Guanine derivatives as promising candidates for the development of purine-based antimalarial drugs.

INTRODUCTION

The increasing resistance of to existing antimalarial drugs drives the urgent need for novel therapeutic strategies. The purine salvage pathway in is essential for the parasite's survival due to its complete reliance on host-derived purines for nucleic acid synthesis and other essential processes. Although the purine salvage system has been intensively researched, no purine-based antimalarial drugs have been taken into preclinical development. The current study evaluated the chemotherapeutic potential of some purine nucleobase analogues against .

METHODS

sensitivity assays were conducted using the 72-hour SYBR Green drug assay on laboratory-adapted strains 3D7 and Dd2. The most potent nucleobase analogues were docked into PfENT1 using the PyRx software suite.

RESULTS

The analogues 8-azaguanine, 7-deazaguanine, and 6-thioguanine exhibited average EC values of 1.71 µM, 14.9 µM and 15.7 µM, respectively, for 3D7 and 5.2 µM, 16.3 µM and 18.6 µM, respectively, for the Dd2 strain, and subsequently tested against field isolates of . These tests showed EC values ranging from 0.5 - 4.5 µM for 8-azaguanine, 3.8 - 12.3 µM for 7-deazaguanine, and 4.1 - 15.0 µM for 6-thioguanine. To understand their cellular targeting, molecular docking of the same analogues was performed using the structure of Equilibrative Nucleoside Transporter 1 (ENT1). This demonstrated that guanine, 8-azaguanine and 7-deazaguanine formed five hydrogen bonds each with the same amino acid residues of ENT1, whereas 6-thioguanine's orientation allowed only two hydrogen bonds with ENT1. The binding pose of inosine was different from these nucleobases.

DISCUSSION

These findings highlight the potential of guanine-based scaffolds, particularly 8-azaguanine and 7-deazaguanine, as promising leads for purine-based antimalarial drug development and the versatility of the ENT1 transporter in the uptake of purine antimetabolites.