enyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-yl)methylene)benzohydrazide) were synthesized from 4-acyl-5-pyrazolone and benzoyl hydrazide and assessed for in silico and in vitro antimalarial activity. One binary zinc(II) complex 1 [Zn(L1)2]DMF was synthesized from L1. Two mixed ligands complexes 2 [Zn(L2)(bpy)(OAc)]EtOH and 3 [Zn(L2)(phen)(H2O)] were synthesized from L2 with 2,2′-bipyridine and 1
两个新颖的4-酰基hydr-5-
吡唑啉酮(L 1 =(Z)-N'-((4-
氯苯基)(3-甲基-5-氧-1-(
对甲苯基)-4,5-二氢-1H -
吡唑-4-基)亚甲基)苯并酰
肼和L 2 = (Z)-N'-(((4-
氯苯基)(1-(3-
氯苯基)-3-甲基-5-氧代-4,5-二氢-由4-酰基-5-
吡唑酮和苯甲酰
肼合成1H-
吡唑-4-基)亚甲基)苯并酰
肼)并评估其计算机和体外抗疟活性。由L 1合成一种二元
锌(II)配合物1 [Zn(L 1)2 ]
DMF。两种混合的
配体络合物2 [Zn(L 2(bpy)(OAc)] EtOH和3 [Zn(L 2)(phen)(H 2 O)]分别由L 2与
2,2'-联吡啶和1,10-
菲咯啉合成。通过1 H NMR,FT-IR,UV-Vis,单晶X射线衍射和电导测量来表征
配体和配合物。所有化合物在体外抗疟活性方面均显示出良好的结果。