4-Substitutedphthalazines and phthalazinones: synthesis, characterization and β-adrenergic blocking activity

被引:8
作者
Abouzid, Khaled A. M. [1 ]
Khalil, Nadia A. [2 ]
Ahmed, Eman M. [2 ]
机构
[1] Ain Shams Univ, Dept Pharmaceut Chem, Fac Pharm, Cairo 11566, Egypt
[2] Cairo Univ, Fac Pharm, Dept Organ Pharmaceut Chem, Cairo, Egypt
关键词
Phthalazines; Phthalazinones; Adrenergic beta-blockers; Arylpiperazine; DERIVATIVES; AGENTS; PYRIDAZINONE; BLOCKERS; RECEPTOR; DISEASE;
D O I
10.1007/s00044-012-0099-6
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Novel 4-(4-bromophenyl)phthalazine and phthalazinone derivatives connected through 2-propanol spacer to N-substituted piperazine residue were synthesized. All the new compounds were screened for their effect on beta-adrenergic blocking activity on the norepinephrine-induced precontracted aortic ring module. Most test compounds displayed appreciable beta-adrenolytic activity compared to propranolol as a reference standard. The results have shown that compounds 3a, 3d, 3e and 7c displayed appreciable inhibition of norepinephrine-induced aortic ring contraction. A novel 4-(4-bromophenyl)phthalazine and phthalazinone derivatives connected through 2-propanol spacer to N-substituted piperazine residue were synthesized. All new compounds were screened for their effect on beta-adrenergic blocking activity on the norepinephrine-induced precontracted aortic ring module.
引用
收藏
页码:1057 / 1064
页数:8
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