76236-10-7 Usage
Uses
Used in Pharmaceutical Industry:
(24S)-24-Ethyl-9β,19-cyclolanosta-25-ene-3β-ol is used as a potential pharmaceutical candidate for drug development due to its structural features and potential medicinal properties. Its unique structure and presence of functional groups may contribute to its biological activities, making it a promising compound for the development of new drugs.
Used in Traditional Medicine:
(24S)-24-Ethyl-9β,19-cyclolanosta-25-ene-3β-ol may have applications in traditional medicine, as it can be found in certain plants that have been used for their therapeutic properties. Its potential pharmacological properties and biological activities could be harnessed to develop treatments for various health conditions.
Used in Cosmetics Industry:
(24S)-24-Ethyl-9β,19-cyclolanosta-25-ene-3β-ol may also have potential applications in the cosmetics industry, as triterpenoids are known for their beneficial effects on the skin. Its presence in certain plants and potential biological activities could make it a valuable ingredient in skincare products for various purposes, such as anti-aging, moisturizing, or soothing the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 76236-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76236-10:
(7*7)+(6*6)+(5*2)+(4*3)+(3*6)+(2*1)+(1*0)=127
127 % 10 = 7
So 76236-10-7 is a valid CAS Registry Number.
76236-10-7Relevant academic research and scientific papers
Dennis, Allen L,Nes, W.David
, p. 7017 - 7021 (2002)
The native SMT from Glycine max (soybean) expressed in Escherichia coli cells catalyzes the step-wise conversion of cycloartenol to 24(28)-methylene cycloartanol to a mixture of stereochemically related Δ24(28)Z-ethylidene-Δ24(28)E-ethylidene- and Δ25(27)-24β-ethylcyclosterols. [27-13C]Cycloartenol was tested as a substrate to determine the C-25 configuration of the Δ24(28)-olefin formed during the first C1-transfer reaction. This substrate yielded (25-R)-[27-13C]24(28)-methylenecycloartanol. These results are entirely consistent with the observed stereochemistries of pathway specific 24-alkyl sterols found in plants and additionally revealed for the first time that a SMT can sequentially C-methylate the Δ24-bond to generate multiple olefins.
