88142-63-6 Usage
Uses
Used in Pharmaceutical Industry:
(+)-Medioresinol 4,4'-O-di-β-D-glucopyranoside is used as a potential therapeutic agent for its antioxidant properties, which may help in combating oxidative stress-related conditions. Its anti-inflammatory effects also suggest potential use in treating inflammatory diseases.
Used in Anticancer Applications:
In the field of oncology, (+)-medioresinol 4,4'-O-di-β-D-glucopyranoside is considered for its anti-cancer properties, possibly serving as a chemopreventive agent or adjunct therapy for various types of cancer. Its mechanisms may involve the modulation of cellular signaling pathways associated with cancer progression and metastasis.
Used in Nutraceutical Industry:
Given its presence in natural plant sources and potential health benefits, (+)-medioresinol 4,4'-O-di-β-D-glucopyranoside could be utilized as an ingredient in nutraceutical products aimed at promoting general health and well-being.
Used in Cosmetic Industry:
The antioxidant and anti-inflammatory properties of (+)-medioresinol 4,4'-O-di-β-D-glucopyranoside may also find applications in the cosmetic industry for skincare products, where it could contribute to anti-aging and skin health improvements.
Check Digit Verification of cas no
The CAS Registry Mumber 88142-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,4 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88142-63:
(7*8)+(6*8)+(5*1)+(4*4)+(3*2)+(2*6)+(1*3)=146
146 % 10 = 6
So 88142-63-6 is a valid CAS Registry Number.
88142-63-6Relevant academic research and scientific papers
Kikuchi, Masao,Onoguchi, Rie,Yaoita, Yasunori,MacHida, Koichi
, p. 202 - 205 (2011)
Two new glycosides, named plicatumoside A (1) and (+)-neomedioresinol 4,4′-di-O-β-d-glucopyranoside (2), together with 13 known compounds, were isolated from the leaves of Viburnum plicatum Thunb. ex Murray var. plicatum f. plicatum. Their structures were established on the basis of NMR, MS, and chemical data.
