TY - JOUR
T1 - Synthesis and evaluation of some 17-acetamidoandrostane and N,N-dimethyl-7-deoxycholic amide derivatives as cytotoxic agents: Structure/activity studies
AU - Huang, Yanmin
AU - Cui, Jianguo
AU - Jia, Linyi
AU - Gan, Chunfang
AU - Song, Huacan
AU - Zeng, Chun
AU - Zhou, Aimin
PY - 2013/7/1
Y1 - 2013/7/1
N2 - Using pregnenolone and 7-deoxycholic acid as starting materials, some 17-acetamidoandrostane and N,N-dimethyl-7-deoxycholic amide derivatives were synthesized. The cytotoxicity of the synthesized compounds was tested in vitro against two tumor cell lines: SGC 7901 (human gastric carcinoma) and Bel 7404 (human liver carcinoma). The result showed that the blockage of the interaction of the amide group with outside groups might cause a decrease of the cytotoxicity, and an O-benzyloximino group at the 3-position of N,N-dimethyl-7-deoxycholic amide could enhance the cytotoxic activity of the compound. The information obtained from the studies provides the structure-activity relationship for these compounds and may be useful for the design of novel chemotherapeutic drugs. © 2013 by the authors.
AB - Using pregnenolone and 7-deoxycholic acid as starting materials, some 17-acetamidoandrostane and N,N-dimethyl-7-deoxycholic amide derivatives were synthesized. The cytotoxicity of the synthesized compounds was tested in vitro against two tumor cell lines: SGC 7901 (human gastric carcinoma) and Bel 7404 (human liver carcinoma). The result showed that the blockage of the interaction of the amide group with outside groups might cause a decrease of the cytotoxicity, and an O-benzyloximino group at the 3-position of N,N-dimethyl-7-deoxycholic amide could enhance the cytotoxic activity of the compound. The information obtained from the studies provides the structure-activity relationship for these compounds and may be useful for the design of novel chemotherapeutic drugs. © 2013 by the authors.
KW - 17-acetamidoandrostane
KW - Antiproliferative activity
KW - N
KW - N-dimethyl-7-deoxycholic amide
KW - Pregnenolone
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U2 - 10.3390/molecules18077436
DO - 10.3390/molecules18077436
M3 - Article
C2 - 23803715
SN - 1420-3049
VL - 18
SP - 7436
EP - 7447
JO - Molecules
JF - Molecules
IS - 7
ER -