前药
神经退行性变
化学
辅酶A
药理学
生物合成
生物化学
激酶
酶
生物
医学
内科学
还原酶
疾病
作者
Giulio Auciello,Annalise Di Marco,Odalys Gonzalez Paz,Savina Malancona,Steven J. Harper,Maria Beconi,Ilaria Rossetti,A Ciammaichella,Paola Fezzardi,Andrea Vecchi,Elena Bracacel,Daniel O. Cicero,Edith Monteagudo,Daniel Elbaum
标识
DOI:10.1021/acs.jmedchem.0c01531
摘要
Mutations in the human PANK2 gene are implicated in neurodegenerative diseases such as pantothenate kinase-associated neurodegeneration (PKAN) and result in low levels of coenzyme-A (CoA) in the CNS due to impaired production of phosphopantothenic acid (PPA) from vitamin B5. Restoration of central PPA levels by delivery of exogenous PPA is a recent strategy to reactivate CoA biosynthesis in PKAN patients. Fosmetpantotenate is an oral PPA prodrug. We report here the development of a new PANk2–/– knockout model that allows CoA regeneration in brain cells to be evaluated and describe two new series of cyclic phosphate prodrugs of PPA capable of regenerating excellent levels of CoA in this system. A proof-of-concept study in mouse demonstrates the potential of this new class of prodrugs to deliver PPA to the brain following oral administration and confirms incorporation of the prodrug-derived PPA into CoA.
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