Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University , Erzurum , Turkey.
J Enzyme Inhib Med Chem. 2013 Oct;28(5):974-80. doi: 10.3109/14756366.2012.700927. Epub 2012 Jul 18.
Two series of 1-(3-aminomethyl-4-hydroxyphenyl)-3-pyridinyl-2-propen-1-ones, designed as novel cytotoxins, were synthesized. The compounds had low CC50 values in the micromolar range against HL-60 promyelocytic leukemic cells and HSC-2, HSC-3 and HSC-4 oral squamous cell carcinomas. The CC50 values of these compounds were higher towards non-malignant HGF (gingival fibroblasts), HPC (pulp cells), and HPLF (periodontal ligament fibroblasts) cells, which reveals the tumour-selectivity of these enones. A representative compound 4c caused cleavage of PARP1 in HSC-2 cells but not in HGF cells, which may be a contributing factor to the tumour-selectivity.
设计了两个系列的 1-(3-氨甲基-4-羟基苯基)-3-吡啶基-2-丙烯-1-酮,作为新型细胞毒素进行合成。这些化合物对 HL-60 早幼粒细胞白血病细胞和 HSC-2、HSC-3 和 HSC-4 口腔鳞状癌细胞的 CC50 值在微摩尔范围内较低。这些化合物对非恶性 HGF(牙龈成纤维细胞)、HPC(牙髓细胞)和 HPLF(牙周韧带成纤维细胞)的 CC50 值较高,这表明这些烯酮具有肿瘤选择性。代表性化合物 4c 在 HSC-2 细胞中引起 PARP1 的裂解,但在 HGF 细胞中没有,这可能是肿瘤选择性的一个促成因素。