发表论文 |
1. Meng L#*, Cao Q#, Du X#, Lv H, Li C, Zhang X, Jiang N, Xiao Y. Structurally diverse bufadienolides from the skins of Bufo bufo gargarizans and their cytotoxicity. Sci Rep. 2024, 14(1):27344. 2. Meng L#, Lv H#, Kong Q, Li S, Jiang N, Yu C, Duan Z*, Xiao Y*, Liu Y*. The combination of paeoniflorin and metformin synergistically inhibits the progression of liver fibrosis in mice. Eur J Pharmacol. 2024, 981:176917. 3. Lv H, Kong Q, Song C, Yang J*, Meng L*. Maytenhoiridosides A and B, two new iridoid glycosides from the branches of Maytenus hookeri. Phytochem Lett. 2024, 62:34-37. 4. Meng L, Kong Q, Xie J, Pan F, Lu K, Li S, Li Y, Zhang D, Liu Y*. Bufogarlides A-C, three new bufadienolides with Δ14,15 double bond from the skins of Bufo bufo gargarizans. Nat Prod Res. 2024, 38(3):470-476. 5. Meng L, Yu C, Hui J, Jiang N, Wang H, Xie J, Xu L, Liu Y*. Three new coumarin derivatives from Maytenus hookeri. Nat Prod Res. 2024, 38(3):365-371. 6. 孟令杰, 孔庆宏, 姜念, 吕慧婧, 黎成锦, 郭朝霞, 刘云. 中华大蟾蜍皮化学成分及其细胞毒活性. 中成药. 2023, 45(11):3622-3626. 7. 孟令杰, 黎成锦, 宋长伟, 李三华, 刘云. 黑眶蟾蜍皮化学成分研究. 中成药. 2023, 45(4):1172-1176. 8. Jiang N, Yu C, Hui J, Xie J, Wang Y, Yang J, Li S*, Meng L*. Chemical constituents from Maytenus hookeri. Biochem Syst Ecol. 2022, 104:104475. 9. Li S#, Kong Q#, Zhang X, Zhu X, Yu C, Yu C, Jiang N, Hui J, Meng L*, Liu Yu*. 3-epi-bufotalin suppresses the proliferation in colorectal cancer cells through the inhibition of the JAK1/STAT3 signaling pathway. Biocell, 2022 46(11): 2425-2432. 10. Meng L, Li S, Kong Q, Wang M, Zhang X, Zhu X, Yu W, Jiang N, Chun Z, Li N, Liu Y*. Two new 19-hydroxy bufadienolides with cytotoxic activity from the skins of Bufo melanosticus, Nat Prod Res, 2021, 35(23):4894-4900. 11. Meng L, Jiang N, Yu C, Li S, Chun Z, Zhu X, Song C, Xiao Y, Hui J, Qin Y, Liu Y*. Bufadienolides from the skins of Bufo melanosticus and their cytotoxic activity, Phytochem Lett. 2019, 31:73-77. 12. Meng LJ, Tuo L*, Yan XR. Cohnella endophytica sp. nov., a novel endophytic bacterium isolated from bark of Sonneratia apetala. Int J Syst Evol Micr. 2019, 69:2004–2009. 13. Meng LJ, Guo QL, Zhu CG, Xu CB, Shi JG*. Isatindigodiphindoside, an alkaloid glycoside with a new diphenylpropylindole skeleton from the root of Isatis indigotica. Chin. Chem. Lett. 2018, 29(1):119–122. 14. Meng L, Guo Q, Chen M, Jiang J, Li Y, Shi J*. Isatindolignanoside A, a glucosidic indole-lignan conjugate from an aqueous extract of the Isatis indigotica roots. Chin. Chem. Lett. 2018, 29(8):1257–1260. 15. Meng L, Guo Q, Liu Y, Shi J*. 8,4¢-Oxyneolignane glucosides from an aqueous extract of “ban lan gen” (Isatis indigotica root) and their absolute configurations. Acta Pharm. Sin. B. 2017, 7(6):638–646. 16. Meng L, Guo Q, Liu Y, Chen M, Li Y, Jiang J, Shi J*. Indole alkaloid sulfonic acids from an aqueous extract of Isatis indigotica roots and their antiviral activity. Acta Pharm. Sin. B. 2017, 7(3):334–341. 17. Meng LJ, Guo QL, Xu CB, Zhu CG, Liu YF, Chen MH, Lin S, Li YH, Jiang JD, Shi JG*. Diglycosidic indole alkaloid derivatives from an aqueous extract of Isatis indigotica roots. J. Asian Nat. Prod. Res. 2017, 19(6):529–540. |