참고문헌
- Nag SA, Qin JJ, Wang W, Wang MH, Wang H, Zhang R. Ginsenosides as anticancer agents: in vitro and in vivo activities, structureeactivity relationships, and molecular mechanisms of action. Front Pharmacol 2012;3:25. https://doi.org/10.3389/fphar.2012.00025
- Wang CZ, Cai Y, Anderson S, Yuan CS. Ginseng metabolites on cancer chemoprevention: an angiogenesis link. Diseases 2015;3:193-204. https://doi.org/10.3390/diseases3030193
- Li KK, Gong XJ. A review on the medicinal potentials of Panax ginseng saponins in diabetes mellitus. RSC Adv 2015;5:47353-66. https://doi.org/10.1039/C5RA05864C
- Lee CH, Kim JH. A review on the medicinal potentials of ginseng and ginsenosides on cardiovascular diseases. J Ginseng Res 2014;38:161-6. https://doi.org/10.1016/j.jgr.2014.03.001
- Ru W, Wang D, Xu Y, He X, Sun YE, Qian L, Zhou X, Qin Y. Chemical constituents and bioactivities of Panax ginseng (C. A. Mey.). Drug Discov Ther 2015;9:23-32. https://doi.org/10.5582/ddt.2015.01004
- Yang WZ, Hu Y, Wu WY, Ye M, Guo DA. Saponins in the genus Panax L. (Araliaceae): a systematic review of their chemical diversity. Phytochemistry 2014;106:7-24. https://doi.org/10.1016/j.phytochem.2014.07.012
- Shin BK, Kwon SW, Park JH. Chemical diversity of ginseng saponins from Panax ginseng. J Ginseng Res 2015;39:287-98. https://doi.org/10.1016/j.jgr.2014.12.005
- Liu J, Chen D, Liu P, He M, Li J, Li J, Hu L. Discovery, synthesis, and structureactivity relationships of 20(S)-protopanaxadiol (PPD) derivatives as a novel class of AMPKa2b1g1 activators. Eur J Med Chem 2014;79:340-9. https://doi.org/10.1016/j.ejmech.2014.04.010
- Xiao S, Chen S, Sun Y, Zhou W, Piao H, Zhao Y. Synthesis and anti-tumor evaluation of panaxadiol halogen-derivatives. Bioorg Med Chem Lett 2017;27:4204-11. https://doi.org/10.1016/j.bmcl.2017.06.061
- Ma LY, Zhou QL, Yang XW. New SIRT1 activator from alkaline hydrolysate of total saponins in the stems-leaves of Panax ginseng. Bioorg Med Chem Lett 2015;25:5321-5. https://doi.org/10.1016/j.bmcl.2015.09.039
- Ma LY, Yang XW. Six new dammarane-type triterpenes from acidic hydrolysate of the stems-leaves of Panax ginseng and their inhibitoryeactivities against three human cancer cell lines. Phytochemistry Lett 2015;13:406-12. https://doi.org/10.1016/j.phytol.2015.08.002
- Yang XW, Ma LY, Zhou QL, Xu W, Zhang YB. SIRT1 activator isolated from artificial gastric juice incubate of total saponins in stems and leaves of Panax ginseng. Bioorg Med Chem Lett 2018;28:240-3. https://doi.org/10.1016/j.bmcl.2017.12.067
- Qiu S, Yang WZ, Yao CL, Shi XJ, Li JY, Lou Y, Duan YN, Wu WY, Guo DA. Malonylginsenosides with potential antidiabetic activities from the flower buds of Panax ginseng. J Nat Prod 2017;80:899-908. https://doi.org/10.1021/acs.jnatprod.6b00789
- Yang XW, Zhou QL. Four new ginsenosides from red ginseng with inhibitory activity on melanogenesis in melanoma cells. Bioorg Med Chem Lett 2015;25:3112-6. https://doi.org/10.1016/j.bmcl.2015.06.017
-
Lee DG, Lee J, Cho IH, Kim HJ, Lee SW, Kim YO, Park CG, Lee S. Ginsenoside
$Rg_{12}$ , a new dammarane-type triterpene saponin from Panax ginseng root. J Ginseng Res 2017;41:531-3. https://doi.org/10.1016/j.jgr.2016.10.002 - Li KK, Yao CM, Yang XW. Four new dammarane-type triterpene saponins from the stems and leaves of Panax ginseng and their cytotoxicity on HL-60 cells. Planta Med 2012;78:189-92. https://doi.org/10.1055/s-0031-1280320
- Li KK, Yang XB, Yang XW, Liu JX, Gong XJ. New triterpenoids from the stems and leaves of Panax ginseng. Fitoterapia 2012;83:1030-5. https://doi.org/10.1016/j.fitote.2012.05.013
- Li KK, Yang XW. A new triterpene natural product from stems and leaves of Panax ginseng. Chin Tradit Herb Drugs 2015;46:169-73.
