Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Assiut University, Assiut, 71526, Egypt.
Arch Pharm Res. 2012 Aug;35(8):1355-68. doi: 10.1007/s12272-012-0805-4. Epub 2012 Sep 1.
Theophylline derivatives have long been recognized as potent bronchodilators for the relief of acute asthma. Recently, it was found that bacterial infection has a role in asthma pathogenesis. The present work involves the design and synthesis of 8-substituted theophylline derivatives as bronchodilators and antibacterial agents. The chemical structures of these compounds were elucidated by IR, (1)H-NMR, mass spectrometry, and elemental analyses. The bronchodilator activity was evaluated using acetylcholine-induced bronchospasm in guinea pigs, and most of the compounds showed significant anti-bronchoconstrictive activity in comparison with standard aminophylline. In addition, the antibacterial activity of all the target compounds was investigated in vitro against Gram-positive and Gram-negative bacteria using ampicillin as a reference drug. Results showed that some of the tested compounds possessed significant antibacterial activity. A pharmacophore model was computed to obtain useful insight into the essential structural features of bronchodilator activity. A structure activity relationship was also discussed.
茶碱衍生物长期以来一直被认为是治疗急性哮喘的有效支气管扩张剂。最近发现,细菌感染在哮喘发病机制中起作用。本工作涉及作为支气管扩张剂和抗菌剂的 8-取代茶碱衍生物的设计和合成。通过 IR、(1)H-NMR、质谱和元素分析阐明了这些化合物的化学结构。使用豚鼠乙酰胆碱诱导的支气管痉挛评估了支气管扩张活性,与标准氨茶碱相比,大多数化合物表现出显著的抗支气管收缩活性。此外,使用氨苄西林作为参考药物,在体外对所有目标化合物进行了针对革兰氏阳性菌和革兰氏阴性菌的抗菌活性研究。结果表明,一些测试化合物具有显著的抗菌活性。计算了药效团模型,以获得对支气管扩张活性的基本结构特征的有用见解。还讨论了构效关系。