AP2359A - Sulfonamide derivatives for the treatment of diseases. - Google Patents

Sulfonamide derivatives for the treatment of diseases.

Info

Publication number
AP2359A
AP2359A AP2006003669A AP2006003669A AP2359A AP 2359 A AP2359 A AP 2359A AP 2006003669 A AP2006003669 A AP 2006003669A AP 2006003669 A AP2006003669 A AP 2006003669A AP 2359 A AP2359 A AP 2359A
Authority
AP
ARIPO
Prior art keywords
diseases
treatment
sulfonamide derivatives
sulfonamide
derivatives
Prior art date
Application number
AP2006003669A
Other languages
English (en)
Other versions
AP2006003669A0 (en
Inventor
Alan Daniel Brown
Mark Edward Bunnage
Paul Alan Glossop
Original Assignee
Pfizer
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=36954179&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AP2359(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from GB0406387A external-priority patent/GB0406387D0/en
Application filed by Pfizer filed Critical Pfizer
Publication of AP2006003669A0 publication Critical patent/AP2006003669A0/xx
Application granted granted Critical
Publication of AP2359A publication Critical patent/AP2359A/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/08Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/18Sulfonamides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C07D217/06Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00Systems containing two condensed rings
    • C07C2602/02Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04One of the condensed rings being a six-membered aromatic ring
    • C07C2602/08One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
AP2006003669A 2004-01-22 2005-01-12 Sulfonamide derivatives for the treatment of diseases. AP2359A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP04290169 2004-01-22
GB0406387A GB0406387D0 (en) 2004-03-22 2004-03-22 Sulfonamide derivatives for the treatment of diseases
US60026004P 2004-08-09 2004-08-09
PCT/IB2005/000086 WO2005080313A2 (fr) 2004-01-22 2005-01-12 Derives de sulfonamides utilises dans le traitement de maladies

Publications (2)

Publication Number Publication Date
AP2006003669A0 AP2006003669A0 (en) 2006-06-30
AP2359A true AP2359A (en) 2012-01-30

Family

ID=36954179

Family Applications (1)

Application Number Title Priority Date Filing Date
AP2006003669A AP2359A (en) 2004-01-22 2005-01-12 Sulfonamide derivatives for the treatment of diseases.

Country Status (30)

Country Link
US (4) US7244766B2 (fr)
EP (1) EP1708991B1 (fr)
JP (1) JP4020954B2 (fr)
AP (1) AP2359A (fr)
AR (1) AR047509A1 (fr)
AT (1) ATE375977T1 (fr)
AU (1) AU2005214153B2 (fr)
BR (1) BRPI0507085A (fr)
CA (1) CA2553789C (fr)
DE (1) DE602005002930T2 (fr)
DK (1) DK1708991T3 (fr)
DO (1) DOP2005000006A (fr)
EA (1) EA011167B1 (fr)
ES (1) ES2293530T3 (fr)
GE (1) GEP20094781B (fr)
MY (1) MY143390A (fr)
NL (1) NL1028087C2 (fr)
NO (1) NO20062983L (fr)
NZ (1) NZ548318A (fr)
OA (1) OA13362A (fr)
PA (1) PA8622001A1 (fr)
PE (1) PE20051136A1 (fr)
PL (1) PL1708991T3 (fr)
PT (1) PT1708991E (fr)
RS (1) RS50561B (fr)
SI (1) SI1708991T1 (fr)
TW (1) TWI341831B (fr)
UA (1) UA84048C2 (fr)
UY (1) UY28721A1 (fr)
WO (1) WO2005080313A2 (fr)

