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Evaluation on the leishmanicidal activity of 2-N,N'-dialkylamino-1,4-naphthoquinone derivatives.
de Araújo, Morgana V; David, Cibelle Cabral; Neto, José Clementino; de Oliveira, Luiz A P L; da Silva, Karoline Cristina Jatobá; Dos Santos, Jefferson Miguel; da Silva, João Kayke S; de A Brandão, Victoria B C; Silva, Tania M S; Camara, Celso A; Alexandre-Moreira, Magna S.
Affiliation
  • de Araújo MV; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720, Maceió, AL, Brazil. Electronic address: morgana_vital@hotmail.com.
  • David CC; Laboratory of Bioactive Compounds Synthesis, Molecular Sciences Department, Federal Rural University of Pernambuco, 52171-900, Recife, PE, Brazil. Electronic address: cibelle.cabral@gmail.com.
  • Neto JC; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720, Maceió, AL, Brazil. Electronic address: Zeca_1989@hotmail.com.
  • de Oliveira LA; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720, Maceió, AL, Brazil. Electronic address: luizpldeoliveira@gmail.com.
  • da Silva KC; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720, Maceió, AL, Brazil. Electronic address: karol.jatobas@gmail.com.
  • Dos Santos JM; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720, Maceió, AL, Brazil. Electronic address: migueljeffersonjm@gmail.com.
  • da Silva JK; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720, Maceió, AL, Brazil.
  • de A Brandão VB; Laboratory of Bioactive Compounds Synthesis, Molecular Sciences Department, Federal Rural University of Pernambuco, 52171-900, Recife, PE, Brazil. Electronic address: vic_aragao@hotmail.com.
  • Silva TM; Laboratory of Bioactive Compounds Synthesis, Molecular Sciences Department, Federal Rural University of Pernambuco, 52171-900, Recife, PE, Brazil. Electronic address: sarmentosilva@gmail.com.
  • Camara CA; Laboratory of Bioactive Compounds Synthesis, Molecular Sciences Department, Federal Rural University of Pernambuco, 52171-900, Recife, PE, Brazil. Electronic address: ccelso@gmail.com.
  • Alexandre-Moreira MS; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720, Maceió, AL, Brazil. Electronic address: suzana.magna@gmail.com.
Exp Parasitol ; 176: 46-51, 2017 May.
Article in En | MEDLINE | ID: mdl-28174101
ABSTRACT
Parasites of the Leishmania genus are the causative agents of leishmaniasis in humans, a disease that affects more than 12 million people worldwide. In this study was evaluated in vitro leishmanicidal activity of 2-N,N'-dialkylamino-1,4-naphthoquinone derivatives, covering a series of fourteen 2-N-morpholino-, 2-N-thiomorpholino, 2-N-piperidino, 2-N-(N4-methyl)-piperazino naphthoquinones (1a-n) derived from nor-lapachol and lawsone, belong to some other di-alkyaminoderivatives. At the cytotoxicity assay on peritoneal macrophages, the compounds possessing larger alkyl groups and N-methyl-piperazino moiety (1d, 1h, 1i and 1k), showed toxic effects similar to the standard drug used pentamidine. However, the other compounds of the series showed no deleterious effect on the host cell. Meanwhile, these cytotoxic derivatives (1d, 1h and 1i) had pronounced leishmanicidal activity against L. amazonensis promastigotes, and treatments with six other compounds (1d, 1e, 1f, 1h, 1k and 1n) had significant effect leishmanicidal against L. chagasi promastigotes. In the assay against L. chagasi amastigotes, eight compounds (1a, 1b, 1c, 1d, 1h, 1i, 1k and 1m) showed significant activity. Moreover, the compounds (1a, 1b, 1c, and 1m) showed effect against amastigotes of L. chagasi and not being toxic to the host cell. These data show the derivatives as promising substances for research leishmanicidal activity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leishmania mexicana / Naphthoquinones / Antiprotozoal Agents Limits: Animals Language: En Journal: Exp Parasitol Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leishmania mexicana / Naphthoquinones / Antiprotozoal Agents Limits: Animals Language: En Journal: Exp Parasitol Year: 2017 Document type: Article
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