کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1396445 | 1501187 | 2010 | 6 صفحه PDF | دانلود رایگان |

Novel fluorinated analogues of goniothalamin 1 and howiinol A 2 have been prepared from trifluorocrotonate derivatives. Trifluoromethyl goniothalamin (R/S) 4 showed a slightly lower activity than 1, while the trifluoromethyl howiinol A 16 exhibited similar activities on several cell lines in the micromolar range. Unlike (R) goniothalamin and howiinol A, trifluoromethyl parent compounds remained unchanged when submitted to biomimetic oxidative systems.
Novel trifluoromethyl analogues of goniothalamin and howiinol A have been prepared and exhibited slightly lower or similar cytotoxicity towards various cancer cell lines. The CF3 group prevented from biomimetic oxidative processes all sites of molecules 4 and 16.Figure optionsDownload as PowerPoint slide
Journal: European Journal of Medicinal Chemistry - Volume 45, Issue 7, July 2010, Pages 3213–3218