MA27497A1 - Compositions ophtalmiques pour le traitement de l'hypertension oculaire. - Google Patents

Compositions ophtalmiques pour le traitement de l'hypertension oculaire.

Info

Publication number
MA27497A1
MA27497A1 MA28316A MA28316A MA27497A1 MA 27497 A1 MA27497 A1 MA 27497A1 MA 28316 A MA28316 A MA 28316A MA 28316 A MA28316 A MA 28316A MA 27497 A1 MA27497 A1 MA 27497A1
Authority
MA
Morocco
Prior art keywords
agent
eye
treatment
vagomimetic
compounds
Prior art date
Application number
MA28316A
Other languages
English (en)
Inventor
James B Doherty
Meng-Hsin Chen
Luping Liu
Swaminathan R Natarajan
Robert M Tynebor
Original Assignee
Merck & Co Inc
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 Merck & Co Inc filed Critical Merck & Co Inc
Publication of MA27497A1 publication Critical patent/MA27497A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6503Five-membered rings
    • C07F9/65031Five-membered rings having the nitrogen atoms in the positions 1 and 2
    • C07F9/65038Five-membered rings having the nitrogen atoms in the positions 1 and 2 condensed with carbocyclic rings or carbocyclic ring systems
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/4161,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Ophthalmology & Optometry (AREA)
  • Diabetes (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

sous forme de solution ou suspension et contenant facultativement de la gomme xanthane ou de la gomme gellane. 11. Une composition conformément à la Revendication 9 oé un ingrédient actif appartient à la famille consistant de: agent bloquant adrénolytique-(beta), agent para-vagomimétique, agent vagomimétique, inhibiteur de l'anhydrase carbonique, agoniste EP4, une prostaglandine ou un dérivé de celle-ci, lipide hypotenseur, neuroprotecteur, et/ou un agoniste du récepteur 5-HT2 est ajouté. L'invention concerne des composés puissants de blocage du canal de potassium de formule I ou une préparation correspondante destinée au traitement de glaucome ou d'autres troubles qui débouchent sur une pression intraoculaire élevée dans l'oeil d'un patient. Cette invention a aussi trait à l'utilisation de tels composés de manière à engendrer un effet neuroprotecteur destiné à l'oeil d'espèces mammaliennes, notamment, des êtres humains
MA28316A 2002-11-08 2005-06-07 Compositions ophtalmiques pour le traitement de l'hypertension oculaire. MA27497A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US42480802P 2002-11-08 2002-11-08
US50009103P 2003-09-04 2003-09-04

Publications (1)

Publication Number Publication Date
MA27497A1 true MA27497A1 (fr) 2005-08-01

Family

ID=32314559

Family Applications (1)

Application Number Title Priority Date Filing Date
MA28316A MA27497A1 (fr) 2002-11-08 2005-06-07 Compositions ophtalmiques pour le traitement de l'hypertension oculaire.

Country Status (22)

