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49802-40-6

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49802-40-6 Usage

Structure

Aromatic ring structure with a naphthalene-dione backbone

Family

Naphthalene-dione

Usage

Production of dyes, pigments, and other organic synthesis processes

Biological activity

Inhibits the growth of certain cancer cells

Pharmacological activity

Anti-inflammatory agent

Industrial and scientific applications

Versatile and important chemical in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 49802-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,0 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 49802-40:
(7*4)+(6*9)+(5*8)+(4*0)+(3*2)+(2*4)+(1*0)=136
136 % 10 = 6
So 49802-40-6 is a valid CAS Registry Number.

49802-40-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methylbutyl)naphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names -

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:49802-40-6 SDS

49802-40-6Downstream Products

49802-40-6Relevant articles and documents

Bioactivity profiles of cytoprotective short-chain quinones

Chear, Sueanne,Feng, Zikai,Gueven, Nuri,Hemasa, Ayman L.,Nadikudi, Monila,Smith, Jason A.,Woolley, Krystel L.

supporting information, (2021/05/31)

Short-chain quinones (SCQs) have been investigated as potential therapeutic candidates against mitochondrial dysfunction, which was largely thought to be associated with the reversible redox characteristics of their active quinone core. We recently reported a library of SCQs, some of which showed potent cytoprotective activity against the mitochondrial complex I inhibitor rotenone in the human hepatocarcinoma cell line HepG2. To better characterize the cytoprotection of SCQs at a molecular level, a bioactivity profile for 103 SCQs with different compound chemistries was generated that included metabolism related markers, redox activity, expression of cytoprotective proteins and oxidative damage. Of all the tested endpoints, a positive correlation with cytoprotection by SCQs in the presence of rotenone was only observed for the NAD(P)H:quinone oxidoreductase 1 (NQO1)-dependent reduction of SCQs, which also correlated with an acute rescue of ATP levels. The results of this study suggest an unexpected mode of action for SCQs that appears to involve a modification of NQO1-dependent signaling rather than a protective effect by the reduced quinone itself. This finding presents a new selection strategy to identify and develop the most promising compounds towards their clinical use.

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