Synthesis Of New Chroman-4-one Based 1,2,3-Triazole Analogues As Antioxidant And Anti-inflammatory Agents

被引:6
作者
Ambala, Shankaraiah [1 ]
Thumma, Vishnu [2 ]
Mallikanti, Veerabhadraiah [1 ]
Bathini, Vineesha [1 ]
Jyothi, K. [3 ]
Pochampally, Jalapathi [1 ]
机构
[1] Osmania Univ, Dept Chem, Hyderabad 500007, Telangana, India
[2] Matrusri Engn Coll, Dept Sci & Humanities, Hyderabad 500059, Telangana, India
[3] St Marys Coll Pharm, Hyderabad 500025, Telangana, India
关键词
Chroman-4-one; anti-inflammatory; antioxidant; molecular docking; NADPH oxidase; INNATE IMMUNITY; DERIVATIVES; FLAVONOIDS; INHIBITORS; DISEASES;
D O I
10.1002/cbdv.202400587
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A library of new chroman-4-one based 1,2,3-triazole analogues were synthesized involving a series of condensation, cyclization, Suzuki coupling and copper catalysed click chemistry protocols. The newly synthesized compounds 8a-l were screened for their invitro antioxidant and anti-inflammatory activities by employing Ascorbic acid and Diclofenac as reference drugs respectively. The compound without any substituent on benzyl ring (8a), compound with -Cl substituent in para position of benzyl ring (8i), and compound with ethoxy substituent in para position of benzyl ring (8k) exhibited potent antioxidant and anti-inflammatory activities with higher percentage of inhibition. To understand their binding affinities, molecular docking study of these three compounds performed against NADPH oxidase with presented outstanding docking scores and promising binding interactions like H-bond and hydrophobic. image
引用
收藏
页数:10
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