68331-86-2 Usage
Description
(8xi,9xi,14xi,25R)-spirostan-3-yl 4-O-alpha-D-glucopyranosyl-alpha-L-idopyranoside is a spirostan steroid glycoside, which is a complex chemical compound derived from plants. It consists of a steroid core with a sugar molecule attached, specifically alpha-D-glucopyranosyl-alpha-L-idopyranoside. The arrangement of hydroxyl groups and sugar moieties, as indicated by the xi and R positions, contributes to its unique properties. This plant steroid glycoside is likely to possess various biological activities, such as antioxidant, anti-inflammatory, or immunomodulatory effects, and may have potential pharmacological and physiological significance in both plants and medicinal applications.
Uses
Used in Pharmaceutical Industry:
(8xi,9xi,14xi,25R)-spirostan-3-yl 4-O-alpha-D-glucopyranosyl-alpha-L-idopyranoside is used as a potential therapeutic agent for various medical conditions due to its biological activities, such as antioxidant, anti-inflammatory, or immunomodulatory effects. The specific arrangement of hydroxyl groups and sugar moieties may contribute to its efficacy and solubility, making it a promising candidate for drug development.
Used in Nutraceutical Industry:
In the nutraceutical industry, (8xi,9xi,14xi,25R)-spirostan-3-yl 4-O-alpha-D-glucopyranosyl-alpha-L-idopyranoside may be utilized as a natural supplement or ingredient in health products, capitalizing on its antioxidant and anti-inflammatory properties to promote overall health and well-being.
Used in Cosmetic Industry:
(8xi,9xi,14xi,25R)-spirostan-3-yl 4-O-alpha-D-glucopyranosyl-alpha-L-idopyranoside could be employed in the cosmetic industry as an active ingredient in skincare products, leveraging its potential anti-inflammatory and immunomodulatory effects to improve skin health and address various skin conditions.
Used in Agricultural Industry:
In agriculture, (8xi,9xi,14xi,25R)-spirostan-3-yl 4-O-alpha-D-glucopyranosyl-alpha-L-idopyranoside may be investigated for its potential applications in enhancing plant growth, stress resistance, or as a natural pesticide due to its biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 68331-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,3 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68331-86:
(7*6)+(6*8)+(5*3)+(4*3)+(3*1)+(2*8)+(1*6)=142
142 % 10 = 2
So 68331-86-2 is a valid CAS Registry Number.
68331-86-2Relevant articles and documents
Antifungal activity of 2α,3β-functionalized steroids stereoselectively increases with the addition of oligosaccharides
Cammarata, Amy,Upadhyay, Sunil Kumar,Jursic, Branko S.,Neumann, Donna M.
supporting information; experimental part, p. 7379 - 7386 (2012/02/13)
Invasive fungal infections pose a significant problem to the immune-compromised. Moreover, increased resistance to common antifungals requires development of novel compounds that can be used to treat invasive fungal infections. Naturally occurring steroid
