本研究主要探討3-苯基喹啉衍生物的合成和其抗增生活性的評估。合成方面,3-苯基喹啉衍生物主要是在C-2上以縮氨硫脲基團和肟基團做取代。抗增生活性方面,主要用人類乳癌細胞株(MB-321)進行抑制腫瘤細胞生長活性測試。 研究結果指出在C-2上以肟基團取代時,並沒有抑制活性。以N,N-二甲基縮氨硫脲基(化合物18a-f)取代時,有明顯較好的抑制活性。
This thesis describes the synthesis and antiproliferative evaluation of 3-phenylquinoline derivatives. The substituted groups of these newly synthesized compounds are thiosemicarbazons group and oxime group. These compounds were evaluated for their antiproliferative activities against breast cancer cell line (MB-231). Result of this study indicated that the substituted groups are oxime groups showed no antiproliferation activities. The derivatives of thiosemicarbazones bearing dimethyl group (18a-f) showed promising antiproliferative activity.