CO6180437A2 - Derivados de sulfonamida como agonistas adrenergicos y antagonistas muscarinicos - Google Patents

Derivados de sulfonamida como agonistas adrenergicos y antagonistas muscarinicos

Info

Publication number
CO6180437A2
CO6180437A2 CO09034044A CO09034044A CO6180437A2 CO 6180437 A2 CO6180437 A2 CO 6180437A2 CO 09034044 A CO09034044 A CO 09034044A CO 09034044 A CO09034044 A CO 09034044A CO 6180437 A2 CO6180437 A2 CO 6180437A2
Authority
CO
Colombia
Prior art keywords
sulfonamide
derivatives
solvate
pharmaceutically acceptable
acceptable salt
Prior art date
Application number
CO09034044A
Other languages
English (en)
Inventor
Lyn Howard Jones
Graham Lunn
David Anthony Price
Original Assignee
Pfizer 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 Pfizer Ltd filed Critical Pfizer Ltd
Publication of CO6180437A2 publication Critical patent/CO6180437A2/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
    • C07D211/40Oxygen atoms
    • C07D211/44Oxygen atoms attached in position 4
    • C07D211/46Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
    • 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
    • A61K31/435Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Pulmonology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

en la que R1 es halo, R2 es H o halo, y Q se selecciona entre -(CH2)9- oo una sal farmacéuticamente aceptable o solvato del mismo. 2.- Un compuesto de acuerdo con la reivindicación 1, o una sal farmacéuticamente aceptable o solvato del mismo, en el que R1 es F. 3.- Un compuesto de acuerdo con la reivindicación 1, o una sal farmacéuticamente aceptable o solvato del mismo, en el que R1 es CI. 4.- Un compuesto de acuerdo con una cualquiera de las reivindicaciones 1 a 3, o una sal farmacéuticamente aceptable o solvato del mismo, en el que Q es -(CH2)9-. 5.- Un compuesto de acuerdo con una cualquiera de las reivindicaciones 1 a 3, o una sal farmacéuticamente aceptable o solvato del mismo, en el que Q es 6.- Un compuesto de acuerdo con una cualquiera de las reivindicaciones 1 a 5, o una sal farmacéuticamente aceptable o solvato del mismo, en el que R2 es H.7.- Un compuesto de acuerdo con una cualquiera de las reivindicaciones 1 a 5, o una sal farmacéuticamente aceptable o solvato del mismo, en el que R2 es F. 8.- El estereoisómero R de un compuesto de acuerdo con una cualquiera de las reivindicaciones 1 a 7, o una sal farmacéuticamente aceptable o solvato del mismo.
CO09034044A 2006-10-04 2009-04-02 Derivados de sulfonamida como agonistas adrenergicos y antagonistas muscarinicos CO6180437A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US82809906P 2006-10-04 2006-10-04

Publications (1)

Publication Number Publication Date
CO6180437A2 true CO6180437A2 (es) 2010-07-19

Family

ID=38947725

Family Applications (1)

Application Number Title Priority Date Filing Date
CO09034044A CO6180437A2 (es) 2006-10-04 2009-04-02 Derivados de sulfonamida como agonistas adrenergicos y antagonistas muscarinicos

Country Status (25)

