Department of Chemistry, Federal University of Mato Grosso, Cuiabá-MT 78068-600, Brazil.
Engineering Institute, Federal University of Mato Grosso, Várzea Grande-MT 78060-900, Brazil.
Molecules. 2018 Oct 19;23(10):2693. doi: 10.3390/molecules23102693.
Eight alkaloids (⁻) were isolated from , and their herbicide activities were evaluated through in vitro, semivivo, and in vivo assays. The most relevant results were observed for Compounds and ⁻ at 150 μM, which decreased dry biomass by 20% and 23%, respectively. These are significant results since they presented similar values with the positive control, commercial herbicide 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU). Based on the performed assays, Compound (graveoline) is classified as an electron-transport inhibitor during the light phase of photosynthesis, as well as a plant-growth regulator. On the other hand, Compounds ⁻ inhibited electron and energy transfers, and are also plant-growth inhibitors. These phytotoxic behaviors based on acridone and quinolone alkaloids may serve as a valuable tool in the further development of a new class of herbicides since natural products represent an interesting alternative to replace commercial herbicides, potentially due their low toxicity.
从 中分离得到 8 种生物碱(⁻),并通过体外、半体内和体内试验评价了它们的除草活性。在 150 μM 时,化合物 和 ⁻ 的观察结果最为相关,分别使干生物量减少了 20%和 23%。这些结果意义重大,因为它们与阳性对照(商业除草剂 3-(3,4-二氯苯基)-1,1-二甲基脲(DCMU))具有相似的值。基于进行的试验,化合物 (gravenoline)被归类为光合作用光阶段的电子传递抑制剂,以及植物生长调节剂。另一方面,化合物 ⁻ 抑制电子和能量转移,也是植物生长抑制剂。基于吖啶酮和喹诺酮生物碱的这些植物毒性行为可能是进一步开发新一类除草剂的有价值工具,因为天然产物代表了替代商业除草剂的有趣选择,这可能是由于它们的低毒性。