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2-(3,5-dimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-chromen-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70460-29-6

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70460-29-6 Usage

Chemical Class

Flavonoids

Physical Form

Yellow crystalline powder

Molecular Weight

402.39 g/mol

Biological Activities

+ Anti-inflammatory
+ Antioxidant
+ Anti-cancer
+ Neuroprotective
+ Cardiovascular protective

Presence in Plants

Commonly found in various plants

Interest for Research

Potential therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 70460-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,6 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70460-29:
(7*7)+(6*0)+(5*4)+(4*6)+(3*0)+(2*2)+(1*9)=106
106 % 10 = 6
So 70460-29-6 is a valid CAS Registry Number.

70460-29-6SDS

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-(3,5-dimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-1-benzopyran-4-one

1.2 Other means of identification

Product number -
Other names 2-(3,5-dimethoxyphenyl)-5,6,7,8-tetramethoxychromen-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:70460-29-6 SDS

70460-29-6Downstream Products

70460-29-6Relevant academic research and scientific papers

B-Ring-modified and/or 5-demethylated nobiletin congeners: Inhibitory activity against pro-MMP-9 production

Oshitari, Tetsuta,Okuyama, Yuji,Miyata, Yoshiki,Kosano, Hiroshi,Takahashi, Hideyo,Natsugari, Hideaki

experimental part, p. 7085 - 7092 (2012/01/02)

Three metabolites and 12 analogues of nobiletin (1) were synthesized. Whereas nobiletin derivatives 2-4 inhibited pro-MMP-9 production similarly in both PMA- and TNF-α-stimulated human lens epithelial cells, the 2′-hydroxylated analogue 5a exerted marked inhibitory effects (IC 50: 0.4 μM) on PMA-treated cells, which were 170-fold more potent than those on TNF-α-treated cells. This activity may be closely related to PKC-mediated transcriptional regulation of pro-MMP-9.

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