4.6 Article

Boron-Based Drug Design

期刊

CHEMICAL RECORD
卷 15, 期 3, 页码 616-635

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/tcr.201402100

关键词

boron; boronic acids; carboranes; drug design; inhibitors

资金

  1. Grants-in-Aid for Scientific Research [26293007, 26102721] Funding Source: KAKEN

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The use of the element boron, which is not generally observed in a living body, possesses a high potential for the discovery of new biological activity in pharmaceutical drug design. In this account, we describe our recent developments in boron-based drug design, including boronic acid containing protein tyrosine kinase inhibitors, proteasome inhibitors, and tubulin polymerization inhibitors, and ortho-carborane-containing proteasome activators, hypoxia-inducible factor 1 inhibitors, and topoisomerase inhibitors. Furthermore, we applied a closo-dodecaborate as a water-soluble moiety as well as a boron-10 source for the design of boron carriers in boron neutron capture therapy, such as boronated porphyrins and boron lipids for a liposomal boron delivery system.

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