Deepika P, Vinusha H M, Begum Muneera, Ramu Ramith, Shirahatti Prithvi S, Nagendra Prasad M N
Department of Chemistry, JSS Science and Technology University, Mysuru, Karnataka, 570 006, India.
PG Department of Chemistry, Sarada Vilas College, Mysuru, 570004, India.
Heliyon. 2022 Jun 6;8(6):e09648. doi: 10.1016/j.heliyon.2022.e09648. eCollection 2022 Jun.
In this current work we have prepared a Schiff base ligand, () derived from 5- nitropyridine-2-amine with 4-hydroxy-3-methoxybenzaldehyde and its Cu(II), and Zn(II) in 2:1 stoichiometric ratio (2HL:M). The formation of the ligand and the metal complexes were evaluated by means of MS, FT-IR, UV-Visible, H-NMR, C-NMR and thermogravimetric methods. The free radical scavenging activity of compounds was evaluated through a sequence of assays viz., DPPH, ABTS and Superoxide where BHA was used as a positive controller. -glucosidase inhibitory activities showed that complexes had considerable inhibitory potential when compared to the ligand.
在当前这项工作中,我们制备了一种席夫碱配体,()它由5-硝基吡啶-2-胺与4-羟基-3-甲氧基苯甲醛反应得到,以及其与铜(II)和锌(II)以2:1化学计量比(2HL:M)形成的配合物。通过质谱(MS)、傅里叶变换红外光谱(FT-IR)、紫外可见光谱(UV-Visible)、氢核磁共振光谱(H-NMR)、碳核磁共振光谱(C-NMR)和热重分析方法对配体和金属配合物的形成进行了评估。通过一系列测定,即二苯基苦味酰基自由基(DPPH)、2,2'-联氮-双-3-乙基苯并噻唑啉-6-磺酸(ABTS)和超氧阴离子测定,评估了化合物的自由基清除活性,其中丁基羟基茴香醚(BHA)用作阳性对照。α-葡萄糖苷酶抑制活性表明,与配体相比,配合物具有相当大的抑制潜力。