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NTIS 바로가기Plants, v.9 no.9, 2020년, pp.1232 -
Qi, Yutong (Department of Life and Nanopharmaceutical Sciences, Graduate School Kyung Hee University, Seoul 02447, Korea) , Choi, Se-In (qiyutong9675@gmail.com (Y.Q.)) , Son, So-Ri (sae_in@daum.net (S.-I.C.)) , Han, Hee-Soo (allosori@khu.ac.kr (S.-R.S.)) , Ahn, Hye Shin (heesu3620@daum.net (H.-S.H.)) , Shin, Yu-Kyong (ktlee@khu.ac.kr (K.-T.L.)) , Lee, Sun Hee (Department of Life and Nanopharmaceutical Sciences, Graduate School Kyung Hee University, Seoul 02447, Korea) , Lee, Kyung-Tae (qiyutong9675@gmail.com (Y.Q.)) , Kwon, Hak Cheol (sae_in@daum.net (S.-I.C.)) , Jang, Dae Sik (allosori@khu.ac.kr (S.-R.S.))
Campanula takesimana Nakai (Campanulaceae; Korean bellflower) is one of the endemic herbs of Korea. The plant has been used as traditional medicines for treating asthma, tonsillitis, and sore throat in Korea. A hot water extract of the leaves of C. takesimana exhibited a significant inhibitory effec...
1. Park K.R. Jung H.J. Isozyme and morphological variation in Campanula punctata and C. takesimana (Campanulaceae) Korean J. Plant Taxon. 2000 30 1 16 10.11110/kjpt.2000.30.1.001
4. Yang G. Lee K. Lee M. Ham I. Choi H.Y. Inhibition of lipopolysaccharide-induced nitric oxide and prostaglandin E 2 production by chloroform fraction of Cudrania tricuspidata in RAW 264.7 macrophages BMC Complement. Altern. Med. 2012 12 250 10.1186/1472-6882-12-250 23228109
5. Agrawal P.K. NMR spectroscopy in the structural elucidation of oligosaccharides and glycosides Phytochemistry 1992 31 3307 3330 10.1016/0031-9422(92)83678-R 1368855
6. Yuda M. Ohtani K. Mizutani K. Kasai R. Tanaka O. Jia M.R. Ling Y.R. Pu X.F. Saruwatari Y.I. Neolignan glycosides from roots of Codonopsis tangshen Phytochemistry 1990 29 1989 1993 10.1016/0031-9422(90)85053-I
7. Mizutani K. Yuda M. Tanaka O. Saruwatari Y.I. Jia M.R. Ling Y.K. Pu X.F. Tanghenosides i and ii from chuan-dangshen, the root of C odonopsis tangshen oliv Chem. Pharm. Bull. 1998 36 2726 2729 10.1248/cpb.36.2726
8. Pieters L. de Bruyne T. Claeys M. Vlietinck A. Calomme M. vanden Berghe D. Isolation of a dihydrobenzofuran lignan from South American dragon’s blood ( Croton spp.) as an inhibitor of cell proliferation J. Nat. Prod. 1993 56 899 906 10.1021/np50096a013 8350090
9. Li L. Seeram N.P. Maple syrup phytochemicals include lignans, coumarins, a stilbene, and other previously unreported antioxidant phenolic compounds J. Agric. Food Chem. 2010 58 11673 11679 10.1021/jf1033398 21033720
10. Calis I. Kirmizibekmez H. Beutler J.A. Donmez A.A. Yalcin F.N. Kilic E. Ozalp M. Ruedi P. Tasdemir D. Secondary metabolites of Phlomis v iscosa and their biological activities Turk. J. Chem. 2005 29 71 81
12. Schumacher B. Scholle S. Holzl J. Khudeir N. Hess S. Muller C.E. Lignans isolated from valerian: Identification and characterization of a new olivil derivative with partial agonistic mactivity at A1 adenosine receptors J. Nat. Prod. 2002 65 1479 1485 10.1021/np010464q 12398547
13. Tan R.X. Ma W.G. Wei H.X. Zhang L.X. Glycosides from Wahlenbergia marginata Phytochemistry 1998 48 1245 1250 10.1016/S0031-9422(97)00928-X
14. Yawadio R. Tanimori S. Morita N. Identification of phenolic compounds isolated from pigmented rices and their aldose reductase inhibitory activities Food Chem. 2007 101 1616 1625 10.1016/j.foodchem.2006.04.016
