PE20030416A1 - 1,8-naftiridin-4(1h)-onas alquin aril sustituidas como inhibidores de fosfodiesterasa-4 - Google Patents
1,8-naftiridin-4(1h)-onas alquin aril sustituidas como inhibidores de fosfodiesterasa-4Info
- Publication number
- PE20030416A1 PE20030416A1 PE2002000819A PE2002000819A PE20030416A1 PE 20030416 A1 PE20030416 A1 PE 20030416A1 PE 2002000819 A PE2002000819 A PE 2002000819A PE 2002000819 A PE2002000819 A PE 2002000819A PE 20030416 A1 PE20030416 A1 PE 20030416A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- phenyl
- naphthyridin
- pyridinyletinyl
- ona
- Prior art date
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- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- 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
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Animal Behavior & Ethology (AREA)
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- Communicable Diseases (AREA)
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- Psychiatry (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
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- Transplantation (AREA)
- Diabetes (AREA)
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- Ophthalmology & Optometry (AREA)
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Abstract
SE REFIERE A 1,8-NAFTIRIDIN-4(1H)-ONAS ALQUIN ARIL SUSTITUIDAS DE FORMULA I, DONDE R ES H, ALQUILO C1-C6, CICLOALQUILO C3-C6; R1 ES H, ALQUILO C1-C6, CICLOALQUILO C3-C6, ALCOXI C1-C6, ALQUENILO C2-C6, ENTRE OTROS; R2 ESTA AUSENTE, H, HALOGENO, ALQUILO C1-C6, CICLOALQUILO C3-C6, FENILO, HETEROARILO, ENTRE OTROS; R3 ESTA AUSENTE, H, OH, N-(ALQUIL C0-C6)(ALQUILO C0-C6), HALOGENO, ENTRE OTROS; R4, R5, R6, R7 SON H, HALOGENO, ALQUILO C1-C6-ALCOXI C1-C6, SOn(ALQUILO C1-C6), NITRO, CN, ENTRE OTROS; R8 ES FENILO, PIRIDILO, PIRIMIDILO, INDOLILO, QUINOLILO, TIENILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS N-ISOPROPIL-1-[3-(2-PIRIDINILETINIL)FENIL]-1,4-DIHIDRO[1,8]NAFTIRIDIN-4-ONA-3-CARBOXAMIDA; N-CICLOPROPIL-1-[3-(3-PIRIDINILETINIL)FENIL]-1,4-DIHIDRO[1,8]NAFTIRIDIN-4-ONA-3-CARBOXAMIDA; N-ISOPROPIL-1-[3-(3-PIRIDINILOETINIL)FENIL]-1,4-DIHIDRO[1,8]NAFTIRIDIN-4-ONA-3-CARBOXAMIDA; ENTRE OTROS. LA COMPOSICION QUE COMPRENDE ADEMAS UN ANTAGONISTA DEL RECEPTOR DE LEUCOTRIENO, INHIBIDOR DE SINTESIS DE LEUCOTRIENO, ANTAGONISTA DE M2/M3, CORTICOSTEROIDE, ANTAGONISTA DE RECEPTOR H1, AGONISTA DE RECEPTOR BETA-2-ADRENERGICO, INHIBIDOR COX2, ESTATINA, FAINE. LOS COMPUESTOS SON INHIBIDORES DE FOSFODIESTERASA 4 Y PUEDEN SER UTILES PARA TRATAMIENTO DE ASMA, BRONQUITIS CRONICA, ENFERMEDAD PULMONAR OBSTRUCTIVA CRONICA, SINDROME DISNEICO AGUDO DEL ADULTO, TOS, ENFERMEDAD PULMONAR OBSTRUCTIVA CRONICA, RINITIS ALERGICA, DEPRESION
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31609301P | 2001-08-29 | 2001-08-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20030416A1 true PE20030416A1 (es) | 2003-05-15 |
Family
ID=23227432
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2002000819A PE20030416A1 (es) | 2001-08-29 | 2002-08-26 | 1,8-naftiridin-4(1h)-onas alquin aril sustituidas como inhibidores de fosfodiesterasa-4 |
Country Status (28)
Country | Link |
---|---|
US (2) | US6743802B2 (es) |
EP (2) | EP1436290B8 (es) |
JP (1) | JP4157035B2 (es) |
KR (1) | KR100928849B1 (es) |
CN (1) | CN100338061C (es) |
AR (1) | AR036365A1 (es) |
AU (1) | AU2002322940B2 (es) |
BR (1) | BR0212042A (es) |
CA (1) | CA2456817C (es) |
DO (1) | DOP2002000456A (es) |
EA (1) | EA006800B1 (es) |
EC (1) | ECSP044992A (es) |
GE (1) | GEP20063805B (es) |
HK (1) | HK1080073B (es) |
HR (1) | HRP20040151A2 (es) |
HU (1) | HUP0401729A3 (es) |
IL (1) | IL160213A0 (es) |
IS (1) | IS7138A (es) |
JO (1) | JO2311B1 (es) |
MX (1) | MXPA04001889A (es) |
NO (1) | NO330521B1 (es) |
NZ (1) | NZ530931A (es) |
PE (1) | PE20030416A1 (es) |
PL (1) | PL367716A1 (es) |
RS (1) | RS17004A (es) |
