Potent aminocyclitol glucocerebrosidase inhibitors are subnanomolar pharmacological chaperones for treating gaucher disease.
Amino-myo-inositol derivatives have been found to be potent inhibitors of glucocerebrosidase (GCase), the β-glucosidase enzyme deficient in Gaucher disease (GD). When tested using lymphoblasts derived from patients with GD homozygous for N370S or L444P mutations, the compounds enhanced GCase activit...
主要な著者: | Trapero, A, González-Bulnes, P, Butters, T, Llebaria, A |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
2012
|
類似資料
-
Polyhydroxylated bicyclic isoureas and guanidines are potent glucocerebrosidase inhibitors and nanomolar enzyme activity enhancers in Gaucher cells.
著者:: Trapero, A, 等
出版事項: (2011) -
Chaperoning glucocerebrosidase: a therapeutic strategy for both Gaucher disease and Parkinsonism
著者:: Benjamin McMahon, 等
出版事項: (2016-01-01) -
Rational design and synthesis of highly potent pharmacological chaperones for treatment of N370S mutant Gaucher disease.
著者:: Wang, G, 等
出版事項: (2009) -
Synthesis of N-substituted ε-hexonolactams as pharmacological chaperones for the treatment of N370S mutant Gaucher disease.
著者:: Wang, G, 等
出版事項: (2012) -
Progranulin Recruits HSP70 to β-Glucocerebrosidase and Is Therapeutic Against Gaucher Disease
著者:: Jinlong Jian, 等
出版事項: (2016-11-01)