537039-44-4Relevant academic research and scientific papers
UREA DERIVATIVE AND USE THEREFOR
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, (2018/07/29)
The purpose of the present invention is to provide a compound with inhibitory activity on Discoidin Domain Receptor 1. The present invention provides a urea derivative represented by the formula (I) below or a pharmaceutically acceptable salt thereof.
UREA DERIVATIVE AND USE THEREFOR
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, (2018/07/29)
The purpose of the present invention is to provide a compound with inhibitory activity on Discoidin Domain Receptor 1. The present invention provides a urea derivative represented by the formula below or a pharmaceutically acceptable salt thereof.
Biaryls as potent, tunable dual neurokinin 1 receptor antagonists and serotonin transporter inhibitors
Degnan, Andrew P.,Tora, George O.,Han, Ying,Rajamani, Ramkumar,Bertekap, Robert,Krause, Rudolph,Davis, Carl D.,Hu, Joanna,Morgan, Daniel,Taylor, Sarah J.,Krause, Kelly,Li, Yu-Wen,Mattson, Gail,Cunningham, Melissa A.,Taber, Matthew T.,Lodge, Nicholas J.,Bronson, Joanne J.,Gillman, Kevin W.,Macor, John E.
, p. 3039 - 3043 (2015/06/22)
Depression is a serious illness that affects millions of patients. Current treatments are associated with a number of undesirable side effects. Neurokinin 1 receptor (NK1R) antagonists have recently been shown to potentiate the antidepressant e
AMINO-PIPERIDINE DERIVATIVES AS CETP INHIBITORS
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Page/Page column 159; 160, (2008/06/13)
The present invention provides a compound of formula (I), wherein the variants R1, R2, R3, R4, R5, R6, R7 are as defined herein, and wherein said compound is an inhibitor of CETP, and thus can be employed for the treatment of a disorder or disease mediated by CETP or responsive to the inhibition of CETP.
NK-1 AND SEROTONIN TRANSPORTER INHIBITORS
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Page/Page column 62, (2010/11/28)
The invention encompasses compounds of Formula I, including pharmaceutically acceptable salts, their pharmaceutical compositions, and their use in treating disorders associated with an excess or imbalance of tachykinins or serotonin or both.
TRISUBSTITUTED AMINE COMPOUND
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Page/Page column 164-165, (2008/06/13)
The present invention relates to a compound of the general formula (1): wherein, Y is a methylene group, and the like; A is an optionally substituted heterocyclic group, and the like; B is an optionally substituted heterocyclic group, and the like; R1 is an optionally substituted alkyl group, wherein the alkyl group further may optionally be substituted by an optionally substituted homocyclic group, and the like; and R2 is an optionally substituted amino group, and the like; or a pharmaceutically acceptable derivative thereof, which has an inhibitory activity against cholesteryl ester transfer protein (CETP), thereby being useful for prophylaxis and/or treatment of arteriosclerotic diseases, hyperlipemia or dyslipidemia, and the like.
A PROCESS FOR PREPARING TETRAHYDROQUINOLINE DERIVATIVES
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Page/Page column 54, (2008/06/13)
The present invention is to provide a process for preparing optically active tetrahydroquinoline derivatives which can be used for the treatment and/or prevention of diseases such as arteriosclerotic diseases, dyslipidemia and the like, and a process for preparing synthetic intermediates thereof. Specifically, (2R,4S)-2-ethyl-6-trifluoromethyl-1,2,3,4-tetrahydroquinolin-4-ylamine or a salt thereof is prepared with fewer steps without using an optical resolution, and the optically active tetrahydroquinoline derivatives are obtained from the amine compound.
CETP INHIBITORS
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Page/Page column 64-65, (2010/02/14)
Compounds of Formula (I), including pharmaceutically acceptable salts of the compounds, are CETP inhibitors, and are useful for raising HDL-cholesterol, reducing LDL-cholesterol, and for treating or preventing atherosclerosis. In the compounds of Formu
