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MA26721A1 - Derives de 2-aminopyridine nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant - Google Patents

Derives de 2-aminopyridine nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant

Info

Publication number
MA26721A1
MA26721A1 MA25912A MA25912A MA26721A1 MA 26721 A1 MA26721 A1 MA 26721A1 MA 25912 A MA25912 A MA 25912A MA 25912 A MA25912 A MA 25912A MA 26721 A1 MA26721 A1 MA 26721A1
Authority
MA
Morocco
Prior art keywords
preparation
pharmaceutical compositions
compositions containing
novel
aminopyridine derivatives
Prior art date
Application number
MA25912A
Other languages
English (en)
Inventor
Adams Lowe John Iii
Original Assignee
Pfizer Prod 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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of MA26721A1 publication Critical patent/MA26721A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/73—Unsubstituted amino or imino radicals
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A—HUMAN NECESSITIES
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    • A—HUMAN NECESSITIES
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    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Addiction (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Dermatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Ophthalmology & Optometry (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Oncology (AREA)
  • Obesity (AREA)
  • Vascular Medicine (AREA)
  • Otolaryngology (AREA)
  • Psychology (AREA)
  • Communicable Diseases (AREA)
  • Immunology (AREA)

Abstract

L'INVENTION CONCERNE DES DÉRIVÉS DE 2-AMINOPYRIDINE DE FORMULE 1 : DANS LAQUELLE A, B, X, Y ET R1 REPRÉSENTENT DIVERS RADICAUX. ELLE CONCERNE ÉGALEMENT UN PROCÉDÉ POUR LEUR PRÉPARATION ET DES COMPOSITIONS PHARMACEUTIQUES LES CONTENANT. APPLICATION : UTILISATION DE CES COMPOSÉS ET COMPOSITIONS, INHIBANT L'ACTIVITÉ DES OXYDE NITRIQUES-SYNTHASES (NOS) , POUR LE TRAITEMENT DE DIVERSES MALADIES, NOTAMMENT DU SYSTèME NERVEUX CENTRAL.
MA25912A 1999-02-25 2000-02-23 Derives de 2-aminopyridine nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant MA26721A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US12159799P 1999-02-25 1999-02-25

Publications (1)

Publication Number Publication Date
MA26721A1 true MA26721A1 (fr) 2004-12-20

Family

ID=22397690

Family Applications (1)

Application Number Title Priority Date Filing Date
MA25912A MA26721A1 (fr) 1999-02-25 2000-02-23 Derives de 2-aminopyridine nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant

Country Status (44)

