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首页> 外文期刊>Journal of the Chemical Society of Pakistan >Synthesis, Characterization, Crystal Structures, Analgesic and Antioxidant Activities of Thiourea Derivatives
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Synthesis, Characterization, Crystal Structures, Analgesic and Antioxidant Activities of Thiourea Derivatives

机译:硫脲衍生物的合成,表征,晶体结构,止痛和抗氧化活性

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摘要

1-(2-chlorobenzoyl)-3-(2,3-dimethyl-5-oxo-1-phenyl-2,5-dihydro-1H-pyrazol-4-yl)thiourea (Cl2AAP) and 1-(2-chlorobenzoyl)-3-(pyridine-2-yl)thiourea (Cl2AP) were synthesized and characterized by spectroscopic methods (FT-IR, H-1 NMR) and single crystal X-ray diffraction. Both compounds crystallized in monoclinic system and solved in P2(1), Z = 4 and P2(1)/c, Z = 12 space groups respectively. Pharmacological screenings of the synthesized compounds have shown comparable analgesic activity to that of the standard diclofenac sodium at 30 mg/kg body weight dose. The DPPH and ABTS free radical scavenging activity of Cl2AAP are more significant than Cl2AP as compared to standard (IC50= 10, 60; 45, 75; and <10 mu g/ml for standard Ascorbic acid respectively).
机译:1-(2-氯苯甲酰基)-3-(2,3-二甲基-5-氧代-1-苯基-2,5-二氢-1H-吡唑-4-基)硫脲和1-(2-氯苯甲酰基)合成)-3-(吡啶-2-基)硫脲(Cl2AP),并通过光谱法(FT-IR,H-1 NMR)和单晶X射线衍射进行表征。两种化合物均在单斜晶系统中结晶,并分别以P2(1)/ n,Z = 4和P2(1)/ c,Z = 12个空间群求解。合成化合物的药理筛选显示,在30 mg / kg体重剂量下,其镇痛活性与标准双氯芬酸钠相当。与标准品相比,Cl2AAP的DPPH和ABTS自由基清除活性比Cl2AP更为显着(标准抗坏血酸的IC50分别为10、60、45、75和<10μg / ml)。

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