| Literature DB >> 15537340 |
Eva Altmann1, Sandra W Cowan-Jacob, Martin Missbach.
Abstract
Starting from the high-throughput screening hit 1a, novel cathepsin K inhibitors have been developed based on a purine scaffold. High-resolution X-ray structures of several derivatives have revealed the binding mode of these unique cysteine protease inhibitors.Entities:
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Year: 2004 PMID: 15537340 DOI: 10.1021/jm0493111
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446