Liquidambarines A − C, three new abietane diterpenoids from Liquidambar formosana Hance and their anti-inflammatory activities

References

• Beek TV, Claassen FW, Dorado J, Godejohann M, Sierra-Alvarez R, Wijnberg JBPA. 2007. Fungal biotransformation products of dehydroabietic acid. J Nat Prod. 70(2):154–159.
   PubMed Web of Science ®Google Scholar
• Cheng ZX, Chen WL, Chen XC, Lin D, Chen H. 2011. Effect of essential oil and ethyl acetate extract of Resina Liquidambaris on vascular active factor of normal mice. China Med Her. 8:37–39.
   Google Scholar
• Dat NT, Lee IS, Cai XF, Shen G, Kim YH. 2004. Oleanane triterpenoids with inhibitory activity against NFAT transcription factor from Liquidambar formosana. Biol Pharm Bull. 27(3):426–428.
   PubMed Web of Science ®Google Scholar
• Feng ZL, Li D, Liu QY, Liu JX, Huang L, Zhang QW, Wang YT, Lin LG. 2017. Anti-inflammatory abietane diterpenoids from the seeds of Podocarpus nagi. Phytochem Lett. 21:260–263.
   Web of Science ®Google Scholar
• Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR, Scalmani G, Barone V, Mennucci B, Petersson GA. 2013. Gaussian, version 09, expanding the limits of computational chemistry. Wallingford (CT): Gaussian, Inc.
   Google Scholar
• Huang XL, Wang DW, Liu YQ, Cheng YX. 2022. Diterpenoids from Blumea balsamifera and their anti-inflammatory activities. Molecules. 27(9):2890–2904.
   PubMed Web of Science ®Google Scholar
• Huang T, Ying S-H, Li J-Y, Chen H-W, Zang Y, Wang W-X, Li J, Xiong J, Hu J-F. 2020. Phytochemical and biological studies on rare and endangered plants endemic to China. Part XV. Structurally diverse diterpenoids and sesquiterpenoids from the vulnerable conifer Pseudotsuga sinensis. Phytochemistry. 169:112184–112114.
   PubMed Web of Science ®Google Scholar
• Iankov LK, Ivanov CP, Fam TTT. 1980. Tritepene acids with lupane and ursane skeletons from the resin of Liquidambar formosana H. Dokl Bolg Akad Nauk. 33:75–78.
   Google Scholar
• Kinouchi Y, Ohtsu H, Tokuda H, Nishino H, Matsunaga S, Tanaka R. 2000. Potential antitumor-promoting diterpenoids from the stem bark of Picea glehni. J Nat Prod. 63(6):817–820.
   PubMed Web of Science ®Google Scholar
• Lee C-L, Chiang L-C, Cheng L-H, Liaw C-C, Abd El-Razek MH, Chang F-R, Wu Y-C. 2009. Influenza A (H1N1) Antiviral and Cytotoxic Agents from Ferula assa-foetida. J Nat Prod. 72(9):1568–1572.
   PubMed Web of Science ®Google Scholar
• Li HL, Song HC, Zhang Y, Chen YG. 2016. Chemical constituents of the barks of Podocarpus macrophyllus. Chem Nat Compd. 52(3):539–541.
   Web of Science ®Google Scholar
• Liu H, Shen MY, He ZH. 1995. Study on the chemical constituent of Liquidambar balsam. Chem Ind Forest Prod. 15:61–66.
   Google Scholar
• Liu C, Xu JF, He QM, Yu QS. 1991. Chemical components of the Liquidambar formosana H. resin. Org Chem. 11:508–510.
   Google Scholar
• Man D, Bai MH, Mu QE, Hu GJL, Xiu BS, Huang SQ, Te MQL. 2020. Molecular docking study of the mechanism of resina Liquidamberis intervention in rheumatoid arthritis. Nat Prod Res Dev. 32(6):9.
   Google Scholar
• Ouyang X, Yi S, Lu H, Wu S, Zhao H. 2016. Liquidambar formosana Hance: a mini-review of chemical constituents and pharmacology. Eur J Med Plants. 17(1):1–11.
   Google Scholar
• Pham TTT, Vien DL. 1975. A new triterpene acid isolated from the resin of Liquidambar formosana. Tap San Hoa Hoc. 13:34–37.
   Google Scholar
• Pharmacopoeia of the People’s Republic of China. 2020. The national pharmacopoeia commission. Beijing (BJ): China Pharmaceutical Science and Technology Press. p. 215.
   Google Scholar
• Qiu CL, Ye ZN, Yan BC, Hu K, Yang J, Yang XZ, Li HM, Li XN, Sun HD, Puno PT. 2022. Structurally Diverse Diterpenoids from Isodon Oresbius and Their Bioactivity. Bioorg Chem. 124:1–11.
   Web of Science ®Google Scholar
• Shang HJ, Li DY, Wang WJ, Li ZL, Hua HM. 2014. Three new diterpenoids from the resin of Liquidambar formosana. Nat Prod Res. 28(1):1–6.
   PubMed Web of Science ®Google Scholar
• Shimozu Y, Kuroda T, Tsuchiya T, Hatano T. 2017. Structures and antibacterial properties of sorugosins H-J, oligomeric ellagitannins from Liquidambar formosana with characteristic bridging groups between sugar moieties. J Nat Prod. 80(10):2723–2733.
   PubMed Web of Science ®Google Scholar
• Sun HD. 2012. Diterpene chemistry. Beijing (BJ): Chemical Industry Press. p. 129–130.
   Google Scholar
• Wang B, Jing J, He XF, Yuan T, Yue JM. 2010. Three new terpenoids from Pinus yunnanensis. Helv Chim Acta. 93(3):490–496.
   Web of Science ®Google Scholar
• Wang K, Pan YM, Wang HS, Zhang Y, Lei Q, Zhu ZR, Li HY, Liang M. 2010. Antioxidant activities of Liquidambar formosana Hance leaf extracts. Med Chem Res. 19(2):166–176.
   Web of Science ®Google Scholar
• Yang NY, Chen JH, Zhou GS, Tang YP, Duan JA, Tian LJ, Liu XH. 2011. Pentacyclic triterpenes from the resin of Liquidambar formosana. Fitoterapia. 82(6):927–931.
   PubMed Web of Science ®Google Scholar
• Yankov LK, Ivanov CP, Fam TTT. 1980. Tritepene acids with oleane skeleton from the resin of Liquidambar formosana H. Dokl Bolg Akad Nauk. 33:357–360.
   Google Scholar
• Yu J, Liu S, Xuan L. 2012. Two new lupene-type triterpenoids from the roots of Liquidambar formosana. Nat Prod Res. 26(7):630–636.
   PubMed Web of Science ®Google Scholar
• Zapata B, Rojas M, Betancur-Galvis L, Mesa-Arango AC, P’erez-Guaita D, Gonz’alez MA. 2013. Cytotoxic, immunomodulatory, antimycotic, and antiviral activities of semisynthetic 14-hydroxyabietane derivatives and triptoquinone C-4 epimers. Med Chem Commun. 4(9):1239–1246.
   Google Scholar
• Zhu Y, Guan Y-J, Chen Q-Z, Yuan L-H, Xu Q-Q, Zhou M-L, Liu H, Lin W, Zhang Z-D, Zhou Z-L, et al. 2021. Pentacyclic triterpenes from the resin of Liquidambar formosana have anti-angiogenic properties. Phytochemistry. 184:112676–112679.
   PubMed Web of Science ®Google Scholar