MXPA06001039A - Derivados de nicotinamida utiles como inhibidores de pde4. - Google Patents
Derivados de nicotinamida utiles como inhibidores de pde4.Info
- Publication number
- MXPA06001039A MXPA06001039A MXPA06001039A MXPA06001039A MXPA06001039A MX PA06001039 A MXPA06001039 A MX PA06001039A MX PA06001039 A MXPA06001039 A MX PA06001039A MX PA06001039 A MXPA06001039 A MX PA06001039A MX PA06001039 A MXPA06001039 A MX PA06001039A
- Authority
- MX
- Mexico
- Prior art keywords
- pde4 inhibitors
- nicotinamide derivatives
- derivatives useful
- derivatives
- nicotinamide
- Prior art date
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- 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
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Abstract
Esta invencion se refiere a derivados de nicotinamida de formula (I) y a procedimientos para la preparacion de, a intermedios usados en la preparacion de, a composiciones farmaceuticas que contienen, y a los usos de tales derivados: (ver Formula (I)) en la que R1 se selecciona entre el grupo compuesto por hidrogeno, metilo o halo; R7 se une a la posicion 3 o 4 del anillo fenilo y es S(O)pR8, R8 es alquilo (C1-C4) opcionalmente sustituido con cicloalquilo (C3-C6); p es 0, 1 o 2; R6 se selecciona entre el grupo compuesto por hidrogeno, halo, alquilo (C1-C3) y alcoxi (C1-C3); m es 0 o 1; L es un anillo carbociclico (C3-C8) no aromatico; R2 es hidrogeno, hidroxi, alcoxi (C1-C3), alquilo (C1-C3) (opcionalmente sustituido con hidroxi o con alcoxi (C1-C3)), CO2R9, NR10R11 o CONR10R11; R3 es hidrogeno o alquilo (C1-C3); R9 es hidrogeno o alquilo (C1-C3), cada uno de R10 y R11 es independiente hidrogeno, o se selecciona entre el grupo compuesto por: alquilo (C1-C6) opcionalmente sustituido con fenilo o un anillo heterociclico de 5 o 6 miembros que tiene de 1 a 3 heteroatomo(s) seleccionados independientemente entre N, O y S, donde el fenilo esta opcionalmente sustituido con uno o mas sustituyentes seleccionados entre hidroxi, halo, alquilo (C1-C3) o alcoxi (C1-C3) y donde el anillo heterociclico esta opcionalmente sustituido con uno o mas sustituyentes seleccionados entre hidroxi, halo, alquilo (C1-C3), alcoxi (C1-C3) u oxo; cicloalquilo (C3-C8); CO(alquilo (C1-C6)) opcionalmente sustituido con hidroxi, halo, cicloalquilo (C3-C8), alcoxi (C1-C3), fenilo o un anillo heterociclico que tiene 5 o 6 miembros que incluye de 1 a 3 heteroatomo(s) seleccionados independientemente entre N, O y S, donde el fenilo esta opcionalmente sustituido con uno o mas sustituyentes seleccionados entre hidroxi, halo, alquilo (C1-C3) o alcoxi (C1-C3) y donde el anillo heterociclico esta opcionalmente sustituido con uno o mas sustituyentes seleccionados entre hidroxi, halo, alquilo (C1-C3), alcoxi (C1-C3) u oxo; CO(R12), donde R12 es cicloalquilo (C3-C8) opcionalmente sustituido con alquilo (C1-C3) o R12 es fenilo o un anillo heterociclico de 5 o 6 miembros que tiene de 1 a 3 heteroatomo(s) seleccionados independientemente entre N, O y S, donde el fenilo esta opcionalmente sustituido con uno o mas sustituyentes seleccionados entre hidroxi, halo, alquilo (C1-C3) o alcoxi (C1-C3) y donde el anillo heterociclico esta opcionalmente sustituido con uno o mas sustituyentes seleccionados entre hidroxi, halo, alquilo (C1-C3), alcoxi (C1-C3) u oxo; y CO2-(alquilo (C1-C3)); o R10 y R11 se toman junto con el atomo de N al que estan unidos para formar una lactama de 5 o 6 miembros.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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GBGB0317516.3A GB0317516D0 (en) | 2003-07-25 | 2003-07-25 | Nicotinamide derivatives useful as PDE4 inhibitors |
PCT/IB2004/002379 WO2005009966A1 (en) | 2003-07-25 | 2004-07-13 | Nicotinamide derivatives useful as pde4 inhibitors |
Publications (1)
Publication Number | Publication Date |
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MXPA06001039A true MXPA06001039A (es) | 2006-04-11 |
Family
ID=27772741
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MXPA06001039A MXPA06001039A (es) | 2003-07-25 | 2004-07-13 | Derivados de nicotinamida utiles como inhibidores de pde4. |
Country Status (8)
Country | Link |
