Two new norsesquiterpenoids with estrogenic activity from the stems and leaves of Dioscorea oppositifolia L

References

• Bai M, Cai Y, Wu SY, Song XP, Chen GY, Zheng CJ, Han CR. 2019. A new norisoprenoid from the leaves of Ficus pumila. Nat Prod Res. 33(9):1292–1297.
   PubMed Web of Science ®Google Scholar
• Chen GY, Zhang B, Zhao T, Nidhal N, Wang JL, Zhou XM, Dai CY. 2019. A new triterpenoid glucoside from Leucas zeylanica. Nat Prod Res. 1–5. doi:https://doi.org/10.1080/14786419.2019.1566820.
   Google Scholar
• Chen YF, Zhu Q, Wu SJ. 2015. Preparation of oligosaccharides from Chinese yam and their antioxidant activity. Food Chem. 173:1107–1110.
   PubMed Web of Science ®Google Scholar
• Cho HK, Suh WS, Kim KH, Kim SY, Lee KR. 2014. Phytochemical constituents of Salsola komarovii and their effects on NGF induction. Nat Prod Sci. 20(2):95–101.
   Google Scholar
• Georgantea P, Ioannou E, Vagias C, Roussis V. 2014. Bisabolane and chamigrane sesquiterpenes from the soft coral Pseudopterogorgia rigida. Phytochem Lett. 8:86–91.
   Web of Science ®Google Scholar
• Giang PM, Son PT, Matsunami K, Otsuka H. 2005. New megastigmane glucosides from Excoecaria cochinchinensis LOUR. var. cochinchinensis. Chem Pharm Bull. 53(12):1600–1603.
   PubMed Web of Science ®Google Scholar
• Guo Y, Zhu S, Wu G, Huang ML, Yan SK, Jin HZ, Zhang WD. 2017. Four new phenylpropanoid glycosides from Clausena dunniana var. robusta and their antiinflammatory activities. Phytochem Lett. 22:138–141.
   Web of Science ®Google Scholar
• Jang H, Lee JW, Kim JG, Hong HR, Le TPL, Hong JT, Kim Y, Lee MK, Hwang BY. 2018. Nitric oxide inhibitory constituents from Siegesbeckia pubescens. Bioorg Chem. 80:81–85.
   PubMed Web of Science ®Google Scholar
• Joy JK, Siddhuraju P. 2017. Studies on nutritional profile and antioxidant potential of different Dioscorea SP with Plectranthus rotundifolius. Int J Curr Pharm Sci Res. 9(4):65–74.
   Google Scholar
• Li M, Zeng MN, Zhang ZG, Zhang JK, Zhang BB, Zhao X, Zheng XK, Feng WS. 2018. Uridine derivatives from the seeds of Lepidium apetalum Willd. and their estrogenic effects. Phytochemistry. 155:45–52.
   PubMed Web of Science ®Google Scholar
• Lam SH, Li YC, Kuo PC, Hwang TL, Yang ML, Wang CC, Tzen J. 2019. Chemical constituents of Vigna luteola and their anti-inflammatory bioactivity. Molecules. 24(7):1–11.
   Web of Science ®Google Scholar
• Ma FY, Zhang Y, Yao YN, Wen YR, Hu WP, Zhang J, Liu XH, Bell AE, Tikkanen-Kaukanen C. 2017. Chemical components and emulsification properties of mucilage from Dioscorea opposita Thunb. Food Chem. 228:315–322.
   PubMed Web of Science ®Google Scholar
• Mazumder S, Shang DJ, Negru DE, Baik MH, Evans PA. 2012. Stereoselective rhodium-catalyzed [3 + 2+1] carbocyclization of alkenylidenecyclopropanes with carbon monoxide: theoretical evidence for a trimethylenemethane metallacycle intermediate. J Am Chem Soc. 134(51):20569–20572.
   PubMed Web of Science ®Google Scholar
• Ni L, Huang W, Shi Y, Wang HS, Qiu YT, Xu HY. 2018. Chemical constituents from the bark of Bauhinia purpurea and their NO inhibitory activities. Nat Prod Res. 1–6. doi:https://doi.org/10.1080/14786419.2018.1543672.
