Synthesis, Molecular Docking and Mosquitocidal Efficacy of Lawsone and its Derivatives Against the Dengue Vector Aedes aegypti L. (Diptera: Culicidae)

被引:3
作者
Stalin, Antony [1 ,2 ]
Dhivya, Paul [3 ]
Lin, Ding [1 ,2 ]
Feng, Yue [4 ]
Asharaja, Antony Cruz [5 ]
Gandhi, Munusamy Rajiv [6 ]
Kannan, Balakrishnan Senthamarai [7 ]
Kandhasamy, Subramani [8 ]
Reegan, Appadurai Daniel [9 ]
Chen, Yuan [1 ,2 ]
机构
[1] Zhejiang A&F Univ, State Key Lab Subtrop Silviculture, Dept Tradit Chinese Med, Hangzhou 311300, Peoples R China
[2] Zhejiang A&F Univ, Zhejiang Prov Key Lab Resources Protect & Innovat, Hangzhou 311300, Peoples R China
[3] Nirmala Coll Women, Dept Chem, Coimbatore 641018, Tamil Nadu, India
[4] Zhejiang Chinese Med Univ, Coll Pharmaceut Sci, Hangzhou, Peoples R China
[5] Pasumpon Muthuramalinga Thevar Coll, PG & Res Dept Zool, Tenkasi 627953, Tamil Nadu, India
[6] Natl Biodivers Author, 5th Floor,CSIR Rd,TICEL Bio Pk, Chennai 600113, Tamil Nadu, India
[7] Tirunelveli Dakshina Mara Nadar Sangam TDMNS Coll, Dept Chem, Tirunelveli 627113, Tamil Nadu, India
[8] Indian Inst Technol Madras, Dept Biotechnol, Stem Cell & Mol Biol Lab, Chennai 600036, Tamil Nadu, India
[9] Natl Ctr Dis Control, NTI Campus,Ballary Rd, Bangalore 560003, Karnataka, India
关键词
Multi-Component Reaction; 2-hydroxy-1; 4-naphthoquinone; Aedes aegypti; Mosquitocidal activity; Molecular; CULEX-QUINQUEFASCIATUS SAY; LARVICIDAL ACTIVITY; IMMATURE STAGES; TRYPANOSOMA-CRUZI; NAPHTHOQUINONES; RESISTANCE; TEMEPHOS; CYTOTOXICITY; INHIBITOR; LAPACHONE;
D O I
10.2174/1573406417666210727121654
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Aedes aegypti is the primary vector of dengue, a significant public health problem in many countries. Controlling of Ae. aegypti is the biggest challenge in the mosquito control programe, and there is a need for finding bioactive molecules to control Ae. aegypti in order to prevent dengue virus transmission. Objective: To assess the mosquitocidal property of lawsone and its 3-methyl-4H-chromen-3-yl-1phenylbenzo[6,7]chromeno[2,3,c]pyrazole-dione derivatives (6a-6h) against various life stages of Ae. aegypti. Besides, to study the mode of action of the active compound by molecular docking and histopathological analysis. Methods: All derivatives were synthesized from the reaction between 2-hydroxy-1,4-naphthoquinone, chromene-3-carbaldehyde, and 1-phenyl-3-methyl-pyrazol-5-one by using one pot sequential multicomponent reaction. The mosquito life stages were subjected to diverse concentrations ranging from 1.25, 2.5, 5.0, and 10 ppm for lawsone and its derivatives. The structure of all synthesized compounds was characterized by spectroscopic analysis. Docking analysis was performed using autodock tools. Midgut sections of Ae. aegypti larvae were analyzed for histopathological effects. Results: Among the nine compounds screened, derivative 6e showed the highest mortality on Ae. aegypti life stages. The analyzed LC50 and LC90 results of derivative 6e were 3.01, 5.87 ppm, and 3.41, 6.28 ppm on larvae and pupae of Ae. aegypti, respectively. In the ovicidal assay, the derivative 6e recorded 47.2% egg mortality after 96-hour post-exposure to 10 ppm concentration. In molecular docking analysis, the derivative 6e confirmed strong binding interaction (-9.09 kcal/mol and -10.17 kcal/mol) with VAL 60 and HIS 62 of acetylcholinesterase 1 (AChE1) model and LYS 255, LYS 263 of kynurenine aminotransferase of Ae. aegypti, respectively. The histopathological results showed that the derivative 6e affected the columnar epithelial cells (CC) and peritrophic membrane (pM). Conclusion: The derivative 6e is highly effective in the life stages of Ae. aegypti mosquito and it could be used in the integrated mosquito management programe.
引用
收藏
页码:170 / 180
页数:11
相关论文
共 53 条
[1]   A method of computing the effectiveness of an insecticide [J].
Abbott, WS .
JOURNAL OF ECONOMIC ENTOMOLOGY, 1925, 18 :265-267
[2]   Current resistance status to temephos in Aedes aegypti from different regions of Argentina [J].
Albrieu Llinas, G. ;
Seccacini, E. ;
Gardenal, C. N. ;
Licastro, S. .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2010, 105 (01) :113-116
[3]  
[Anonymous], 2005, GLOBAL CARIES DATA 1, P1
[4]  
[Anonymous], 2016, Press release
[5]   Antitumour quinones [J].
Asche, C .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2005, 5 (05) :449-467
[6]   New 1,2,3,4-tetrahydro-1-aza-anthraquinones and 2-aminoalkyl compounds from norlapachol with molluscicidal activity [J].
Barbosa, TP ;
Camara, CA ;
Silva, TMS ;
Martins, RM ;
Pinto, AC ;
Vargas, MD .
BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (23) :6464-6469
[7]  
Chen CD, 2013, TROP BIOMED, V30, P220
[8]   A new chromone glycoside from Rhododendron spinuliferum [J].
Chen, Gang ;
Jin, Hui Zi ;
Li, Xue Feng ;
Zhang, Qi ;
Shen, Yun Heng ;
Yan, Shi Kai ;
Zhang, Wei Dong .
ARCHIVES OF PHARMACAL RESEARCH, 2008, 31 (08) :970-972
[9]   Multiple Modes of Action of the Squamocin in the Midgut Cells of Aedes aegypti Larvae [J].
Costa, Marilza da Silva ;
de Paula, Sergio Oliveira ;
Martins, Gustavo Ferreira ;
Zanuncio, Jose Cola ;
Goulart Santana, Antonio Euzebio ;
Serrao, Jose Eduardo .
PLOS ONE, 2016, 11 (08)
[10]   Naphthoquinoidal [1,2,3]-triazole, a new structural moiety active against Trypanosoma cruzi [J].
da Silva, Eufranio N., Jr. ;
Menna-Barreto, Rubem F. S. ;
Pinto, Maria do Carmo F. R. ;
Silva, Raphael S. F. ;
Teixeira, Daniel V. ;
de Souza, Maria Cecilia B. V. ;
De Simone, Carlos Alberto ;
De Castro, Solange L. ;
Ferreira, Vitor F. ;
Pinto, Antonio V. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2008, 43 (08) :1774-1780