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10-methoxy-1,4,6,9-tetramethylpyrido[3,2-g]quinoline-2,8(1H,9H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63791-97-9

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63791-97-9 Usage

Chemical family

Pyridoquinoline family

Type of compound

Derivative of pyridoquinoline

Structure

Pyridoquinoline ring fused with a quinoline ring and a methoxy group attached to the 10th position

Physical appearance

Yellow crystalline solid

Main use

Research and scientific studies

Application

Fluorescent probe and imaging agent for studying biological processes and structures

Potential biological activities

Antimicrobial, antiviral, and anticancer properties

Interest in fields

Medicinal chemistry and drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 63791-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,9 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63791-97:
(7*6)+(6*3)+(5*7)+(4*9)+(3*1)+(2*9)+(1*7)=159
159 % 10 = 9
So 63791-97-9 is a valid CAS Registry Number.

63791-97-9SDS

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 10-methoxy-1,4,6,9-tetramethylpyrido[3,2-g]quinoline-2,8-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:63791-97-9 SDS

63791-97-9Downstream Products

63791-97-9Relevant academic research and scientific papers

COMPOUNDS AND ANTI-TUMOR NQO1 SUBSTRATES

-

, (2013/04/25)

Compounds of Formula (I) can be selectively lethal toward a variety of different cancer cell types. The compounds are useful for the management, treatment, control, or adjunct treatment of diseases, where the selective lethality is beneficial in chemotherapeutic therapy.

Chemistry and biology of deoxynyboquinone, a potent inducer of cancer cell death

Bair, Joseph S.,Palchaudhuri, Rahul,Hergenrother, Paul J.

supporting information; experimental part, p. 5469 - 5478 (2010/07/03)

Deoxynyboquinone (DNQ) is a potent antineoplastic agent with an unknown mechanism of action. Here we describe a facile synthetic route to this anthraquinone, and we use this material to determine the mechanism by which DNQ induces death in cancer cells. DNQ was synthesized in seven linear steps through a route employing three palladium-mediated coupling reactions. Experiments performed on cancer cells grown in hypoxia and normoxia strongly suggest that DNQ undergoes bioreduction to its semiquinone, which then is re-oxidized by molecular oxygen, forming superoxide that induces cell death. Furthermore, global transcript profiling of cells treated with DNQ shows elevation of transcripts related to oxidative stress, a result confirmed at the protein level by Western blotting. In contrast to most other antineoplastic agents that generate reactive oxygen species (ROS), DNQ potently induces death of cancer cells in culture, with IC50 values between 16 and 210 nM. In addition, unlike the experimental therapeutic elesclomol, DNQ is still able to induce cancer cell death under hypoxic conditions. This mechanistic understanding of DNQ will allow for a more comprehensive evaluation of the potential of direct ROS generation as an anticancer strategy, and DNQ itself has potential as a novel anticancer agent.

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