   Google Scholar
• Posta M, Light ME, Papenfus HB, Van Staden J, Kohout L. 2013. Structure-activity relationships of analogs of 3,4,5-trimethylfuran-2(5H)-one with germination inhibitory activities. J Plant Physiol. 170(14):1235–1242.
   PubMed Web of Science ®Google Scholar
• Ren YJ, Zeng MN, Cao YG, Zhang BB, Guo MM, Qi M, Zhang YL, Zhao X, Zheng XK, Feng WS. 2019. A new diphenylethane and a new dibenz[b,f]oxepin with estrogenic activity from the stems and leaves of Dioscorea oppositifolia L. Phytochem Lett. 33:26–30.
   Web of Science ®Google Scholar
• Shu P, Wei X, Xue Y, Li W, Zhang J, Xiang M, Zhang M, Luo Z, Li Y, Yao G, et al. 2013. Wilsonols A-L, megastigmane sesquiterpenoids from the leaves of Cinnamomum wilsonii. J Nat Prod. 76(7):1303–1312.
   PubMed Web of Science ®Google Scholar
• Su L, Wang YM, Zhong KR, Tu GZ, Jiang YY, Liu B. 2019. Chemical constituents of Mentha haplocalyx. Chem Nat Compd. 55(2):351–353.
   Web of Science ®Google Scholar
• Wang SJ, Gao WY, Liu HY, Chen HX, Yu JG, Xiao P. 2006. Studies on the physicochemical, morphological, thermal and crystalline properties of starches separated from different Dioscorea opposita cultivars. Food Chem. 99(1):38–44.
   Web of Science ®Google Scholar
• Wu XY, Xiong J, Liu XH, Hu JF. 2016. Chemical constituents of the rare cliff plant Oresitrophe rupifraga and their antineuroinflammatory activity. Chem Biodiversity. 13(8):1030–1037.
   PubMed Web of Science ®Google Scholar
• Xiong HP, Mi JL, Le JM, Wu ZJ, Chen WS. 2017. Chemical constituents of Ampelopsis japonica. Chem Nat Compd. 53(4):791–793.
   Web of Science ®Google Scholar
• Yang B-Y, Yin X, Liu Y, Sun Y, Guan W, Zhou Y-Y, Kuang H-X. 2019. Terpenes and lignans from the roots of Solanum melongena L. Nat Prod Res. (2):1–10.
   Web of Science ®Google Scholar
• Yang HH, Oh KE, Jo YH, Ahn JH, Liu Q, Turk A, Jang JY, Hwang BY, Lee KY, Lee MK. 2018. Characterization of tyrosinase inhibitory constituents from the aerial parts of Humulus japonicus using LC-MS/MS coupled online assay. Bioorg Med Chem. 26(2):509–515.
   PubMed Web of Science ®Google Scholar
• Zeng RT, He YR, Shen YH. 2015. Sesquiterpenoids from branches and leaves of Cephalotaxus lanceolata. Chin Tradit Herb Drugs. 46(3):320–324.
   Google Scholar
• Zhao X, Guo Y, Zhang Y, Xie YG, Yan SK, Jin HZ, Zhang WD. 2017. Monoterpene derivatives from the flowers of the Hemerocallis minor Mill. Phytochem Lett. 21:134–138.
   Web of Science ®Google Scholar
• Zhang L, Ng TB, Lam JKW, Wang SW, Lao LX, Zhang KLY, Sze S. 2019. Research and development of proteins and peptides with therapeutic potential from Yam tubers. Curr Protein Peptide Sci. 20(3):277–284.
   PubMed Web of Science ®Google Scholar
• Zhang ZS, Wang XM, Liu CB, Li JF. 2016. The degradation, antioxidant and antimutagenic activity of the mucilage polysaccharide from Dioscorea opposite. Carbohydr Polym. 150:227–231.
   PubMed Web of Science ®Google Scholar
• Zhu MM, Wang SL, Fan MT, Li J. 2016. In vitro study of the carotenoid-cleavage enzyme from Staphylococcus pasteuri TS-82 revealed substrate specificities and generation of norisoprenoid flavors. Food Sci Biotechnol. 25(1):221–227.
   PubMed Web of Science ®Google Scholar