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Updated: Dec 18, 2025

Defining Substrate Specificities for Lipase and Phospholipase Candidates
Published on: November 23, 2016
Stereospecific synthesis of phosphatidylglycerol using a cyanoethyl phosphoramidite precursor
Zachary J Struzik1, Ashley N Weerts1, Judith Storch2
1Department of Chemistry, Purdue University, Multi-disciplinary Cancer Research Facility, Bindley Bioscience Center, 1203 W. State Street, West Lafayette, IN 47907, United States.
Abstract:
Phosphatidylglycerols (PG) are a family of naturally occurring phospholipids that are responsible for critical operations within cells. PG are characterized by an (R) configuration in the diacyl glycerol backbone and an (S) configuration in the phosphoglycerol head group. Herein, we report a synthetic route to provide control over the PG stereocenters as well as control of the acyl chain identity.
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