College of Pharmacy, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Republic of Korea.
Bioorg Med Chem Lett. 2012 Oct 1;22(19):6116-9. doi: 10.1016/j.bmcl.2012.08.029. Epub 2012 Aug 14.
In spite of the critical role of the natural products in drug discovery, surprising little attention has been placed on endangered and rare plant species that could play a pivotal role in pharmaceutical and fiber development. Protein tyrosine phosphatase-1B (PTP1B), which blocks insulin signaling, has been gaining interest to be a promising therapeutic target for the treatment of type 2 diabetes mellitus. Bioassay-guided fractionation on the leaves of Rhododendron brachycarpum G. Don (Ericaceae) yielded seven PTP1B inhibitory triterpenoids, including a new triterpene, rhododendric acid A (1). Their PTP1B inhibitory potency and their lipophilicity were investigated to provide a feasible scaffold that may overcome the innate limitation of the previously reported PTP1B inhibitors.
尽管天然产物在药物发现中起着至关重要的作用,但对于可能在制药和纤维开发中发挥关键作用的濒危和珍稀植物物种,人们关注得惊人地少。蛋白酪氨酸磷酸酶-1B(PTP1B)能阻断胰岛素信号转导,它作为治疗 2 型糖尿病的一个很有前途的治疗靶点,引起了人们的兴趣。对短柱杜鹃(Ericaceae)叶进行基于生物活性的分离,得到了 7 种具有 PTP1B 抑制活性的三萜类化合物,包括一种新的三萜酸 rhododendric acid A(1)。研究了它们对 PTP1B 的抑制活性和脂溶性,以提供一个可行的支架,可能克服以前报道的 PTP1B 抑制剂的固有局限性。