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US (1) | US7141586B2 (es) |
EP (1) | EP1651609A1 (es) |
JP (1) | JP2006528660A (es) |
BR (1) | BRPI0412903A (es) |
CA (1) | CA2534262A1 (es) |
GB (1) | GB0317516D0 (es) |
MX (1) | MXPA06001039A (es) |
WO (1) | WO2005009966A1 (es) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
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DE60317466T2 (de) * | 2002-02-11 | 2008-03-06 | Pfizer Inc. | Nicotinamidderivate, die als PDE4--Inhibitoren einsetzbar sind |
AR049384A1 (es) | 2004-05-24 | 2006-07-26 | Glaxo Group Ltd | Derivados de purina |
GB0514809D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
BRPI0617673C1 (pt) * | 2005-10-19 | 2012-05-22 | Ranbaxy Lab Ltd | composições de inibidores de fosfodiesterase do tipo iv |
TWI498115B (zh) * | 2007-12-27 | 2015-09-01 | Daiichi Sankyo Co Ltd | 咪唑羰基化合物 |
US8273774B2 (en) | 2008-05-27 | 2012-09-25 | Astrazeneca Ab | Phenoxypyridinylamide compounds |
EP2397482A1 (en) | 2010-06-15 | 2011-12-21 | Almirall, S.A. | Heteroaryl imidazolone derivatives as jak inhibitors |
JP2014001199A (ja) * | 2012-01-25 | 2014-01-09 | Ishihara Sangyo Kaisha Ltd | 有害生物防除剤 |
WO2013161980A1 (ja) * | 2012-04-27 | 2013-10-31 | 東レ株式会社 | シクロヘキサンジアミド誘導体及びその医薬用途 |
EA201790317A1 (ru) | 2014-09-10 | 2018-07-31 | Эпизим, Инк. | Ингибиторы smyd |
US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
CA3128468A1 (en) | 2017-10-05 | 2019-04-11 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce dux4 and downstream gene expression for the treatment of fshd |
WO2023119230A1 (en) | 2021-12-22 | 2023-06-29 | L'oreal | Coagulation pathway and nicotinamide-adenine dinucleotide pathway modulating compositions and methods of their use |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EA003528B1 (ru) | 1997-04-04 | 2003-06-26 | Пфайзер Продактс Инк. | Производные никотинамида, их применение, фармацевтическая композиция, способ лечения и способ ингибирования изоферментов фдэ4 d |
US20020111495A1 (en) * | 1997-04-04 | 2002-08-15 | Pfizer Inc. | Nicotinamide acids, amides, and their mimetics active as inhibitors of PDE4 isozymes |
BR0107964A (pt) | 2000-01-31 | 2002-10-29 | Pfizer Prod Inc | Derivados de nicotinamida benzofundida com heterociclica úteis como inibidores seletivos de isozimas pde4 |
DE60103976T2 (de) | 2000-01-31 | 2005-07-21 | Pfizer Products Inc., Groton | Pyrimidinylcarboxamiden als inhibitoren der pde4 isoenzyme |
MXPA03006886A (es) * | 2001-01-31 | 2003-11-13 | Pfizer Prod Inc | Derivados amida de acido tiazolilico, oxazolilico, pirrolilico e imidazolilico utiles como inhibidores de las isozimas pde4. |
SK8792003A3 (en) * | 2001-01-31 | 2004-09-08 | Pfizer Prod Inc | Nicotinamide biaryl derivatives useful as inhibitors of PDE4 isozymes and pharmaceutical composition containing them |
ATE305467T1 (de) * | 2001-01-31 | 2005-10-15 | Pfizer Prod Inc | Als inhibitoren von pde4-isozymen geeignete etherderivate |
DE60317466T2 (de) * | 2002-02-11 | 2008-03-06 | Pfizer Inc. | Nicotinamidderivate, die als PDE4--Inhibitoren einsetzbar sind |
GB0203193D0 (en) * | 2002-02-11 | 2002-03-27 | Pfizer Ltd | Nicotinamide derivatives useful as pde4 inhibitors |
-
2003
- 2003-07-25 GB GBGB0317516.3A patent/GB0317516D0/en not_active Ceased
-
2004
- 2004-07-13 MX MXPA06001039A patent/MXPA06001039A/es not_active Application Discontinuation
- 2004-07-13 BR BRPI0412903-2A patent/BRPI0412903A/pt not_active IP Right Cessation
- 2004-07-13 WO PCT/IB2004/002379 patent/WO2005009966A1/en not_active Application Discontinuation
- 2004-07-13 EP EP04744037A patent/EP1651609A1/en not_active Withdrawn
- 2004-07-13 CA CA002534262A patent/CA2534262A1/en not_active Abandoned
- 2004-07-13 JP JP2006521686A patent/JP2006528660A/ja active Pending
- 2004-07-20 US US10/896,315 patent/US7141586B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US7141586B2 (en) | 2006-11-28 |
WO2005009966A1 (en) | 2005-02-03 |
BRPI0412903A (pt) | 2006-09-26 |
GB0317516D0 (en) | 2003-08-27 |
US20050032838A1 (en) | 2005-02-10 |
CA2534262A1 (en) | 2005-02-03 |
EP1651609A1 (en) | 2006-05-03 |
JP2006528660A (ja) | 2006-12-21 |
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