WO2006014968A3 - Propargyl nitroxydes and indanyl nitroxides and their use for the treatment of neurologic diseases and disorders - Google Patents

Propargyl nitroxydes and indanyl nitroxides and their use for the treatment of neurologic diseases and disorders Download PDF

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Publication number
WO2006014968A3
WO2006014968A3 PCT/US2005/026510 US2005026510W WO2006014968A3 WO 2006014968 A3 WO2006014968 A3 WO 2006014968A3 US 2005026510 W US2005026510 W US 2005026510W WO 2006014968 A3 WO2006014968 A3 WO 2006014968A3
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WO
WIPO (PCT)
Prior art keywords
alkyl
compounds
methods
nitroxydes
nitroxides
Prior art date
Application number
PCT/US2005/026510
Other languages
French (fr)
Other versions
WO2006014968A2 (en
Inventor
Jeffrey Sterling
Benjamin Sklarz
Yaacov Herzig
David Lerner
Eliezer Falb
Haim Ovadia
Original Assignee
Teva Pharma
Teva Pharmaceutical Usa Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Teva Pharma, Teva Pharmaceutical Usa Inc filed Critical Teva Pharma
Publication of WO2006014968A2 publication Critical patent/WO2006014968A2/en
Publication of WO2006014968A3 publication Critical patent/WO2006014968A3/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/94Oxygen atom, e.g. piperidine N-oxide

Abstract

Disclosed are compounds having the structure wherein Z is -OH or O ; and A is wherein X and Y are independently NR1or O, where R1 is H or C1-C4 alkyl ; and R2 is H, C1-C4 alkyl or t-butoxycarbonyl, wherein W is C3-C4 alkynyl ; and R1 is H or C1-C4 alkyl, or wherein R1 is H, C1-C4 alkyl, or C3-C4 alkynyl ; and R3 is H, OH, O (C1-C4 alkyl) , or a halogen, optically active enantiomers, pharmaceutically acceptable salts of the compounds, pharmaceutical compositions containing such compounds or salts, and processes for their preparation. The subject invention also provides methods of alleviating symptoms of neurologic, autoimmune, and inflammatory disorders caused by the presence of reactive oxygen species, methods of preventing oxidation of lipids, proteins, or deoxyribonucleic acids on a cellular level, and methods of protecting human red blood cells from lysis by 02 radicals.
PCT/US2005/026510 2004-07-27 2005-07-26 Propargyl nitroxydes and indanyl nitroxides and their use for the treatment of neurologic diseases and disorders WO2006014968A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US90098404A 2004-07-27 2004-07-27
US10/900,984 2004-07-27

Publications (2)

Publication Number Publication Date
WO2006014968A2 WO2006014968A2 (en) 2006-02-09
WO2006014968A3 true WO2006014968A3 (en) 2006-11-09

Family

ID=35787775

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2005/026510 WO2006014968A2 (en) 2004-07-27 2005-07-26 Propargyl nitroxydes and indanyl nitroxides and their use for the treatment of neurologic diseases and disorders

Country Status (1)

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WO (1) WO2006014968A2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009023707A1 (en) * 2007-08-14 2009-02-19 Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services Method of treating disease involving myelin and/or axonal loss
IT1392914B1 (en) * 2009-01-22 2012-04-02 Dipharma Francis Srl PROCEDURE FOR THE PREPARATION OF (R) -N-PROPARGIL-1-AMMINOINDHANE AND ITS SALTS
AU2013243875B2 (en) 2012-04-03 2017-11-30 Schindler, William Succinimide-activated nitroxyl compounds and methods for the use thereof for nitroxylation of proteins

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5457133A (en) * 1990-01-03 1995-10-10 Teva Pharmaceutical Industries Ltd. R-enantiomers of N-propargyl-aminoindan compounds, their preparation and pharmaceutical compositions containing them
US6303650B1 (en) * 1996-12-18 2001-10-16 Yissum Research Development Company Of The Hebrew University Of Jerusalem Aminoindan derivatives
US6956060B2 (en) * 1990-01-03 2005-10-18 Teva Pharmaceutical Industries, Ltd. Use of R-enantiomer of N-propargyl-1-aminoindan, salts, and compositions thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5457133A (en) * 1990-01-03 1995-10-10 Teva Pharmaceutical Industries Ltd. R-enantiomers of N-propargyl-aminoindan compounds, their preparation and pharmaceutical compositions containing them
US6956060B2 (en) * 1990-01-03 2005-10-18 Teva Pharmaceutical Industries, Ltd. Use of R-enantiomer of N-propargyl-1-aminoindan, salts, and compositions thereof
US6303650B1 (en) * 1996-12-18 2001-10-16 Yissum Research Development Company Of The Hebrew University Of Jerusalem Aminoindan derivatives

Also Published As

Publication number Publication date
WO2006014968A2 (en) 2006-02-09

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