A, W., N, T., J, W., C, O., X, Z., Z, H., . . . A, G. (2021). Discovery of 6-substituted thieno[2,3-d]pyrimidine analogs as dual inhibitors of glycinamide ribonucleotide formyltransferase and 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase in de novo purine nucleotide biosynthesis in folate receptor expressing human tumors. Bioorganic & medicinal chemistry, 37, 116093. https://doi.org/10.1016/j.bmc.2021.116093
Chicago Style (17th ed.) CitationA, Wallace-Povirk, et al. "Discovery of 6-substituted Thieno[2,3-d]pyrimidine Analogs as Dual Inhibitors of Glycinamide Ribonucleotide Formyltransferase and 5-aminoimidazole-4-carboxamide Ribonucleotide Formyltransferase in De Novo Purine Nucleotide Biosynthesis in Folate Receptor Expressing Human Tumors." Bioorganic & Medicinal Chemistry 37 (2021): 116093. https://doi.org/10.1016/j.bmc.2021.116093.
MLA (9th ed.) CitationA, Wallace-Povirk, et al. "Discovery of 6-substituted Thieno[2,3-d]pyrimidine Analogs as Dual Inhibitors of Glycinamide Ribonucleotide Formyltransferase and 5-aminoimidazole-4-carboxamide Ribonucleotide Formyltransferase in De Novo Purine Nucleotide Biosynthesis in Folate Receptor Expressing Human Tumors." Bioorganic & Medicinal Chemistry, vol. 37, 2021, p. 116093, https://doi.org/10.1016/j.bmc.2021.116093.