Country Link
US (2) US6211208B1 (fr)
EP (1) EP1155000B1 (fr)
JP (1) JP3825636B2 (fr)
KR (1) KR20010114213A (fr)
CN (1) CN1341099A (fr)
AP (1) AP2001002251A0 (fr)
AR (1) AR018979A1 (fr)
AT (1) ATE245143T1 (fr)
AU (1) AU767593B2 (fr)
BG (1) BG105855A (fr)
BR (1) BR0008569A (fr)
CA (1) CA2364719C (fr)
CO (1) CO5160241A1 (fr)
CR (1) CR6438A (fr)
CZ (1) CZ20013036A3 (fr)
DE (1) DE60003893T2 (fr)
DK (1) DK1155000T3 (fr)
DZ (1) DZ3017A1 (fr)
EA (1) EA003941B1 (fr)
EE (1) EE200100454A (fr)
ES (1) ES2200813T3 (fr)
GT (1) GT200000021A (fr)
HN (1) HN2000000016A (fr)
HR (1) HRP20010597A2 (fr)
HU (1) HUP0200163A3 (fr)
ID (1) ID29892A (fr)
IL (1) IL144308A0 (fr)
IS (1) IS6005A (fr)
MA (1) MA26721A1 (fr)
MX (1) MXPA01008671A (fr)
NO (1) NO20014095L (fr)
NZ (1) NZ512912A (fr)
OA (1) OA11841A (fr)
PA (1) PA8490901A1 (fr)
PE (1) PE20001482A1 (fr)
PL (1) PL350219A1 (fr)
PT (1) PT1155000E (fr)
SK (1) SK12022001A3 (fr)
SV (1) SV2002000026A (fr)
TN (1) TNSN00034A1 (fr)
TR (1) TR200102481T2 (fr)
WO (1) WO2000050400A1 (fr)
YU (1) YU58301A (fr)
ZA (1) ZA200106974B (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20010049379A1 (en) * 1997-08-27 2001-12-06 Lowe John Adams 2-aminopyridines containing fused ring substituents
AP2001002251A0 (en) * 1999-02-25 2001-09-30 Pfizer Prod Inc 2-aminopyridines containing fused ring substituents.
EP1268427A1 (fr) 2000-03-31 2003-01-02 Cocensys, Inc. Aminopyridines et leur utilisation en tant qu'anticonvulsants et inhibiteurs du canal sodium
US20040092741A1 (en) * 2002-11-08 2004-05-13 Pfizer Inc Substituted pyridines via boronic acid coupling
US8729107B2 (en) * 2002-12-06 2014-05-20 Purdue Research Foundation Pyridines for treating injured mammalian nerve tissue
JP4903385B2 (ja) * 2002-12-06 2012-03-28 パーデュー・リサーチ・ファウンデーション 損傷した哺乳類神経組織を治療するためのピリジン類
US20050192321A1 (en) * 2003-09-15 2005-09-01 Meythaler Jay M. Treatment of neuropathy with rapid release aminopyridine
US9120750B2 (en) 2013-03-07 2015-09-01 Northwestern University 2-Aminopyridine-based selective neuronal nitric oxide synthase inhibitors
US10759791B2 (en) 2014-11-04 2020-09-01 Northwestern University Mammalian and bacterial nitric oxide synthase inhibitors
WO2016073623A2 (fr) 2014-11-04 2016-05-12 Northwestern University Inhibiteurs d'oxyde nitrique synthase d'origine bactérienne et mammalienne
US9585867B2 (en) 2015-08-06 2017-03-07 Charles Everett Ankner Cannabinod formulation for the sedation of a human or animal
US12213973B2 (en) 2021-10-18 2025-02-04 Northwestern University Bacterial nitric oxide synthase inhibitors

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU4515696A (en) * 1994-12-12 1996-07-03 Merck & Co., Inc. Substituted 2-aminopyridines as inhibitors of nitric oxide synthase
JPH101435A (ja) * 1995-09-14 1998-01-06 Nippon Kayaku Co Ltd ２−アミノピリジン類を有効成分とする一酸化窒素合成酵素阻害剤
EA002270B1 (ru) * 1996-03-29 2002-02-28 Пфайзер Инк. Производные 6-фенилпиридил-2-амина
HN1997000027A (es) 1996-12-06 1997-06-05 Pfizer Prod Inc Derivados de 6-fenil piridil - 2 amina
TR199901917T2 (xx) * 1997-02-10 1999-12-21 Pfizer Products Inc. 2-Amino-6-(2-ikame edilmi�-4-fenoksi)-ikame edilmi� piridinler
HN1998000118A (es) * 1997-08-27 1999-02-09 Pfizer Prod Inc 2 - aminopiridinas que contienen sustituyentes de anillos condensados.
HN1998000125A (es) * 1997-08-28 1999-02-09 Pfizer Prod Inc 2-aminopiridinas con sustituyentes alcoxi ramificados
AU765851B2 (en) * 1998-06-03 2003-10-02 Pfizer Products Inc. 2-aminopyridines containing fused ring substituents as nitric oxide synthase inhibitors
AP2001002251A0 (en) * 1999-02-25 2001-09-30 Pfizer Prod Inc 2-aminopyridines containing fused ring substituents.

Also Published As

Publication number Publication date
JP2002537381A (ja) 2002-11-05
DE60003893D1 (de) 2003-08-21
IL144308A0 (en) 2002-05-23
HUP0200163A2 (en) 2002-06-29
ATE245143T1 (de) 2003-08-15
NO20014095D0 (no) 2001-08-23
US6372768B2 (en) 2002-04-16
IS6005A (is) 2001-07-13
HN2000000016A (es) 2001-02-02
HRP20010597A2 (en) 2002-08-31
KR20010114213A (ko) 2001-12-31
AU2124300A (en) 2000-09-14
PE20001482A1 (es) 2001-01-03
EA003941B1 (ru) 2003-10-30
CN1341099A (zh) 2002-03-20
CZ20013036A3 (cs) 2002-03-13
PL350219A1 (en) 2002-11-18
TNSN00034A1 (fr) 2005-11-10
GT200000021A (es) 2001-08-17
DK1155000T3 (da) 2003-10-13
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