发明名称 |
Thiadiazolidinediones as GSK-3 inhibitors |
摘要 |
The present invention relates to new thiadiazolidinediones of formula (I), or any pharmaceutically acceptable salt, solvate or prodrug thereof, and its use in the treatment of a disease in which glycogen synthase kinase 3 (GSK-3) is involved, particularly neurodegenerative diseases, inflammatory and autoimmune diseases and cardiovascular disorders. Additionally, there is provided a process for preparing such compounds, as well as pharmaceutical compositions comprising them. |
申请公布号 |
US9371299(B2) |
申请公布日期 |
2016.06.21 |
申请号 |
US201314380623 |
申请日期 |
2013.02.22 |
申请人 |
ASD THERAPEUTICS PARTNERS, LLC |
发明人 |
Medina Padilla Miguel;Domínguez Correa Juan Manuel;De Cristobal Blanco Javier;Fuertes Huerta Ana;Sánchez-Quesada Jorge;López Ogalla Javier;Herrero Santos Susana;Pérez de la Cruz Moreno María Ángeles;Martínez Montero Olga;Rodríguez Salguero Beatriz;Palomo Nicolau Francisco |
分类号 |
C07D285/08;C07D417/06 |
主分类号 |
C07D285/08 |
代理机构 |
Moore & Van Allen, PLLC |
代理人 |
Fuierer Tristan A.;Moore & Van Allen, PLLC |
主权项 |
1. A compound of Formula (I): wherein: Ra is an unsubstituted ethyl, or a methyl group or an ethyl group substituted with hydroxyl, heterocyclyl or C(O)OR′, wherein R′ is an alkyl group which is a linear hydrocarbon chain radical consisting of 1 to 6 carbon atoms; Rb is —(CHR1)n—(Z)m-aryl, wherein n is 1, m is 1 or 2, and R1 is —CO(O)R″, wherein R″ is an alkyl group; Z is —C(R2)(R3)—, wherein R2 and R3 are independently selected from hydrogen and alkyl; or any pharmaceutically acceptable salt, solvate or prodrug thereof. |
地址 |
Warren NJ US |