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Phenotypic, chemical and functional characterization of cyclic nucleotide phosphodiesterase 4 (PDE4) as a potential anthelmintic drug target.

PLoS Negl Trop Dis. 2017; 
Long Thavy,Rojo-Arreola Liliana,Shi Da,El-Sakkary Nelly,Jarnagin Kurt,Rock Fernando,Meewan Maliwan,Rascón Alberto A,Lin Lin,Cunningham Katherine A,Lemieux George A,Podust Larissa,Abagyan Ruben,Ashrafi Kaveh,McKerrow James H,Caffrey Con
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Peptide Synthesis domain of SmPDE4A (Smp_134140; XM_002573613; residues 668–1,060 in Fig 2) was synthesized (Genscript Get A Quote

摘要

Reliance on just one drug to treat the prevalent tropical disease, schistosomiasis, spurs the search for new drugs and drug targets. Inhibitors of human cyclic nucleotide phosphodiesterases (huPDEs), including PDE4, are under development as novel drugs to treat a range of chronic indications including asthma, chronic obstructive pulmonary disease and Alzheimer's disease. One class of huPDE4 inhibitors that has yielded marketed drugs is the benzoxaboroles (Anacor Pharmaceuticals).

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