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HIV-1 Reverse Transcriptase: a potential target for marine products
Miceli, Leonardo A.; Souza, Alessandra M. T. de; Rodrigues, Carlos R.; Paixão, Izabel C. N. P.; Teixeira, Valéria L.; Castro, Helena C..
Affiliation
  • Miceli, Leonardo A.; Universidade Federal Fluminense, Brazil. Instituto de Biologia. Programa de Pós-graduação em Biologia das Interações. BR
  • Souza, Alessandra M. T. de; Universidade Federal do Rio de Janeiro. Instituto Macaé de Metrologia. Laboratório de Modelagem Molecular e Pesquisa em Ciências Farmacêuticas. BR
  • Rodrigues, Carlos R.; Universidade Federal do Rio de Janeiro. Laboratório de Modelagem Molecular. BR
  • Paixão, Izabel C. N. P.; Universidade Federal Fluminense, Brazil. Instituto de Biologia. Programa de Pós-graduação em Biologia das Interações. BR
  • Teixeira, Valéria L.; Universidade Federal Fluminense, Brazil. Instituto de Biologia. Programa de Pós-graduação em Biologia das Interações. BR
  • Castro, Helena C.; Universidade Federal Fluminense, Brazil. Instituto de Biologia. Programa de Pós-graduação em Biologia das Interações. BR
Rev. bras. farmacogn ; 22(4): 881-888, jul.-ago. 2012. ilus
Article in En | LILACS | ID: lil-640356
Responsible library: BR1.1
ABSTRACT
HIV-1 reverse transcriptase (HIV-1 RT) is a therapeutic target for the treatment of HIV-positive individuals or those already showing AIDS symptoms. In this perspective, the identification of new inhibitors for this enzyme is of great importance in view of the growing viral resistance to the existing treatments. This resistance has compromised the quality of life of those infected with multidrug-resistant strains, whose treatment options are already limited, putting at risk these individuals lives. The literature has recognized marine organisms and their products as natural sources for the identification of new therapeutic options for different pathologies. In this brief review, we consider the structure of HIV-1 RT and its most common inhibitors, as well as some marine diterpenes originally reported as HIV-1 RT inhibitors to encourage the identification and development of new marine antiviral prototypes.
Key words

Full text: 1 Collection: 01-internacional Database: LILACS Aspects: Patient_preference Language: En Journal: Rev. bras. farmacogn Journal subject: FARMACIA Year: 2012 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: LILACS Aspects: Patient_preference Language: En Journal: Rev. bras. farmacogn Journal subject: FARMACIA Year: 2012 Document type: Article Affiliation country:
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