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CPT-11 is a clinically used cancer drug, and it is a prodrug of the potent topoisomerase I inhibitor, SN-38 (7-ethyl-10-hydroxycamptothecin). To bypass the need for the in vivo conversion of CPT-11 and increase the therapeutic index, bifunctional derivatives of SN-38 were prepared for use in antibody-based targeted therapy of cancer. The general synthetic scheme incorporated an acetylene-azide click cycloaddition step in the design, a short polyethylene glycol spacer for aqueous solubility, and a maleimide group for conjugation. Conjugates of a humanized anti-CEACAM5 monoclonal antibody, hMN-14, prepared using these SN-38 derivatives were evaluated in vitro for stability in buffer and human serum and for antigen-binding and cytotoxicity in a human colon adenocarcinoma cell line. Conjugates of hMN-14 and SN-38 derivatives 16 and 17 were found promising for further development.
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Moon et al. (Wed,) studied this question.
www.synapsesocial.com/papers/6a082b069a6c4ba6e610821b — DOI: https://doi.org/10.1021/jm800719t
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Sung-Ju Moon
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Journal of Medicinal Chemistry
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Immunomedics (United States)
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