ES2341813T3 - 4-bencil-1 (2h)-ftalazinonas como antagonistas del receptor h1. - Google Patents

4-bencil-1 (2h)-ftalazinonas como antagonistas del receptor h1. Download PDF

Info

Publication number
ES2341813T3
ES2341813T3 ES07857765T ES07857765T ES2341813T3 ES 2341813 T3 ES2341813 T3 ES 2341813T3 ES 07857765 T ES07857765 T ES 07857765T ES 07857765 T ES07857765 T ES 07857765T ES 2341813 T3 ES2341813 T3 ES 2341813T3
Authority
ES
Spain
Prior art keywords
methyl
quad
chlorophenyl
pyrrolidinyl
oxo
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
ES07857765T
Other languages
English (en)
Spanish (es)
Inventor
Paul Martin Gore
Michael Joachim Kranz
Brian Edgar Looker
Sadie Vile
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Glaxo Group Ltd
Original Assignee
Glaxo Group Ltd
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 Glaxo Group Ltd filed Critical Glaxo Group Ltd
Application granted granted Critical
Publication of ES2341813T3 publication Critical patent/ES2341813T3/es
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/02Nasal agents, e.g. decongestants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/26Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
    • C07D237/30Phthalazines
    • C07D237/32Phthalazines with oxygen atoms directly attached to carbon atoms of the nitrogen-containing ring

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
ES07857765T 2006-12-20 2007-12-18 4-bencil-1 (2h)-ftalazinonas como antagonistas del receptor h1. Active ES2341813T3 (es)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US87087506P 2006-12-20 2006-12-20
US870875P 2006-12-20
US97844707P 2007-10-09 2007-10-09
US978447P 2007-10-09
US99122707P 2007-11-30 2007-11-30
US991227P 2007-11-30

Publications (1)

Publication Number Publication Date
ES2341813T3 true ES2341813T3 (es) 2010-06-28

Family

ID=39536783

Family Applications (1)

Application Number Title Priority Date Filing Date
ES07857765T Active ES2341813T3 (es) 2006-12-20 2007-12-18 4-bencil-1 (2h)-ftalazinonas como antagonistas del receptor h1.

Country Status (10)

Country Link
US (1) US20100184770A1 (enExample)
EP (1) EP2091538B1 (enExample)
JP (1) JP2010513393A (enExample)
AR (1) AR064424A1 (enExample)
AT (1) ATE459358T1 (enExample)
DE (1) DE602007005167D1 (enExample)
ES (1) ES2341813T3 (enExample)
PE (1) PE20081657A1 (enExample)
TW (1) TW200831493A (enExample)
WO (1) WO2008074803A2 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090042879A1 (en) * 2005-04-21 2009-02-12 Nippon Shinyaku Co., Ltd. Phthalazinone derivatives and pharmaceutical compositions comprising the same
US8466150B2 (en) 2006-12-28 2013-06-18 Abbott Laboratories Inhibitors of poly(ADP-ribose)polymerase
PH12012501544A1 (en) * 2006-12-28 2024-06-03 Abbvie Inc Inhibitors of poly (adp-ribose) polymerase
ATE525370T1 (de) * 2007-10-11 2011-10-15 Glaxo Group Ltd Phthalazin- und pyridoä3,4- düpyridazinverbindungen als h1-rezeptor- antagonisten
WO2009150101A1 (en) * 2008-06-09 2009-12-17 Glaxo Group Limited Pharmaceutical compositions comprising n-[2-((2r)-2-{[4-[(4-chlorophenyl)methyl]-l-oxo-2(ih)-phthalaz inyl]methyl}-l- pyrrolidinyl)ethyl]-4-(methyloxy)butanamide
CA2733128C (en) * 2008-08-13 2016-05-24 Boehringer Ingelheim International Gmbh Phthalazinone compounds as chymase inhibitors
WO2012045729A1 (en) 2010-10-05 2012-04-12 Glaxo Group Limited Imidazo [1, 2 -a] pyridine and pyrazolo [1, 5 -a] pyridine derivatives as trpv1 antagonists
WO2012072512A1 (en) 2010-11-29 2012-06-07 Glaxo Group Limited N-cyclobutyl-imidazopyridine or -pyrazolopyridine carboxamides as trpv1 antagonists
US8754101B2 (en) 2011-04-11 2014-06-17 Glaxo Group Limited N-cyclobutyl-imidazopyridine-methylamine as TRPV1 antagonists
JP2024521818A (ja) * 2021-05-27 2024-06-04 シュレーディンガー, インコーポレイテッド ヘテロ環式化合物およびその使用方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0222191B1 (de) * 1985-11-11 1991-01-30 ASTA Pharma AG 4-Benzyl-1-(2H)-phthalazinon-Derivate
DE3634942A1 (de) * 1985-11-11 1987-05-14 Asta Werke Ag Chem Fab Neue 4-benzyl-1-(2h)-phthalazinon-derivate
CZ199593A3 (en) * 1992-10-02 1994-04-13 Asta Medica Ag Phthalazinone derivatives exhibiting anti-arrhythmic and analgesic activity and eliminating resistance to a plurality of medicaments (mdr)
PT997474E (pt) * 1998-08-14 2004-01-30 Pfizer Agentes antitromboticos
WO2002064584A1 (en) * 2001-02-15 2002-08-22 Altana Pharma Ag Phthalayinone-piperidino-derivatives as pde4 inhibitors
TWI347845B (en) * 2002-03-06 2011-09-01 Nycomed Gmbh Pharmaceutical compositions,combinations,and kits for the treatment of respiratory diseases and use of the same
US7553841B2 (en) * 2003-03-18 2009-06-30 Merck & Co., Inc. Amino cyclobutylamide modulators of chemokine receptor activity
WO2005007644A1 (ja) * 2003-06-27 2005-01-27 Banyu Pharmaceutical Co., Ltd ヘテロアリールオキシ含窒素飽和へテロ環誘導体
US20090042879A1 (en) * 2005-04-21 2009-02-12 Nippon Shinyaku Co., Ltd. Phthalazinone derivatives and pharmaceutical compositions comprising the same
EA200801996A1 (ru) * 2006-04-20 2009-04-28 Глаксо Груп Лимитед 2-замещенные производные 4-бензилфталазинонов в качестве гистаминовых h1- и h3-антагонистов

