AR037233A1 - Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento - Google Patents
Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamentoInfo
- Publication number
- AR037233A1 AR037233A1 ARP020103213A ARP020103213A AR037233A1 AR 037233 A1 AR037233 A1 AR 037233A1 AR P020103213 A ARP020103213 A AR P020103213A AR P020103213 A ARP020103213 A AR P020103213A AR 037233 A1 AR037233 A1 AR 037233A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- group
- alkyl
- formula
- hydrogen
- Prior art date
Links
Classifications
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- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
- A61P23/02—Local anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- 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
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- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/14—Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
- Y10T436/145555—Hetero-N
Abstract
Un compuesto piridina aril sustituida que tiene la fórmula (1), o una sal, profármaco o solvato farmacéuticamente aceptable del mismo, en donde: Ar se selecciona entre el grupo que consiste en Ar1, Ar2, Ar3 y Ar4, en donde; Ar1 es de fórmula (2); Ar2 es de fórmula (3); Ar3 es de fórmula (4); Ar5 es de fórmula(5);R1 se selecciona entre el grupo que consiste en un alquilo opcionalmente sustituido, amino, alquiltiol, C(O)R10, SO2R10, OC(O)NH2, 2-imidazolinilo, 2-imidazolilo, 3-pirazolilo, 5-isoxazolilo y 3-(1,2,4)-triazolilo; R2, R3 y R4 se selecciona en forma independiente entre el grupo que consiste en hidrógeno, alquilo, alquenilo o alquinilo opcionalmente sustituido, halógeno, hidroxi, cicloalquilo, ciano, amino, alquilamino, dialquilamino, alcoxi, aminocarbonilo, alquilaminocarbonilo, arilaminocarbonilo, aralquilaminocarbonilo, alquilcarbonilamino, arilcarbonilamino y aralquilcarbonilamino; siempre y cuando que 1) el anillo piridilo no sea 2,6-disustituido con respecto a Ar y R1, o cualquiera de R2-R4 que no es hidrógeno; y 2) cuando Ar es Ar2 o Ar3, entonces R1 es C(O)R10; 3) cuando Ar es Ar4, entonces R1 es aminocarbonilo o un heterocicloalquilaminocarbonilo opcionalmente sustituido; R5, R6, R7 y R8 se seleccionan en forma independiente entre el grupo que consiste en hidrógeno, alquilo, alquenilo, alquinilo, halógeno, haloalquilo, hidroxialquilo, hidroxi, nitro, amino, ciano, amida, carboxialquilo, alcoxialquilo, ureído, acilamino, tiol, aciloxi, azido, alcoxi, carboxi, carbonilamido y alquiltiol; R9 es un alquilo opcionalmente sustituido; R10 se selecciona entre el grupo que consiste en alquilo, alquenilo, alquinilo, OR11, amino, alquilamino, dialquilamino, alquenilamino, dialquilaminoalquenilo, dialquilaminoalquilamino, dialquilaminoalquenilamino, alquilaminoalquenilamino, hidroxiaminoalquenilamino, cicloalquilo, heterocicloalquilo, cicloalquilalquilamino, heterocicloalquilamino, arilo, arilalquilo, arialquenilo, arilalquinilo y arilalquilamino, todos los cuales pueden ser opcionalmente sustituidos, siempre y cuando que R10 no sea OR11 cuando R1 es SO2R10; en donde R11 se selecciona entre el grupo que consiste en hidrógeno, alquilo, opcionalmente sustituido y un metal alcalino; y X es uno de O, S, NH, o CH2 cuando Ar es Ar1; o X es una de O, S, NH, o está ausente (un enlace covalente) cuando Ar es Ar4, con las condiciones de que : 4) cuando Ar es Ar1, X es O, R5, R6 y R7 es cada uno hidrógeno, y R1 es un grupo alquilo, entonces R8 no es un grupo alcoxi opcionalmente sustituido; y 5) cuando Ar es Ar4, y X es O ó está ausente y R1 es aminocarbonilo, entonces R9 no es grupo alquilo de cadena recta opcionalmente monosustituido con halógeno, carboxi, alcoxi, un fenilo