ginsenoside-m1 and 1-3-diisopropylcarbodiimide

ginsenoside-m1 has been researched along with 1-3-diisopropylcarbodiimide* in 1 studies

Other Studies

1 other study(ies) available for ginsenoside-m1 and 1-3-diisopropylcarbodiimide

Article	Year
Synthesis of esters of ginsenoside metabolite M1 and their cytotoxicity on MGC80-3 cells. Molecules (Basel, Switzerland), 2013, Mar-25, Volume: 18, Issue:4 Monoesters of ginsenoside metabolite M1 at the 3-OH, 4-OH and 6-OH positions of the glucose moiety at M1 were synthesized via the reaction of M1 with acyl chloride, or acid-N,N'-diisopropylcarbodiimide in the presence of DMAP. Their structures were fully characterized by spectral methods. The cytotoxicity of these compounds against then MGC80-3 human gastric cancer cell line was also assessed. High inhibitory effects were found at a concentration of 100 μg/mL. Topics: Antineoplastic Agents; Carbodiimides; Cell Line, Tumor; Ginsenosides; Humans; Molecular Structure; Pyridines	2013

Article

Year

Synthesis of esters of ginsenoside metabolite M1 and their cytotoxicity on MGC80-3 cells.

Molecules (Basel, Switzerland), 2013, Mar-25, Volume: 18, Issue:4

Monoesters of ginsenoside metabolite M1 at the 3-OH, 4-OH and 6-OH positions of the glucose moiety at M1 were synthesized via the reaction of M1 with acyl chloride, or acid-N,N'-diisopropylcarbodiimide in the presence of DMAP. Their structures were fully characterized by spectral methods. The cytotoxicity of these compounds against then MGC80-3 human gastric cancer cell line was also assessed. High inhibitory effects were found at a concentration of 100 μg/mL.

Topics: Antineoplastic Agents; Carbodiimides; Cell Line, Tumor; Ginsenosides; Humans; Molecular Structure; Pyridines

2013