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2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)-3-(2-isopropoxy-5-(piperazin-1-ylmethyl)phenyl)qiuinazolin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1538593-71-3

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1538593-71-3 Usage

Chemical class

Quinazolinone derivative

Explanation

The compound is based on a quinazolinone core structure, which is a known class of chemical compounds with potential pharmacological properties.

Explanation

The compound has a complex structure with various substituents and functional groups, such as a piperazine group, a chlorophenyl moiety, an isopropoxy group, and a piperazin-1-ylmethyl group.

Explanation

The piperazine group is a five-membered nitrogen-containing ring that is often found in pharmaceutical compounds due to its diverse biological activities and ability to form hydrogen bonds.

Explanation

The chlorophenyl moiety is a phenyl group (a six-membered carbon ring with delocalized pi electrons) that has a chlorine atom attached to it. This group can influence the compound's lipophilicity, stability, and biological activity.

Explanation

The isopropoxy substituent is a methoxy group (-OCH3) attached to an isopropyl group (a propyl group with a branching at the second carbon). This group can affect the compound's solubility and bioavailability.

Explanation

The compound's complex structure and various substituents contribute to its potential pharmacological properties. These properties could be of interest for further investigation in medicinal chemistry and drug development.

Explanation

The synthesis of 2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)-3-(2-isopropoxy-5-(piperazin-1-ylmethyl)phenyl)qiuinazolin-4(3H)-one and its potential biological activities are important aspects to explore for potential applications in medicinal chemistry and drug development. Further research could lead to the discovery of new therapeutic agents.

Complex structure

Multiple substituents and functional groups

Piperazine group

Five-membered nitrogen-containing ring

Chlorophenyl moiety

Chlorine-substituted phenyl group

Isopropoxy substituent

Methoxy group attached to an isopropyl group

Piperazin-1-ylmethyl substituent

Methyl group attached to a piperazine ring

Potential pharmacological properties

Diverse structural features

Synthesis and biological activities

Interest for further investigation

Check Digit Verification of cas no

The CAS Registry Mumber 1538593-71-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,8,5,9 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1538593-71:
(9*1)+(8*5)+(7*3)+(6*8)+(5*5)+(4*9)+(3*3)+(2*7)+(1*1)=203
203 % 10 = 3
So 1538593-71-3 is a valid CAS Registry Number.

1538593-71-3Downstream Products

1538593-71-3Relevant academic research and scientific papers

QUINAZOLINONE-BASED ONCOGENIC-RAS-SELECTIVE LETHAL COMPOUNDS AND THEIR USE

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, (2014/02/15)

The present invention provides, inter alia, compounds having the structure (1) compositions containing such compounds are also provided. Methods for using such compounds or compositions for treating or ameliorating the effects of a cancer having a cell that harbors an oncogenic RAS mutation, for modulating a lipoxygenase in a ferroptosis cell death pathway, and for depleting reduced glutathione (GSH) in a cell harboring an oncogenic RAS mutation are further provided.

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