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1201902-04-6

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1201902-04-6 Usage

Chemical class

Quinazoline derivative

Activity

Potential antineoplastic (anti-cancer) activity

Mechanism of action

Potent and selective inhibitor of the poly (ADP-ribose) polymerase (PARP) enzyme

Role in DNA repair

PARP enzyme plays a key role in DNA repair

Effect on cancer cells

Inhibiting PARP disrupts DNA repair, leading to the accumulation of DNA lesions and inducing apoptosis (cell death)

Preclinical studies

Shown promising anti-tumor activity

Potential use

Investigation for the treatment of various types of cancer

Check Digit Verification of cas no

The CAS Registry Mumber 1201902-04-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,9,0 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1201902-04:
(9*1)+(8*2)+(7*0)+(6*1)+(5*9)+(4*0)+(3*2)+(2*0)+(1*4)=86
86 % 10 = 6
So 1201902-04-6 is a valid CAS Registry Number.

1201902-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [6-(4-methyl-1H-imidazol-1-yl)-2-(4-methoxyphenyl)]quinazoline

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:1201902-04-6 SDS

1201902-04-6Upstream product

1201902-04-6Downstream Products

1201902-04-6Relevant articles and documents

6-1H-IMIDAZO-QUINAZOLINE AND QUINOLINES DERIVATIVES, NEW MAO INHIBITORS AND IMIDAZOLINE RECEPTOR LIGANDS

-

Page/Page column 30, (2010/01/12)

The present invention is directed to 6-(1H-imidazo-1-yl)-2-aryl and 2-heteroaryl quinazoline and quinolines derivatives, compounds of formula (I), their pharmaceutical acceptable salts and solvates and corresponding pharmaceutical compositions, that acts

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