Novel scaffold for cathepsin K inhibitors.
Teno, Naoki, Miyake, Takahiro, Ehara, Takeru, Irie, Osamu, Sakaki, Junichi, Ohmori, Osamu, Gunji, Hiroki, Matsuura, Naoko, Masuya, Keiichi, Hitomi, Yuko, Nonomura, Kazuhiko, Horiuchi, Miyuki, Gohda, Keigo, Iwasaki, Atsuko, Umemura, Ichiro, Tada, Sachiyo, Kometani, Motohiko, Iwasaki, Genji, Cowan-Jacob, Sandra, Missbach, Martin, Lattmann, Rene and Betschart, Claudia (2007) Novel scaffold for cathepsin K inhibitors. Bioorganic & Medicinal Chemistry Letters, 17 (22). pp. 6096-6100. ISSN 0960-894X
Abstract
Pyrrolopyrimidine, a novel scaffold, allows to adjust interactions within the S3 subsite of cathepsin K. The core intermediate 10 facilitated the P3 optimization and identified highly potent and selective cathepsin K inhibitors 11-20.
Item Type: | Article |
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Additional Information: | author can archive post-print (ie final draft post-refereeing); Publisher's version/PDF cannot be used |
Keywords: | Cathepsin K inhibitors; Pyrrolopyrimidine; Novel scaffold |
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Date Deposited: | 14 Dec 2009 14:01 |
Last Modified: | 31 Jan 2013 01:18 |
URI: | https://oak.novartis.com/id/eprint/360 |