Convenient preparation of N-8-quinolinyl benzenesultams as novel NF-κB inhibitors
摘要:
An efficient synthesis of a series of N-8-quinolinyl benzenesultarns as novel NF-kappa B inhibitors was described via diazotization-induced cyclization of easily accessible N-8-quinolinyl-2-aminobenzenesulfonamides. (C) 2008 Elsevier Ltd. All rights reserved.
The present invention relates to novel hepcidin antagonists, pharmaceutical compositions comprising them and the use thereof as medicaments for the use in the treatment of iron metabolism disorders, such as, in particular, iron deficiency diseases and anemias, in particular anemias in connection with chronic inflammatory diseases.
The present invention relates to novel hepcidin antagonists, pharmaceutical compositions comprising them and the use thereof as medicaments for the use in the treatment of iron metabolism disorders, such as, in particular, iron deficiency diseases and anemias, in particular anemias in connection with chronic inflammatory diseases.
Convenient preparation of N-8-quinolinyl benzenesultams as novel NF-κB inhibitors
作者:Yuli Xie、Gangli Gong、Yidong Liu、Shixian Deng、Alison Rinderspacher、Lars Branden、Donald W. Landry
DOI:10.1016/j.tetlet.2008.01.136
日期:2008.3
An efficient synthesis of a series of N-8-quinolinyl benzenesultarns as novel NF-kappa B inhibitors was described via diazotization-induced cyclization of easily accessible N-8-quinolinyl-2-aminobenzenesulfonamides. (C) 2008 Elsevier Ltd. All rights reserved.