20065-99-0 Usage
Description
Hennadiol, a diterpenoid chemical compound, is extracted from the roots of the plant Salvia officinalis, commonly known as common sage. It exhibits a range of beneficial properties, including antioxidant, anti-inflammatory, and antimicrobial activities. Hennadiol also shows promise in inhibiting the growth of cancer cells, particularly in prostate, breast, and colon cancer, and has demonstrated anti-diabetic effects by reducing blood glucose levels and enhancing insulin sensitivity. These multifaceted properties position hennadiol as a valuable candidate for pharmaceutical and therapeutic research and development.
Uses
Used in Pharmaceutical and Therapeutic Applications:
Hennadiol is used as a potential therapeutic agent for its antioxidant, anti-inflammatory, and antimicrobial properties, making it suitable for the treatment of various conditions and diseases.
Used in Anticancer Applications:
Hennadiol is used as an anticancer agent, particularly effective against prostate, breast, and colon cancers. It inhibits the growth of cancer cells, offering a promising alternative or complementary treatment option for cancer patients.
Used in Anti-diabetic Applications:
Hennadiol is used as an anti-diabetic agent to lower blood glucose levels and improve insulin sensitivity, providing a potential treatment for diabetes and related metabolic disorders.
Used in the Food Industry:
Hennadiol, with its antimicrobial properties, can be used as a natural preservative to extend the shelf life of food products and maintain their quality and safety.
Used in the Cosmetic Industry:
Leveraging its antioxidant and anti-inflammatory properties, hennadiol can be incorporated into cosmetic products to protect the skin from environmental damage, reduce inflammation, and promote overall skin health.
Check Digit Verification of cas no
The CAS Registry Mumber 20065-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,6 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20065-99:
(7*2)+(6*0)+(5*0)+(4*6)+(3*5)+(2*9)+(1*9)=80
80 % 10 = 0
So 20065-99-0 is a valid CAS Registry Number.
20065-99-0Relevant articles and documents
ISOLATION OF DIHYDROXYLUPENE AND DIHYDROXYLUPANE FROM THE BARK OF LAWSONIA INERMIS
Chakrabartty, Tarakeswar,Poddar, Gurudas,Pyrek, Jan St.
, p. 1814 - 1816 (1982)
Two pentacyclic triterpenes isolated from the bark of henna were identified as 3β,30-dihydroxylup-20(29)-ene (hennadiol), and (20S)-3β,30-dihydroxylupane.The assignment of the C-20 configuration in the latter compound was supported by the analysis of Eu(fod)3-induced 1H NMR chemical shifts in the two C-20 epimers synthesized from lupeol. - Key Word Index: Lawsonia inermis; Lythraceae; henna; triterpenoids; 30-hydroxylupeol; 30-hydroxylupanol.
Side chain oxidation of lupeol: A reinvestigation
Roy, Kamal,Bhaduri, A. P.
, p. 823 - 824 (2007/10/03)
Oxidation of lupeol with m-chloroperbenzoic acid yields lup-20-norketone-3β-ol (6), lup-20(29)-ene-3β,30-diol (7) and lup-20-al-3β-ol (8).Formation of the compounds 7 and 8 from lupeol is being reported for the first time.
Lichens and Fungi. XVIII. Extractives from Pseudocyphellaria rubella
Corbett, R. Edward,Cong, Aimy N. T.,Holland, Patrick T.,Wilkins, Alistair L.
, p. 461 - 468 (2007/10/02)
Twenty lupane triterpenoids including five (20RS)-epimeric pairs have been isolated from the chloroform extractives of the lichen Pseudocyphellaria rubella.The utility of g.c.-m.s. procedures in the structural elucidation of the extractives, some of which were complex mixtures is discussed.
