The ReFRAME library as a comprehensive drug repurposing library and its application to the treatment of cryptosporidiosis

被引:136
作者
Janes, Jeff [1 ]
Young, Megan E. [1 ]
Chen, Emily [1 ]
Rogers, Nicole H. [1 ]
Burgstaller-Muehlbacher, Sebastian [2 ]
Hughes, Laura D. [2 ]
Love, Melissa S. [1 ]
Hull, Mitchell V. [1 ]
Kuhen, Kelli L. [1 ]
Woods, Ashley K. [1 ]
Joseph, Sean B. [1 ]
Petrassi, H. Michael [1 ]
McNamara, Case W. [1 ]
Tremblay, Matthew S. [1 ]
Su, Andrew I. [2 ]
Schultz, Peter G. [1 ]
Chatterjee, Arnab K. [1 ]
机构
[1] Calif Inst Biomed Res, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Integrat Struct & Computat Biol, La Jolla, CA 92037 USA
基金
比尔及梅琳达.盖茨基金会;
关键词
drug repositioning; phenotypic screening; Cryptosporidium; drug discovery; neglected tropical diseases; BUMPED-KINASE INHIBITORS; PARVUM; THERAPY;
D O I
10.1073/pnas.1810137115
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The chemical diversity and known safety profiles of drugs previously tested in humans make them a valuable set of compounds to explore potential therapeutic utility in indications outside those originally targeted, especially neglected tropical diseases. This practice of "drug repurposing" has become commonplace in academic and other nonprofit drug-discovery efforts, with the appeal that significantly less time and resources are required to advance a candidate into the clinic. Here, we report a comprehensive open-access, drug repositioning screening set of 12,000 compounds (termed ReFRAME; Repurposing, Focused Rescue, and Accelerated Medchem) that was assembled by combining three widely used commercial drug competitive intelligence databases (Clarivate Integrity, GVK Excelra GoStar, and Citeline Pharmaprojects), together with extensive patent mining of small molecules that have been dosed in humans. To date, 12,000 compounds (similar to 80% of compounds identified from data mining) have been purchased or synthesized and subsequently plated for screening. To exemplify its utility, this collection was screened against Cryptosporidium spp., a major cause of childhood diarrhea in the developing world, and two active compounds previously tested in humans for other therapeutic indications were identified. Both compounds, VB-201 and a structurally related analog of ASP-7962, were subsequently shown to be efficacious in animal models of Cryptosporidium infection at clinically relevant doses, based on available human doses. In addition, an open-access data portal (https://reframedb.org) has been developed to share ReFRAME screen hits to encourage additional follow-up and maximize the impact of the ReFRAME screening collection.
引用
收藏
页码:10750 / 10755
页数:6
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