Leuprorelin三苯基甲醇偶联物的合成及抗增殖活性研究

R. Beni, W. Boadi, Kaleh Karim, Jawzah Alnakhli, Samiyah Alhamed
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引用次数: 0

摘要

Leuprorelin®(LEP)是FDA批准的用于治疗乳腺癌和前列腺癌的药物。在LEP治疗期间,有一些报道的不良反应,如短暂性高血压、流涎过多和排尿困难增加。本研究通过给药系统调节LEP的理化性质,对其药效和毒性进行了修饰。为此,合成了Leuprorelin®的三苯基甲醇衍生物(TPMs)缀合物作为前药。对比抗增殖实验表明,LEP-TPMs结合物对人浸润性导管癌(BT-549)、人前列腺癌(PC3)、人肺癌(A549)和小鼠前脂肪细胞(3T3-L1)的抗增殖活性显著高于相应的TPMs和LEP非共价物理混合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Antiproliferative Activities of Triphenylmethanol Conjugates of Leuprorelin
Leuprorelin® (LEP) is an FDA drug for breast cancer and prostate cancer treatment. There are several reported adverse effects such as transient hypertension, excessive salivation, and increased dysuria during treatment with LEP. In this study, the efficacy and toxicity of LEP were modified by using a drug delivery system to adjust the physicochemical properties. In this regard, Leuprorelin® conjugates of triphenylmethanol derivatives (TPMs) were synthesized as prodrugs. Comparative antiproliferative assays showed that LEP-TPMs conjugates had significantly higher antiproliferative activities than the corresponding non-covalent physical mixtures of the TPMs and LEP against human invasive ductal carcinoma (BT-549), human prostate carcinoma (PC3), human lung cancer (A549) and mouse pre-adipocytes (3T3-L1) cells.
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来源期刊
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