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Browse by: INVENTOR PATENT HOLDER PATENT NUMBER DATE
 
 
Inventor:
Lee; Hee-Yoon
Address:
Daejeon, KR
No. of patents:
5
Patents:












Patent Number Title Of Patent Date Issued
8236806 Piperazinyl-propyl-pyrazole derivatives as dopamine D4 receptor antagonists, and pharmaceutical August 7, 2012
The present invention relates to a novel piperazinyl-propyl-pyrazole derivative, a method of its preparation and a pharmaceutically acceptable composition comprising the same. The novel piperazinyl-propyl-pyrazole derivative of the present invention has superior selective affinity for
7846963 2-oxo-heterocyclic compounds and the pharmaceutical compositions comprising the same December 7, 2010
The present invention is related to new 2-oxo-cyclic compound the process for preparing them and a pharmaceutical composition comprising the same. The present invention provides a pharmaceutical composition for preventing and treating the inflammatory disease comprising the pain or i
7723376 2-oxo-heterocyclic compounds and pharmaceutical compositions May 25, 2010
The present invention is related to novel use of 2-oxo-heterocyclic compounds having anticancer activity and the process for preparing them and a pharmaceutical composition comprising the same. The present invention provides a pharmaceutical composition for preventing and treating th
6723724 Isoxazolylalkylpiperazine derivatives having selective biological activity at dopamine D3 or D4 April 20, 2004
The present invention relates to isoxazolylalkylpiperazine derivatives having selective biological activity at dopamine D.sub.3 or D.sub.4 receptors represented by the following formula (1), and its preparation method through reductive amination reaction in the presence of reducing a
6673800 4,5,-dihydroisoxazolylakylpiperazine derivatives having selective biological activity at dopamin January 6, 2004
The present invention relates to 4,5-dihydroisoxazolylalkylpiperazine derivatives having selective biological activity at dopamine D.sub.3 and D.sub.4 receptors represented by the following Formula (1), and its preparation method through reductive amination reaction in the presence of










 
 
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