-
Yang XW, Li KK, Zhou QL. 20(S)-Ginsenoside-
$Rr_{2}$ , a novel triterpenoid saponin from stems and leaves of Panax ginseng. Chin Tradit Herb Drugs 2015;46:3137-45. -
Li KK, Xu F, Gong XJ. Isolation, purification and quantification of ginsenoside
$F_{5}$ and$F_{3}$ isomeric compounds from crude extracts of flower buds of Panax ginseng. Molecules 2016;21:315. https://doi.org/10.3390/molecules21030315 - Li SS, Li KK, Xu F, Tao L, Yang L, Chen SX, Gong XJ. A strategy for simultaneous isolation of less polar ginsenosides, including a pair of new 20-methoxyl isomers, from flower buds of Panax ginseng. Molecules 2017;22:442. https://doi.org/10.3390/molecules22030442
- Yoshikawa M, Morikawa T, Kashima Y, Ninomiya K, Matsuda H. Structures of new dammarane-type triterpene saponins from the flower buds of Panax notoginseng and hepatoprotective effects of principal ginseng saponins. J Nat Prod 2003;66:922-7. https://doi.org/10.1021/np030015l
- Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods 1983;65:55-63. https://doi.org/10.1016/0022-1759(83)90303-4
-
Ko SR, Choi KJ, Suzuki K, Suzuki Y. Enzymatic preparation of ginsenosides
$Rg_{2}$ ,$Rh_{1}$ , and$F_{1}$ . Chem Pharm Bull 2003;51:404-8. https://doi.org/10.1248/cpb.51.404 -
Sanada S, Kondo N, Shoji J, Tanaka O, Shibata S. Studies on the saponins of ginseng. I. structures of ginsenoside-Ro,
$-Rb_{1}$ ,$-Rb_{2}$ , -Rc and -Rd. Chem Pharm Bull 1974;22:421-8. https://doi.org/10.1248/cpb.22.421 - Zhu GY, Li YW, Hau DK, Jiang ZH, Yu ZL, Fong WF. Acylated protopanaxadioltype ginsenosides from the root of Panax ginseng. Chem Biodivers 2011;8:1853-63. https://doi.org/10.1002/cbdv.201000196
- Tang Y, Zhao ZZ, Li ZH, Feng T, Chen HP, Liu JK, Irpexoates A-D. Four triterpenoids with malonyl modifications from the fruiting bodies of the medicinal fungus Irpex lacteus. Nat Prod Bioprospect 2018;8:171-6. https://doi.org/10.1007/s13659-018-0160-3
- Gu J, Li GY, Yang T, Fang DM, Huang TF. Phytochemical study on Holboellia latifolia. Nat Prod Res Dev 2013;25:1362-6.
- Panov DA, Grishkovets VI, Kachala VV, Shashkov AS. Triterpene glycosides from Kalopanax septemlobum. VII. Minor glycosides from stems of Kalopanax septemlobum var. maximowiczii and Kalopanax septemlobum var. typicum. Chem Nat Compd 2006;42:61-6. https://doi.org/10.1007/s10600-006-0036-3
-
Lee DY, Kim HG, Lee YG, Kim JH, Lee JW, Choi BR, Jang IB, Kim GS, Baek NI. Isolation and quantification of ginsenoside
$Rh_{23}$ , a new anti-melanogenic compound from the leaves of Panax ginseng. Molecules 2018;23:267. https://doi.org/10.3390/molecules23020267 - Yoshikawa M, Murakami T, Yashiro K, Yamahara J, Matsuda H, Saijoh R, Tanaka O. Bioactive saponins and glycosides. XI. Structures of new dammarane-type triterpene oligoglycosides, quinquenosides I, II, III, IV, and V, from American ginseng, the roots of Panax quinquefolium L. Chem Pharm Bull 1998;46:647-54. https://doi.org/10.1248/cpb.46.647
- Shangguan WJ, Li H, Zhang YH. Induction of G2/M phase cell cycle arrest and apoptosis by ginsenoside Rf in human osteosarcoma MG-63 cells through the mitochondrial pathway. Oncol Rep 2014;31:305-13. https://doi.org/10.3892/or.2013.2815
- Wang P, Du X, Xiong M, Cui J, Yang Q, Wang W, Chen Y, Zhang T. Ginsenoside Rd attenuates breast cancer metastasis implicating derepressing microRNA-18a-regulated Smad2 expression. Sci Rep 2016;6:33709. https://doi.org/10.1038/srep33709
- Zheng X, Chen W, Hou H, Li J, Li H, Sun X, Zhao L, Li X. Ginsenoside 20(S)-Rg3 induced autophagy to inhibit migration and invasion of ovarian cancer. Biomed Pharmacother 2017;85:620-6. https://doi.org/10.1016/j.biopha.2016.11.072
피인용 문헌
- Comprehensive Quality Evaluation of American Ginseng for Different Parts and Abnormal Trait Based on the Major Ginsenoside Contents and Morphological Characteristics vol.2021, 2020, https://doi.org/10.1155/2021/8831080
- Characteristic Malonyl Ginsenosides from the Leaves of Panax notoginseng as Potential Quality Markers for Adulteration Detection vol.69, pp.16, 2020, https://doi.org/10.1021/acs.jafc.1c00382