154461-65-1 Usage
Uses
Used in Pharmaceutical Applications:
Sinapaldehyde glucoside is used as a pharmaceutical ingredient for its potential antioxidant, anti-inflammatory, and antimicrobial properties. These characteristics make it a valuable component in the development of various health supplements and medications.
Used in Cosmetic and Skincare Applications:
Sinapaldehyde glucoside is used as an active ingredient in cosmetic and skincare products due to its antioxidant attributes. Its ability to protect the skin from oxidative stress and promote overall skin health makes it a sought-after component in the beauty industry.
Used in Health Supplements:
Sinapaldehyde glucoside is used as a dietary supplement for its potential health benefits. It is often included in formulations that aim to support the immune system, reduce inflammation, and provide antioxidant protection. However, it is essential to consider the appropriate dosage and individual health conditions when incorporating Sinapaldehyde glucoside into a supplement regimen.
Check Digit Verification of cas no
The CAS Registry Mumber 154461-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,4,6 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 154461-65:
(8*1)+(7*5)+(6*4)+(5*4)+(4*6)+(3*1)+(2*6)+(1*5)=131
131 % 10 = 1
So 154461-65-1 is a valid CAS Registry Number.
154461-65-1Relevant articles and documents
Total Syntheses and Anti-inflammatory Activities of Syringin and Its Natural Analogues
Dong, Hongbo,Du, Weihong,He, Yujiao,Shi, Zheng,Wang, Yingying,Wu, Min
, p. 2866 - 2874 (2021/11/12)
Syringin (1), a natural bioactive glucoside isolated from the root of Acanthopanax senticosus (Rupr. Maxim.) Harms, possesses significant anti-inflammatory activity. In this study, we have accomplished the total syntheses of syringin (1), along with its natural analogues 2-12, from a common starting material, syringaldehyde (13), in 4-8 steps with an overall yields of 11.8-61.3%. The anti-inflammatory activities of these compounds were determined against NO production in the LPS-stimulated RAW264.7 cells. Among them, compounds 1-5, 7, and 9 exhibited different levels of anti-inflammatory activity.
Coniferyl alcohol metabolism in conifers - I. Glucosidic turnover of cinnamyl aldehydes by UDPG: Coniferyl alcohol glucosyltransferase from pine cambium
Steeves, Valerie,Foerster, Hartmut,Pommer, Ulrich,Savidge, Rodney
, p. 1085 - 1093 (2007/10/03)
UDPG: coniferyl alcohol glucosyltransferase (CAGT; EC 2.4.1.111) isolated from cambial tissues of Pinus strobus was able to convert cinnamyl aldehydes as well as dihydroconiferyl alcohol into their corresponding 4-O-β-D-glucosides in vitro, Cinnamyl aldeh
