化学
生物利用度
双环分子
广告
酰胺
立体化学
组合化学
哌嗪
胺气处理
方向(向量空间)
化学合成
有机化学
甲酰胺
结构-活动关系
硫代氨基甲酸酯类
苯并咪唑
水解
前药
酰胺
作者
Murugaiah A. M. Subbaiah,Shruti Surendran,Gaurav Saini,Lavanya Billava Ramappa,Sivashankaran Raju,Joyson Nandha,Himangshu Bhowmik,Enugurthi Hari Krishna,Sushmita Janrao,V. Anil Kumar,S. Choubey,Joothipriya Subramanian,Bhuvaneshwaran Anandamoorthy,Sukanta Kumar Sahoo,Raghavendra Veerapuram,Korlepara Vamsi Krishna,Manohar Yelleswarapu,Y.K. Gupta,Muthalagu Vetrichelvan,Anuradha Gupta
标识
DOI:10.1021/acs.jmedchem.5c03656
摘要
Replacing phenyl rings with saturated bridged bicyclic scaffolds can mitigate liabilities inherent in planar aromatic rings. We evaluated the retro-isosteric impact of phenyl-to-bridged bicyclic substitution on bioactivation and ADME/PK using phenyl prototype 2b that displayed rapid microsomal turnover, glutathione-adduct formation, high plasma protein binding, poor solubility, and modest oral bioavailability. Bridged bicyclic analogues abolished reactive metabolite formation and improved metabolic stability (2–6-fold), while bridgehead substitution delivered greater improvements (up to 58-fold). In mice, fluoro-BCHex improved bioavailability to 30%, whereas oxa-BCHex achieved 100% bioavailability with 10× higher exposure than 2b, consistent with enhanced microsomal stability, solubility, and permeability. MMP analysis revealed that amide reversal significantly reduced the MLM half-life, plasma fraction unbound, and solubility, while HLM t 1/2 and permeability were unaffected. These findings position bridged bicycles as effective benzene mimetics for mitigating bioactivation with incremental ADME benefits, with bridgehead functionalization, heteroatom incorporation, and amide orientation as tunable handles for further ADME/PK optimization.
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