期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 51, 期 20, 页码 6259-6262出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm800914n
关键词
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A high-throughput screen at 100.mu M inhibitor concentration for the BACE-1 enzyme revealed a novel spiropiperidine iminohydantoin aspartyl protease inhibitor template. An X-ray cocrystal structure with BACE-1 revealed a novel mode of binding whereby the inhibitor interacts with the catalytic aspartates via bridging water molecules. Using the crystal structure as a guide, potent compounds with good brain penetration were designed.
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