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135106-52-4

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135106-52-4 Usage

General Description

5-Methoxyquinazolin-4-ol is a chemical compound belonging to the category of quinazolinone derivatives. It is a heterocyclic compound with a quinazoline core structure and a methoxy group attached to the fourth position of the ring. This chemical may have potential pharmaceutical applications due to its structural features, particularly in the field of medicinal chemistry. Quinazolinone derivatives have been studied for their potential biological activities, including anticancer, antibacterial, antiviral, and antifungal properties. Further research and studies on the biological and pharmacological activities of 5-Methoxyquinazolin-4-ol may reveal its potential as a drug candidate or lead to the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 135106-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135106-52:
(8*1)+(7*3)+(6*5)+(5*1)+(4*0)+(3*6)+(2*5)+(1*2)=94
94 % 10 = 4
So 135106-52-4 is a valid CAS Registry Number.

135106-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-1H-quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 5-Methoxy-3H-chinazolin-4-on

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:135106-52-4 SDS

135106-52-4Relevant articles and documents

4- (IH-INDAZOL-S-YL-AMINO)-QUINAZOLINE COMPOUNDS AS ERBB RECEPTOR TYROSINE KINASE INHIBITORS FOR THE TREATMENT OF CANCER

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Page/Page column 79, (2008/06/13)

A quinazoline derivative of the Formula I: wherein the substituents are as defined in the text for use in the production of an anti proliferative effect which effect is produced alone or in part by inhibiting erbB2 receptor tyrosine kinase in a warm blood

N-(5-chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy] -5-(tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine, a novel, highly selective, orally available, dual-specific c-Src/Abl kinase inhibitor

Hennequin, Laurent F.,Allen, Jack,Breed, Jason,Curwen, Jon,Fennell, Michael,Green, Tim P.,Lambert-Van Der Brempt, Christine,Morgentin, Rémy,Norman, Richard A.,Olivier, Annie,Otterbein, Ludovic,Plé, Patrick A.,Warin, Nicolas,Costello, Gerard

, p. 6465 - 6488 (2007/10/03)

Src family kinases (SFKs) are nonreceptor tyrosine kinases that are reported to be critical for cancer progression. We report here a novel subseries of C-5-substituted anilinoquinazolines that display high affinity and specificity for the tyrosine kinase domain of the c-Src and Abl enzymes. These compounds exhibit high selectivity for SFKs over a panel of recombinant protein kinases, excellent pharmacokinetics, and in vivo activity following oral dosing. N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5- (tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine (AZD0530) inhibits c-Src and Abl enzymes at low nanomolar concentrations and is highly selective over a range of kinases. AZD0530 displays excellent pharmacokinetic parameters in animal preclinically and in man (t1/2 = 40 h). AZD0530 is a potent inhibitor of tumor growth in a c-Src-transfected 3T3-fibroblast xenograft model in vivo and led to a significant increase in survival in a highly aggressive, orthotopic model of human pancreatic cancer when dosed orally once daily. AZD0530 is currently undergoing clinical evaluation in man.

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