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ChemInform Abstract: Design and Synthesis of Monocyclic β-Lactams as Mechanism-Based Inhibitors of Human Cytomegalovirus Protease.

✍ Scribed by A. D. BORTHWICK; G. WEINGARTEN; T. M. HALEY; M. TOMASZEWSKI; W. WANG; Z. HU; J. BEDARD; H. JIN; L. YUEN; T. S. MANSOUR


Publisher
John Wiley and Sons
Year
2010
Weight
33 KB
Volume
29
Category
Article
ISSN
0931-7597

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✦ Synopsis


Design and Synthesis of Monocyclic β-Lactams as Mechanism-Based Inhibitors of Human Cytomegalovirus Protease. -Starting from monocyclic β-lactams novel human cytomegalovirus protease inhibitors, e.g. (III), (VII),and (VIII), are developed. The most potent one among them is the derivative (VII) with good stability to hydrolysis and good selectivity in low µmol ranges. -(BORTHWICK, A.


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