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6-Methoxyluteolin, a natural flavonoid compound, is derived from plants such as Desmodium gangeticum and Solidago canadensis. It is recognized for its potential anti-inflammatory, antioxidant, and anticancer properties, making it a promising candidate for the development of new therapeutic agents for treating cancer, inflammation, and oxidative stress-related diseases.

520-11-6

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520-11-6 Usage

Uses

Used in Pharmaceutical Industry:
6-Methoxyluteolin is used as an anti-inflammatory agent for its ability to inhibit the production of pro-inflammatory cytokines, which can help in reducing inflammation in the body.
6-Methoxyluteolin is used as an antioxidant for its capacity to protect cells from oxidative damage, which can contribute to the prevention and treatment of oxidative stress-related diseases.
Used in Oncology:
6-Methoxyluteolin is used as an anticancer agent for its ability to inhibit the growth of certain cancer cells and induce apoptosis, offering potential therapeutic benefits in the treatment of various types of cancer.
Used in Drug Development:
6-Methoxyluteolin is used as a lead compound in the development of new therapeutic agents targeting inflammation, oxidative stress, and cancer, due to its multifaceted biological activities and potential for further research and formulation into effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 520-11-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 520-11:
(5*5)+(4*2)+(3*0)+(2*1)+(1*1)=36
36 % 10 = 6
So 520-11-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O7/c1-22-16-11(20)6-13-14(15(16)21)10(19)5-12(23-13)7-2-3-8(17)9(18)4-7/h2-6,17-18,20-21H,1H3

520-11-6SDS

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 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4H-chromen-4-one

1.2 Other means of identification

Product number -
Other names 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxychromen-4-one

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:520-11-6 SDS

520-11-6Relevant academic research and scientific papers

New Flavonoids and Turkesterone-2-O-Cinnamate from Leaves of Rhaponticum uniflorum

Olennikov,Kashchenko

, p. 256 - 264 (2019/05/06)

Leaves of Rhaponticum uniflorum (L.) DC. (Asteraceae) afforded 46 compounds including seven new flavonoids that were identified using UV, IR, and NMR spectroscopy and mass spectrometry as 6-hydroxyluteolin-7-O-(2′-O-caffeoyl)-β-D-glucopyranoside (rhaunoside A, 1), 6-hydroxyluteolin-7-O-(6″-O-cinnamoyl)-β-D-glucopyranoside (rhaunoside B, 2), 6-hydroxyluteolin-4′-O-β-D-glucopyranoside (rhaunoside C, 3), nepetin-7-O-(6″-O-caffeoyl)-β-D-glucopyranoside (rhaunoside D, 4), nepetin-7-O-(6″-O-cinnamoyl)-β-D-glucopyranoside (rhaunoside E, 5), nepetin-3′-O-β-D-glucopyranoside (rhaunoside F, 6), and luteolin-7-O-(2″-O-caffeoyl)-β-D-glucopyranoside (rhaunoside G, 7) and the new ecdysteroid turkesterone-2-O-cinnamate (8).

Chemical constituents from cassia occidentalis Linn

Yadava,Satnami

body text, p. 1112 - 1118 (2011/10/09)

The present paper deals with the isolation and structural elucidation of three new compounds 1, 2 and 3 from the seeds of Cassia occidentalis Linn. These compounds have been characterized as 5, 7-dihydroxyflavone-5-O-β-D- xylopyranosyl-7-O-α-L-rhamnopyranosyl-(1→3)-O-α-L- arabinopyranoside (1), 3, 5, 7, 3′,4′-pentahydroxy flavone-3-O-α-L-rhamnopyranosyl-7-O-β-D-glucopyranosyl-(1→3) -O-β-D-xylopyranoside (2) and 5, 7, 3′, 4′-tetrahydroxy-6- methoxyflavone-5-O-α-L-ara-binopyranosyl-(1→4)-O-α-L- rhamnopyranosyl-(1→3)-O-β-D-galactopyranoside (3) respectively by various colour reactions, chemical degradations and spectral analysis. These compounds have been evaluated against various bacteria and fungi which showed good results.

Gastroprotective flavone/flavanone compounds with therapeutic effect on inflammatory bowel disease

-

, (2008/06/13)

PCT No. PCT/KR97/00144 Sec. 371 Date Jan. 14, 1999 Sec. 102(e) Date Jan. 14, 1999 PCT Filed Jul. 25, 1997 PCT Pub. No. WO98/04541 PCT Pub. Date Feb. 5, 1998The present invention relates to novel flavone/flavanone compounds or their pharmaceutically acceptable salts and process for preparation thereof for protecting gastrointestinal tracts against gastritis, ulcers and inflammatory bowel disease.

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