To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability (2014)
- Authors:
- Autor USP: PARISE FILHO, ROBERTO - FCF
- Unidade: FCF
- Subjects: BIODISPONIBILIDADE; FÁRMACOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of Pharmacy and Pharmaceutical Sciences
- ISSN: 1482-1826
- Volume/Número/Paginação/Ano: v. 17, n. 4, p. 532-540, 2014
-
ABNT
DAMIÃO, Mariana Celestina Frojuello Costa Bernstorff et al. To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability. Journal of Pharmacy and Pharmaceutical Sciences, v. 17, n. 4, p. 532-540, 2014Tradução . . Disponível em: http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/23063. Acesso em: 14 fev. 2026. -
APA
Damião, M. C. F. C. B., Pasqualoto, K. F. M., Polli, M. C., & Parise Filho, R. (2014). To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability. Journal of Pharmacy and Pharmaceutical Sciences, 17( 4), 532-540. Recuperado de http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/23063 -
NLM
Damião MCFCB, Pasqualoto KFM, Polli MC, Parise Filho R. To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability [Internet]. Journal of Pharmacy and Pharmaceutical Sciences. 2014 ; 17( 4): 532-540.[citado 2026 fev. 14 ] Available from: http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/23063 -
Vancouver
Damião MCFCB, Pasqualoto KFM, Polli MC, Parise Filho R. To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability [Internet]. Journal of Pharmacy and Pharmaceutical Sciences. 2014 ; 17( 4): 532-540.[citado 2026 fev. 14 ] Available from: http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/23063 - Potential antineoplasics: synthesis of new selective metalloproteinase inhibitors
- Planejamento, síntese e avaliação da atividade de anticolinesterásica de análogos arilsulfonil-hidrazônicos
- Design and synthesis of capsaicin-like sulfonamide analogues as potential antitumor agents
- Oleanolic acid (OA) as an antileishmanial agent: Biological evaluation and in silico mechanistic insights
- Design and synthesis of capsaicin analogues with potential antitumor activity
- Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells: design, synthesis and molecular modeling
- Design, synthesis and antitumor evaluation of bioisosteric capsaicin-like compounds
- Analysis of the applicability and use of lipinski's rule for central nervous system drugs
- Antifúngicos
- Synthesis and purification of N-(benzodioxol-5-ylmethylene) aryl-sulfonylhydrazones
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
