Invention Application
WO9637199A8 USE OF R-ENANTIOMER OF N-PROPARGYL-1-AMINOINDAN, SALTS, AND COMPOSITIONS THEREOF
审中-公开
N-丙基-1-氨基茚的R-增效剂,其盐及其组合物的使用
- Patent Title: USE OF R-ENANTIOMER OF N-PROPARGYL-1-AMINOINDAN, SALTS, AND COMPOSITIONS THEREOF
- Patent Title (中): N-丙基-1-氨基茚的R-增效剂,其盐及其组合物的使用
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Application No.: PCT/US9607465Application Date: 1996-05-22
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Publication No.: WO9637199A8Publication Date: 1999-08-12
- Inventor: YOUDIM MOUSSA B H , FINBERG JOHN P M , LEVY RUTH , STERLING JEFFREY , LERNER DAVID , YELLIN HAIM , VEINBERD ALEX
- Applicant: TEVA PHARMA , TECHNION RES & DEV FOUNDATION , YOUDIM MOUSSA B H , FINBERG JOHN P M , LEVY RUTH , STERLING JEFFREY , LERNER DAVID , YELLIN HAIM , VEINBERG ALEX
- Assignee: TEVA PHARMA,TECHNION RES & DEV FOUNDATION,YOUDIM MOUSSA B H,FINBERG JOHN P M,LEVY RUTH,STERLING JEFFREY,LERNER DAVID,YELLIN HAIM,VEINBERG ALEX
- Current Assignee: TEVA PHARMA,TECHNION RES & DEV FOUNDATION,YOUDIM MOUSSA B H,FINBERG JOHN P M,LEVY RUTH,STERLING JEFFREY,LERNER DAVID,YELLIN HAIM,VEINBERG ALEX
- Priority: US44643995 1995-05-22
- Main IPC: A61P9/10
- IPC: A61P9/10 ; A61K20060101 ; A61K31/135 ; A61K31/136 ; A61K31/137 ; A61K31/195 ; A61K31/215 ; A61K45/06 ; A61P20060101 ; A61P9/00 ; A61P25/00 ; A61P25/08 ; A61P25/16 ; A61P25/18 ; A61P25/20 ; A61P25/24 ; A61P25/28 ; C07C20060101 ; C07C211/30 ; C07C211/38 ; C07C211/42
Abstract:
The subject invention provides R(+)-N-propargyl-1-aminoindan and pharmaceutically acceptable salts thereof, as well as pharmaceutical compositions containing same. The subject invention also provides methods of treating a subject afflicted with Parkinson's disease, a memory disorder, dementia, depression, hyperactive syndrome, an effective illness, a neurodegenerative disease, a neurotoxic injury, stroke, brain ischemia, a head trauma injury, a spinal trauma injury, neurotrauma, schizophrenia, an attention deficit disorder, multiple sclerosis, or withdrawal symptoms, using R(+)-N-propargyl-1-aminoindan or the pharmaceutically acceptable salt of the subject invention. The subject invention further provides a method of preventing nerve damage in a subject. Finally, the subject invention provides methods of preparing R(+)-N-propargyl-1-aminoindan, a salt thereof, and racemic N-propargyl-1-aminoindan.
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