Identification of Active Compounds against Melanoma Growth by Virtual Screening for Non-Classical Human DHFR Inhibitors (2022)
- Authors:
- Autor USP: PACHÓN, DIEGO MAURICIO RIAÑO - CENA
- Unidade: CENA
- DOI: 10.3390/ijms232213946
- Subjects: FÁRMACOS; MELANOMA; FARMACOTERAPIA; PROTEÍNAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: International Journal of Molecular Sciences
- ISSN: 1422-0067
- Volume/Número/Paginação/Ano: v. 23, art. 13946, 2022
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
VÁSQUEZ, Andrés Felipe et al. Identification of Active Compounds against Melanoma Growth by Virtual Screening for Non-Classical Human DHFR Inhibitors. International Journal of Molecular Sciences, v. 23, 2022Tradução . . Disponível em: https://doi.org/10.3390/ijms232213946. Acesso em: 16 abr. 2024. -
APA
Vásquez, A. F., Gómez, L. A., González Barrios, A., & Riaño-Pachón, D. M. (2022). Identification of Active Compounds against Melanoma Growth by Virtual Screening for Non-Classical Human DHFR Inhibitors. International Journal of Molecular Sciences, 23. doi:10.3390/ijms232213946 -
NLM
Vásquez AF, Gómez LA, González Barrios A, Riaño-Pachón DM. Identification of Active Compounds against Melanoma Growth by Virtual Screening for Non-Classical Human DHFR Inhibitors [Internet]. International Journal of Molecular Sciences. 2022 ; 23[citado 2024 abr. 16 ] Available from: https://doi.org/10.3390/ijms232213946 -
Vancouver
Vásquez AF, Gómez LA, González Barrios A, Riaño-Pachón DM. Identification of Active Compounds against Melanoma Growth by Virtual Screening for Non-Classical Human DHFR Inhibitors [Internet]. International Journal of Molecular Sciences. 2022 ; 23[citado 2024 abr. 16 ] Available from: https://doi.org/10.3390/ijms232213946 - Shedding light on the dynamic role of the “target of rapamycin” kinase in the fast-growing C4 species Setaria viridis, a suitable model for biomass crops
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Informações sobre o DOI: 10.3390/ijms232213946 (Fonte: oaDOI API)
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