通过硅学毒性和药物特性获得抗肿瘤药物候选物

Dewa Ayu Made Adnyaswari, A. W. Indrayani, I. G. A. Artini
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摘要

背景:药物代谢是医疗实践和药理学的一个重要方面,涉及药物在体内各系统的转化,以产生更容易排出体外的化合物。据报道,索拉非尼对接受手术切除的肝细胞癌患者是一种有效的辅助治疗药物。然而,索拉非尼的药代动力学特性较差,如水溶性有限、消除和代谢速度快,导致其生物利用度较低,限制了其进一步的临床应用。迷迭香叶中的迷迭香酸可溶于乙醇,对癌症、糖尿病、炎症性疾病、神经退行性疾病和肝脏疾病有治疗作用。 方法:硅学是使用计算机模拟方法进行实验或测试的术语。硅学测试已成为探索新型药物化合物或提高现有化合物疗效的重要方法。这种方法包括通过虚拟仿真进行预测、提出假设,以及发现医学和治疗方面的潜在突破。结果:索拉非尼配体的 Caco2 值为 0.762。白桦脂酸的 Caco2 值最高,香豆素酸的 Caco2 值最低。熊果酸的样本 HIA 值最高,而迷迭香酸的样本 HIA 值最低。与此同时,索拉非尼的 HIA 值为 85 494。卡诺索尔和罗司洛尔等配体的分布量较高,而萨玛卡诺索酸、熊果酸和白桦脂酸的分布量较低。玫瑰茄酸配体的分布容积为 0.393,分布容积较好,而索拉非尼的分布容积值为-0.009。卡诺索尔的 BBB 样本值最高,罗香豆酸的 BBB 样本值最低。所有配体(如卡诺酸、卡诺醇、洛斯曼醇、熊果酸、白桦脂酸、迷迭香酸)都没有致突变性和细胞毒性作用,但对免疫力有影响。对比配体索拉非尼对肝毒性、免疫和细胞毒性有影响。结论在药代动力学研究中,迷迭香中的六种酚酸化合物与参考配体索拉非尼相比表现出更优越的特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In silico Toxicity and Pharmaceutical Properties to Get Candidates for Antitumor Drug
Background: Drug metabolism is a crucial aspect of medical practice and pharmacology, involving the transformation of drugs by various bodily systems to create compounds that are more easily eliminated from the body. Sorafenib was reported as a useful adjuvant treatment in patients with hepatocellular carcinoma who underwent surgical resection. However, poor pharmacokinetic properties such as limited water solubility, rapid elimination and metabolism lead to low bioavailability, restricting its further clinical application. Rosmarinic acid, soluble in ethanol and found in Rosemary leaves, has demonstrated therapeutic benefits in conditions such as cancer, diabetes, inflammatory disorders, neurodegenerative disorders, and liver disease.  Method: In silico is a term for experiments or tests carried out using computer simulation methods. In silico testing has emerged as a valuable approach for initiating the exploration of novel drug compounds or enhancing the efficacy of existing ones. This method involves predicting, generating hypotheses, and uncovering potential breakthroughs in medicine and therapy through virtual simulations. Results: Caco2 value of Sorafenib ligand as a comparison, namely 0.762. The highest Caco2 value is owned by Betulinic Acid and the value The lowest Caco2 is owned by Rosmarinic Acid. The highest sample HIA value was owned by Ursolic Acid and the lowest was owned by Rosmarinic Acid. Meanwhile, Sorafenib's HIA value is 85,494. ligands such as Carnosol and rosmanol have a high distribution volume, while the Sama carnosic league, ursolic acid and betulinic acid have a low distribution volume. The Rosmarinic acid ligand has a good distribution volume of 0.393, while the distribution volume value of Sorafenib is -0.009. The highest BBB sample value was owned by Carnosol and the lowest was owned by Rosmarinic acid. Meanwhile, the comparison ligand has a value of -1.473 and is considered less distributed in the brain. all ligands such as Carnosic Acid, Carnosol, Rosmanol, Ursolic Acid, Betulinic Acid, Rosmarinic acid do not have mutagenicity and Cytotoxic effects, but have an effect on immunity. The comparison ligand Sorafenib turned out to have effects on hepatotoxicity, immunity and cytotoxicity. Conclusion: In pharmacokinetic research, the six phenolic acid compounds in Rosemary exhibited superior properties compared to the reference ligand Sorafenib.
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