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41514-64-1

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41514-64-1 Usage

General Description

3,4,5-Trimethoxyphenyl β-D-glucopyranoside is a chemical compound that consists of a glucose molecule linked to a phenyl group with three methoxy groups attached to it. It can be found in various plant sources and has been utilized in traditional medicine for its potential antioxidant and anti-inflammatory properties. 3,4,5-TRIMETHOXYPHENYL B-D-GLUCOPYRANOSIDE has also been studied for its potential antidiabetic and anticancer effects. Additionally, it has shown promise in the field of cosmetics and skincare due to its antioxidant properties. Research on 3,4,5-Trimethoxyphenyl β-D-glucopyranoside is ongoing to explore its potential uses in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 41514-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,1 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41514-64:
(7*4)+(6*1)+(5*5)+(4*1)+(3*4)+(2*6)+(1*4)=91
91 % 10 = 1
So 41514-64-1 is a valid CAS Registry Number.

41514-64-1Downstream Products

41514-64-1Relevant articles and documents

In vitro antiplasmodial activity of extracts of tristaniopsis species and identification of the active constituents: Ellagic acid and 3,4,5-trimethoxyphenyl-(6'-O-galloyl)-O-/?-D-glucopyranoside

Verotta, Luisella,Dell'Agli, Mario,Giolitot, Andrea,Guerrini, Marco,Cabalion, Pierre,Bosisio, Enrica

, p. 603 - 607 (2007/10/03)

Screening of plants from New Caledonia for antiplasmodial activity against Plasmodium falciparum revealed that methanolic extracts of the leaves and bark of Tristaniopsis calobuxus, T. yateensis, and T. glauca inhibited the growth of chloroquine-sensitive and -resistant clones. Ellagic acid and the new compound 3,4,5-trimethoxyphenyl-(6'-O-galloyl)-O-β-D-glucopyranoside were identified as the active constituents (ICso 0.5 and 3.2 /M, respectively). The growth inhibition of both clones was comparable. The compounds showed negligible or very low cytotoxicity to human skin fibroblasts and Hep G2 cells when tested at concentrations ranging from 0.5 to 100 πM.

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