152110-17-3 Usage
Description
Teuclatriol, a naturally occurring diterpene glycoside, is found predominantly in Teucrium species of plants. It possesses a complex structure that endows it with potential pharmaceutical properties, including anti-inflammatory, antioxidant, and anti-cancer activities. Its unique chemical composition and diverse biological functions make teuclatriol a compelling subject for further exploration in pharmacology and medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
Teuclatriol is used as a pharmaceutical agent for its anti-inflammatory properties, which can help in reducing inflammation and associated symptoms in various conditions.
Teuclatriol is used as an antioxidant agent for its ability to neutralize free radicals, thereby protecting cells from oxidative damage and potentially reducing the risk of various diseases associated with oxidative stress.
Teuclatriol is used as an anti-cancer agent for its potential to inhibit the growth and proliferation of cancer cells, making it a promising candidate for the development of new cancer therapies.
Used in Cosmetics Industry:
Teuclatriol is used as an ingredient in cosmetic products for its anti-inflammatory and antioxidant properties, which can contribute to skin health and protection against environmental stressors.
Used in Nutraceutical Industry:
Teuclatriol is used as a nutraceutical supplement for its health-promoting properties, including its potential to support immune function and overall well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 152110-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,1,1 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 152110-17:
(8*1)+(7*5)+(6*2)+(5*1)+(4*1)+(3*0)+(2*1)+(1*7)=73
73 % 10 = 3
So 152110-17-3 is a valid CAS Registry Number.
152110-17-3Relevant articles and documents
Traceless Stereoinduction for the Enantiopure Synthesis of Substituted-2-Cyclopentenones
Arisetti, Nanaji,Reiser, Oliver
supporting information, p. 94 - 97 (2015/07/28)
The pseudoenantiomeric 4-O-Boc- and 4-OPMP-cyclopent-2-enones, readily available from hydroxymethylenefurane on multigram scale, are demonstrated to be exceptional building blocks for the synthesis of enantiopure 4-alkyl-5-(1′-hydroxyalkyl) substituted 2-cyclopentenones and derivatives thereof. The 4-OR substituent acts as a traceless stereoinducing element, conferring not only 1,2- but also 1,4-stereocontrol with excellent selectivity. The methodology developed here was applied for the rapid synthesis of natural products and biologically active 2-cyclopentenones such as TEI-9826, guaianes, and pseudoguaianolides. (Figure Presented).
