1. Academic Validation
  2. Synthesis and evaluation of novel dolastatin 10 derivatives for versatile conjugations

Synthesis and evaluation of novel dolastatin 10 derivatives for versatile conjugations

  • Bioorg Med Chem. 2018 May 1;26(8):1643-1652. doi: 10.1016/j.bmc.2018.02.011.
Shinya Yokosaka 1 Akiko Izawa 1 Chizuka Sakai 1 Eri Sakurada 1 Yasuhiro Morita 1 Yukihiro Nishio 2
Affiliations

Affiliations

  • 1 Toray Industries Inc., Pharmaceutical Research Laboratories, 6-10-1 Tebiro, Kamakura, Kanagawa 248-8555, Japan.
  • 2 Toray Industries Inc., Pharmaceutical Research Laboratories, 6-10-1 Tebiro, Kamakura, Kanagawa 248-8555, Japan. Electronic address: yukihiro_nishio@nts.toray.co.jp.
Abstract

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.

Keywords

Cytotoxicity; Dolastatin 10; Tubulin inhibitor.

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