Country Link
US (2) US7196082B2 (fr)
EP (1) EP1562909B1 (fr)
JP (2) JP4456072B2 (fr)
KR (1) KR20050072805A (fr)
AR (1) AR041991A1 (fr)
AU (2) AU2003286884A1 (fr)
BR (1) BR0316040A (fr)
CA (1) CA2505086C (fr)
CL (1) CL2003002293A1 (fr)
DO (1) DOP2003000747A (fr)
EC (1) ECSP055781A (fr)
HR (1) HRP20050409A2 (fr)
IS (1) IS7822A (fr)
MA (1) MA27497A1 (fr)
MX (1) MXPA05004889A (fr)
NO (1) NO20052751D0 (fr)
NZ (1) NZ539593A (fr)
PE (1) PE20040692A1 (fr)
PL (1) PL377172A1 (fr)
RU (1) RU2005117627A (fr)
TW (1) TWI250873B (fr)
WO (2) WO2004043932A1 (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20040028469A (ko) 2002-09-30 2004-04-03 엘지전자 주식회사 1 회 기록 가능한 광디스크의 디펙트 영역 관리방법
US7135575B2 (en) * 2003-03-03 2006-11-14 Array Biopharma, Inc. P38 inhibitors and methods of use thereof
AU2004272546B2 (en) * 2003-09-04 2007-10-18 Merck Sharp & Dohme Corp. Ophthalmic compositions for treating ocular hypertension
CA2574078A1 (fr) * 2004-07-20 2006-02-23 Merck & Co., Inc. Compositions ophtalmiques traitant l'hypertension oculaire
EP1647549A1 (fr) 2004-10-14 2006-04-19 Laboratoire Theramex Indazoles, benzisoxazoles et benzisothiazoles en tant qu'agents oestrogéniques
SI1981851T1 (sl) * 2006-01-31 2012-05-31 Array Biopharma Inc Kinazni inhibitorji in postopki za njihovo uporabo
CA2644716A1 (fr) * 2006-03-13 2007-09-27 Merck & Co., Inc. Compositions ophtalmiques pour le traitement de l'hypertension oculaire
CN101437519A (zh) * 2006-03-31 2009-05-20 艾博特公司 吲唑化合物
EP2352501B1 (fr) * 2008-11-03 2014-01-01 ChemoCentryx, Inc. Composés pour l'utilisation dans le traitement de l'ostéoporose
WO2012071369A2 (fr) 2010-11-24 2012-05-31 The Trustees Of Columbia University In The City Of New York Antagoniste rbp4 non rétinoïde pour le traitement de la dégénérescence maculaire liée à l'âge et de la maladie de stargardt
WO2013166037A1 (fr) 2012-05-01 2013-11-07 The Trustees Of Columbia University In The City Of New York Antagonistes non rétinoïdes pour le traitement de troubles oculaires
WO2014151959A1 (fr) 2013-03-14 2014-09-25 The Trustees Of Columbia University In The City Of New York N-alkyl-2-phénoxyéthanamines, leurs préparation et utilisation
US9637450B2 (en) 2013-03-14 2017-05-02 The Trustees Of Columbia University In The City Of New York Octahydrocyclopentapyrroles, their preparation and use
US9944644B2 (en) 2013-03-14 2018-04-17 The Trustees Of Columbia University In The City Of New York Octahydropyrrolopyrroles their preparation and use
EP3495357B1 (fr) 2013-03-14 2021-05-05 The Trustees of Columbia University in the City of New York 4-phénylpipéridines, leur préparation et leur utilisation
BR112016025356B1 (pt) 2014-04-30 2023-04-18 The Trustees Of Columbia University In The City Of New York Compostos de 4-fenilpiperidinas substituídas, composições e seus usos
CN104211638A (zh) * 2014-08-13 2014-12-17 李增 一种脂肪氨基取代的芸香碱类衍生物及其制备和作为抗阿尔兹海默症的药物中的应用
US20190016680A1 (en) 2016-01-14 2019-01-17 Beth Israel Deaconess Medical Center, Inc. Mast-cell modulators and uses thereof

