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Ginsenosides Ginsenoside

Much less is known about the cytotoxic and antiproliferative effects of the 20(S)-PPT family of ginsenosides. Ginsenoside Rhi has been reported to inhibit proliferation of the NIH 3T3 mouse fibroblast cell line but did... [Pg.66]

Fig. 5.1 Chemical structures of ginsenosides. Ginsenosides can be separated into protopanaxadi-ols (a) or protopanaxatriols (b), depending on the presence or absence of a substituent group at carbon 6. Individual ginsenosides differ according to their sugar moieties, as indicated by Ri and R2 in the table... Fig. 5.1 Chemical structures of ginsenosides. Ginsenosides can be separated into protopanaxadi-ols (a) or protopanaxatriols (b), depending on the presence or absence of a substituent group at carbon 6. Individual ginsenosides differ according to their sugar moieties, as indicated by Ri and R2 in the table...
Figure 3. HPLC Analysis of Ginsenosides. Ginsenosides were isolated from spent broth in which either no organism (upper trace), Trichoderma hamatum (middle trace) or Pythium irregulare (lower trace) had been cultured for five days at 25 °C in the dark. Ginsenosides were chromatographed on a Microsorb-MV C-18 column (150 x 4.6 mm, 5 mm) using an acetonitrile H20 gradient (Nicol et al., 2002), and detected at 203 nm. The in the lower trace indicates the unknown metabolite found in the spent broth of Py. irregulare. Figure 3. HPLC Analysis of Ginsenosides. Ginsenosides were isolated from spent broth in which either no organism (upper trace), Trichoderma hamatum (middle trace) or Pythium irregulare (lower trace) had been cultured for five days at 25 °C in the dark. Ginsenosides were chromatographed on a Microsorb-MV C-18 column (150 x 4.6 mm, 5 mm) using an acetonitrile H20 gradient (Nicol et al., 2002), and detected at 203 nm. The in the lower trace indicates the unknown metabolite found in the spent broth of Py. irregulare.
Use of biochemical and biological information for bioprocesses is also significant to the advancement of BRE. Here, the information on the signal transduction from external Ca was utilized for regulation of ginsenoside biosynthetic pathway of cultured cells of P. notoginseng. A quantitative study on the effects of external calcium and calcium sensors was conducted to... [Pg.92]

Fig. 3. A proposed signal transduction pathway regarding the external Ca effect on ginsenoside Rb synthesis by P. notoginseng cells. Ca signal changes are triggered by external Ca concentrations. The calcium signatures are decoded by calcium sensors, CaM and CDPK. UGRdGT is possibly modulated by the sensors in a direct or indirect (dashed lines) way. Changes of CDPK activity may result from increased synthesis or posttranslational modification of the enzyme (shown as CDPK ). Fig. 3. A proposed signal transduction pathway regarding the external Ca effect on ginsenoside Rb synthesis by P. notoginseng cells. Ca signal changes are triggered by external Ca concentrations. The calcium signatures are decoded by calcium sensors, CaM and CDPK. UGRdGT is possibly modulated by the sensors in a direct or indirect (dashed lines) way. Changes of CDPK activity may result from increased synthesis or posttranslational modification of the enzyme (shown as CDPK ).
Radad K, Gille G, Moldzio R, Saito H, Ishige K, Rausch WD. Ginsenosides Rbl and Rgl effects on survival and neurite growth of MPP +-affected mesencephalic dopaminergic cells. J Neural Transm 2004 111 37-45. [Pg.162]

Furthermore, in a recent study by Takei and colleagues, the ginsenoside metabolites Ml (Compound K) and M4 (20(S)-Protopanaxatriol) were demonstrated to promote the maturation of human monocyte-derived DCs [48], M4, and to a lesser extent Ml, increased the DC expression of key costimulatory molecules, decreased their endocytic activity, and induced their production of IL-12. Moreover, these effects had the end result of generating mature DCs that could induce potent Thl polarization. Unfortunately, it was not clearly defined in this study if the ginsenoside metabolites were used at physiologically relevant concentrations, a variable that would be expected to have significant implications on the interpretation of these results. [Pg.191]

Liu, P. et al., Developmental toxicity research of ginsenoside Rbl using a whole mouse embryo culture model, Birth Defects Res B Dev Reprod Toxicol, 74, 207, 2005. [Pg.200]

Park, E.K. et al., Ginsenoside Rhl possesses antiallergic and anti-inflammatory activities, Int Arch Allergy Immunol, 133, 113, 2004. [Pg.200]

Luo, Y.M., Cheng, X.J., and Yuan, W.X., Effects of ginseng root saponins and ginsenoside Rbl on immunity in cold water swim stress mice and rats, Zhongguo Yao Li Xue Bao, 14, 401, 1993. [Pg.201]

Kenarova, B. et al., Immunomodulating activity of ginsenoside Rgl from Panax ginseng,... [Pg.201]

H. Hasegawa, K. S. Lee, T. Nagaoka, Y. Tezuka, M. Uchiyama, S. Kadota, I. Saiki, Pharmacokinetics of Ginsenoside Deglycosylated by Intestinal Bacteria and Its Transformation to Biologically Active Fatty Acid Esters , Biol. Pharm. Bull. 2000, 23, 298 -304. [Pg.755]

Ginsenosides are triterpenoid saponins found nearly exclusively in ginseng and they have been the target of a lot of research as they are believed to be the main active principles behind the claims of ginsengs efficacy. Ginseng refers to species within the genus Panax (Araliaceae... [Pg.2]


See other pages where Ginsenosides Ginsenoside is mentioned: [Pg.190]    [Pg.66]    [Pg.231]    [Pg.472]    [Pg.486]    [Pg.91]    [Pg.93]    [Pg.93]    [Pg.93]    [Pg.94]    [Pg.163]    [Pg.736]    [Pg.130]    [Pg.215]    [Pg.190]    [Pg.190]    [Pg.191]    [Pg.192]    [Pg.197]    [Pg.200]    [Pg.200]    [Pg.365]    [Pg.687]    [Pg.2]    [Pg.3]    [Pg.3]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.4]   
See also in sourсe #XX -- [ Pg.2 , Pg.224 ]




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