Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors (2018)
Source: Bioorganic Chemistry. Unidade: IQSC
Subjects: MOLÉCULA, QUÍMICA MÉDICA
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CIANNI, Lorenzo et al. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors. Bioorganic Chemistry, p. 285-292, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2018.04.006. Acesso em: 18 out. 2024.APA
Cianni, L., Satori, G. R., Rosini, F., De Vitta, D., Pires, G. L. de P., Lopes, B. R., et al. (2018). Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors. Bioorganic Chemistry, 285-292. doi:10.1016/j.bioorg.2018.04.006NLM
Cianni L, Satori GR, Rosini F, De Vitta D, Pires GL de P, Lopes BR, Leitão A, Burtoloso ACB, Montanari CA. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors [Internet]. Bioorganic Chemistry. 2018 ; 285-292.[citado 2024 out. 18 ] Available from: https://doi.org/10.1016/j.bioorg.2018.04.006Vancouver
Cianni L, Satori GR, Rosini F, De Vitta D, Pires GL de P, Lopes BR, Leitão A, Burtoloso ACB, Montanari CA. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors [Internet]. Bioorganic Chemistry. 2018 ; 285-292.[citado 2024 out. 18 ] Available from: https://doi.org/10.1016/j.bioorg.2018.04.006