Zink M, Lanig H, Troschütz R (2004)
Publication Status: Published
Publication Type: Journal article, Original article
Publication year: 2004
Book Volume: 39
Pages Range: 1079-88
Journal Issue: 12
URI: https://www.sciencedirect.com/science/article/pii/S022352340400176X?via%3Dihub
DOI: 10.1016/j.ejmech.2004.09.001
Piritrexim (PTX) (1), a lipophilic inhibitor of the human dihydrofolate reductase, has been evaluated as an anticancer agent. The synthesis of four structural variations (2-5) of PTX is reported. The PTX analogues 2-5 were obtained by reaction of suitable C3-building blocks with pyrimidine-2,4,6-triamine (14) or with cyanacetamide (7) and guanidine (10). The evaluation of 2-4 for antitumor activity against a panel of 60 human cancer cell lines showed inhibitory effects on the growth of the cell lines. These data are supported by molecular modeling and docking studies, which show that compounds 2-4 share the same binding mode within the DHFR active site. Moreover, the estimated ligand binding energies are in good agreement with the experimental activity data.
APA:
Zink, M., Lanig, H., & Troschütz, R. (2004). Structural variations of piritrexim, a lipophilic inhibitor of human dihydrofolate reductase: synthesis, antitumor activity and molecular modeling investigations. European Journal of Medicinal Chemistry, 39(12), 1079-88. https://doi.org/10.1016/j.ejmech.2004.09.001
MLA:
Zink, Mario, Harald Lanig, and Reinhard Troschütz. "Structural variations of piritrexim, a lipophilic inhibitor of human dihydrofolate reductase: synthesis, antitumor activity and molecular modeling investigations." European Journal of Medicinal Chemistry 39.12 (2004): 1079-88.
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