10219-75-7 Usage
Description
EREMOPHILENE is a naturally occurring compound found in Alpinia oxyphylla essential oil, which is known for its diverse applications in various industries, particularly in the fields of cancer research, food, and pharmaceuticals. It possesses unique properties that make it a valuable component for different applications.
Uses
Used in Cancer Research:
EREMOPHILENE is used as a component in the in vitro cytotoxicity of human cancer cell lines, demonstrating its potential as a therapeutic agent against cancer. Its presence in Alpinia oxyphylla essential oil contributes to the overall effectiveness of the oil in combating cancer cells.
Used in the Food Industry:
EREMOPHILENE is used as a valuable component in the food industry, where it contributes to the unique flavor and aroma of certain food products. Its presence in essential oils derived from Alpinia oxyphylla makes it a sought-after ingredient for enhancing the sensory qualities of various dishes.
Used in the Pharmaceutical Industry:
EREMOPHILENE is used as a potential therapeutic agent in the pharmaceutical industry, thanks to its cytotoxic properties against cancer cells. Its inclusion in essential oils and other medicinal formulations can lead to the development of novel treatments for various diseases, including cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 10219-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,1 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10219-75:
(7*1)+(6*0)+(5*2)+(4*1)+(3*9)+(2*7)+(1*5)=67
67 % 10 = 7
So 10219-75-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-11(2)13-8-9-14-7-5-6-12(3)15(14,4)10-13/h7,12-13H,1,5-6,8-10H2,2-4H3/t12-,13+,15+/m0/s1
10219-75-7Relevant articles and documents
Structure and absolute configuration of kusunol.
Hikino,Suzuki,Takemoto
, p. 832 - 838 (1968)
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Biotransformation of aristolane- and 2,3-secoaromadendrane-type sesquiterpenoids having a 1,1-dimethylcyclopropane ring by Chlorella fusca var. vacuolata, Mucor species, and Aspergillus niger
Furusawa, Mai,Hashimoto, Toshihiro,Noma, Yoshiaki,Asakawa, Yoshinori
, p. 861 - 868 (2007/10/03)
Biotransformation of the aristolane-type sesquiterpene hydrocarbon (+)-1(10)-aristolene (1) from the crude drug Nardostachys chinensis and of the 2,3-secoaromadendrane-type sesquiterpene lactone plagiochilide (2) from the liverwort Plagiochila fruticosa by three microorganisms, Chlorella fusca var. vacuolata, Mucor species, and Aspergillus niger was investigated. C. fusca var. vacuolata and Mucor sp. introduced oxygen function into the cyclohexane ring of aristolene while A. niger oxidized stereoselectively one methyl of the 1,1-dimethyl group on the cyclopropane ring of aristolanes and 2,3-secoaromadendrane to give C-12 primary alcohol and C-12 carboxylic acid. The possible metabolic pathway of the formation of new metabolites is discussed. The stereostructures of new metabolites were established by a combination of NMR spectroscopy including HMBC and NOESY, X-ray crystallographic analysis, and chemical reaction.
