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Description
Many of them are overexpressed in tumor cells
The difference in recovery time can be remarkable
In vitro experiments demonstrated that the reported -CD Val-Lys-conjugate polyrotaxane significantly impeded the cellular uptake of a Gly-Sar dipeptide, a known human peptide transporter substrate, without being absorbed themselves
G.HendersonP
focused on improving the in vivo efficacy of T-6932 by reducing its lipophilicity
Most therapeutic peptides exist in what we call a "gray area" of FDA regulation
