2012
DOI: 10.1016/j.fitote.2012.03.008
|View full text |Cite
|
Sign up to set email alerts
|

Steroidal saponins from Fritillaria pallidiflora Schrenk

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
15
0
1

Year Published

2014
2014
2023
2023

Publication Types

Select...
6
1
1

Relationship

0
8

Authors

Journals

citations
Cited by 31 publications
(17 citation statements)
references
References 12 publications
1
15
0
1
Order By: Relevance
“…Other compounds with anticancer activity were chosen definitely less often and these include: actinomycin D, adriamycin, beta-L-(-)-dioxalane-cytidine (-)-OddC, camptothecin, elipticin, etoposide, 5-FU, mitamycin C, mitoxantrone, nimustine (ACNU), podophyllotoxin, staurosporine, tamoxifen, and troxacitabine. In one study resveratrol, which is not an approved anticancer drug, served as the control (Shen et al 2012).…”
Section: Introductionmentioning
confidence: 99%
“…Other compounds with anticancer activity were chosen definitely less often and these include: actinomycin D, adriamycin, beta-L-(-)-dioxalane-cytidine (-)-OddC, camptothecin, elipticin, etoposide, 5-FU, mitamycin C, mitoxantrone, nimustine (ACNU), podophyllotoxin, staurosporine, tamoxifen, and troxacitabine. In one study resveratrol, which is not an approved anticancer drug, served as the control (Shen et al 2012).…”
Section: Introductionmentioning
confidence: 99%
“…Steroidal saponins consist of a steroidal aglycone, a C27 spirostane skeleton, generally comprising of a six-ring structure (Figure 4.3). Four saponins showed cytotoxicity against C6 and HeLa cell lines with IC 50 values 5.1-75.8 mM (Shen et al, 2012a). Four saponins showed cytotoxicity against C6 and HeLa cell lines with IC 50 values 5.1-75.8 mM (Shen et al, 2012a).…”
Section: Saponins and Terpenoidsmentioning
confidence: 95%
“…Further purification was performed using reverse phase (RP) preparative HPLC chromatography and other methods, and finally, sixteen saponins were isolated from SRS. On the basis of the analytical methods such as UV, IR, MS and extensive 1 H and 13 C NMR spectra analysis and comparison with data in literature (Huang et al, 2006;Kang et al, 2012;Li et al, 2006;Matsuda et al, 2003;Mimaki et al, 2000;Shao et al, 2007;Shen et al, 2012;Zhao et al, 2007), the sixteen saponins were identified as parisyunnanoside A, smilaxchinoside A, protogracillin, parisaponin I, parisyunnanoside C, pseudoproto-pb, riparoside B, parisyunnanoside E, parisyunnanoside D, smilaxchinoside C, paris H, timosaponin J, paris D, timosaponin K, parisvietnaside A and pallidfloside D. The structures of these sixteen saposins are shown in Fig. 1.…”
Section: Isolation and Identification Of Compounds From Srsmentioning
confidence: 99%