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Oral Administration of Peptide-Based Drugs: Beyond Lipinski's Rule

机译:肽基药物的口服给药:超越Lipinski规则

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The use of peptides in therapy presents several limitations, from physicochemical characteristics to inadequate pharmacokinetic profiles for oral absorption. As peptides are gaining importance in the therapeutic arsenal, there is an increasing need to rationalize the main characteristics of this compound class in the market. Therefore, we performed an extensive analysis of all known peptide drugs and clinical candidates based on their peptide features, physicochemical and structural properties, and correlated these with their administration route and therapeutic classes. Peptide drugs are widely distributed across drug and pharmacological space, covering several therapeutic areas with structural diversity and complexity, distributed between groups of cyclic and linear compounds. Although structural and physicochemical properties are clear within these groups, we counter the consensus that cyclic peptides have better oral availability than linear peptides, as most of the orally administrated peptides have linear structures. This study and review furnishes information that could support peptide drug design, with a new cutoff of known descriptors that go beyond the Rule of Five.
机译:从理化特征到口服吸收的药代动力学特征不足,多肽在治疗中的使用受到一些限制。由于肽在治疗武库中变得越来越重要,因此越来越需要在市场上合理化这种化合物类别的主要特征。因此,我们根据所有已知的肽类药物及其肽类特征,理化和结构特性对所有已知的肽类药物和临床候选药物进行了广泛的分析,并将它们与给药途径和治疗类别相关联。肽类药物广泛分布于药物和药理学领域,涵盖具有结构多样性和复杂性的多个治疗领域,分布在环状和线性化合物的组之间。尽管在这些组中结构和物理化学性质均很清楚,但我们反驳了以下共识:环状肽比线性肽具有更好的口服利用率,因为大多数口服肽具有线性结构。这项研究和综述提供了可以支持肽类药物设计的信息,并提供了一个超越五规则的已知描述符的新界限。

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