Synthesis and In-vivo Bioactivity Studies of Some New Hydrazide Schiff Bases and Mannich Bases of Indole Derivatives

被引:0
|
作者
Subramanyam, S. [1 ]
Samineni, Ramu [1 ]
Kadiri, Sunil Kumar [2 ]
Yanadaiah, J. P. [3 ]
Jonnalagedda, Phaneendranath [4 ]
Chikkula, Krishna Veni [5 ]
Gouru, Sampath A. [6 ]
机构
[1] Vignans Fdn Sci Technol & Res, Dept Pharmaceut Sci, Sch Biotechnol & Pharmaceut Sci, Guntur, Andhra Pradesh, India
[2] Davananda Sagar Univ, Coll Pharmaceut Sci, Dept Pharm, K S Layout, Bengaluru, Karnataka, India
[3] Erstwhile Sree Vidyanikethan Coll Pharm, Dept Pharm, Mohan Babu Sch Pharmaceut Sci, Tirupati, Andhra Pradesh, India
[4] Agati Clin Informat LLP, Lead Stat Programmer, Bengaluru, Karnataka, India
[5] Sarojini Naidu Vanita Pharm Maha Vidyalaya, Dept Pharmaceut Chem, Secunderabad, Telangana, India
[6] EQRX Int Inc, Dept Qual Assurance, Cambridge, MA 02139 USA
关键词
Indole derivatives; Hydrazide Schiff bases; Mannich bases; Anti-inflammatory; Analgesic; Antiulcer; ANTI-HIV;
D O I
10.59467/IJHC.2023.33.299
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The anti-inflammatory, analgesic, and antiulcer activities of eight new hydrazide Schiff bases and eight new Mannich bases of indole derivatives were investigated. 2-Methyl-1H-indole-3-carboxylate (III) on hydrazinolysis gave 2-methyl-1H-indole-3-carbohydrazide (IV), which on reaction with aldehydes gave corresponding hydrazide Schiff bases Va-Vh. The reaction of IV with formaldehyde, different aliphatic, aromatic, and heterocyclic amines afforded the Mannich bases of indole derivatives (VIa-VIe). The results of biological studies revealed that Schiff bases with 2,4-dichlorobenzaldehyde (Vh) and 2-chlorobenzaldehyde (Vb) were potent anti-inflammatory, analgesic, and antiulcer activities. Mannich bases (VIh and VIc) having -NO2 and -Cl groups in the paralocation of the heterocyclic nucleus displayed effective anti-inflammatory, analgesic, and antiulcer activities.
引用
收藏
页码:299 / 309
页数:11
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