School of Pharmaceutical Sciences, Southern Medical University, 1838 Guangzhou Avenue North, Guangzhou 510515, PR China.
Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158, PR China.
Fitoterapia. 2021 Apr;150:104835. doi: 10.1016/j.fitote.2021.104835. Epub 2021 Jan 29.
Seven new limonoids, named krishnolides E-K (1-7), including three khayanolides, two mexicanolides, a derivative of trangmolin A, and an andirobin, were isolated from seeds of the Indian Krishna mangrove, Xylocarpus moluccensis. The structures of these limonoids were established by HRESIMS, extensive NMR investigations, and X-ray crystallography. Most notably, the absolute configurations of 1, 5, 6, and 7 were unequivocally determined by single-crystal X-ray diffraction analyses (Cu Kα). Krishnolide F (2) exhibited significant agonistic effects on human pregnane-X-receptor (hPXR) at the concentration of 10.0 μM. Molecular docking revealed that 2 could bind a helix near the region of the Helix 12 of hPXR. Polar contribution could be electrostatic effects from the formation of two stable protein-ligand hydrogen bonds between Gln285/1-OH and His407/1-OH, respectively. This is the first report of agonistic effects of a khayanolide-type limonoid on hPXR.
从印度克里希纳红树林,木果楝 Xylocarpus moluccensis 的种子中分离得到了 7 种新的柠檬苦素,分别命名为 krishnolide E-K(1-7),包括 3 种 khayanolide、2 种 mexicanolide、trangmolin A 的衍生物和 andirobin。这些柠檬苦素的结构通过高分辨质谱(HRESIMS)、广泛的 NMR 研究和 X 射线晶体学确定。最值得注意的是,通过单晶 X 射线衍射分析(Cu Kα)明确确定了 1、5、6 和 7 的绝对构型。Krishnolide F(2)在 10.0 μM 的浓度下对人孕烷 X 受体(hPXR)表现出显著的激动作用。分子对接表明,2 可以结合 hPXR 螺旋 12 附近区域的一个螺旋。极性贡献可能是 Gln285/1-OH 和 His407/1-OH 之间形成的两个稳定的蛋白-配体氢键的静电效应。这是 khayanolide 型柠檬苦素对 hPXR 表现出激动作用的首次报道。