: Ganoderic acid N is a natural terpenoid isolated from the Fungus Ganoderma lucidum[1][2].

Cat. No. Product Name Purity Description
HY-123100 Ganoderic acid N 99.81% Ganoderic acid N is a natural terpenoid isolated from the Fungus Ganoderma lucidum.
HY-123100R Ganoderic acid N (Standard) ≥98% Isoxepac (Standard) is the analytical standard of Isoxepac. This product is intended for research and analytical applications. Isoxepac (HP 549) is a nonsteroidal anti-inflammatory agent (NSAID) with anti-inflammatory, analgesic and antipyretic activity. Isoxepac has been studied in rat, rabbit, dog, rhesus monkey, etc.

References

[1]. Zhenhao Li, et al. Screening Immunoactive Compounds of Ganoderma lucidum Spores by Mass Spectrometry Molecular Networking Combined With in vivo Zebrafish Assays. Front Pharmacol. 2020 Mar 18;11:287. [Content Brief]
[2]. Baosong Chen, et al. Triterpenes and meroterpenes from Ganoderma lucidum with inhibitory activity against HMGs reductase, aldose reductase and α-glucosidase. Fitoterapia. 2017 Jul;120:6-16. [Content Brief]

Keywords:

Ganoderic acid NGanoderic acid N (Standard)