Synthesis and Evaluation of Biological Activity of Homodrimane Sesquiterpenoids Bearing Hydrazinecarbothioamide or 1,2,4-Triazole Unit

被引:0
作者
Lidia Lungu
Alexandru Ciocarlan
Alic Barba
Sergiu Shova
Serghei Pogrebnoi
Ionel Mangalagiu
Costel Moldoveanu
Nicoleta Vornicu
Michele D’Ambrosio
Maria V. Babak
Vladimir B. Arion
Aculina Aricu
机构
[1] Institute of Chemistry,
[2] Laboratory “Chemistry of Natural and Biologically Active Compounds”,undefined
[3] ”P. Poni” Institute of Macromolecular Chemistry,undefined
[4] ”Al. I. Cuza” University of Iasi,undefined
[5] Faculty of Chemistry,undefined
[6] Metropolitan Center of Research T.A.B.O.R.,undefined
[7] University of Trento,undefined
[8] Laboratory of Bioorganic Chemistry,undefined
[9] National University of Singapore,undefined
[10] Department of Chemistry,undefined
[11] University of Vienna,undefined
[12] Institute of Inorganic Chemistry,undefined
来源
Chemistry of Heterocyclic Compounds | 2019年 / 55卷
关键词
homodrimane sesquiterpenoid; hydrazinecarbothioamide; 1,2,4-triazole; antibacterial activity; anticancer activity; antifungal activity; microwave irradiation;
D O I
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学科分类号
摘要
Synthesis of novel (+)-sclareolide-based homodrimane sesquiterpenoids bearing hydrazinecarbothioamide or N-substituted 1,2,4-triazole unit has been reported. These heterocyclic compounds demonstrate promising in vitro antifungal and antibacterial activities toward fungal species Aspergillus niger, Fusarium solani, Penicillium chrysogenum, Penicillium frequentans, and Alternaria alternata and bacteria strains Bacillus sp. and Pseudomonas aeruginosa at minimum inhibitory concentration level of μg/ml. In addition, two homodrimane sesquiterpenoids with hydrazinecarbothioamide fragment show cytotoxicity toward human ovarian carcinoma cells A2780 and A2780cis with half maximal inhibitory concentration values in range of 9–15 μM.
引用
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页码:716 / 724
页数:8
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