Biagi G, Dell'Omodarme G, Ferretti M, Giorgi I, Livi O, Scartoni V
Istituto di Chimica Farmaceutica e Tossicologica, Università di Pisa, Italy.
Farmaco. 1992 Mar;47(3):335-44.
This paper reports further structural modifications concerning the 1,2,3-triazole ring of the compound A, an effective in vitro inhibitor of prostaglandin synthesis. The introduction of different heterocyclic rings provided further information about of the role of the heterocyclic ring in enzymatic inhibition, as regards the number and position of the nitrogen atoms, the electronic effects, basicity, steric hindrance and hydrophilicity. The benzimidazole derivative 4e proved to possess a high enzymatic inhibitory activity.
本文报道了关于化合物A(一种有效的前列腺素合成体外抑制剂)的1,2,3 - 三唑环的进一步结构修饰。引入不同的杂环提供了关于杂环在酶抑制作用中作用的更多信息,涉及氮原子的数量和位置、电子效应、碱性、空间位阻和亲水性。苯并咪唑衍生物4e被证明具有高酶抑制活性。