MA27132A1 - Composes de n-(3-amino-2hydroxy-propyl)alkylamide substitues - Google Patents

Composes de n-(3-amino-2hydroxy-propyl)alkylamide substitues

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Publication number
MA27132A1
MA27132A1 MA27510A MA27510A MA27132A1 MA 27132 A1 MA27132 A1 MA 27132A1 MA 27510 A MA27510 A MA 27510A MA 27510 A MA27510 A MA 27510A MA 27132 A1 MA27132 A1 MA 27132A1
Authority
MA
Morocco
Prior art keywords
compounds
2hydroxy
propyl
amino
substituted
Prior art date
Application number
MA27510A
Other languages
English (en)
Inventor
Gailunas Andrea
Tenbrink Ruth
Mickelson John
A Tucker John
Original Assignee
Elan Pharm Inc
Upjohn Co
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 Elan Pharm Inc, Upjohn Co filed Critical Elan Pharm Inc
Publication of MA27132A1 publication Critical patent/MA27132A1/fr

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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/34Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
    • C07C233/35Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
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    • C07C233/34Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
    • C07C233/35Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/40Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07C2602/00Systems containing two condensed rings
    • C07C2602/02Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04One of the condensed rings being a six-membered aromatic ring
    • C07C2602/10One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline

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Abstract

Sont exposés les composés de la formule (I): utile dans le traitement de la maladie d'Aizheimer et d'autres maladies semblables. Ces composés incluent des inhibiteurs de l'enzyme bêta-sécrétase, utiles dans le traitement de la maladie d'Alzheimer et d'autres maladies caractérisées par le dépôt du peptide A bêta chez le mammifère. Les composés inventés sont utiles dans les compositions pharmaceutiques et les méthodes de traitement pour réduire la formation du peptide A bêta.
MA27510A 2001-07-11 2004-02-04 Composes de n-(3-amino-2hydroxy-propyl)alkylamide substitues MA27132A1 (fr)

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US30452501P 2001-07-11 2001-07-11
US30875601P 2001-07-30 2001-07-30
US34141601P 2001-12-17 2001-12-17
US34134101P 2001-12-17 2001-12-17
US38057401P 2001-12-21 2001-12-21
US34487201P 2001-12-21 2001-12-21

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HR (1) HRP20040069A2 (fr)
IL (1) IL159808A0 (fr)
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CA2453503A1 (fr) 2003-01-23
US20060194817A1 (en) 2006-08-31
BR0211119A (pt) 2005-12-13
EA200400162A1 (ru) 2005-06-30
IS7109A (is) 2004-01-12
WO2003006423A1 (fr) 2003-01-23
JP4278511B2 (ja) 2009-06-17
EP1409450B1 (fr) 2009-12-09
AP2004002952A0 (en) 2004-03-31
GEP20074221B (en) 2007-10-25
US20100048590A1 (en) 2010-02-25
RS13004A (en) 2006-10-27
TNSN04017A1 (en) 2006-06-01
HRP20040069A2 (en) 2005-02-28
CO5560553A2 (es) 2005-09-30
NZ530646A (en) 2008-01-31
EP1409450A1 (fr) 2004-04-21
OA12698A (en) 2006-06-22
ATE451348T1 (de) 2009-12-15
AU2002320490B2 (en) 2008-10-02
ZA200400243B (en) 2005-02-23
MXPA04000334A (es) 2004-09-28
PL368052A1 (en) 2005-03-21
IL159808A0 (en) 2004-06-20
DE60234696D1 (de) 2010-01-21
KR20040063110A (ko) 2004-07-12
JP2005504737A (ja) 2005-02-17
US7589094B2 (en) 2009-09-15
CN101068772A (zh) 2007-11-07
NO20040139L (no) 2004-02-26

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