Country Link
US (1) US20080090873A1 (es)
EP (1) EP2074094A1 (es)
JP (1) JP2010505810A (es)
KR (1) KR20090050104A (es)
CN (1) CN101522622A (es)
AP (1) AP2009004791A0 (es)
AR (1) AR063118A1 (es)
AU (1) AU2007303909A1 (es)
BR (1) BRPI0719270A2 (es)
CA (1) CA2665385A1 (es)
CL (1) CL2007002791A1 (es)
CO (1) CO6180437A2 (es)
CR (1) CR10700A (es)
EA (1) EA200900337A1 (es)
IL (1) IL197244A0 (es)
MA (1) MA30778B1 (es)
MX (1) MX2009002209A (es)
NO (1) NO20090910L (es)
PE (1) PE20080831A1 (es)
RS (1) RS20090137A (es)
TN (1) TN2009000112A1 (es)
TW (1) TW200823185A (es)
UY (1) UY30617A1 (es)
WO (1) WO2008041095A1 (es)
ZA (1) ZA200901320B (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW201036957A (en) 2009-02-20 2010-10-16 Astrazeneca Ab Novel salt 628
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
WO2011061527A1 (en) 2009-11-17 2011-05-26 Astrazeneca Ab Combinations comprising a glucocorticoid receptor modulator for the treatment of respiratory diseases
WO2011081937A1 (en) 2009-12-15 2011-07-07 Gilead Sciences, Inc. Corticosteroid-beta-agonist-muscarinic antagonist compounds for use in therapy
ITRM20110083U1 (it) 2010-05-13 2011-11-14 De La Cruz Jose Antonio Freire Piastra per la costruzione di carrelli per aeroplani
EP2386555A1 (en) 2010-05-13 2011-11-16 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activities
GB201016912D0 (en) 2010-10-07 2010-11-24 Astrazeneca Ab Novel combination
EP2592078A1 (en) 2011-11-11 2013-05-15 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and M3 muscarinic antagonist activities
MA38260B1 (fr) 2012-12-18 2018-04-30 Almirall Sa Nouveaux dérivés de cyclohexyl et quinuclidinyl carbamate ayant une activité d'agoniste adrénergique beta2 et une activité d'antagoniste muscarinique m3
TWI643853B (zh) 2013-02-27 2018-12-11 阿爾米雷爾有限公司 同時具有β2腎上腺素受體促效劑和M3毒蕈鹼受體拮抗劑活性之2-氨基-1-羥乙基-8-羥基喹啉-2(1H)-酮衍生物之鹽類
TW201517906A (zh) 2013-07-25 2015-05-16 Almirall Sa 含有maba化合物和皮質類固醇之組合
TWI641373B (zh) 2013-07-25 2018-11-21 阿爾米雷爾有限公司 具有蕈毒鹼受體拮抗劑和β2腎上腺素受體促效劑二者之活性的2-胺基-1-羥乙基-8-羥基喹啉-2(1H)-酮衍生物之鹽
TW201617343A (zh) 2014-09-26 2016-05-16 阿爾米雷爾有限公司 具有β2腎上腺素促效劑及M3蕈毒拮抗劑活性之新穎雙環衍生物
CN106336406B (zh) * 2015-07-10 2020-01-03 四川海思科制药有限公司 具有β2受体激动及M受体拮抗活性的八氢并环戊二烯衍生物及其在医药上的用途
CN110087729B (zh) 2016-12-14 2022-04-05 北京硕佰医药科技有限责任公司 一类具有季铵盐结构的双功能化合物
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
CN114748622A (zh) 2017-10-05 2022-07-15 弗尔康医疗公司 P38激酶抑制剂降低dux4和下游基因表达以用于治疗fshd
EP3720852A1 (en) * 2017-12-04 2020-10-14 Friedrich-Alexander-Universität Erlangen-Nürnberg Fluorophenyl substituted muscarinic receptor ligands with selectivity for m3 over m2
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

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5776983A (en) * 1993-12-21 1998-07-07 Bristol-Myers Squibb Company Catecholamine surrogates useful as β3 agonists
PE20040950A1 (es) * 2003-02-14 2005-01-01 Theravance Inc DERIVADOS DE BIFENILO COMO AGONISTAS DE LOS RECEPTORES ADRENERGICOS ß2 Y COMO ANTAGONISTAS DE LOS RECEPTORES MUSCARINICOS
JP4767842B2 (ja) * 2003-04-01 2011-09-07 セラヴァンス, インコーポレーテッド β2アドレナリン作用性レセプターアゴニスト活性およびムスカリン性レセプターアンタゴニスト活性を有するジアリールメチル化合物および関連化合物
ES2329133T3 (es) * 2003-05-28 2009-11-23 Theravance, Inc. Compuestos azabicicloalcanicos como antagonistas de receptores de muscarinicos.
PT1708992E (pt) * 2004-01-22 2007-11-16 Pfizer Derivados de sulfonamida para o tratamento de doenças
US7320990B2 (en) * 2004-02-13 2008-01-22 Theravance, Inc. Crystalline form of a biphenyl compound
TWI374883B (en) * 2004-08-16 2012-10-21 Theravance Inc Crystalline form of a biphenyl compound

Also Published As

Publication number Publication date
AR063118A1 (es) 2008-12-30
IL197244A0 (en) 2009-12-24
CL2007002791A1 (es) 2008-04-11
CN101522622A (zh) 2009-09-02
EP2074094A1 (en) 2009-07-01
TW200823185A (en) 2008-06-01
JP2010505810A (ja) 2010-02-25
WO2008041095A1 (en) 2008-04-10
TN2009000112A1 (fr) 2010-08-19
NO20090910L (no) 2009-03-24
MA30778B1 (fr) 2009-10-01
BRPI0719270A2 (pt) 2014-03-11
PE20080831A1 (es) 2008-06-20
US20080090873A1 (en) 2008-04-17
CR10700A (es) 2009-04-24
RS20090137A (en) 2010-06-30
AU2007303909A1 (en) 2008-04-10
ZA200901320B (en) 2010-04-28
KR20090050104A (ko) 2009-05-19
MX2009002209A (es) 2009-03-16
UY30617A1 (es) 2008-05-31
EA200900337A1 (ru) 2009-10-30
CA2665385A1 (en) 2008-04-10
AP2009004791A0 (en) 2009-04-30

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