Design, synthesis and biological evaluation of deuterated Vismodegib for improving pharmacokinetic properties

被引:8
|
作者
Wang, Fangying [1 ]
Jiang, Hongxia [1 ]
Deng, Yufang [1 ]
Yu, Jiang [1 ]
Zhan, Miao [4 ]
Zhao, Lifeng [3 ]
Chen, Yuanwei [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, West China Med Sch, State Key Lab Biotherapy & Canc Ctr,Collaborat In, Chengdu 610041, Sichuan, Peoples R China
[2] Hinova Pharmaceut Inc, Suite 402,Bldg B,5 South KeYuan Rd, Chengdu 610041, Sichuan, Peoples R China
[3] Chengdu Univ, Sichuan Ind Inst Antibiot, Chengdu 610052, Sichuan, Peoples R China
[4] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian 710054, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Vismodegib; Hedgehog signaling pathway; Basal cell carcinoma; Deuterated drug; Deuterium-hydrogen replacement; Pharmacokinetic properties; HEDGEHOG SIGNALING PATHWAY; INHIBITOR GDC-0449; HEAVY DRUGS; CANCER; DEUTERIUM; ABSORPTION; DISCOVERY; DISEASE;
D O I
10.1016/j.bmcl.2018.06.025
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Vismodegib is an oral and high selective hedgehog (Hh) inhibitor used for the treatment of basal cell carcinoma (BCC). In this work, analogs of Vismodegib with deuterium-for-hydrogen replacement at certain metabolically active sites were prepared and found to have a better pharmacokinetic properties in mice. In particular, deuterated compound SKLB-C2211 obviously altered the blood circulation behavior compared to its prototype, which was demonstrated by significantly prolonged blood circulation half-life time (t(1/2)) and increased AUC(0 ->infinity). These results suggested SKLB-C2211 had the potential to be a long-acting inhibitor against Hh signaling pathway, and laid the foundation for the further research of its druggability.
引用
收藏
页码:2399 / 2402
页数:4
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