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Updated: Jun 11, 2026

Defining Substrate Specificities for Lipase and Phospholipase Candidates
Published on: November 23, 2016
Synthesis and evaluation of novel phosphate ester analogs as neutral sphingomyelinase inhibitors
Hiroshi Imagawa1, Masataka Oda, Takayuki Takemoto
1Tokushima Bunri University, Japan. imagawa@ph.bunri-u.ac.jp
Abstract:
A novel sphingomyelin inhibitor RY221B-a, which contains a bipyridyl moiety as a metal coordination site was designed based upon the mechanism of phosphate ester hydrolysis. RY221B-a was synthesized from N-Boc-sphingosine in three steps via selective etherification using stannyl acetal. Synthesized RY221B-a exhibited relatively-strong inhibitory activity against Bc-SMase (IC(50)=1.2microM).
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