ZA200807667B - Use of inhibitors of Jun N-terminal kinases to treat glaucoma - Google Patents
Use of inhibitors of Jun N-terminal kinases to treat glaucomaInfo
- Publication number
- ZA200807667B ZA200807667B ZA200807667A ZA200807667A ZA200807667B ZA 200807667 B ZA200807667 B ZA 200807667B ZA 200807667 A ZA200807667 A ZA 200807667A ZA 200807667 A ZA200807667 A ZA 200807667A ZA 200807667 B ZA200807667 B ZA 200807667B
- Authority
- ZA
- South Africa
- Prior art keywords
- jun
- inhibitors
- treat glaucoma
- terminal kinases
- kinases
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- 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
- A61K31/41—Heterocyclic 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
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- 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
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ophthalmology & Optometry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/394,893 US7803824B2 (en) | 2004-10-29 | 2006-03-31 | Use of inhibitors of Jun N-terminal kinases to treat glaucoma |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200807667B true ZA200807667B (en) | 2010-07-28 |
Family
ID=38523463
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200807667A ZA200807667B (en) | 2006-03-31 | 2007-03-14 | Use of inhibitors of Jun N-terminal kinases to treat glaucoma |
Country Status (13)
Country | Link |
---|---|
US (3) | US7803824B2 (fr) |
EP (1) | EP2004158A2 (fr) |
JP (1) | JP5241033B2 (fr) |
KR (1) | KR20080108503A (fr) |
CN (1) | CN101415407B (fr) |
AR (1) | AR060222A1 (fr) |
AU (1) | AU2007235111B2 (fr) |
BR (1) | BRPI0710099A2 (fr) |
CA (1) | CA2644721A1 (fr) |
MX (1) | MX2008011319A (fr) |
TW (1) | TWI419694B (fr) |
WO (1) | WO2007117849A2 (fr) |
ZA (1) | ZA200807667B (fr) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7803824B2 (en) * | 2004-10-29 | 2010-09-28 | Alcon, Inc. | Use of inhibitors of Jun N-terminal kinases to treat glaucoma |
US20060094753A1 (en) * | 2004-10-29 | 2006-05-04 | Alcon, Inc. | Use of inhibitors of Jun N-terminal kinases for the treatment of glaucomatous retinopathy and ocular diseases |
US20090202524A1 (en) * | 2007-10-31 | 2009-08-13 | Alcon Research, Ltd. | Pai-1 expression and activity inhibitors for the treatment of ocular disorders |
US20100056609A1 (en) * | 2008-08-26 | 2010-03-04 | Washington University | Methods and compositions for inhibition of axonal degeneration by modulation of the dlk/jnk pathway |
US20120077753A1 (en) * | 2009-06-25 | 2012-03-29 | Laxman Gangwani | Jnk inhibitors for use in treating spinal muscular atrophy |
JP2014511391A (ja) * | 2011-03-07 | 2014-05-15 | フォンダッツィオーネ・テレソン | Tfebリン酸化阻害剤およびその使用 |
US10624948B2 (en) * | 2013-06-26 | 2020-04-21 | Xigen Inflammation Ltd. | Use of cell-permeable peptide inhibitors of the JNK signal transduction pathway for the treatment of various diseases |
