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3-(6-O-α-L-Rhamnopyranosyl-β-D-galactopyranosyloxy)-3'-methoxy-4',5,7-trihydroxyflavone is a flavonoid compound characterized by the presence of a rhamnose and a galactose sugar molecule attached to a flavone backbone. This highly functionalized molecule also features a methoxy group and three hydroxyl groups, contributing to its diverse chemical properties and potential health benefits. Flavonoids, in general, are recognized for their antioxidant properties and are being studied for their anti-inflammatory and anti-cancer effects. The specific sugar moieties in 3-(6-O-α-L-Rhamnopyranosyl-β-D-galactopyranosyloxy)-3'-methoxy-4',5,7-trihydroxyflavone may influence its bioavailability and metabolism within the body. 3-(6-O-α-L-Rhamnopyranosyl-β-D-galactopyranosyloxy)-3'-methoxy-4',5,7-trihydroxyflavone is naturally found in plants and is synthesized for use in pharmaceutical and research applications.

53584-69-3

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53584-69-3 Usage

Uses

Used in Pharmaceutical Applications:
3-(6-O-α-L-Rhamnopyranosyl-β-D-galactopyranosyloxy)-3'-methoxy-4',5,7-trihydroxyflavone is utilized as a pharmaceutical agent for its potential antioxidant, anti-inflammatory, and anti-cancer properties. The presence of sugar moieties may enhance its bioavailability and effectiveness in treating various health conditions.
Used in Research Applications:
In the field of research, 3-(6-O-α-L-Rhamnopyranosyl-β-D-galactopyranosyloxy)-3'-methoxy-4',5,7-trihydroxyflavone serves as a subject of study for understanding the mechanisms of flavonoid action, particularly in relation to their health benefits and potential therapeutic uses.
Used in Nutraceutical Applications:
3-(6-O-α-L-Rhamnopyranosyl-β-D-galactopyranosyloxy)-3'-methoxy-4',5,7-trihydroxyflavone may also be incorporated into nutraceutical products, where it can be used as a dietary supplement for its potential health-promoting effects, including support for immune function and general well-being.
Used in Cosmetic Applications:
Due to its antioxidant properties, 3-(6-O-α-L-Rhamnopyranosyl-β-D-galactopyranosyloxy)-3'-methoxy-4',5,7-trihydroxyflavone can be used in cosmetic formulations to protect the skin from oxidative stress and potentially reduce signs of aging.
Used in Food and Beverage Industry:
In the food and beverage sector, this flavonoid may be used as a natural additive to enhance the nutritional value and health benefits of products, capitalizing on the antioxidant and potential anti-inflammatory properties of flavonoids.

Check Digit Verification of cas no

The CAS Registry Mumber 53584-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,8 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53584-69:
(7*5)+(6*3)+(5*5)+(4*8)+(3*4)+(2*6)+(1*9)=143
143 % 10 = 3
So 53584-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C28H32O16/c1-9-18(32)21(35)23(37)27(41-9)40-8-16-19(33)22(36)24(38)28(43-16)44-26-20(34)17-13(31)6-11(29)7-15(17)42-25(26)10-3-4-12(30)14(5-10)39-2/h3-7,9,16,18-19,21-24,27-33,35-38H,8H2,1-2H3/t9-,16+,18-,19-,21+,22-,23+,24+,27+,28?/m0/s1

53584-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Isorhamnetin 3-O-rutinoside

1.2 Other means of identification

Product number -
Other names isorhamnetin 3-rutinoside

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:53584-69-3 SDS

53584-69-3Upstream product

53584-69-3Relevant academic research and scientific papers

Flavonoid and benzophenone glycosides from Coleogyne ramosissima

Ito, Hideyuki,Nishitani, Eisei,Konoshima, Takao,Takasaki, Midori,Kozuka, Mutsuo,Yoshida, Takashi

, p. 695 - 700 (2007/10/03)

A benzophenone glucoside and two flavonol glycosides were isolated together with 27 known polyphenols from the aerial parts of Coleogyne ramosissima, and their structures were elucidated by spectroscopic and chemical methods as iriflophenone 2-O-β-glucopyranoside, isorhamnetin 3-O-2(G)-rhamnopyranosylrutinoside-7-O-α-rhamnopyranoside and limocitrin 3-O-rutinoside-7-O-β-glucopyranoside, respectively. (C) 2000 Elsevier Science Ltd.

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