734-44-1

Upstream product

• 740-37-4 2-methyl-3-(2-methylphenyl)-7-nitro-4(3H)-quinazolinone 
• 95-53-4 o-toluidine 
• 619-17-0 4-Nitroanthranilic acid 

Downstream Products

• 1364664-37-8 2-methyl-3-(2-methylphenyl)-7-(furan-2-ylmethyleneamino)-4(3H)-quinazolinone 
• 1364664-45-8 2-methyl-3-(2-methylphenyl)-7-maleimido-4(3H)-quinazolinone 
• 1364664-44-7 2-methyl-3-(2-methylphenyl)-7-succinimido-4(3H)-quinazolinone 
• 1364664-28-7 2-methyl-3-(2-methylphenyl)-7-[thiophen-2-carbonylamino]-4(3H)-quinazolinone 
• 1364664-41-4 [2-methyl-3-(2-methylphenyl)-7-phthalimido]-4(3H)-quinazolinone 
• 1364664-46-9 2,2'-dimethyl-3'-(2-methylphenyl)-3,7'-biquinazoline-4,4'-(3H,3'H)-dione 
• 1364664-47-0 6-chloro-2,2'-dimethyl-3'-(2-methylphenyl)-3,7'-biquinazoline-4,4'-(3H,3'H)-dione 
• 1364664-42-5 [2-methyl-3-(2-methylphenyl)-7-(4,5,6,7-tetrbromophthalimido)]-4(3H)-quinazolinone 
• 1364664-43-6 [2-methyl-3-(2-methylphenyl)-7-(4,5,6,7-tetrchlorophthalimido)]-4(3H)-quinazolinone 
• 1364664-22-1 2-methyl-3-(2-methylphenyl)-7-ethoxycarbonylamino-4(3H)-quinazolinone 
• 1364664-35-6 2-methyl-3-(2-methylphenyl)-7-(4-flourobenzylideneamino)-4(3H)-quinazolinone 
• 1364664-36-7 2-methyl-3-(2-methylphenyl)-7-(4-chlorobenzylideneamino)-4(3H)-quinazolinone 
• 1364664-34-5 2-methyl-3-(2-methylphenyl)-7-(benzylideneamino)-4(3H)-quinazolinone 
• 1364664-26-5 2-methyl-3-(2-methylphenyl)-7-[4-chlorophenylcarbonylamino]-4(3H)-quinazolinone 

Relevant academic research and scientific papers

Design and synthesis of novel 7-aminoquinazoline derivatives: Antitumor and anticonvulsant activities

A novel series of 7-substituted-4(3H)-quinazolinone were designed, synthesized and evaluated for their antitumor and anticonvulsant activity. Compound 7 revealed broad-spectrum antitumor effectiveness toward numerous cell lines that belong to different tumor subpanels, whereas compounds 9 and 18 possess selective activity toward leukemia cell lines. Additionally, compounds 3, 15, 16, 18, 19 and 20 showed advanced anticonvulsant activity as well as lower neurotoxicity than reference drugs. The achieved results proved that the distinctive compounds could be valuable as a model for future devise, acclimatization and investigation to construct more active analogues.