ES2949982T3 (es) * | 2014-06-26 | 2023-10-04 | Xigen Inflammation Ltd | Inhibidores peptídicos permeables en células de la ruta de transducción de señales de JNK para el tratamiento de la cistitis |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE398459T1 (de) * | 1996-04-26 | 2008-07-15 | Univ Ottawa | Verwendung von naip oder iap für die behandlung und vorbeugung von neuronalen erkrankungen |
WO2000021531A1 (fr) * | 1998-10-13 | 2000-04-20 | Kyowa Hakko Kogyo Co., Ltd. | Medicaments pour maladies oculaires |
CN1147486C (zh) | 1998-12-17 | 2004-04-28 | 霍夫曼-拉罗奇有限公司 | 4-和5-炔基羟吲哚和4-和5-烯基羟吲哚 |
WO2000064872A1 (fr) | 1999-04-23 | 2000-11-02 | Vertex Pharmaceuticals Incorporated | Inhibiteurs des c-jun n-terminal kinases (jnk) |
CZ2002534A3 (cs) | 1999-08-13 | 2002-07-17 | Vertex Pharmaceuticals Incorporated | Inhibitory protein-kináz, farmaceutické prostředky, které je obsahují, a jejich pouľití |
JP2003532626A (ja) | 1999-08-19 | 2003-11-05 | シグナル ファーマシューティカルズ, インコーポレイテッド | Jnk阻害剤としてのピラゾロアントロン及びその誘導体並びにそれらの組成物 |
US20040072888A1 (en) * | 1999-08-19 | 2004-04-15 | Bennett Brydon L. | Methods for treating inflammatory conditions or inhibiting JNK |
EP1088822A1 (fr) | 1999-09-28 | 2001-04-04 | Applied Research Systems ARS Holding N.V. | Dérivés de sulfonyl hydrazides pharmaceutiquement actifs |
EP1088815A1 (fr) | 1999-09-28 | 2001-04-04 | Applied Research Systems ARS Holding N.V. | Dérivés d'acides amines sulphonyle pharmaceutiquement actifs |
EP1088821A1 (fr) | 1999-09-28 | 2001-04-04 | Applied Research Systems ARS Holding N.V. | Derives des sulfamides pharmaceutiquement actifs |
EP1110957A1 (fr) | 1999-12-24 | 2001-06-27 | Applied Research Systems ARS Holding N.V. | Dérivés de benzazole et leur utilisation comme modulateurs de JNK |
AU2001266611A1 (en) | 2000-06-01 | 2001-12-11 | Merck & Co., Inc. | Use of (di-substituted-phenyl)-pyrimidinyl-imidazole derivatives as jnk-inhibitors |
EP1193256A1 (fr) | 2000-09-27 | 2002-04-03 | Applied Research Systems ARS Holding N.V. | Derivés de benzénesulphonamide pharmaceutiquemant actifs comme inhibiteurs de protéines JNK |
US7129242B2 (en) | 2000-12-06 | 2006-10-31 | Signal Pharmaceuticals, Llc | Anilinopyrimidine derivatives as JNK pathway inhibitors and compositions and methods related thereto |
WO2002062792A1 (fr) | 2001-02-02 | 2002-08-15 | Takeda Chemical Industries, Ltd. | Inhibiteur de jnk |
GB0108770D0 (en) | 2001-04-06 | 2001-05-30 | Eisai London Res Lab Ltd | Inhibitors |
CA2440842A1 (fr) | 2001-04-16 | 2002-10-24 | Eisai Co., Ltd. | Nouveau compose a base de 1h-indazoles |
US20040254189A1 (en) | 2001-08-23 | 2004-12-16 | Hideaki Nagaya | Jnk inhibitors |
MXPA04002243A (es) | 2001-09-19 | 2004-06-29 | Aventis Pharma Sa | Compuestos quimicos. |
JP2003129190A (ja) | 2001-10-19 | 2003-05-08 | Sumitomo Metal Ind Ltd | マルテンサイト系ステンレス鋼およびその製造方法 |
US20030138819A1 (en) | 2001-10-26 | 2003-07-24 | Haiqing Gong | Method for detecting disease |
US7390797B2 (en) * | 2002-02-28 | 2008-06-24 | Eisai Co., Ltd. | Fused indazole compounds |
KR20040104566A (ko) * | 2002-04-30 | 2004-12-10 | 알콘, 인코퍼레이티드 | 안압 저하 및 녹내장성 망막병증/시신경병증 치료를 위한특유의 수단으로서의 결합 조직 성장 인자 (ctgf)의활성 및/또는 발현 조절, 저해, 또는 변조제 |
