New lignan from the rattan stems of Schisandra chinensis

References

• CHIBA M, HISADA S, Thieme H. 1977. The position of glucose linkage in phillyrin. Chem Pharm Bull (Tokyo). 25:3435–3436.10.1248/cpb.25.3435
   Web of Science ®Google Scholar
• El-Domiaty MM, El-Shafae AM, Abdel-Aal MM, Abou-Hashem MM. 2002. The first report on the occurrence of furofuranoid lignan glucosides in Acanthaceae. Pharm Biol. 40:96–102.10.1076/phbi.40.2.96.5848
   Web of Science ®Google Scholar
• Greger H, Hofer O. 1980. New unsymmetrically substituted tetrahydrofurofuran lignans from Artemisia absinthium: assignment of the relative stereochemistry by lanthanide induced chemical shifts. Tetrahedron. 36:3551–3558.10.1016/0040-4020(80)88051-3
   Web of Science ®Google Scholar
• He WJ, Fu ZH, Han HJ, Yan H, Zeng GZ, Ji CJ, Chu HB, Zhang YM, Tan NH. 2011. Benzoic acid allopyranosides and lignan glycosides from the twigs of Keteleeria evelyniana. Zeitschrift für Naturforschung B. 66:0733–733739.10.5560/ZNB.2011.66b0733
   Google Scholar
• Kim KH, Lee KH, Choi SU, Kim YH, Lee KR. 2008. Terpene and phenolic constituents of Lactuca indica L. Arch Pharm Res. 31:983–988.10.1007/s12272-001-1256-8
   PubMed Web of Science ®Google Scholar
• Kim MR, Moon HT, Lee DG, Woo ER. 2007. A new lignan glycoside from the stem bark of styrax japonica s. et Z. Arch Pharm Res. 30:425–430.10.1007/BF02980215
   PubMed Web of Science ®Google Scholar
• Kuang HX, Xia YG, Yang BY, Wang QH, Lü SW. 2009. Lignan constituents from Chloranthus japonicus Sieb. Arch Pharm Res. 32:329–334.10.1007/s12272-009-1303-1
   PubMed Web of Science ®Google Scholar
• Lee DG, Lee SM, Bang MH, Park HJ, Lee TH, Kim YH, Kim JY, Baek NI. 2011. Lignans from the flowers of Osmanthus fragrans var. aurantiacus and their inhibition effect on NO production. Archives of Pharmacal Research. 34:2029–2035.10.1007/s12272-011-1204-y
   PubMed Web of Science ®Google Scholar
• Li RT, Han QB, Zheng YT, Wang RR, Yang LM, Lu Y, Sang SQ, Zheng QT, Zhao QS, Sun HD. 2005. Structure and anti-HIV activity of micrandilactones B and C, new nortriterpenoids possessing a unique skeleton from Schisandra micrantha. Chem Commun. 23:2936–2938.10.1039/b501932j
   Google Scholar
• Lin SY, Ko HH, Lee SJ, Chang HS, Lin CH, Chen IS. 2015. Biological evaluation of secondary metabolites from the root of Machilus obovatifolia. Chem Biodivers. 12:1057–1067.10.1002/cbdv.v12.7
   PubMed Web of Science ®Google Scholar
• Liu CS, Cao FH, Peng XJ, Luo JJ, Zeng C. 2012. Chemical constituents from Gentiana striata. J Chinese Med Mater. 35:908–910.
   Google Scholar
• Li W, Liu Y, Wang Z, Yu T, Lu Q, Chen H. 2015. Suppression of MAPK and NF-κB pathways by schisandrin B contributes to attenuation of DSS-induced mice model of inflammatory bowel disease. Pharmazie. 70:598–603.
   PubMed Web of Science ®Google Scholar
• Matsuda N, Kikuchi M. 1996. Studies on the Constituents of Lonicera Species. X. Neolignan Glycosides from the Leaves of Lonicera gracilipes var. glandulosa MAXIM. Chem Pharm Bull. 44:1676–1679.10.1248/cpb.44.1676
   Web of Science ®Google Scholar
• Mosmann T. 1983. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 65:55–63.10.1016/0022-1759(83)90303-4
   PubMed Web of Science ®Google Scholar
• Nakanishi T, Iida N, Inatomi Y, Murata H, Inada A, Murata J, Lang FA, Linuma M, Tanaka T. 2004. Neolignan and flavonoid glycosides in Juniperus communis var. depressa. Phytochemistry. 65:207–213.10.1016/j.phytochem.2003.10.025
   PubMed Web of Science ®Google Scholar
• Panossian A, Wikman G. 2008. Pharmacology of Schisandra chinensis Bail.: An overview of Russian research and uses in medicine. J Ethnopharmacol. 118:183–212.10.1016/j.jep.2008.04.020
   PubMed Web of Science ®Google Scholar
• Pelter A, Ward RS, Rao EV, Sastry kV. 1976. General methods for the assignment of stereochemistry to 2,6-diaryl-3,7-dioxabicyclo [3.3.0] octane lignans. Tetrahedron. 32:2783–2788.10.1016/0040-4020(76)80123-8
   Web of Science ®Google Scholar
• Shao ZX. 1995. Edible and medicinal value and utilization of schisandrae Chin. Wild Plant Resour. 4:33.
