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

IF 0.2 4区 化学 Q4 CHEMISTRY, ORGANIC Indian Journal of Heterocyclic Chemistry Pub Date : 2023-09-30 DOI:10.59467/ijhc.2023.33.289
S. Subramanyam, Ramu Samineni, Sunil Kumar Kadiri, J. P. Yanadaiah, Phaneendranath Jonnalagedda, Krishna Veni Chikkula, Sampath A. Gouru
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Abstract

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.
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吲哚衍生物中一些新的酰肼席夫碱和曼尼希碱的合成及其体内生物活性研究
研究了吲哚衍生物中8个新的酰肼席夫碱和8个新的曼尼希碱的抗炎、镇痛和抗溃疡活性。2-甲基- 1h -吲哚-3-羧酸酯(III)与肼水解得到2-甲基- 1h -吲哚-3-羧酸酯(IV),与醛反应得到相应的肼希夫碱Va-Vh。吲哚与甲醛、不同的脂肪族胺、芳香族胺和杂环胺反应生成了吲哚衍生物的曼尼希碱(VIa-VIe)。生物学研究结果表明,希夫碱与2,4-二氯苯甲醛(Vh)和2-氯苯甲醛(Vb)具有有效的抗炎、镇痛和抗溃疡活性。在杂环核旁位具有-NO2和-Cl基团的曼尼希碱(VIh和VIc)显示出有效的抗炎、镇痛和抗溃疡活性。
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来源期刊
CiteScore
0.40
自引率
33.30%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Indian Journal of Heterocyclic Chemistry is exclusively devoted to research in the area of heterocyclic chemistry. The journal publishes invited review articles and original research papers pertaining to structure and synthesis, mechanism of reactions, spectral studies, biologically active compounds, bio-chemical studies, physicochemical work, phytochemistry etc.
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