opcionalmente sustituido, o un aminocarbonilo opcionalmente sustituido. Además está dirigida a composiciones farmacéuticas y al uso de compuestos de la fórmula (1) para la elaboración de medicamentos para el tratamiento de dano neuronal como consecuencia de isquemia global y focal, para el tratamiento o prevención de condiciones neurodegenerativas tales como esclerosis lateral amiotrófica (ELA) y para el tratamiento, prevención o mejoría tanto de dolor agudo como crónico, como agentes antitinnitus, como anticonvulsivos, y como depresivos antimaníacos, como anestésicos locales, como antiarrítmicos y para el tratamiento o prevención de neuropatía diabética.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31752601P | 2001-09-07 | 2001-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR037233A1 true AR037233A1 (es) | 2004-11-03 |
Family
ID=23234074
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP020103213A AR037233A1 (es) | 2001-09-07 | 2002-08-27 | Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento |
Country Status (12)
Country | Link |
---|---|
US (3) | US7105549B2 (es) |
EP (1) | EP1432419A1 (es) |
JP (1) | JP2005506981A (es) |
KR (1) | KR20040031053A (es) |
AR (1) | AR037233A1 (es) |
BR (1) | BR0212338A (es) |
CA (1) | CA2459527A1 (es) |
HU (1) | HUP0500131A3 (es) |
IL (1) | IL160716A0 (es) |
MX (1) | MXPA04002171A (es) |
RU (1) | RU2004110721A (es) |
WO (1) | WO2003022276A1 (es) |
Families Citing this family (61)
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AR037233A1 (es) * | 2001-09-07 | 2004-11-03 | Euro Celtique Sa | Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento |
GB0124939D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
GB0124934D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
GB0124931D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
GB0124938D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
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-
2002
- 2002-08-27 AR ARP020103213A patent/AR037233A1/es unknown
- 2002-09-06 EP EP02773292A patent/EP1432419A1/en not_active Withdrawn
- 2002-09-06 HU HU0500131A patent/HUP0500131A3/hu unknown
- 2002-09-06 BR BR0212338-0A patent/BR0212338A/pt active Pending
- 2002-09-06 US US10/235,673 patent/US7105549B2/en not_active Expired - Lifetime
- 2002-09-06 RU RU2004110721/04A patent/RU2004110721A/ru not_active Application Discontinuation
- 2002-09-06 CA CA002459527A patent/CA2459527A1/en not_active Abandoned
- 2002-09-06 KR KR10-2004-7003314A patent/KR20040031053A/ko not_active Application Discontinuation
- 2002-09-06 MX MXPA04002171A patent/MXPA04002171A/es unknown
- 2002-09-06 JP JP2003526405A patent/JP2005506981A/ja not_active Withdrawn
- 2002-09-06 IL IL16071602A patent/IL160716A0/xx unknown
- 2002-09-06 WO PCT/US2002/028298 patent/WO2003022276A1/en not_active Application Discontinuation
-
2006
- 2006-09-11 US US11/518,448 patent/US7579367B2/en not_active Expired - Fee Related
-
2009
- 2009-08-24 US US12/546,572 patent/US7943643B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2005506981A (ja) | 2005-03-10 |
CA2459527A1 (en) | 2003-03-20 |
HUP0500131A3 (en) | 2005-07-28 |
US20070010554A1 (en) | 2007-01-11 |
EP1432419A1 (en) | 2004-06-30 |
US7579367B2 (en) | 2009-08-25 |
US20030055088A1 (en) | 2003-03-20 |
WO2003022276A1 (en) | 2003-03-20 |
US7943643B2 (en) | 2011-05-17 |
BR0212338A (pt) | 2004-09-21 |
US20100048626A1 (en) | 2010-02-25 |
MXPA04002171A (es) | 2004-07-23 |
US20080194627A9 (en) | 2008-08-14 |
HUP0500131A2 (hu) | 2005-05-30 |
IL160716A0 (en) | 2004-08-31 |
RU2004110721A (ru) | 2005-10-10 |
US7105549B2 (en) | 2006-09-12 |
KR20040031053A (ko) | 2004-04-09 |
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