Identification of a potent benzoxaborole drug candidate for treating cryptosporidiosis

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作者
Christopher S. Lunde
Erin E. Stebbins
Rajiv S. Jumani
Md Mahmudul Hasan
Peter Miller
John Barlow
Yvonne R. Freund
Pamela Berry
Rianna Stefanakis
Jiri Gut
Philip J. Rosenthal
Melissa S. Love
Case W. McNamara
Eric Easom
Jacob J. Plattner
Robert T. Jacobs
Christopher D. Huston
机构
[1] Anacor Pharmaceuticals,Department of Medicine
[2] University of Vermont Robert R. Larner College of Medicine,Department of Microbiology and Molecular Genetics
[3] University of Vermont College of Agriculture and Life Sciences,Department of Animal and Veterinary Sciences
[4] University of Vermont College of Agriculture and Life Sciences,Department of Medicine
[5] University of California San Francisco,undefined
[6] Calibr at Scripps Research,undefined
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Nature Communications | / 10卷
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摘要
Cryptosporidiosis is a leading cause of life-threatening diarrhea in young children and causes chronic diarrhea in AIDS patients, but the only approved treatment is ineffective in malnourished children and immunocompromised people. We here use a drug repositioning strategy and identify a promising anticryptosporidial drug candidate. Screening a library of benzoxaboroles comprised of analogs to four antiprotozoal chemical scaffolds under pre-clinical development for neglected tropical diseases for Cryptosporidium growth inhibitors identifies the 6-carboxamide benzoxaborole AN7973. AN7973 blocks intracellular parasite development, appears to be parasiticidal, and potently inhibits the two Cryptosporidium species most relevant to human health, C. parvum and C. hominis. It is efficacious in murine models of both acute and established infection, and in a neonatal dairy calf model of cryptosporidiosis. AN7973 also possesses favorable safety, stability, and PK parameters, and therefore, is an exciting drug candidate for treating cryptosporidiosis.
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