Takehiro Nishimura, Yuto Yamauchi, Naoko Yoshida, Ulises G Castillo, Karla Alas, Gabriel Cerén, Toshihiro Mita, Junko Nakajima-Shimada, Marvin J Núñez, Haruhisa Kikuchi
These findings highlight pimarane-type diterpenes as structurally distinct, sp3-rich scaffolds with favorable selectivity profiles and potential as leads for the development of new antitrypanosomal agents.
Chemical investigation of the methanolic extract of Guarea glabra Vahl (Meliaceae) led to the isolation of a new amide alkaloid containing a pyrrolidine moiety (1) and a dihydro-α-pyrone derivative (2), together with two known pimarane-type diterpenes (3, 4). The structures of the new compounds were elucidated using comprehensive spectroscopic analyses, including 1D and 2D NMR experiments. The absolute configuration of 2 was determined by comparing experimental and calculated electronic circular dichroism spectra. Compounds 1-4 demonstrated antitrypanosomal activity against the epimastigote form of Trypanosoma cruzi, with IC50 values ranging from 0.66 to 2.3 µM; compound 4 exhibited submicromolar activity. In the intracellular assay, compound 3 reduced the number of intracellular amastigotes at 10 µM. None of the isolated compounds showed significant antimalarial activity under the tested conditions. Compounds 1-4 exhibited favorable selectivity for T. cruzi over mammalian HT1080 cells. These findings highlight pimarane-type diterpenes as structurally distinct, sp3-rich scaffolds with favorable selectivity profiles and potential as leads for the development of new antitrypanosomal agents.