959237-34-4

Usage

Uses

Used in Pharmaceutical Industry:
2,4-Dichloro-7-iodoquinazoline is utilized as a building block for the synthesis of various biologically active compounds, contributing to the development of new drugs with potential therapeutic benefits.
Used in Organic Chemistry and Materials Science Research:
2,4-Dichloro-7-iodoquinazoline serves as a valuable research tool, aiding scientists in understanding the properties and behaviors of similar chemical structures, thus advancing the fields of organic chemistry and materials science.
Used in Agricultural Applications:
2,4-Dichloro-7-iodoquinazoline has been investigated for its pesticidal properties, suggesting its potential use in agriculture to develop new and effective pest control solutions.

InChI:InChI=1/C8H3Cl2IN2/c9-7-5-2-1-4(11)3-6(5)12-8(10)13-7/h1-3H

Upstream product

• 626-01-7 3-Iodoaniline 
• 1039736-05-4 2-(ethylthio)-7-iodoquinazolin-4(3H)-one 
• 1039736-04-3 ethyl {[(3-iodophenyl)amino]carbonothioyl}carbamate 
• 959236-72-7 7-iodoquinazoline-2,4(1H,3H)-dione 

Downstream Products

• 1039736-06-5 N-(4-{[(2-chloro-7-iodoquinazolin-4-yl)amino]methyl}phenyl)-4-fluorobenzamide 
• 1039736-14-5 C₂₈H₂₇ClIN₅O 
• 1039733-08-8 N-[4-({[2-(dimethylamino)-7-formylquinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide 
• 1039733-00-0 N-[4-({[2-(dimethylamino)-7-iodoquinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide 
• 1039735-10-8 N-[4-({[2-(dimethylamino)-7-vinylquinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide 
• 1039733-10-2 N-[4-({[7-acetyl-2-(dimethylamino)quinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide 
• 1039735-15-3 N-[4-({[2-(dimethylamino)-7-(hydroxymethyl)quinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide 
• 1039736-13-4 1-benzyl-N-[4-({[2-(dimethylamino)-7-iodoquinazolin-4-yl]amino}methyl)phenyl]piperidine-4-carboxamide 
• 1039733-68-0 1-benzyl-N-[4-({[2-(dimethylamino)-7-vinylquinazolin-4-yl]amino}methyl)phenyl]piperidine-4-carboxamide 
• 1039733-05-5 N-[4-({[7-cyano-2-(dimethylamino)quinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide hydrochloride 
• 1039733-03-3 N-[4-({[2-(dimethylamino)-7-vinylquinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide hydrochloride 
• 1039733-04-4 N-[4-({[2-(dimethylamino)-7-ethylquinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide hydrochloride 
• 1039733-13-5 N-{4-[({2-(dimethylamino)-7-[(1Z)-prop-1-en-1-yl]quinazolin-4-yl}amino)methyl]phenyl}-4-fluorobenzamide hydrochloride 
• 1039733-11-3 N-[4-({[2-(dimethylamino)-7-(1-hydroxyethyl)quinazolin-4-yl]amino}methyl)phenyl]-4-fluorobenzamide hydrochloride 

Relevant academic research and scientific papers

Design and synthesis of novel diaminoquinazolines with in vivo efficacy for β-catenin/t-cell transcriptional factor 4 pathway inhibition

We are introducing a novel series of 2,4-diaminoquinazolines as β-catenin/Tcf4 inhibitors which were identified by ligand-based design. Here we elucidate the SAR of this series and explain how we were able to improve key molecular properties such as solubility and cLogP leading to compound 9. Analogue 9 exhibited better biological activity and improved physical and pharmacological properties relative to the HTS hit 49. Furthermore, 9 demonstrated good cell growth inhibition against several human colorectal cancer lines such as LoVo and HT29. In addition, treatment with compound 9 led to gene expression changes that overlapped significantly with the transcriptional profile resulting from the pathway inhibition by siRNA knockdown of β-catenin or Tcf4. Subsequently, 9 was tested for efficacy in a β-catenin/RKE-mouse xenograft, where it led to more then 50% decrease in tumor volume. 2009 American Chemical Society.

AMINO-SUBSTITUTED QUINAZOLINE DERIVATIVES AS INHIBITORS OF β-CANTENIN/TCF-4 PATHWAY AND CANCER TREATMENT AGENTS

The present invention relates to amino-substituted quinazoline derivatives as inhibitors of β-catenin/tcf-4 pathway, which can be useful in the treatment of cancer; to processes for their preparation; to pharmaceutical compositions comprising them; and to methods of using them.