Active Compounds of Sembung Leaves (Blumea balsamifera DC) in Silico Screening as Antihypertensives

Ahmad Sjahriza, Fyrda Shellia, Dyah Iswantini
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Abstract

Hypertension is a structural or functional change in the arteries or the organs it supplies caused by increased blood pressure. Angiotensin-converting enzyme (ACE) can increase blood pressure by converting inactive angiotensin I to active (angiotensin II). Captopril is a hypertension drug that can inhibit ACE activity. Sembung leaf (Blumea balsamifera DC) is a plant that can potentially have antihypertensive activity. This study aims to identify the interaction of active compounds in sembung leaves against ACE as antihypertensive drug candidates through an in silico test based on pharmacodynamic and pharmacokinetic parameters using two docking software, Autodock Vina and PyRx. The results showed that Luteolin was the best test ligand besides having lower ΔG and Ki than control ligands and higher Kd than control ligands.  Luteolin was identified to interact with Zn and hydrogen bond interactions at the active site and met the criteria in Lipinski analysis, ADME, and toxicity, so this compound is relatively safe to be used as a drug candidate for the treatment of hypertension.
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硅学筛选胜榜叶(Blumea balsamifera DC)中作为抗高血压药的活性化合物
高血压是由血压升高引起的动脉或其供应器官的结构或功能变化。血管紧张素转换酶(ACE)可将非活性血管紧张素 I 转换为活性(血管紧张素 II),从而使血压升高。卡托普利是一种能抑制血管紧张素转换酶活性的高血压药物。森蓬叶(Blumea balsamifera DC)是一种具有潜在抗高血压活性的植物。本研究旨在利用 Autodock Vina 和 PyRx 两种对接软件,通过基于药效学和药代动力学参数的硅测试,确定仙蓬叶中的活性化合物与 ACE 的相互作用,并将其作为抗高血压候选药物。结果表明,与对照配体相比,木犀草素的ΔG和Ki较低,Kd较高,是最佳的试验配体。 经鉴定,木犀草素在活性位点上与 Zn 和氢键相互作用,并符合利宾斯基分析、ADME 和毒性标准,因此该化合物作为治疗高血压的候选药物是相对安全的。
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来源期刊
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3
审稿时长
16 weeks
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