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RS50561B (sr) * 2004-01-22 2010-05-07 Pfizer Inc. Derivati sulfonamida za lečenje bolesti
GB0425054D0 (en) * 2004-03-23 2004-12-15 Pfizer Ltd Formamide derivatives for the treatment of diseases
GT200500281A (es) 2004-10-22 2006-04-24 Novartis Ag Compuestos organicos.
EP1695973A1 (fr) * 2005-02-24 2006-08-30 Neuro3D Sel d'Ocaperidone et composition pharmaceutique le contenant.
WO2007010356A2 (fr) * 2005-07-18 2007-01-25 Pfizer Limited Procede pour la preparation de derives de sulfonamide
GB0516313D0 (en) 2005-08-08 2005-09-14 Argenta Discovery Ltd Azole derivatives and their uses
BRPI0614290A2 (pt) 2005-08-08 2011-03-22 Argenta Discovery Ltd derivados de biciclo [ 2.2.1 ] hept-7-ilamina e seus usos
GB0601951D0 (en) 2006-01-31 2006-03-15 Novartis Ag Organic compounds
ATE549337T1 (de) 2006-04-21 2012-03-15 Novartis Ag Purinderivate zur verwendung als adenosin-a2a- rezeptoragonisten
JP4948913B2 (ja) * 2006-06-16 2012-06-06 上野製薬株式会社 ナフタレンカルボン酸アミドの製造方法
MX2010007604A (es) 2008-01-11 2010-08-02 Novartis Ag Pirimidinas como inhibidores de cinasa.
US8236786B2 (en) 2008-08-07 2012-08-07 Pulmagen Therapeutics (Inflammation) Limited Respiratory disease treatment
SG172444A1 (en) 2008-12-30 2011-07-28 Pulmagen Therapeutics Inflammation Ltd Sulfonamide compounds for the treatment of respiratory disorders
WO2010136940A1 (fr) 2009-05-29 2010-12-02 Pfizer Limited Nouveaux agonistes du récepteur des glucocorticoïdes
WO2010150014A1 (fr) 2009-06-24 2010-12-29 Pulmagen Therapeutics (Inflammation) Limited Glitazones 5r-5–deutérés pour le traitement de maladies respiratoires
JP5801997B2 (ja) 2009-07-07 2015-10-28 ファイザー・リミテッドPfizer Limited 薬品の組合せを吸入するための投薬ユニット、投薬ユニットのパック、および吸入器
GB0918924D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Azaindole derivatives
GB0918923D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Aminothiazole derivatives
GB0918922D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Aminopyridine derivatives
WO2011098746A1 (fr) 2010-02-09 2011-08-18 Pulmagen Therapeutics (Inflammation) Limited Sels d'addition acide cristallins de l'énantiomère (5r) de la pioglitazone
GB201002224D0 (en) 2010-02-10 2010-03-31 Argenta Therapeutics Ltd Respiratory disease treatment
GB201002243D0 (en) 2010-02-10 2010-03-31 Argenta Therapeutics Ltd Respiratory disease treatment
UY33597A (es) 2010-09-09 2012-04-30 Irm Llc Compuestos y composiciones como inhibidores de la trk
WO2012034095A1 (fr) 2010-09-09 2012-03-15 Irm Llc Composés et compositions comme inhibiteurs de trk
BR112013021638A2 (pt) 2011-02-25 2016-08-02 Irm Llc "compostos inibidores de trk, seu uso e composições que os compreendem"
WO2013021309A1 (fr) 2011-08-11 2013-02-14 Pfizer Limited Intermédiaire et procédé de préparation d'un dérivé sulfonamide
AU2021296221A1 (en) 2020-06-26 2023-02-02 Mylan Pharma Uk Limited Formulations including 5-(3-(3-hydroxyphenoxy)azetidin-1-yl)-5-methyl-2,2-diphenylhexanamide

Citations (5)

* Cited by examiner, † Cited by third party
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EP0659737A2 (fr) * 1993-12-21 1995-06-28 Bristol-Myers Squibb Company Substituts pour Catécholamines utiles comme agonistes B3
US20020143034A1 (en) * 1998-12-30 2002-10-03 Fujisawa Pharmaceutical Co. Ltd. Aminoalcohol derivatives and their use as beta 3 adrenergic agonists
WO2003099764A1 (fr) * 2002-05-28 2003-12-04 Theravance, Inc. Agonistes du recepteur adrenergique $g(b)2 alcoxy aryle
US20030229058A1 (en) * 2001-11-13 2003-12-11 Moran Edmund J. Aryl aniline beta2 adrenergic receptor agonists
WO2004100950A1 (fr) * 2003-05-15 2004-11-25 Pfizer Limited Derives de (2-hydroxy-2-(4-hydroxy-3-hydoxymethylphenyl)-ethylamino)-propylphenyle utilises comme beta2 agonistes

