reference/12579488

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contentType	Journal Article
endingPage	4902
issn	0960-894X
issueIdentifier	19
pageRange	4897-4902
publicationName	Bioorganic & Medicinal Chemistry Letters
startingPage	4897
bibliographicCitation	Barrett DG, Catalano JG, Deaton DN, Hassell AM, Long ST, Miller AB, Miller LR, Shewchuk LM, Wells-Knecht KJ, Willard DH, Wright LL. Potent and selective P2–P3 ketoamide inhibitors of cathepsin K with good pharmacokinetic properties via favorable P1′, P1, and/or P3 substitutions. Bioorganic & Medicinal Chemistry Letters. 2004 Oct;14(19):4897–902. doi: 10.1016/j.bmcl.2004.07.031.
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date	2004-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/15341947 https://doi.org/10.1016/j.bmcl.2004.07.031
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Potent and selective P2–P3 ketoamide inhibitors of cathepsin K with good pharmacokinetic properties via favorable P1′, P1, and/or P3 substitutions
discusses	http://id.nlm.nih.gov/mesh/M0003661 http://id.nlm.nih.gov/mesh/M0000897 http://id.nlm.nih.gov/mesh/M0528260 http://id.nlm.nih.gov/mesh/M0024280 http://id.nlm.nih.gov/mesh/M0501641
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