Tătărîngă Gabriela, Dorneanu Olivia, Stefănescu Eugenia, Dorneanu Maria
Gr.T.Popa University of Medicine and Pharmacy Iaşi, School of Pharmacy.
Rev Med Chir Soc Med Nat Iasi. 2008 Jan-Mar;112(1):246-8.
The scientific literature states that isatin and its derivatives exhibit antibacterial, antifungal, anticonvulsant, cytotoxic and anti-HIV activities. The aim of our study was to enlarge the number of isatin derivatives.
We synthesized some new hydrazones and then, the corresponding bishydrazones using salicylaldehyde. By condensing isatin and its derivatives (methyl-, nitro-, brom-) with hydrazine, corresponding hydrazones were obtained. The bishydrazones were synthesized by refluxing the obtained hydrazones with salicylaldehyde in methanolic solution. The structure of new compounds was confirmed by elemental and spectral analysis. The lipophilicity of the synthesized derivatives was expressed by clog P values. The antibacterial and antifungal activities of the compounds were determined using disk-diffusion method against Gram positive, Gram negative bacteria, and Candida albicans.
New bishydrazines derived from isatin have been synthesized; their structures have been confirmed by elemental and spectral analysis.
科学文献表明,异吲哚酮及其衍生物具有抗菌、抗真菌、抗惊厥、细胞毒性和抗HIV活性。我们研究的目的是增加异吲哚酮衍生物的数量。
我们合成了一些新的腙,然后使用水杨醛合成了相应的双腙。通过将异吲哚酮及其衍生物(甲基、硝基、溴代)与肼缩合,得到了相应的腙。双腙是通过将所得腙与水杨醛在甲醇溶液中回流合成的。新化合物的结构通过元素分析和光谱分析得以确认。合成衍生物的亲脂性用clog P值表示。使用纸片扩散法测定了这些化合物对革兰氏阳性菌、革兰氏阴性菌和白色念珠菌的抗菌和抗真菌活性。
合成了源自异吲哚酮的新双肼;其结构已通过元素分析和光谱分析得以确认。