发明名称 |
Bis-(aryl/heteroaryl)-methylene compounds, pharmaceutical compositions containing same and their use for treating cancer |
摘要 |
The present disclosure relates to novel compounds having vitamin D receptor agonist and histone deacetylase inhibitory efficacy as well as methods for reducing or inhibiting the proliferation of cancer cells or for treating cancer.; |
申请公布号 |
US9428447(B2) |
申请公布日期 |
2016.08.30 |
申请号 |
US201214367375 |
申请日期 |
2012.12.20 |
申请人 |
The Royal Institution for the Advancement of Learning/McGill University |
发明人 |
Gleason James L.;White John H.;Kaldre Dainis;Fischer Joshua |
分类号 |
A61K31/42;C07C259/06;C07D263/32;C07D209/18;C07D333/16;C07D333/24;C07D209/12 |
主分类号 |
A61K31/42 |
代理机构 |
Buchanan Ingersoll & Rooney P.C. |
代理人 |
Buchanan Ingersoll & Rooney P.C. |
主权项 |
1. A compounds of formulaor a pharmaceutically acceptable salt thereof, wherein
the dotted line is an optional double bond; A and B are each independently an aryl; R1 is hydrogen, an alkyl or cycloalkyl; R2 is absent when the dotted line is a double bond or R2 is hydrogen, an alkyl or cycloalkyl when the dotted line is absent; W is OH when the dotted line is absent or W is O when the dotted line is a double bond; X is O, CH2, CHR7 or CR7R7, where R7 is in an alkyl or fluoroalkyl; Y is NR10(CO), (CO)NR10, O, CH2, CHR7 or CR7R7, where R7 is in an alkyl or fluoroalkyl and R10 is H or an alkyl; R3 and R4 are each independently hydrogen, an alkyl or fluoroalkyl; R5 and R6 are each independently an optional substituent; when p is greater than 0, R″ is H and one of said R″ is optionally OH; n and p are each an integer from 0 to 6. |
地址 |
Montreal, Quebec CA |