Fragment-Merging strategies with known pyrimidine scaffolds targeting dihydrofolate reductase from mycobacterium tuberculosis (2023)
- Authors:
- Autor USP: DIAS, MARCIO VINÍCIUS BERTACINE - ICB
- Unidade: ICB
- DOI: 10.1002/cmdc.202300240
- Subjects: MICROBIOLOGIA; MYCOBACTERIUM TUBERCULOSIS; BACTÉRIAS GRAM-POSITIVAS; INFECÇÕES BACTERIANAS GRAM-POSITIVAS; COMPOSTOS ORGÂNICOS; CRISTALOGRAFIA QUÍMICA; BENZENO
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher: Wiley-VCH Verlag
- Publisher place: Weinheim
- Date published: 2023
- Source:
- Título: ChemMedChem
- ISSN: 1860-7187
- Volume/Número/Paginação/Ano: e202300240, 2023
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by
-
ABNT
KIRKMAN, Tim et al. Fragment-Merging strategies with known pyrimidine scaffolds targeting dihydrofolate reductase from mycobacterium tuberculosis. ChemMedChem, 2023Tradução . . Disponível em: https://doi.org/10.1002/cmdc.202300240. Acesso em: 27 dez. 2025. -
APA
Kirkman, T., Tan, S. F., Chavez-Pacheco, S. M., Hammer, A., Abell, C., Tosin, M., et al. (2023). Fragment-Merging strategies with known pyrimidine scaffolds targeting dihydrofolate reductase from mycobacterium tuberculosis. ChemMedChem. doi:10.1002/cmdc.202300240 -
NLM
Kirkman T, Tan SF, Chavez-Pacheco SM, Hammer A, Abell C, Tosin M, Anthony G. Coyne, Dias MVB. Fragment-Merging strategies with known pyrimidine scaffolds targeting dihydrofolate reductase from mycobacterium tuberculosis [Internet]. ChemMedChem. 2023 ;[citado 2025 dez. 27 ] Available from: https://doi.org/10.1002/cmdc.202300240 -
Vancouver
Kirkman T, Tan SF, Chavez-Pacheco SM, Hammer A, Abell C, Tosin M, Anthony G. Coyne, Dias MVB. Fragment-Merging strategies with known pyrimidine scaffolds targeting dihydrofolate reductase from mycobacterium tuberculosis [Internet]. ChemMedChem. 2023 ;[citado 2025 dez. 27 ] Available from: https://doi.org/10.1002/cmdc.202300240 - Enzymology of pyran ring A formation in salinomycin biosynthesis
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Informações sobre o DOI: 10.1002/cmdc.202300240 (Fonte: oaDOI API)
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