CA2487948A1 (fr) | 2002-06-14 | 2003-12-24 | Applied Research Systems Ars Holding N.V. | Derives de cyanure d'azole methylidene et leur utilisation comme modulateurs de proteine kinase |
EP1542768A1 (fr) * | 2002-09-20 | 2005-06-22 | Alcon, Inc. | Utilisation d'inhibiteurs de la synthese des cytokines dans le traitement des troubles associes a la keratoconjonctivite seche |
US20040092568A1 (en) * | 2002-10-31 | 2004-05-13 | Zeldis Jerome B. | Methods for the treatment, prevention and management of macular degeneration |
US20060094753A1 (en) | 2004-10-29 | 2006-05-04 | Alcon, Inc. | Use of inhibitors of Jun N-terminal kinases for the treatment of glaucomatous retinopathy and ocular diseases |
US7803824B2 (en) * | 2004-10-29 | 2010-09-28 | Alcon, Inc. | Use of inhibitors of Jun N-terminal kinases to treat glaucoma |
WO2006102333A2 (fr) * | 2005-03-21 | 2006-09-28 | Alcon Manufacturing, Ltd. | Utilisation d'agents inhibiteurs de liaison et de signalisation du facteur de croissance de tissus conjonctifs (ctgf) via le complexe recepteur trka/p75ntr pour la prevention de troubles oculaires lies au cgtf |
-
2006
- 2006-03-31 US US11/394,893 patent/US7803824B2/en not_active Expired - Fee Related
-
2007
- 2007-03-14 CA CA002644721A patent/CA2644721A1/fr not_active Abandoned
- 2007-03-14 AU AU2007235111A patent/AU2007235111B2/en not_active Ceased
- 2007-03-14 ZA ZA200807667A patent/ZA200807667B/xx unknown
- 2007-03-14 MX MX2008011319A patent/MX2008011319A/es active IP Right Grant
- 2007-03-14 JP JP2009503137A patent/JP5241033B2/ja not_active Expired - Fee Related
- 2007-03-14 CN CN2007800116928A patent/CN101415407B/zh not_active Expired - Fee Related
- 2007-03-14 WO PCT/US2007/063961 patent/WO2007117849A2/fr active Application Filing
- 2007-03-14 BR BRPI0710099-0A patent/BRPI0710099A2/pt not_active IP Right Cessation
- 2007-03-14 EP EP07758510A patent/EP2004158A2/fr not_active Withdrawn
- 2007-03-14 KR KR1020087023895A patent/KR20080108503A/ko not_active Application Discontinuation
- 2007-03-19 TW TW096109322A patent/TWI419694B/zh not_active IP Right Cessation
- 2007-03-29 AR ARP070101334A patent/AR060222A1/es not_active Application Discontinuation
-
2010
- 2010-08-18 US US12/858,739 patent/US20100311716A1/en not_active Abandoned
-
2011
- 2011-09-14 US US13/232,410 patent/US20120004274A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
EP2004158A2 (fr) | 2008-12-24 |
TWI419694B (zh) | 2013-12-21 |
US7803824B2 (en) | 2010-09-28 |
KR20080108503A (ko) | 2008-12-15 |
JP2009532373A (ja) | 2009-09-10 |
MX2008011319A (es) | 2008-09-19 |
AU2007235111A1 (en) | 2007-10-18 |
US20100311716A1 (en) | 2010-12-09 |
TW200744601A (en) | 2007-12-16 |
WO2007117849A3 (fr) | 2008-04-10 |
CN101415407B (zh) | 2011-05-11 |
CN101415407A (zh) | 2009-04-22 |
BRPI0710099A2 (pt) | 2011-08-02 |
US20060172991A1 (en) | 2006-08-03 |
AU2007235111B2 (en) | 2012-03-22 |
WO2007117849A2 (fr) | 2007-10-18 |
CA2644721A1 (fr) | 2007-10-18 |
JP5241033B2 (ja) | 2013-07-17 |
AR060222A1 (es) | 2008-06-04 |
US20120004274A1 (en) | 2012-01-05 |
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