10567-22-3
10567-22-3
Chemical Structure
3-O-Octadecyl-sn-glycerol
- CAS No.: 10567-22-3
- Formula:C21H44O3
- Molecular Weight:344.57
InChIKey: OGBUMNBNEWYMNJ-OAQYLSRUSA-N
SMILES: CCCCCCCCCCCCCCCCCCOC[C@H](O)CO
Biological Activity: 3-O-Octadecyl-sn-glycerol is an ether lipid that serves as an enantiopure substrate for evaluating the stereoselectivity of lipases in oleic acid esterification reactions. 3-O-Octadecyl-sn-glycerol can be used for the synthesis of AZT-lipid-PFA antiviral dual drugs. 3-O-Octadecyl-sn-glycerol acts as a biochemical reagent for research in various fields[1][2].
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3-O-Octadecyl-sn-glycerol | 3-O-Octadecyl-sn-glycerol is an ether lipid that serves as an enantiopure substrate for evaluating the stereoselectivity of lipases in oleic acid esterification reactions. 3-O-Octadecyl-sn-glycerol can be used for the synthesis of AZT-lipid-PFA antiviral dual drugs. 3-O-Octadecyl-sn-glycerol acts as a biochemical reagent for research in various fields. | |||||||||||||||||||||
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References
- [1]. Schott H, et al. Synthesis and in vitro activities of a new antiviral duplex drug linking Zidovudine (AZT) and Foscarnet (PFA) via an octadecylglycerol residue. Bioorganic & medicinal chemistry. 2009 Jan 01;17(1):303-10. [Content Brief]
- [2]. Meusel D, et al. Stereoselectivity of lipases: esterification reactions of octadecylglycerol. Chemistry and physics of lipids. 1992 Apr;61(2):193-8. [Content Brief]
Keywords
