![Furan,3-[(1E)-2-[(1S,4aS,8aS)-decahydro-5,5,8a-trimethyl-2-methylene-1-naphthalenyl]ethenyl]-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F316173-furan-3-1e-2-1s-4as-8as-decahydro-558a-trimethyl-2-methylene-1-naphthalenyl-ethenyl.webp&w=3840&q=75)
CAS 117591-81-8: Furan,3-[(1E)-2-[(1S,4aS,8aS)-decahydro-5,5,8a-trimethyl-2-methylene-1-naphthalenyl]ethenyl]-
Formula:C20H28O
Synonyms:- Furan,3-[2-(decahydro-5,5,8a-trimethyl-2-methylene-1-naphthalenyl)ethenyl]-, [1S-[1a(E),4ab,8aa]]-
- (+)-Coronarin E
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Coronarin E
CAS:Coronarin E is a diterpene compound, which is a secondary metabolite derived from the plant genus Hedychium, commonly known as ginger lilies. The source of Coronarin E is particularly found in the rhizomes of these plants, which are native to tropical regions. This compound acts by modulating various biochemical pathways, often showing inhibitory effects on inflammatory mediators and enzymes. Its mode of action also includes potential interference with cellular signaling pathways that regulate apoptosis and proliferation. This makes Coronarin E a subject of interest in the study of cancer and inflammatory diseases. The uses and applications of Coronarin E are primarily in the field of pharmacological research. It is being investigated for its anti-inflammatory, anti-cancer, and antimicrobial properties. Scientists are particularly interested in its capability to inhibit tumor growth and metastasis in vitro and in vivo. Further research is necessary to fully understand its therapeutic potential and molecular targets, as well as its safety and efficacy in clinical settings.Formula:C20H28OPurity:Min. 95%Molecular weight:284.4 g/molCoronarin E
CAS:Coronarin E exhibits weak antimicrobial activity.Formula:C20H28OPurity:98%Color and Shape:SolidMolecular weight:284.44