发明名称 |
INHIBITORS OF THE ENZYME UDP-GLUCOSE: N-ACYL-SPHINGOSINE GLUCOSYLTRANSFERASE |
摘要 |
This invention relates to novel inhibitors of UDP-glucose: N-acyl-sphingosine glucosyltransferase and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering inhibitors of UDP-glucose: N-acyl-sphingosine glucosyltransferase. |
申请公布号 |
US2016068519(A1) |
申请公布日期 |
2016.03.10 |
申请号 |
US201514853900 |
申请日期 |
2015.09.14 |
申请人 |
Concert Pharmaceuticals, Inc. |
发明人 |
Harbeson Scott L. |
分类号 |
C07D405/10 |
主分类号 |
C07D405/10 |
代理机构 |
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代理人 |
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主权项 |
1. A compound of Formula I: or a pharmaceutically acceptable salt thereof, wherein each Y1 is the same and is hydrogen or deuterium; each Y2 is the same and is hydrogen or deuterium; Y3 is hydrogen or deuterium; Y4 is hydrogen or deuterium; each Y5 is the same and is hydrogen or deuterium; each Y6 is the same and is hydrogen or deuterium; and each Y7 is the same and is hydrogen or deuterium; R1 is wherein each X1 is the same and is hydrogen or deuterium; each X2 is the same and is hydrogen or deuterium; each X3 is the same and is hydrogen or deuterium; each X4 is the same and is hydrogen or deuterium; each X5 is the same and is hydrogen or deuterium; each X6 is the same and is hydrogen or deuterium; and each Z is the same and is hydrogen or deuterium; provided that if each Y is hydrogen and each X is hydrogen, then each Z is deuterium. |
地址 |
Lexington MA US |