UA (1) | UA75957C2 (es) |
WO (1) | WO2003018579A1 (es) |
ZA (1) | ZA200400952B (es) |
Families Citing this family (49)
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JO2311B1 (en) * | 2001-08-29 | 2005-09-12 | ميرك فروست كندا ليمتد | Alkyl inhibitors Ariel phosphodiesterase-4 |
US7452911B2 (en) | 2002-10-31 | 2008-11-18 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds |
US7351719B2 (en) | 2002-10-31 | 2008-04-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Amide compounds having MCH-antagonistic activity and medicaments comprising these compounds |
DE10250708A1 (de) * | 2002-10-31 | 2004-05-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel |
AU2003291418A1 (en) * | 2002-11-15 | 2004-06-15 | Merck And Co., Inc. | Use of pde4 inhibitors as adjunct therapy for psychiatric disorders |
AR042194A1 (es) * | 2002-11-22 | 2005-06-15 | Merck & Co Inc | Metodo para preparar inhibidores de fosfodiesterasa - 4 |
WO2004047836A1 (en) * | 2002-11-22 | 2004-06-10 | Merck Frosst Canada & Co. | Use of phosphodiesterase-4 inhibitors as enhancers of cognition |
GB0307863D0 (en) * | 2003-04-04 | 2003-05-14 | Merck Sharp & Dohme | Therapeutic treatment |
GB0322726D0 (en) * | 2003-09-27 | 2003-10-29 | Glaxo Group Ltd | Compounds |
GB0322722D0 (en) * | 2003-09-27 | 2003-10-29 | Glaxo Group Ltd | Compounds |
US7592373B2 (en) | 2003-12-23 | 2009-09-22 | Boehringer Ingelheim International Gmbh | Amide compounds with MCH antagonistic activity and medicaments comprising these compounds |
US7524862B2 (en) | 2004-04-14 | 2009-04-28 | Boehringer Ingelheim International Gmbh | Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds |
DE102004017930A1 (de) * | 2004-04-14 | 2005-11-03 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel |
DE102004017934A1 (de) | 2004-04-14 | 2005-11-03 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel |
US20080119509A1 (en) * | 2004-04-26 | 2008-05-22 | Sophie-Dorothee Clas | Altenrative Forms Of The Phosphodeisterase -4 Inhibitor N-Cyclopropyl-1- -3{3-[(1-Oxidopyryidin-3-Yl) Phenyl]-4-Oxo-1,4-Dihydro-1,8-Naphthyridine-3-Carboxyamide |
JP4264388B2 (ja) * | 2004-07-01 | 2009-05-13 | 富士通株式会社 | 半導体チップの接合方法および接合装置 |
WO2006004191A1 (en) * | 2004-07-05 | 2006-01-12 | Astellas Pharma Inc. | Pyrrolopyridazine derivatives which inhibit pde iv and tnf alfa |
US7687490B2 (en) * | 2005-04-12 | 2010-03-30 | Meiji Seika Kaisha, Ltd. | 2-thioethenyl substituted carbapenem derivatives |
JP2006016407A (ja) * | 2005-06-15 | 2006-01-19 | Yamaha Motor Co Ltd | ホスホジエステラーゼ阻害剤 |
EP2258358A3 (en) | 2005-08-26 | 2011-09-07 | Braincells, Inc. | Neurogenesis with acetylcholinesterase inhibitor |
EP2275095A3 (en) | 2005-08-26 | 2011-08-17 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
JP2009509980A (ja) * | 2005-09-28 | 2009-03-12 | メルク フロスト カナダ リミテツド | 篩分けされたラクトースを含むエアゾール粉末製剤 |
JP2009512711A (ja) | 2005-10-21 | 2009-03-26 | ブレインセルス,インコーポレイティド | Pde阻害による神経新生の調節 |
CA2625210A1 (en) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
EP1963321A2 (en) | 2005-12-13 | 2008-09-03 | Wyeth a Corporation of the State of Delaware | Dibenzonaphthyridine derivatives and methods of use thereof |
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AU2007249435A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | 5 HT receptor mediated neurogenesis |
WO2007134136A2 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
KR20090064418A (ko) | 2006-09-08 | 2009-06-18 | 브레인셀즈 인코퍼레이션 | 4-아실아미노피리딘 유도체 포함 조합물 |
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EP2170065A4 (en) | 2007-06-20 | 2011-11-23 | Merck Sharp & Dohme | DIPHENYL SUBSTITUTED ALKANES |
CA2701956A1 (en) * | 2007-10-25 | 2009-04-30 | Merck Frosst Canada Ltd. | Combination therapy |
US8461389B2 (en) | 2008-04-18 | 2013-06-11 | University College Dublin, National University Of Ireland, Dublin | Psycho-pharmaceuticals |
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