Substituted 2-pyrones, 2-pyridones, and other congeners of elasnin as potential agents for the treatment of chronic obstructive lung diseases
WC Groutas, MA Stanga, MJ Brubaker…
Index: Groutas, William C.; Stanga, Michael A.; Brubaker, Michael J.; Huang, Tien L.; Moi, Min K.; Carroll, Robert T. Journal of Medicinal Chemistry, 1985 , vol. 28, # 8 p. 1106 - 1109
Full Text: HTML
Citation Number: 47
Abstract
Several congeners of elasnin (I) have been synthesized and shown to inhibit human leukocyte elastase (HLE). The C-3 alkyl substituted 2-pyrones 11 and 12 were found to be the most effective inhibitors of the enzyme. These compounds are highly specific in their inhibitory activity.
Related Articles:
[Giddens, Anna C.; Nielsen, Lone; Boshoff, Helena I.; Tasdemir, Deniz; Perozzo, Remo; Kaiser, Marcel; Wang, Feng; Sacchettini, James C.; Copp, Brent R. Tetrahedron, 2008 , vol. 64, # 7 p. 1242 - 1249]
[Lokot, Igor P.; Pashkovsky, Felix S.; Lakhvich, Fedor A. Tetrahedron, 1999 , vol. 55, # 15 p. 4783 - 4792]
[Lokot, Igor P.; Pashkovsky, Felix S.; Lakhvich, Fedor A. Tetrahedron, 1999 , vol. 55, # 15 p. 4783 - 4792]
[Lokot, Igor P.; Pashkovsky, Felix S.; Lakhvich, Fedor A. Tetrahedron, 1999 , vol. 55, # 15 p. 4783 - 4792]
[Lokot, Igor P.; Pashkovsky, Felix S.; Lakhvich, Fedor A. Tetrahedron, 1999 , vol. 55, # 15 p. 4783 - 4792]