2020
DOI: 10.1016/j.bioorg.2020.104097
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Ten new glycosides, carissaedulosides A–J from the root barks of Carissa edulis and their cytotoxicities

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Cited by 6 publications
(8 citation statements)
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“…The free TCG showed 25, 22, and 17 % cytotoxicity compared with 26, 20, and 11 % for LMWC‐Cbl‐TCG at a concentration of 100, 10, and 1 μg/ml, respectively (Figure 6). The half‐maximal inhibitory concentration (IC50) values expressing the concentrations responsible for 50 % growth inhibition were also calculated [29] . The results indicated insignificant cytotoxicity, in which the IC50 obtained for all samples containing TCG, LMWC‐Cbl, and LMWC‐Cbl‐TCG was >200 μg/ml against the HEK 293 cell lines.…”
Section: Resultsmentioning
confidence: 99%
“…The free TCG showed 25, 22, and 17 % cytotoxicity compared with 26, 20, and 11 % for LMWC‐Cbl‐TCG at a concentration of 100, 10, and 1 μg/ml, respectively (Figure 6). The half‐maximal inhibitory concentration (IC50) values expressing the concentrations responsible for 50 % growth inhibition were also calculated [29] . The results indicated insignificant cytotoxicity, in which the IC50 obtained for all samples containing TCG, LMWC‐Cbl, and LMWC‐Cbl‐TCG was >200 μg/ml against the HEK 293 cell lines.…”
Section: Resultsmentioning
confidence: 99%
“…Kaunda et al [94] isolated three furofuran lignans (carissaeduloside H, carissaeduloside I, and carissaeduloside J ( 26)) together with 12 analogues (sarhamnoloside (22)…”
Section: Lignansmentioning
confidence: 99%
“…C. spinarum). Out of these compounds, sarhamnoloside (22) and [(1S,2S,3S)-1,2,3,4tetrahydro-3,7-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-(hydroxyl-methyl)-6-methoxy-2naphthalen-yl] methyl β-D-glucopyranoside (51) exhibited anticancer activity against lung and breast cancer cell lines [94] (Table 5).…”
Section: Lignansmentioning
confidence: 99%
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