Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377113 | Bioorganic & Medicinal Chemistry Letters | 2008 | 5 Pages |
Abstract
Tumor targeting peptides are promising vehicles for site-directed cancer therapy. Pep42, a cyclic 13-mer oligopeptide that specifically binds to glucose-regulated protein 78 (GRP78) and internalized into cancer cells, represents an excellent vehicle for tumor cell-specific chemotherapy. Here, we report the synthesis and evaluation of Pep42-prodrug conjugates that contain a cathepsin B-cleavable linker, resulting in the traceless release of drug inside the cancer cells.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yoshiyuki Yoneda, Sebastian C.J. Steiniger, Kateřina Čapková, Jenny M. Mee, Ying Liu, Gunnar F. Kaufmann, Kim D. Janda,