Analysis of Structure–Activity Relationships of Novel Inhibitors of the Macrophage Infectivity Potentiator (Mip) Proteins of Neisseria meningitidis, Neisseria gonorrhoeae, and Burkholderia pseudomallei
ACE-2 modulating compounds and methods of use thereof
申请人:——
公开号:US20040082496A1
公开(公告)日:2004-04-29
ACE-2 modulating compounds for the treatment of body weight disorders are disclosed. Methods of using the compounds and pharmaceutical compositions containing the compounds are also claimed.
Among the hapalosin derivatives synthesized, the compounds carrying methyl (5a), methylthioethyl (5d) and phenylmethyl (5e) groups at the C12 position possess only the cis-peptide structure, in contrast to the cases of 5b and 5c. In addition to their conformational stability, the biological activities of the compounds were determined in relation of the P-glycoprotein-mediated MDR-reversing activity
The present disclosure generally relates to pipecolic acid derived compounds, in particular pipecolic acid derived compounds of Formula (I), and to formulations and compositions comprising the same. The present disclosure also relates to methods and uses of these compounds, compositions and/or formulations in treating and/or preventing a disease or condition mediated by a pathogen which is responsive to inhibition of macrophage infectivity potentiator (Mip) proteins, and/or a disease or condition mediated in which Mip protein is a virulence factor.