16975-61-4

Upstream product

• 76-83-5 trityl chloride 
• 67-64-1 acetone 
• 14347-78-5 1,2-O-isopropylidene-D-glycerol 
• 60456-21-5 methyl (4S)-2,2-dimethyl-1,3-dioxolane-4-carboxylate 

Downstream Products

• 14347-78-5 1,2-O-isopropylidene-D-glycerol 
• 17327-05-8 (S)-3-(trityloxy)propane-1,2-diol 
• 13397-92-7 (Z)-(R)-3-(trityloxy)propane-1,2-diyl dioleate 
• 16990-53-7 (S)-1-Z-Ala-3-O-benzyl-3-O-trityl-glycerin 
• 17086-77-0 (S)-1-Z-Ala-3-O-trityl-glycerin 
• 16975-62-5 (R)-3-(trityloxy)propane-1,2-diol 

Relevant academic research and scientific papers

Synthesis of Phosphatidylserine and Its Stereoisomers: Their Role in Activation of Blood Coagulation

Natural phosphatidylserine (PS), which contains two chiral centers, enhances blood coagulation. However, the process by which PS enhanced blood coagulation is not completely understood. An efficient and flexible synthetic route has been developed to synthesize all of the possible stereoisomers of PS. In this study, we examined the role of PS chiral centers in modulating the activity of the tissue factor (TF)-factor VIIa coagulation initiation complex. Full length TF was relipidated with phosphatidylcholine, and the synthesized PS isomers were individually used to estimate the procoagulant activity of the TF-FVIIa complex via a FXa generation assay. The results revealed that the initiation complex activity was stereoselective and had increased sensitivity to the configuration of the PS glycerol backbone due to optimal protein-lipid interactions.