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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1962 2
1963 3
1965 1
1966 1
1975 3
1976 3
1977 3
1978 3
1979 7
1980 6
1981 4
1982 7
1983 7
1984 11
1985 16
1986 22
1987 25
1988 19
1989 20
1990 24
1991 24
1992 27
1993 34
1994 30
1995 37
1996 40
1997 39
1998 43
1999 55
2000 53
2001 80
2002 65
2003 118
2004 106
2005 156
2006 173
2007 169
2008 184
2009 230
2010 242
2011 282
2012 367
2013 407
2014 464
2015 490
2016 477
2017 509
2018 527
2019 606
2020 559
2021 49
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5,942 results
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Ginsenosides, potent inhibitors of sialyltransferase.
Huang W, Sun L, Wang B, Ma Y, Yao D, Han W, Wang L. Huang W, et al. Z Naturforsch C J Biosci. 2020 Jan 28;75(1-2):41-49. doi: 10.1515/znc-2019-0150. Z Naturforsch C J Biosci. 2020. PMID: 32031984
In this study, we assessed that the antitumor inhibitors of 20(S)-ginsenosides Rg3, 20(R)-ginsenosides Rg3, 20(S)-ginsenosides Rh2, and 20(R)-ginsenosides Rh2 could block the sialoglycans in liver cancer cells HepG2. ...Meanwhile, the results of the mo …
In this study, we assessed that the antitumor inhibitors of 20(S)-ginsenosides Rg3, 20(R)-ginsenosides Rg3, 20(S)-ginsenosi
Study on Transformation of Ginsenosides in Different Methods.
Zheng MM, Xu FX, Li YJ, Xi XZ, Cui XW, Han CC, Zhang XL. Zheng MM, et al. Biomed Res Int. 2017;2017:8601027. doi: 10.1155/2017/8601027. Epub 2017 Dec 14. Biomed Res Int. 2017. PMID: 29387726 Free PMC article. Review.
Studies have showed that the major ginsenosides could be converted into rare ginsenosides, which played a significant role in exerting pharmacological activity. However, the contents of some rare ginsenosides are very little. So it is very important to find t …
Studies have showed that the major ginsenosides could be converted into rare ginsenosides, which played a significant role in …
Ginsenosides: are any of them candidates for drugs acting on the central nervous system?
Nah SY, Kim DH, Rhim H. Nah SY, et al. CNS Drug Rev. 2007 Winter;13(4):381-404. doi: 10.1111/j.1527-3458.2007.00023.x. CNS Drug Rev. 2007. PMID: 18078425 Free PMC article. Review.
Ginsenosides inhibit voltage-dependent Ca(2+), K(+), and Na(+) channel activities in a stereospecific manner. ...This review will introduce recent findings and advances on ginsenoside-induced regulation of ion channel activities in the CNS, and will further expand t
Ginsenosides inhibit voltage-dependent Ca(2+), K(+), and Na(+) channel activities in a stereospecific manner. ...This review will int
Biosynthesis and biotechnological production of ginsenosides.
Kim YJ, Zhang D, Yang DC. Kim YJ, et al. Biotechnol Adv. 2015 Nov 1;33(6 Pt 1):717-35. doi: 10.1016/j.biotechadv.2015.03.001. Epub 2015 Mar 6. Biotechnol Adv. 2015. PMID: 25747290 Review.
Ginsenosides belong to a group of triterpene saponins (also called ginseng saponins) that are found almost exclusively in Panax species and accumulated especially in the plant roots. In this review, we update the conserved and diversified pathway/enzyme biosynthesizing
Ginsenosides belong to a group of triterpene saponins (also called ginseng saponins) that are found almost exclusively in Panax speci
Various Multicharged Anions of Ginsenosides in Negative Electrospray Ionization with QTOF High-Resolution Mass Spectrometry.
Zhao N, Cheng M, Huang S, Liu D, Zhao Q, Bai Y, Zhang X. Zhao N, et al. J Am Soc Mass Spectrom. 2019 Mar;30(3):403-418. doi: 10.1007/s13361-018-2089-5. Epub 2019 Jan 14. J Am Soc Mass Spectrom. 2019. PMID: 30644055
Our investigation using 14 pure ginsenosides affirmed that the multicharged anions were formed by ginsenosides rather than other types of ingredients in ginseng. Various anions could be observed for each ginsenoside. These anions contain ions ([M-2H](2-), [M+ …
Our investigation using 14 pure ginsenosides affirmed that the multicharged anions were formed by ginsenosides rather than oth …
Comparative analysis of ginsenosides in human glucocorticoid receptor binding, transactivation, and transrepression.
