Selective antagonist of formyl peptide receptor 2 (FPR2) signaling. Inhibits WKYMVm binding to FPR2 (IC50 = 0.23 μM) and inhibits intracellular calcium release induced by WKYMVm, MMK 1, amyloid β42, and F peptide. Also inhibits FPR2-mediated signaling in human neutrophils; blocks chemotactic migration and superoxide generation by amyloid β42 peptide.

GGTI 298 是一种香叶基香叶基转移酶 I 抑制剂，能够将人类肿瘤细胞阻滞在细胞周期的 G1 期并诱导细胞凋亡。

黄色结晶粉末，用作工业和有机中间体。