Also Published As

Publication number Publication date
TW200831493A (en) 2008-08-01
JP2010513393A (ja) 2010-04-30
EP2091538B1 (en) 2010-03-03
ATE459358T1 (de) 2010-03-15
US20100184770A1 (en) 2010-07-22
EP2091538A2 (en) 2009-08-26
AR064424A1 (es) 2009-04-01
WO2008074803A2 (en) 2008-06-26
WO2008074803A3 (en) 2008-09-18
PE20081657A1 (es) 2008-12-23
WO2008074803A8 (en) 2009-05-14
DE602007005167D1 (de) 2010-04-15

Similar Documents

Publication Publication Date Title
ES2341813T3 (es) 4-bencil-1 (2h)-ftalazinonas como antagonistas del receptor h1.
JP4489143B2 (ja) ヒスタミンh1及びh3アンタゴニストとしての2−置換4−ベンジルフタラジノン誘導体
ES2566339T3 (es) Derivados de 4-carboxamida indazol útiles como inhibidores de PI3-quinasas
ES2543426T3 (es) Compuestos 7-(1H-pirazol-4-il)-1,6-naftiridina como inhibidores de Syk
ES2548036T3 (es) Polimorfos y sales de N-[5-[4-(5-{[(2R,6S)-2,6-dimetil-4-morfolinil]metil}-1,3-oxazol-2-il)-1H-indazol-6-il]-2-(metiloxi)-3-piridinil]metanosulfonamida
ES2241891T3 (es) Derivados de quinazolona como antagonistas de receptores adrenergicos alfa-1a/b.
EP2185542A2 (en) Substituted quinoline derivatives as h1 receptor antagonists
ES2541530T3 (es) Derivados piridinil- y piperazinil-metiloxi-arílicos útiles como inhibidores de tirosina quinasa de bazo (SYK)
US20080275027A1 (en) Piperazinone Derivatives Useful as Histamine H3 Receptor Antagonists and/or Inverse Agonists
ES2339400T3 (es) Antagonistas del receptor de histamina que comprenden un nucleo de azepina.
ES2337187T3 (es) Acido 3-(4-((4-(4-((3-(3,3-dimetil-1-piperidinil)propil(oxi)fenil)-1-piperidinilcarbonil)-1-naftalenil) propanoico o propenoico como antagonistas de receptor h1 y h3 para el tratamiento de trastornos inflamatorios y/o alergicos.
ES2369320T3 (es) Compuestos de ftalazina y pirido(3,4-d)piridazina como antagonistas del receptor h1.
ES2330472T3 (es) Compuestos.
ES2354180T3 (es) Derivados de 4-bencilftalazinona 2-sistituidos como antagonistas de las histaminas h1 y h3.
US20100222349A1 (en) Quinoline derivatives used to treat inflammatory and allergic diseases
ES2358299T3 (es) Compuestos pirrolo[2,3-b]piridin-4-il-bencenosulfonamida como inhibidores de ikk2.
MX2008008141A (es) Acido 3-(4-{[4-(4-{[3-(3,3-dimetil-1-piperidinil)propil)oxi}fenil)-1-piperidinil]carbonil}-1-naftalenil)propanoico o propenoico como antagonistas del receptor h1 y h3 para el tratamiento de discunciones inflamatorias y/o alergicas