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1
7 H-Pyrrolo[2,3- d]pyrimidin-4-amine-Based Inhibitors of Calcium-Dependent Protein Kinase 1 Have Distinct Inhibitory and Oral Pharmacokinetic Characteristics Compared with 1 H-Pyrazolo[3,4- d]pyrimidin-4-amine-Based Inhibitors.与基于1H-吡唑并[3,4-d]嘧啶-4-胺的抑制剂相比,基于7H-吡咯并[2,3-d]嘧啶-4-胺的钙依赖性蛋白激酶1抑制剂具有不同的抑制特性和口服药代动力学特征。
ACS Infect Dis. 2018 Apr 13;4(4):516-522. doi: 10.1021/acsinfecdis.7b00224. Epub 2018 Mar 16.
2
Advances in bumped kinase inhibitors for human and animal therapy for cryptosporidiosis. bumped 激酶抑制剂在人类和动物隐孢子虫病治疗中的研究进展。
Int J Parasitol. 2017 Oct;47(12):753-763. doi: 10.1016/j.ijpara.2017.08.006. Epub 2017 Sep 9.
3
Necessity of Bumped Kinase Inhibitor Gastrointestinal Exposure in Treating Cryptosporidium Infection.激酶抑制剂胃肠道暴露在治疗隐孢子虫感染中的必要性。
J Infect Dis. 2017 Jul 1;216(1):55-63. doi: 10.1093/infdis/jix247.
4
5-Aminopyrazole-4-Carboxamide-Based Compounds Prevent the Growth of Cryptosporidium parvum.基于5-氨基吡唑-4-甲酰胺的化合物可抑制微小隐孢子虫的生长。
Antimicrob Agents Chemother. 2017 Jul 25;61(8). doi: 10.1128/AAC.00020-17. Print 2017 Aug.
5
Bumped-Kinase Inhibitors for Cryptosporidiosis Therapy.用于隐孢子虫病治疗的撞击激酶抑制剂
J Infect Dis. 2017 Apr 15;215(8):1275-1284. doi: 10.1093/infdis/jix120.
6
Novel Bumped Kinase Inhibitors Are Safe and Effective Therapeutics in the Calf Clinical Model for Cryptosporidiosis.新型碰撞激酶抑制剂在犊牛隐孢子虫病临床模型中是安全有效的治疗药物。
J Infect Dis. 2016 Dec 15;214(12):1856-1864. doi: 10.1093/infdis/jiw488. Epub 2016 Oct 17.
7
5-Aminopyrazole-4-carboxamide analogues are selective inhibitors of Plasmodium falciparum microgametocyte exflagellation and potential malaria transmission blocking agents.5-氨基吡唑-4-甲酰胺类似物是恶性疟原虫小配子体体外受精的选择性抑制剂及潜在的疟疾传播阻断剂。
Bioorg Med Chem Lett. 2016 Nov 15;26(22):5487-5491. doi: 10.1016/j.bmcl.2016.10.014. Epub 2016 Oct 10.
8
A Novel Calcium-Dependent Kinase Inhibitor, Bumped Kinase Inhibitor 1517, Cures Cryptosporidiosis in Immunosuppressed Mice.一种新型钙依赖性激酶抑制剂——碰撞激酶抑制剂1517,可治愈免疫抑制小鼠的隐孢子虫病。
J Infect Dis. 2016 Dec 15;214(12):1850-1855. doi: 10.1093/infdis/jiw481. Epub 2016 Oct 12.
9
Development of an Orally Available and Central Nervous System (CNS) Penetrant Toxoplasma gondii Calcium-Dependent Protein Kinase 1 (TgCDPK1) Inhibitor with Minimal Human Ether-a-go-go-Related Gene (hERG) Activity for the Treatment of Toxoplasmosis.开发一种口服可用且能穿透中枢神经系统(CNS)的弓形虫钙依赖性蛋白激酶1(TgCDPK1)抑制剂,其对人醚孔相关基因(hERG)的活性最小,用于治疗弓形虫病。
J Med Chem. 2016 Jul 14;59(13):6531-46. doi: 10.1021/acs.jmedchem.6b00760. Epub 2016 Jul 1.
10
SAR Studies of 5-Aminopyrazole-4-carboxamide Analogues as Potent and Selective Inhibitors of CDPK1.5-氨基吡唑-4-甲酰胺类似物作为CDPK1强效和选择性抑制剂的构效关系研究
ACS Med Chem Lett. 2015 Oct 22;6(12):1184-1189. doi: 10.1021/acsmedchemlett.5b00319. eCollection 2015 Dec 10.

基于 5-氨基吡唑-4-甲酰胺的 bumped-kinase 抑制剂的开发用于隐孢子虫病的治疗。

Development of 5-Aminopyrazole-4-carboxamide-based Bumped-Kinase Inhibitors for Cryptosporidiosis Therapy.

机构信息

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.

出版信息

J Med Chem. 2019 Mar 28;62(6):3135-3146. doi: 10.1021/acs.jmedchem.9b00069. Epub 2019 Mar 15.

DOI:10.1021/acs.jmedchem.9b00069
PMID:30830766
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6559944/
Abstract

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.

摘要

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。