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仿生色谱系统中抗癌硫代卡巴肼的保留行为及计算模拟。

Retention Behavior of Anticancer Thiosemicarbazides in Biomimetic Chromatographic Systems and In Silico Calculations.

机构信息

Department of Physical Chemistry, Institute of Chemical Sciences, Faculty of Chemistry, Maria Curie-Skłodowska University, 20-031 Lublin, Poland.

Independent Radiopharmacy Unit, Medical University of Lublin, Chodzki 4a, 20-093 Lublin, Poland.

出版信息

Molecules. 2023 Oct 16;28(20):7107. doi: 10.3390/molecules28207107.

Abstract

Chromatographic methods, apart from in silico ones, are commonly used rapid techniques for the evaluation of certain properties of biologically active compounds used for their prediction of pharmacokinetic processes. Thiosemicarbazides are compounds possessing anticancer, antimicrobial, and other valuable biological activities. The aim of the investigation was to estimate the lipophilicity of 1-aryl-4-(phenoxy)acetylthiosemicarbazides, to predict their oral adsorption and the assessment of their % plasma-protein binding (%PPB). RP-HPLC chromatographic techniques with five diversified HPLC systems, including columns with surface-bonded octadecylsilanes (C-18), phosphatidylcholine (immobilized artificial membrane, IAM), cholesterol (Chol), and α1-acid glycoprotein (AGP) and human serum albumin (HSA), were applied. The measured lipophilicity of all investigated compounds was within the range recommended for potential drug candidates. However, some derivatives are strongly bonded to HSA (%PPB ≈ 100%), which may limit some pharmacokinetic processes. HPLC determined lipophilicity descriptors were compared with those obtained by various computational approaches.

摘要

色谱方法,除了计算机模拟方法外,通常也被用于评估用于预测药代动力学过程的生物活性化合物的某些性质的快速技术。硫代氨基脲类化合物具有抗癌、抗菌和其他有价值的生物活性。本研究的目的是评估 1-芳基-4-(苯氧基)乙酰基硫代氨基脲的亲脂性,预测它们的口服吸附,并评估它们的%血浆蛋白结合(%PPB)。应用了五种不同的 HPLC 系统的反相 HPLC 色谱技术,包括具有表面键合十八烷基硅烷(C-18)、磷脂酰胆碱(固定化人工膜,IAM)、胆固醇(Chol)和α1-酸性糖蛋白(AGP)以及人血清白蛋白(HSA)的柱子。所有研究化合物的测量亲脂性都在潜在药物候选物的推荐范围内。然而,一些衍生物与 HSA 强烈结合(%PPB≈100%),这可能限制某些药代动力学过程。通过各种计算方法获得的 HPLC 确定的亲脂性描述符与那些描述符进行了比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77d8/10608985/333e39659fdf/molecules-28-07107-g001.jpg

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