首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >1-(3-Aminomethyl-4-hydroxyphenyl)-3-pyridinyl-2-propen-1-ones: A novel group of tumour-selective cytotoxins
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1-(3-Aminomethyl-4-hydroxyphenyl)-3-pyridinyl-2-propen-1-ones: A novel group of tumour-selective cytotoxins

机译:1-(3-氨基甲基-4-羟基苯基)-3-吡啶基-2-丙烯-1-酮:一组新的肿瘤选择性细胞毒素

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Abstract 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.
机译:摘要合成了被设计为新型细胞毒素的两个系列的1-(3-氨基甲基-4-羟基苯基)-3-吡啶基-2-丙烯-1-酮。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口腔鳞状细胞癌在微摩尔范围内具有较低的CC 50 值。这些化合物对非恶性HGF(牙龈成纤维细胞),HPC(牙髓细胞)和HPLF(牙周膜成纤维细胞)细胞的CC 50 值较高,这揭示了这些烯酮的肿瘤选择性。代表性化合物4c导致HSC-2细胞中PARP1的裂解,但HGF细胞中没有,这可能是导致肿瘤选择性的一个因素。

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