Article ID Journal Published Year Pages File Type
10586260 Bioorganic & Medicinal Chemistry Letters 2015 6 Pages PDF
Abstract
We report here a new series of prodrugs of paclitaxel containing self-immolative disulfide linkers with improved water-solubility, in vitro anticancer activity and oral bioavailability when compared to those of paclitaxel. The disulfide bond in these prodrugs can undergo sulfhydryl-assisted cleavage to release paclitaxel in vivo by a plausible mechanism as shown in the scheme.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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