Department of Medicine, Division of Allergy & Infectious Disease, Center for Emerging & Re-Emerging Infectious Disease (CERID) , University of Washington , Seattle , Washington 98109 , United States.
Fred Hutchinson Cancer Research Center , Seattle , Washington 98109 , United States.
J Med Chem. 2019 Mar 28;62(6):3135-3146. doi: 10.1021/acs.jmedchem.9b00069. Epub 2019 Mar 15.
Cryptosporidium is a leading cause of pediatric diarrhea worldwide. Currently, there is neither a vaccine nor a consistently effective drug available for this disease. Selective 5-aminopyrazole-4-carboxamide-based bumped-kinase inhibitors (BKIs) are effective in both in vitro and in vivo models of Cryptosporidium parvum. Potential cardiotoxicity in some BKIs led to the continued exploration of the 5-aminopyrazole-4-carboxamide scaffold to find safe and effective drug candidates for Cryptosporidium. A series of newly designed BKIs were tested for efficacy against C. parvum using in vitro and in vivo (mouse infection model) assays and safety issues. Compound 6 (BKI 1708) was found to be efficacious at 8 mg/kg dosed once daily (QD) for 5 days with no observable signs of toxicity up to 200 mg/kg dosed QD for 7 days. Compound 15 (BKI 1770) was found to be efficacious at 30 mg/kg dosed twice daily (BID) for 5 days with no observable signs of toxicity up to 300 mg/kg dosed QD for 7 days. Compounds 6 and 15 are promising preclinical leads for cryptosporidiosis therapy with acceptable safety parameters and efficacy in the mouse model of cryptosporidiosis.
隐孢子虫是全世界儿童腹泻的主要原因。目前,针对这种疾病既没有疫苗也没有始终有效的药物。基于选择性 5-氨基吡唑-4-甲酰胺的 bumped-kinase 抑制剂(BKIs)在隐孢子虫的体外和体内模型中都有效。一些 BKIs 存在潜在的心脏毒性,这导致人们继续探索 5-氨基吡唑-4-甲酰胺支架,以寻找安全有效的隐孢子虫候选药物。使用体外和体内(小鼠感染模型)测定法以及安全性问题,测试了一系列新设计的 BKIs 对隐孢子虫的疗效。发现化合物 6(BKI 1708)在每天 1 次 8 毫克/千克剂量(QD)给药 5 天,每天 1 次 200 毫克/千克剂量给药 7 天,没有观察到毒性迹象,具有疗效。化合物 15(BKI 1770)在每天 2 次 30 毫克/千克剂量给药 5 天,没有观察到毒性迹象,每天 1 次 300 毫克/千克剂量给药 7 天,具有疗效。化合物 6 和 15 是具有前景的隐孢子虫病治疗的临床前先导化合物,具有可接受的安全性参数和在隐孢子虫病小鼠模型中的疗效。