کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1231148 | 1495273 | 2012 | 4 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Synthesis, spectral characterization and larvicidal activity of acridin-1(2H)-one analogues Synthesis, spectral characterization and larvicidal activity of acridin-1(2H)-one analogues](/preview/png/1231148.png)
Acridin-1(2H)-one analogue of 7-chloro-3,4-dihydro-9-phenyl-2-[(pyridine-2yl) methylene] acridin-1(2H)-one, 5 was prepared by using 7-chloro-3,4-dihydro-9-phenylacridin-1(2H)-one, 3 and picolinaldehyde, 4 in the presence of KOH at room temperature. These compounds were characterized by analytical and spectral analyses. The purpose of the present study was to assess the efficacy of larvicidal and repellent activity of synthesized 7-chloro-3,4-dihydro-9-phenyl-acridin-1(2H)-one analogues such as compounds 3 and 5 against the early fourth instar larvae of filariasis vector, Culex quinquefasciatus and Japanese encephalitis vector, Culex gelidus (Diptera: Culicidae). The compound exhibited high larvicidal effects at 50 mg/L against both the mosquitoes with LC50 values of 25.02 mg/L (r2 = 0.998) and 26.40 mg/L (r2 = 0.988) against C. quinquefasciatus and C. gelidus, respectively. The 7-chloro-3,4-dihydro-9-phenyl-acridin-1(2H)-one analogues that are reported for the first time to our best of knowledge can be better explored for the control of mosquito population. This is an ideal ecofriendly approach for the control of Japanese encephalitis vectors, C. quinquefasciatus and C. gelidus.
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► To synthesis of Acridin-1(2H)-one analogues and its spectral characterization.
► To assess the efficacy of larvicidal and repellent activity of 7-chloro-3,4-dihydro-9-phenyl-acridin-1(2H)-ones.
► The early fourth instar larvae of filariasis and Japanese encephalitis vectors were used.
► The compound exhibited high larvicidal effects at 50 mg/L against both the mosquitoes.
Journal: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy - Volume 95, September 2012, Pages 442–445