15. Sakakibara N. Nakatsubo T. Suzuki S. Shibata D. Shimada M. Umezawa T. Metabolic analysis of the cinnamate/monolignol pathway in Carthamus tinctorius seeds by a stable-isotope-dilution method Org. Biomol. Chem. 2007 5 802 815 10.1039/b616705e 17315067
16. Peng W. Fu X. Li Y. Xiong Z. Shi X. Zhang F. Huo G. Li B. Phytochemical study of stem and leaf of Clausena lansium Molecules 2019 24 3124 10.3390/molecules24173124
18. Chiang H. Lo Y. Lu F. Xanthine oxidase inhibitors from the leaves of Alsophila s pinulosa (Hook) Tryon J. Enzym. Inhib. 1994 8 61 71 10.3109/14756369409040777 7539070
19. Cheng X. Tang X. Guo C. Zhang C. Yang Q. New flavonol glycosides from the seeds of Desmodium styracifolium Chem. Nat. Compd. 2018 54 846 850 10.1007/s10600-018-2496-7
20. Kazuma K. Noda N. Suzuki M. Malonylated flavonol glycosides from the petals of Clitoria ternatea Phytochemistry 2003 62 229 237 10.1016/S0031-9422(02)00486-7 12482461
21. Markham K.R. Ternai B. Stanley R. Geiger H. Mabry T.J. Carbon-13 NMR Studies of flavonoids―III: Naturally occurring flavonoid glycosides and their acylated derivatives Tetrahedron 1978 34 1389 1397 10.1016/0040-4020(78)88336-7
22. Aisyah L.S. Yun Y.F. Herlina T. Julaeha E. Zainuddin A. Nurfarida I. Hidayat A.T. Supratman U. Shiono Y. Flavonoid compounds from the leaves of Kalanchoe prolifera and their cytotoxic activity against P-388 murine leukimia cells Nat. Prod. Sci. 2017 23 139 145 10.20307/nps.2017.23.2.139
23. Nathan C. Points of control in inflammation Nature 2002 420 846 852 10.1038/nature01320 12490957
24. Hotamisligil G.S. Inflammation and metabolic disorders Nature 2006 444 860 867 10.1038/nature05485 17167474
25. Hammer K.D. Hillwig M.L. Solco A.K. Dixon P.M. Delate K. Murphy P.A. Wurtele E.S. Birt D.F. Inhibition of prostaglandin E 2 production by anti-inflammatory Hypericum perforatum extracts and constituents in RAW264. 7 mouse macrophage cells J. Agric. Food Chem. 2007 55 7323 7331 10.1021/jf0710074 17696442
26. Liu Q. Huang X. Bai M. Chang X. Yan X. Zhu T. Zhao W. Peng Y. Song S. Antioxidant and anti-inflammatory active dihydrobenzofuran neolignans from the Seeds of Prunus tomentosa J. Agric. Food Chem. 2014 62 7796 7803 10.1021/jf502171z 25019337
27. Yao J. Zou Z. Wang X. Ji X. Yang J. Pinoresinol diglucoside alleviates oxLDL-induced dysfunction in human umbilical vein endothelial cells Evid. Based Complement. Alternat. Med. 2016 2016 10 10.1155/2016/3124519
28. Yoo S. Jeong S. Lee N. Shin H. Seo C. Simultaneous determination and anti-inflammatory effects of four phenolic compounds in Dendrobii herba Nat. Prod. Res. 2017 31 2923 2926 10.1080/14786419.2017.1300798 28281361
29. Wu X. Zhang L. He J. Li G. Ding L. Gao X. Dong L. Song L. Li Y. Zhao Q. Two new diterpenoids from Excoecaria acerifolia J. Asian Nat. Prod. Res. 2013 15 151 157 10.1080/10286020.2012.757596 23323987
30. Li L. Popko J.L. Umezawa T. Chiang V.L. 5-hydroxyconiferyl aldehyde modulates enzymatic methylation for syringyl monolignol formation, a new view of monolignol biosynthesis in angiosperms J. Biol. Chem. 2000 275 6537 6545 10.1074/jbc.275.9.6537 10692459
31. Tanaka T. Tatsuya N. Toshihisa U. Kenji T. Isao K. Facile discrimination of aldose enantiomers by reversed-phase HPLC Chem. Pharm. Bull. 2007 55 899 901 10.1248/cpb.55.899 17541189
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