Taguchi_2003_Bioorg.Med.Chem.Lett_13_3681

Reference

Title : Biological evaluation of sphingomyelin analogues as inhibitors of sphingomyelinase - Taguchi_2003_Bioorg.Med.Chem.Lett_13_3681
Author(s) : Taguchi M , Goda K , Sugimoto K , Akama T , Yamamoto K , Suzuki T , Tomishima Y , Nishiguchi M , Arai K , Takahashi K , Kobori T
Ref : Bioorganic & Medicinal Chemistry Lett , 13 :3681 , 2003
Abstract : Seeking neutral sphingomyelinase inhibitors, we designed and synthesized hydrolytically stable analogues of sphingomyelin. These novel analogues replace the phosphodiester moiety of sphingomyelin with carbamate and urea moiety, resulting in inhibition of neutral sphingomyelinase. Compound 1 prevented ceramide generation and apoptotic neuronal cell death in a model of ischemia based on organotypic hippocampal slice cultures.
ESTHER : Taguchi_2003_Bioorg.Med.Chem.Lett_13_3681
PubMedSearch : Taguchi_2003_Bioorg.Med.Chem.Lett_13_3681
PubMedID: 14552757

Related information

Citations formats

Taguchi M, Goda K, Sugimoto K, Akama T, Yamamoto K, Suzuki T, Tomishima Y, Nishiguchi M, Arai K, Takahashi K, Kobori T (2003)
Biological evaluation of sphingomyelin analogues as inhibitors of sphingomyelinase
Bioorganic & Medicinal Chemistry Lett 13 :3681

Taguchi M, Goda K, Sugimoto K, Akama T, Yamamoto K, Suzuki T, Tomishima Y, Nishiguchi M, Arai K, Takahashi K, Kobori T (2003)
Bioorganic & Medicinal Chemistry Lett 13 :3681