20198-40-7Relevant academic research and scientific papers
Regioselective synthesis and biological evaluation of: N -substituted 2-aminoquinazolin-4-ones
Liao, Zhen-Yuan,Yeh, Wen-Hsiung,Liao, Pen-Yuan,Liu, Yu-Ting,Chen, Ying-Cheng,Chen, Yi-Hung,Hsieh, Tsung-Han,Lin, Chia-Chi,Lu, Ming-Hsuan,Chen, Yi-Song,Hsu, Ming-Chih,Li, Tsai-Kun,Chien, Tun-Cheng
supporting information, p. 4482 - 4494 (2018/06/29)
The reaction of methyl anthranilates with N-arylcyanamides in the presence of p-TsOH in t-BuOH under reflux afforded predominantly 3-arylquinazolin-4-ones. In contrast, the reaction of the same reactants with TMSCl in t-BuOH at 60 °C followed by the Dimro
Substituted isoquinolines and quinazolines as potential antiinflammatory agents. Synthesis and biological evaluation of inhibitors of tumor necrosis factor α
Chao, Qi,Deng, Lynn,Shih, Hsiencheng,Leoni, Lorenzo M.,Genini, Davide,Carson, Dennis A.,Cottam, Howard B.
, p. 3860 - 3873 (2007/10/03)
A series of isoquinolin-1-ones and quinazolin-4-ones and related derivatives were prepared and evaluated for their ability to inhibit tumor necrosis factor α (TNFα) production in human peripheral blood monocytes stimulated with bacterial lipopolysaccharide (LPS). In an effort to optimize the TNFα inhibitory activity, a homologous series of N-alkanoic acid esters was prepared. Several electrophilic and nucleophilic substitutions were also carried out. Alkanoic acid esters of four carbons were found to be optimum for activity in both the isoquinoline and quinazoline series. Ring substituents such as fluoro, bromo, nitro, acetyl, and aminomethyl on the isoquinoline ring resulted in a significant loss of activity. Likewise, similar groups on the quinazoline ring also reduced inhibitory activity. However, the 6- and 7-aminoquinazoline derivatives, 75 and 76, were potent inhibitors, with IC50 values in the TNFα in vitro assay of approximately 5 μM for each. An in vivo mouse model of pulmonary inflammation was then used to evaluate promising candidate compounds identified in the primary in vitro assay. Compound 75 was selected for further study in this inhalation model, and was found to reduce the level of TNFα in brochoalveolar lavage fluid of LPS-treated mice by about 50% that of control mice. Thus, compounds such as 75, which can effectively inhibit proinflammatory cytokines such as TNFα in clinically relevant animal models of inflammation and fibrosis, may have potential as new antiinflammatory agents. Finally, a quinazoline derivative suitable to serve as a photoaffinity radiolabeled compound was prepared to help identify the putative cellular target(s) for these TNFα inhibitors.