   Google Scholar
• Šmejkal K, Šlapetová T, Krmenčík P, Babula P, Dall'Acqua S, Innocenti G, Vančo J, Casarin E, Carrara M, Kalvarová K, et al. 2010. Evaluation of cytotoxic activity of Schisandra chinensis lignans. Planta Med. 76:1672–1677.10.1055/s-0030-1249861
   PubMed Web of Science ®Google Scholar
• Tabopda TK, Mitaine-Offer AC, Paululat T, Delemasure S, Dutartre P, Ngadjui BT, Lacaille-Dubois MA. 2016. Steroidal saponins from Chlorophytum deistelianum. Phytochemistry. 126:34–40.10.1016/j.phytochem.2016.03.003
   PubMed Web of Science ®Google Scholar
• Takeda Y, Ooiso Y, Masuda T, Honda G, Otsuka H, Sezik E, Yesilada E. 1998. Iridoid and eugenol glycosides from Nepeta cadmea. Phytochemistry. 49:787–791.10.1016/S0031-9422(98)00125-3
   Web of Science ®Google Scholar
• Tran TD, Pham NB, Booth R, Forster PI, Quinn RJ. 2016. Lignans from the Australian endemic plant Austrobaileya scandens. J Nat Prod. 79:1514–1523.10.1021/acs.jnatprod.5b00988
   PubMed Web of Science ®Google Scholar
• Wu SB, Meyer RS, Whitaker BD, Litt A, Kennelly EJ. 2012. Antioxidant glucosylated caffeoylquinic acid derivatives in the invasive tropica soda apple. Solanum viarum J Nat Prod. 75:2246–2250.10.1021/np300553t
   PubMed Web of Science ®Google Scholar
• Xiao WL, Li RT, Li SH, Li XL, Sun HD, Zheng YT, Wang RR, Lu Y, Wang C, Zheng QT. 2005. Lancifodilactone F: a novel nortriterpenoid possessing a unique skeleton from Schisandra lancifolia and its anti-HIV activity. Org Lett. 7:1263–1266.10.1021/ol0473187
   PubMed Web of Science ®Google Scholar
• Xue Y, Li X, Du X, Li X, Wang W, Yang J, Chen J, Pu J, Sun H. 2015. Isolation and anti-hepatitis B virus activity of dibenzocyclooctadiene lignans from the fruits of Schisandra chinensis. Phytochemistry. 116:253–261.10.1016/j.phytochem.2015.03.009
   PubMed Web of Science ®Google Scholar
• Yang BY, Guo JT, Li ZY, Wang CF, Wang ZB, Wang QH, Kuang HX. 2016. New thymoquinol glycosides and neuroprotective dibenzocyclooctane lignans from the rattan stems of Schisandra chinensis. Chem Biodivers. 13:1118–1125.10.1002/cbdv.v13.9
   PubMed Web of Science ®Google Scholar
• Yang BY, Liu Y, Jiang HB, Xu ZP, Guo R, Wang R, Li XM, Kuang HX. 2017. Phenylpropanoids from the fruits of Nicandra physaloides and their anti-inflammatory activities. Nat Prod Res. 31:2634–2640.10.1080/14786419.2017.1289202
   PubMed Web of Science ®Google Scholar
• Yang JQ, He WJ, Tan NH, Chu HB, Zhang YM, Mei WL, Dai HF. 2009. Chemical constituents of Pedicularis cephalantha Franch and P. siphonantha Don. Nat Prod Res Dev. 21:600–603.
   Google Scholar
• Yang BY, Guo JT, Wang ZB, Li ZY, Zheng GX, Wang QH, Kuang HX. in press. Monoterpenoid glycosides from the rattan stems of Schisandra chinensis.
   Google Scholar
• Zheng MS, Li G, Li Y, Seo CS, Lee YK, Jung JS, Song DK, Bae HB, Kwak AH, Chang HW, Kim JR. 2011. Protective constituents against sepsis in mice from the root barks of Ulmus davidiana var. japonica. Arch Pharm Res. 34:1443–1450.10.1007/s12272-011-0905-6
   PubMed Web of Science ®Google Scholar
• Zhu L, Li B, Liu X, Huang G, Meng X. 2015. Purification of six lignans from the stems of Schisandra chinensis by using high-speed counter-current chromatography combined with preparative high-performance liquid chromatography. Food Chem. 186:146–152.10.1016/j.foodchem.2014.09.008
   PubMed Web of Science ®Google Scholar
• Zu XP, Zhang WD, Han ZZ, Li HL. 2014. Water soluble chemical constituents of Valeriana officinalis Linn. var. latiofolia Miq. Acad J Second Mil Med Univ. 35:161–170.10.3724/SP.J.1008.2014.00161
   Google Scholar