Chemistry and biology of dihydroisoxazole derivatives: Selective inhibitors of human transglutaminase 2

Kihang Choi, Matthew Siegel, Justin L. Piper, Liya Yuan, Eun Cho, Pavel Strnad, Bishr Omary, Keith M. Rich, Chaitan Khosla

Research output: Contribution to journalArticle

131 Citations (Scopus)

Abstract

3-Halo-4,5-dihydroisoxazoles are attractive warheads for the selective inhibition of nucleophilic active sites in biological systems. A series of 3-bromo-4,5-dihydroisoxazole compounds were prepared and tested for their ability to irreversibly inhibit human transglutaminase 2 (TG2), an enzyme that plays an important role in the pathogenesis of diverse disorders including Celiac Sprue and certain types of cancers. Several compounds showed high specificity for human TG2 (kinh/KI > 2000 min -1M-1) but essentially no reactivity (k < 1 min -1M-1) toward physiological thiols such as glutathione. The pharmacokinetic and pharmacodynamic properties of a prototype dihydroisoxazole inhibitor, 1b, were evaluated; in mice the compound showed good oral bioavailability, short serum half-life and efficient TG2 inhibition in small intestinal tissue, and low toxicity. It also showed excellent synergism with N,N′-bis(2-chloroethyl)-N-nitrosourea (BCNU, carmustine) against refractory glioblastoma tumors in mice. A fluorescent dihydroisoxazole inhibitor 5 facilitated microscopic visualization of TG2 endocytosis from the extracellular surface of HCT-116 cells. Together, these findings demonstrate the promise of dihydroisoxazole compounds as probes for the biology of TG2 and its role in human disease.

Original languageEnglish
Pages (from-to)469-475
Number of pages7
JournalChemistry and Biology
Volume12
Issue number4
DOIs
Publication statusPublished - 2005 Apr

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Pharmacology
  • Drug Discovery
  • Clinical Biochemistry

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    Choi, K., Siegel, M., Piper, J. L., Yuan, L., Cho, E., Strnad, P., Omary, B., Rich, K. M., & Khosla, C. (2005). Chemistry and biology of dihydroisoxazole derivatives: Selective inhibitors of human transglutaminase 2. Chemistry and Biology, 12(4), 469-475. https://doi.org/10.1016/j.chembiol.2005.02.007