4.7 Article

Synthesis and evaluation of novel dolastatin 10 derivatives for versatile conjugations

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BIOORGANIC & MEDICINAL CHEMISTRY
卷 26, 期 8, 页码 1643-1652

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2018.02.011

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Dolastatin 10; Tubulin inhibitor; Cytotoxicity

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Dolastatin 10 (1) is a highly potent cytotoxic microtubule inhibitor (cytotoxicity IC50 < 5.0 nM) and several of its analogs have recently been used as payloads in antibody drug conjugates. Herein, we describe the design and synthesis of a series of novel dolastatin 10 analogs useful as payloads for conjugated drugs. We explored analogs containing functional groups at the thiazole moiety at the C-terminal of dolastatin 10. The functional groups included amines, alcohols, and thiols, which are representative structures used in known conjugated drugs. These novel analogs showed excellent potency in a tumor cell proliferation assay, and thus this series of dolastatin 10 analogs is suitable as versatile payloads in conjugated drugs. Insights into the structure-activity relationships of the analogs are also discussed. (c) 2018 Elsevier Ltd. All rights reserved.

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