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Novel scaffold for cathepsin K inhibitors.

Authors :
Teno N
Miyake T
Ehara T
Irie O
Sakaki J
Ohmori O
Gunji H
Matsuura N
Masuya K
Hitomi Y
Nonomura K
Horiuchi M
Gohda K
Iwasaki A
Umemura I
Tada S
Kometani M
Iwasaki G
Cowan-Jacob SW
Missbach M
Lattmann R
Betschart C
Source :
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2007 Nov 15; Vol. 17 (22), pp. 6096-100. Date of Electronic Publication: 2007 Sep 15.
Publication Year :
2007

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.

Details

Language :
English
ISSN :
0960-894X
Volume :
17
Issue :
22
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
17911019
Full Text :
https://doi.org/10.1016/j.bmcl.2007.09.047