| Literature DB >> 11728187 |
B G Szczepankiewicz1, G Liu, H S Jae, A S Tasker, I W Gunawardana, T W von Geldern, S L Gwaltney, J R Wu-Wong, L Gehrke, 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, A K Claiborne, Q Li, S H Rosenberg.
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.Entities:
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Year: 2001 PMID: 11728187 DOI: 10.1021/jm010231w
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446