Hu C, Lau AJ, Wang R, Chang TKH. Hu C, et al. Eur J Pharmacol. 2017 Nov 15;815:501-511. doi: 10.1016/j.ejphar.2017.10.019. Epub 2017 Oct 12. Eur J Pharmacol. 2017. PMID: 29031898
We investigated the effect of 20(S)-protopanaxadiol (PPD), PPD-type ginsenosides (Rb1, Rb2, Rc, Rd, Rh2, and Compound K), 20(S)-protopanaxatriol (PPT), and PPT-type ginsenosides (Re, Rf, Rg1, and Rh1) on glucocorticoid receptor binding, transactivation, and transrep …
We investigated the effect of 20(S)-protopanaxadiol (PPD), PPD-type ginsenosides (Rb1, Rb2, Rc, Rd, Rh2, and Compound K), 20(S)-proto …
A literature update elucidating production of Panax ginsenosides with a special focus on strategies enriching the anti-neoplastic minor ginsenosides in ginseng preparations.
Biswas T, Mathur AK, Mathur A. Biswas T, et al. Appl Microbiol Biotechnol. 2017 May;101(10):4009-4032. doi: 10.1007/s00253-017-8279-4. Epub 2017 Apr 14. Appl Microbiol Biotechnol. 2017. PMID: 28411325 Review.
The minor ginsenosides under current scientific scrutiny include diol ginsenosides such as Rg3, Rh2, compound K, and triol ginsenosides Rg2 and Rh1, which are being touted as the next "anti-neoplastic pharmacophores," with better bioavailability and potency a …
The minor ginsenosides under current scientific scrutiny include diol ginsenosides such as Rg3, Rh2, compound K, and triol …
Ginsenosides: prospective for sustainable biotechnological production.
Murthy HN, Georgiev MI, Kim YS, Jeong CS, Kim SJ, Park SY, Paek KY. Murthy HN, et al. Appl Microbiol Biotechnol. 2014;98(14):6243-54. doi: 10.1007/s00253-014-5801-9. Epub 2014 May 25. Appl Microbiol Biotechnol. 2014. PMID: 24859520 Review.
Field cultivation of the ginseng plant is a time-consuming and labor-intensive process. Ginsenosides, a group of glycosylated triterpenes, also known as saponins, are the principal bioactive constituents of ginseng. ...Cells and adventitious roots have been cultured in lar …
Field cultivation of the ginseng plant is a time-consuming and labor-intensive process. Ginsenosides, a group of glycosylated triterp …
[Research achievements on ginsenosides biosynthesis from Panax ginseng].
Lin YP, Zhang MP, Wang KY, Sun CY, Wang Y. Lin YP, et al. Zhongguo Zhong Yao Za Zhi. 2016 Dec;41(23):4292-4302. doi: 10.4268/cjcmm20162302. Zhongguo Zhong Yao Za Zhi. 2016. PMID: 28933103 Review. Chinese.
Panax ginseng is one of the famous rare medicinal herbs, and ginsenosides are the main active ingredient of ginseng is ginsenoside.They can be divided into three chemotypes: oleanane type, protopanaxadiol (PPD) type and the protopanaxatriol (PPT)type. Ginsenoside
Panax ginseng is one of the famous rare medicinal herbs, and ginsenosides are the main active ingredient of ginseng is ginsenoside
Retention behavior of ginsenosides in a sulfo-based high performance liquid chromatography column.
Qu B, Zhang L, Wang S, Quan Y, Wu X. Qu B, et al. J Chromatogr A. 2020 Jan 11;1610:460542. doi: 10.1016/j.chroma.2019.460542. Epub 2019 Sep 14. J Chromatogr A. 2020. PMID: 31558273
We herein report the use of a sulfo-based column and hydrophilic interaction chromatography (HILIC) to separate 14 ginsenosides, namely Rb1, Rb2, Rb3, Rc, Rd, Rf, Re, Rg1, Rg2, Rg3, Rh1, Rh2, F(2), and C-K. In addition to its rapid and efficient ability to separate these …
We herein report the use of a sulfo-based column and hydrophilic interaction chromatography (HILIC) to separate 14 ginsenosides, name …
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