1. Academic Validation
  2. Syntheses and applications of fluorescent and biotinylated epolactaene derivatives: Epolactaene and its derivative induce disulfide formation

Syntheses and applications of fluorescent and biotinylated epolactaene derivatives: Epolactaene and its derivative induce disulfide formation

  • Bioorg Med Chem. 2008 May 1;16(9):5039-49. doi: 10.1016/j.bmc.2008.03.029.
Kouji Kuramochi 1 Shunsuke Yukizawa Seiki Ikeda Takashi Sunoki Satoshi Arai Rie Matsui Akinori Morita Yoshiyuki Mizushina Kengo Sakaguchi Fumio Sugawara Masahiko Ikekita Susumu Kobayashi
Affiliations

Affiliation

  • 1 Department of Applied Biological Science, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
Abstract

Epolactaene, isolated from cultured Penicillium sp. BM 1689-P mycelium, induces neurite outgrowth and arrests the cell cycle of the human neuroblastoma cell line, SH-SY5Y, at the G1 phase. We have found that epolactaene and its derivatives induce Apoptosis in the human leukemia B-cell line, BALL-1. In this study, we prepared fluorescent and biotinylated epolactaene derivatives. We characterized the cellular location and the identification of BALL-1 proteins that reacted with these compounds. The results obtained from the reaction of epolactaene or its derivative with N-acetylcysteine methyl ester indicate that these compounds induce the disulfide formation and the alpha-position of the epoxylactam core is the reactive site.

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