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4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)is a flavonoid glycoside with a benzopyranone core structure. It features a glucopyranosyl group at the 7-position and a 2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl) moiety, with a stereochemistry of (2S). 4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)is known for its potential biological activities, including antioxidant, anti-inflammatory, and anti-cancer properties. It is commonly found in plants and natural products, making it a promising candidate for pharmaceutical and medicinal applications.

14982-11-7

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14982-11-7 Usage

Uses

Used in Pharmaceutical Industry:
4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)is used as a pharmaceutical compound for its potential antioxidant, anti-inflammatory, and anti-cancer properties. Its natural occurrence in plants and natural products makes it a promising candidate for the development of new drugs and therapies.
Used in Nutraceutical Industry:
In the nutraceutical industry, 4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)is used as a dietary supplement or functional food ingredient due to its antioxidant and anti-inflammatory properties. These benefits can contribute to overall health and well-being, as well as support the prevention of certain diseases.
Used in Cosmetic Industry:
4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)is used as an active ingredient in cosmetic products for its antioxidant and anti-inflammatory properties. It can help protect the skin from environmental stressors, reduce inflammation, and promote a healthy, youthful appearance.
Used in Agricultural Industry:
In the agricultural industry, 4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)can be used as a natural pesticide or growth promoter. Its antioxidant and anti-inflammatory properties may help protect plants from stress and promote healthy growth, reducing the need for synthetic chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 14982-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,8 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14982-11:
(7*1)+(6*4)+(5*9)+(4*8)+(3*2)+(2*1)+(1*1)=117
117 % 10 = 7
So 14982-11-7 is a valid CAS Registry Number.

14982-11-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name homoeriodictyol-7-O-β-Glc

1.2 Other means of identification

Product number -
Other names Hedt-II

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14982-11-7 SDS

14982-11-7Downstream Products

14982-11-7Relevant academic research and scientific papers

Identification of a flavonoid 7-O-glucosyltransferase from Andrographis paniculata

Li, Yuan,Gao, Wei,Huang, Lu-Qi

, p. 279 - 286 (2019/11/21)

Andrographis paniculata is an important traditional medicinal herb in which flavonoids are part of the primary specialized metabolites. A flavonoid glucosyltransferase with broad substrate spectrum (named ApUGT3) was successfully identified by screening homologous glycosyltransferase genes from A. paniculata. The enzyme displayed glycosylation activity toward multiple flavonoids in?vitro, and the major products were identified as 7-O-glucosides. Phylogenetic analysis revealed that ApUGT3 is the first reported glycosyltransferase from the Acanthaceae family that belongs to cluster I, suggesting that ApUGT3 is a new flavonoid glycosyltransferase of this subcluster. This enzyme is potentially useful as powerful glycosylation catalysts to modify flavonoid-like compounds and improve their biological activities. (Figure presented.).

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