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US4540581A (en) 1984-01-31 1985-09-10 Bristol-Myers Company Topical nonsteroidal anti-inflammatory compositions and uses
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
US5264067A (en) 1992-04-23 1993-11-23 Geber Garment Technology, Inc. Adjustable length carriage compatible for use with differing spreading table widths and types
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JPH10218861A (ja) 1997-02-04 1998-08-18 Yamanouchi Pharmaceut Co Ltd 新規なフェネタノール誘導体又はその塩
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
BR9810456A (pt) * 1997-06-27 2001-09-25 Fujisawa Pharmaceutical Co Composto de sulfonamida, método para sua obtenção e seu uso farmacêutico
US6541669B1 (en) 1998-06-08 2003-04-01 Theravance, Inc. β2-adrenergic receptor agonists
AUPQ841300A0 (en) 2000-06-27 2000-07-20 Fujisawa Pharmaceutical Co., Ltd. New aminoalcohol derivatives
US6465501B2 (en) 2000-07-17 2002-10-15 Wyeth Azolidines as β3 adrenergic receptor agonists
HRP20000765A2 (en) * 2000-11-10 2002-06-30 Pliva D D Compositions of n-(1-methylethylaminocarbonyl)-4-(3-methylphenylamino)-3-pyridylsulfonamide and cyclic oligosaccharides with increased release
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RS50561B (sr) * 2004-01-22 2010-05-07 Pfizer Inc. Derivati sulfonamida za lečenje bolesti

Patent Citations (6)

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Publication number Priority date Publication date Assignee Title
EP0659737A2 (fr) * 1993-12-21 1995-06-28 Bristol-Myers Squibb Company Substituts pour Catécholamines utiles comme agonistes B3
US5776983A (en) * 1993-12-21 1998-07-07 Bristol-Myers Squibb Company Catecholamine surrogates useful as β3 agonists
US20020143034A1 (en) * 1998-12-30 2002-10-03 Fujisawa Pharmaceutical Co. Ltd. Aminoalcohol derivatives and their use as beta 3 adrenergic agonists
US20030229058A1 (en) * 2001-11-13 2003-12-11 Moran Edmund J. Aryl aniline beta2 adrenergic receptor agonists
WO2003099764A1 (fr) * 2002-05-28 2003-12-04 Theravance, Inc. Agonistes du recepteur adrenergique $g(b)2 alcoxy aryle
WO2004100950A1 (fr) * 2003-05-15 2004-11-25 Pfizer Limited Derives de (2-hydroxy-2-(4-hydroxy-3-hydoxymethylphenyl)-ethylamino)-propylphenyle utilises comme beta2 agonistes

Also Published As

Publication number Publication date
RS50561B (sr) 2010-05-07
US7767715B2 (en) 2010-08-03
SI1708991T1 (sl) 2008-02-29
OA13362A (en) 2007-04-13
UA84048C2 (ru) 2008-09-10
WO2005080313A2 (fr) 2005-09-01
EP1708991B1 (fr) 2007-10-17
US20100273758A1 (en) 2010-10-28
NO20062983L (no) 2006-07-24
PT1708991E (pt) 2007-12-14
NL1028087C2 (nl) 2006-05-09
PL1708991T3 (pl) 2008-02-29
GEP20094781B (en) 2009-09-25
TWI341831B (en) 2011-05-11
US20050182091A1 (en) 2005-08-18
WO2005080313A3 (fr) 2005-12-01
MY143390A (en) 2011-05-13
EA011167B1 (ru) 2009-02-27
AU2005214153B2 (en) 2008-09-18
US8013019B2 (en) 2011-09-06
DOP2005000006A (es) 2005-07-31
ATE375977T1 (de) 2007-11-15
EP1708991A2 (fr) 2006-10-11
ES2293530T3 (es) 2008-03-16
US20080267970A1 (en) 2008-10-30
AR047509A1 (es) 2006-01-25
AP2006003669A0 (en) 2006-06-30
NZ548318A (en) 2009-03-31
US7244766B2 (en) 2007-07-17
JP4020954B2 (ja) 2007-12-12
DE602005002930D1 (de) 2007-11-29
US20090197912A1 (en) 2009-08-06
US7528170B2 (en) 2009-05-05
EA200601223A1 (ru) 2006-12-29
DE602005002930T2 (de) 2008-07-24
PE20051136A1 (es) 2006-02-18
BRPI0507085A (pt) 2007-06-19
UY28721A1 (es) 2005-08-31
CA2553789C (fr) 2011-07-19
PA8622001A1 (es) 2005-08-30
WO2005080313A9 (fr) 2006-08-31
DK1708991T3 (da) 2008-01-14
JP2007518789A (ja) 2007-07-12
AU2005214153A1 (en) 2005-09-01
NL1028087A1 (nl) 2005-07-25
CA2553789A1 (fr) 2005-09-01
TW200530165A (en) 2005-09-16

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