New antimitotic agents with activity in multi-drug-resistant cell lines and in vivo efficacy in murine tumor models

B. G bruce g Szczepankiewicz, W. J. Chiou, R. B. Credo, J. D. Alder, M. A. Nukkala, N. A. Zielinski, K. Jarvis, K. W. Mollison, D. J. Frost, J. L. Bauch, Y. H. Hui, G. bruce g Liu, A. K. Claiborne, Q. Li, S. H. Rosenberg, H. S. Jae, A. S. Tasker, I. W. Gunawardana, T. W. Von Geldern, S. L. GwaltneyJ. R. Wu-Wong, L. Gehrke

Research output: Contribution to journalArticlepeer-review

63 Scopus citations

Abstract

During a screen for compounds that could inhibit cell proliferation, a series of new tubulin-binding compounds was identified with the discovery of oxadiazoline 1 (A-105972). This compound showed good cytotoxic activity against non-multi-drug-resistant and multi-drug-resistant cancer cell lines, but its utility in vivo was limited by a short half-life. Medicinal chemistry efforts led to the discovery of indolyloxazoline 22g (A-259745), which maintained all of the in vitro activity seen with oxadiazoline 1, but also demonstrated a better pharmacokinetic profile, and dose-dependent in vivo activity. Over a 28 day study, indolyloxazoline 22g increased the life span of tumor-implanted mice by up to a factor of 3 upon oral dosing. This compound, and others of its structural class, may prove to be useful in the development of new chemotherapeutic agents to treat human cancers.

Original languageEnglish (US)
Pages (from-to)4416-4430
Number of pages15
JournalJournal of Medicinal Chemistry
Volume44
Issue number25
DOIs
StatePublished - Dec 6 2001

ASJC Scopus subject areas

  • Molecular Medicine
  • Drug Discovery

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