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2534580A1 (fr) 1982-10-13 1984-04-20 Synthelabo Derives de phenyl-1 piperidino-2 propanol, leur preparation, et medicaments qui les contiennent
US5151444B1 (en) 1987-09-18 1999-07-06 R Tech Ueno Ltd Ocular hypotensive agents
AU3693789A (en) 1988-05-10 1989-11-29 Leo Pharmaceutical Products Ltd. A/S (Lovens Kemiske Fabrik Produktionsaktieselskab) New ophthalmic preparation for treating glaucoma
ES2317964T5 (es) 1988-09-06 2015-02-20 Pfizer Health Ab Derivado de prostaglandina-F2alfa para el tratamiento de glaucoma o hipertensión ocular
US5296504A (en) 1988-09-06 1994-03-22 Kabi Pharmacia Prostaglandin derivatives for the treatment of glaucoma or ocular hypertension
US5352708A (en) 1992-09-21 1994-10-04 Allergan, Inc. Non-acidic cyclopentane heptanoic acid, 2-cycloalkyl or arylalkyl derivatives as therapeutic agents
US5922773A (en) 1992-12-04 1999-07-13 The Children's Medical Center Corp. Glaucoma treatment
FR2701026B1 (fr) 1993-02-02 1995-03-31 Adir Nouveaux dérivés de l'indole, de l'indazole et du benzisoxazole, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.
JP3208210B2 (ja) * 1993-03-17 2001-09-10 旭化成株式会社 結晶性芳香族ポリカーボネートプレポリマーの製造方法及び芳香族ポリカーボネートの製造方法
CA2164733A1 (fr) 1993-06-08 1994-12-22 Nino Sorgente Methodes et compositions pour abaisser la pression intraoculaire
US5510383A (en) 1993-08-03 1996-04-23 Alcon Laboratories, Inc. Use of cloprostenol, fluprostenol and their salts and esters to treat glaucoma and ocular hypertension
US5573758A (en) 1995-04-28 1996-11-12 Allergan Method for reducing intraocular pressure in the mammalian eye by administration of potassium channel blockers
AP1147A (en) * 1996-05-03 2003-02-25 Pfizer Substituted indazole derivatives and related compounds.
US5925342A (en) 1996-11-13 1999-07-20 Allergan Method for reducing intraocular pressure in the mammalian eye by administration of potassium channel blockers
GB2321455A (en) * 1997-01-24 1998-07-29 Norsk Hydro As Lipophilic derivatives of biologically active compounds
EP1114816A4 (fr) 1998-09-14 2002-09-04 Ono Pharmaceutical Co DERIVES E DE PHENYL-PROSTAGLANDINE A SUBSTITUTION-$g(V) ET MEDICAMENTS LES CONTENANT COMME INGREDIENT ACTIF
EA005293B1 (ru) 1999-12-22 2004-12-30 Пфайзер Продактс Инк. Производные пирролидин-2-она и их применение при лечении остеопороза
EP1251862B1 (fr) 2000-01-18 2008-10-01 Merck & Co., Inc. Compositions ophthalmiques pour traiter l'hypertension oculaire
PL358481A1 (en) 2000-03-17 2004-08-09 Alcon Inc. 6-hydroxy-indazole derivatives for treating glaucoma
US6956036B1 (en) * 2000-03-17 2005-10-18 Alcon, Inc. 6-hydroxy-indazole derivatives for treating glaucoma
WO2001070701A1 (fr) 2000-03-17 2001-09-27 Alcon, Inc. Derives d'indazole 5-hydroxy permettant de traiter le glaucome
WO2001072268A1 (fr) 2000-03-31 2001-10-04 Toray Industries, Inc. Agents de régulation de la pousse du cheveu ou de sa formation
WO2002024647A1 (fr) 2000-09-21 2002-03-28 Ono Pharmaceutical Co., Ltd. Agonistes du recepteur de l'ep4 comprenant comme principe actif des derives de la 8-azaprostaglandine
EA200300379A1 (ru) 2000-11-27 2003-08-28 Пфайзер Продактс Инк. Селективные агонисты рецептора ep4 в лечении остеопороза
FR2827861B1 (fr) 2001-07-27 2004-04-02 Aventis Pharma Sa Derives des indazoles ou des indoles, leur utilisation en medecine humaine et plus particulierement en cancerologie

Also Published As

Publication number Publication date
NO20052751L (no) 2005-06-07
US7547720B2 (en) 2009-06-16
PL377172A1 (pl) 2006-01-23
JP5061293B2 (ja) 2012-10-31
EP1562909B1 (fr) 2012-06-27
HRP20050409A2 (en) 2006-02-28
IS7822A (is) 2005-04-25
AU2003286884A1 (en) 2004-06-03
JP4456072B2 (ja) 2010-04-28
JP2006508190A (ja) 2006-03-09
BR0316040A (pt) 2005-09-13
AU2003287506B2 (en) 2009-04-23
US20040097575A1 (en) 2004-05-20
CA2505086C (fr) 2009-08-25
AR041991A1 (es) 2005-06-08
TW200501949A (en) 2005-01-16
CL2003002293A1 (es) 2005-01-14
KR20050072805A (ko) 2005-07-12
TWI250873B (en) 2006-03-11
ECSP055781A (es) 2005-09-20
DOP2003000747A (es) 2004-05-31
EP1562909A1 (fr) 2005-08-17
CA2505086A1 (fr) 2004-05-27
WO2004043933A1 (fr) 2004-05-27
AU2003287506B8 (en) 2009-05-28
AU2003287506A1 (en) 2004-06-03
RU2005117627A (ru) 2006-01-20
US20070129418A1 (en) 2007-06-07
US7196082B2 (en) 2007-03-27
MXPA05004889A (es) 2005-07-22
JP2010006825A (ja) 2010-01-14
WO2004043932A1 (fr) 2004-05-27
PE20040692A1 (es) 2004-10-08
NO20052751D0 (no) 2005-06-07
NZ539593A (en) 2006-12-22

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