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1 Ergebnisse
1
Design and Synthesis of Novel 3‑Nitro‑1 H ‑1,2,4-triazole-1..:
Bruno I. Pelizaro
;
Jaqueline C. Z. Batista
;
Gisele B. Portapilla
...
doi:10.1021/acs.jmedchem.3c01745.s002. , 2024
Link:
https://doi.org/10.1021/acs.jmedchem.3c01745.s002
RT Journal T1
Design and Synthesis of Novel 3‑Nitro‑1 H ‑1,2,4-triazole-1,2,3-triazole-1,4-disubstituted Analogs as Promising Antitrypanosomatid Agents: Evaluation of In Vitro Activity against Chagas Disease and Leishmaniasis
UL https://suche.suub.uni-bremen.de/peid=base-ftgriffithunifig:oai:figshare.com:article_25134433&Exemplar=1&LAN=DE A1 Bruno I. Pelizaro A1 Jaqueline C. Z. Batista A1 Gisele B. Portapilla A1 Amarith R. das Neves A1 Fernanda Silva A1 Diego B. Carvalho A1 Cristiane Y. K. Shiguemoto A1 Lucas R. Pessatto A1 Edgar J. Paredes-Gamero A1 Iara A. Cardoso A1 Pedro H. Luccas A1 M. Cristina Nonato A1 Norberto P. Lopes A1 Fernanda Galvão A1 Kelly M. P. Oliveira A1 Nadla S. Cassemiro A1 Denise B. Silva A1 Eliane M. Piranda A1 Carla C. P. Arruda A1 Sergio de Albuquerque A1 Adriano C. M. Baroni YR 2024 K1 Biochemistry K1 Neuroscience K1 Developmental Biology K1 Science Policy K1 Environmental Sciences not elsewhere classified K1 Chemical Sciences not elsewhere classified K1 Physical Sciences not elsewhere classified K1 tulahuen lacz strain K1 showed nonmutagenic potential K1 salmonella typhimurium strains K1 relevant selectivity index K1 promising antitrypanosomatid candidate K1 promising antitrypanosomatid agents K1 likely potential mechanism K1 analogs demonstrated relevant K1 50 </ sub K1 vitro antitrypanosomatid activity K1 outstanding antichagasic activity K1 15g </ b K1 1 </ sub K1 vitro activity K1 antichagasic activity K1 h </ K1 disubstituted analogs K1 vivo studies K1 trypanosoma cruzi K1 topliss set K1 ta102 ) K1 suitable lipe K1 excellent yields K1 chagas disease K1 appropriate substrate K1 >‑ 1 K1 >- 1 K1 28 compounds K1 15 μm K1 09 μm K1 ) K1 contributing JF doi:10.1021/acs.jmedchem.3c01745.s002 LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.3c01745.s002 DO https://doi.org/10.1021/acs.jmedchem.3c01745.s002 SF ELIB - SuUB Bremen
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