Synthesis and biological activity of N-substituted aminocarbonyl-1,3-dioxolanes as VLA-4 antagonists
摘要:
A novel set of compounds with a 1,3-dioxolane ring which acts as a proline bioisostere have been successfully designed as VLA-4 receptor antagonists. Compounds (18e), (28j), and (35g) were shown to have high receptor affinities. (C) 2010 Elsevier Ltd. All rights reserved.
[EN] DIOXOLANE DERIVATIVES AS CELL ADHESION INHIBITORS<br/>[FR] DERIVES DE DIOXOLANE COMME INHIBITEURS DE L'ADHESION CELLULAIRE
申请人:RANBAXY LAB LTD
公开号:WO2005026163A1
公开(公告)日:2005-03-24
The present invention relates to dioxolane derivatives as cell adhesion inhibitors. These compounds can be useful for inhibition and prevention of cell adhesion and cell adhesion-mediated pathologies, including inflammatory and autoimmune diseases such as bronchial asthma, rheumatoid arthritis, type I diabetes, multiple sclerosis, allograft rejection or psoriasis. This invention also relates to pharmacological compositions containing the compounds of the present invention, and the methods of treating bronchial asthma, rheumatoid arthritis, multiple sclerosis, type I diabetes, psoriasis, allograft rejection, and other inflammatory and/or autoimmune disorders, using the compounds.
Synthesis and biological activity of N-substituted aminocarbonyl-1,3-dioxolanes as VLA-4 antagonists
作者:Abdul Rehman、Ajay Soni、Keshav Naik、Sreeji Nair、Venkata P. Palle、Sunanda Dastidar、Abhijit Ray、M.S. Alam、Mohammad Salman、Ian A. Cliffe、Viswajanani Sattigeri
DOI:10.1016/j.bmcl.2010.07.069
日期:2010.9
A novel set of compounds with a 1,3-dioxolane ring which acts as a proline bioisostere have been successfully designed as VLA-4 receptor antagonists. Compounds (18e), (28j), and (35g) were shown to have high receptor affinities. (C) 2010 Elsevier Ltd. All rights reserved.