Discovery of small-molecule allosteric inhibitors of PfATC as antimalarials (2022)
- Authors:
- USP affiliated authors: WRENGER, CARSTEN - ICB ; KRÜGER, ARNE - ICB
- Unidade: ICB
- DOI: 10.1021/jacs.2c08128
- Subjects: PARASITOLOGIA; ANTIMALÁRICOS; PLASMODIUM MALARIAE; PLASMODIUM FALCIPARUM; CATALASE; ATIVAÇÃO ENZIMÁTICA; AMINOÁCIDOS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2022
- Source:
- Título: Journal of American Chemical Society
- ISSN: 1520-5126
- Volume/Número/Paginação/Ano: p. 1-8, 2022
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by
-
ABNT
WANG, Chao et al. Discovery of small-molecule allosteric inhibitors of PfATC as antimalarials. Journal of American Chemical Society, p. 1-8, 2022Tradução . . Disponível em: https://doi.org/10.1021/jacs.2c08128. Acesso em: 27 dez. 2025. -
APA
Wang, C., Zhang, B., Krüger, A., Du, X., Visser, L., Dömling, A. S. S., et al. (2022). Discovery of small-molecule allosteric inhibitors of PfATC as antimalarials. Journal of American Chemical Society, 1-8. doi:10.1021/jacs.2c08128 -
NLM
Wang C, Zhang B, Krüger A, Du X, Visser L, Dömling ASS, Wrenger C, Groves MR. Discovery of small-molecule allosteric inhibitors of PfATC as antimalarials [Internet]. Journal of American Chemical Society. 2022 ; 1-8.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1021/jacs.2c08128 -
Vancouver
Wang C, Zhang B, Krüger A, Du X, Visser L, Dömling ASS, Wrenger C, Groves MR. Discovery of small-molecule allosteric inhibitors of PfATC as antimalarials [Internet]. Journal of American Chemical Society. 2022 ; 1-8.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1021/jacs.2c08128 - Novel highlight in malarial drug discovery: aspartate transcarbamoylase
- Aptamer applications in emerging viral diseases
- High target homology does not guarantee inhibition: aminothiazoles emerge as inhibitors of Plasmodium falciparum
- Transporter-mediated solutes uptake as drug target in Plasmodium falciparum
- Inibidores da via de síntese de vitamina B6 entregues por associação com nanopartículas contra Plasmodium spp
- Cytometric quantification of singlet oxygen in the human malaria parasite Plasmodium falciparum
- Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target?
- Exploring aspartate transcarbamoylase: a promising broad-spectrum target for drug development
- The crystal structure of the Plasmodium falciparum PdxK provides an experimental model for pro-drug activation
- Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases
Informações sobre o DOI: 10.1021/jacs.2c08128 (Fonte: oaDOI API)
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