Wills Veronica S, Metzger Joseph I, Allen Cheryl, Varney Michelle L, Wiemer David F, Holstein Sarah A
Department of Chemistry, University of Iowa, Iowa City, IA 52242-1294, USA.
Department of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Bioorg Med Chem. 2017 Apr 15;25(8):2437-2444. doi: 10.1016/j.bmc.2017.02.066. Epub 2017 Mar 4.
Protein geranylgeranylation reactions are dependent on the availability of geranylgeranyl diphosphate (GGDP), which serves as the isoprenoid donor. Inhibition of GGDP synthase (GGDPS) is of interest from a drug development perspective as GGDPS inhibition results in impaired protein geranylgeranylation, which in multiple myeloma, disrupts monoclonal protein trafficking and induces apoptosis. We have recently reported a series of isoprenoid triazole bisphosphonates and have demonstrated that a 3:1 mixture of homogeranyl and homoneryl isomers potently, and in a synergistic manner, inhibits GGDPS. We now present the synthesis and biological evaluation of a novel series of bishomoisoprenoid triazoles which furthers our understanding of the structure-function relationship of this class. These studies demonstrate the importance of chain length and olefin stereochemistry on inhibitory activity.
蛋白质香叶基香叶基化反应依赖于香叶基香叶基二磷酸(GGDP)的可用性,GGDP作为类异戊二烯供体。从药物开发的角度来看,抑制GGDP合酶(GGDPS)是有意义的,因为抑制GGDPS会导致蛋白质香叶基香叶基化受损,在多发性骨髓瘤中,这会破坏单克隆蛋白运输并诱导细胞凋亡。我们最近报道了一系列类异戊二烯三唑双膦酸盐,并证明了均香叶基和均壬基异构体的3:1混合物以协同方式有效抑制GGDPS。我们现在展示了一系列新型双高异戊二烯三唑的合成和生物学评估,这进一步加深了我们对这类化合物结构 - 功能关系的理解。这些研究证明了链长和烯烃立体化学对抑制活性的重要性。