Novel pi3k inhibitors: synthesis and molecular docking of wortmanninoid analogues (2017)
- Authors:
- Autor USP: PARISE FILHO, ROBERTO - FCF
- Unidade: FCF
- Subjects: NEOPLASIAS; METABÓLITOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Brazilian Journal of Pharmaceutical Sciences
- ISSN: 1984-8250
- Volume/Número/Paginação/Ano: v. 53, suppl. 1, p. 56 res. FCF107, 2017
- Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo
-
ABNT
CARVALHO, Camila Felix de e TAVARES, Maurício Temotheo e PARISE FILHO, Roberto. Novel pi3k inhibitors: synthesis and molecular docking of wortmanninoid analogues. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 02 out. 2024. , 2017 -
APA
Carvalho, C. F. de, Tavares, M. T., & Parise Filho, R. (2017). Novel pi3k inhibitors: synthesis and molecular docking of wortmanninoid analogues. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. -
NLM
Carvalho CF de, Tavares MT, Parise Filho R. Novel pi3k inhibitors: synthesis and molecular docking of wortmanninoid analogues. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 56 res. FCF107.[citado 2024 out. 02 ] -
Vancouver
Carvalho CF de, Tavares MT, Parise Filho R. Novel pi3k inhibitors: synthesis and molecular docking of wortmanninoid analogues. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 56 res. FCF107.[citado 2024 out. 02 ] - Potential candidates for new anticancer agents: synthesis and evaluation of antitumor activity of tioureidics and ureidics analogs of capsaicin
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