Synthesis of Coumarin-Based, Esterase-Sensitive Cyclic Prodrugs of Opioid Peptides with Enhanced Mem
With the discovery of an increasing number of biologically active peptides and p
With the discovery of an increasing number of biologically active peptides and peptide mimetics (1 –3 ), there is a pressing need for the development of strategies to deliver these biologically active compounds to the desired site of action. The preceding two chapters have described two methods of making esterase-sensitive cyclic prodrugs of peptides. In this chapter, we wish to describe a third method of making esterase-sensitive cyclic prodrugs of peptides using DADLE, an opioid peptide (4 –7 ), as an example.
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Primed Synthesis and Direct Sequencing in the Isolation of cDNA Clones Using Short Oligonucleotides
With the development of improved techniques for the construc...
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Solid-Phase Guanidinylation of Peptidyl Amines Compatible with Standard Fmoc-Chemistry: Formation of
With the growing importance of peptides and peptidomimetics ...
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