AR041262A1 - Metodos para tratar los trastornos de ojo seco - Google Patents
Metodos para tratar los trastornos de ojo secoInfo
- Publication number
- AR041262A1 AR041262A1 ARP030103339A ARP030103339A AR041262A1 AR 041262 A1 AR041262 A1 AR 041262A1 AR P030103339 A ARP030103339 A AR P030103339A AR P030103339 A ARP030103339 A AR P030103339A AR 041262 A1 AR041262 A1 AR 041262A1
- Authority
- AR
- Argentina
- Prior art keywords
- norleucil
- inhibitors
- kinase inhibitors
- dry eye
- trifluomethyl
- Prior art date
Links
Classifications
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- 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
- A61K31/60—Salicylic acid; Derivatives thereof
- A61K31/612—Salicylic acid; Derivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid
- A61K31/616—Salicylic acid; Derivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid by carboxylic acids, e.g. acetylsalicylic acid
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- 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
-
- 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
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/08—Peptides having 5 to 11 amino acids
-
- 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
- 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)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Gastroenterology & Hepatology (AREA)
- Immunology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Ophthalmology & Optometry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Reivindicación 1: El uso de una composición que comprende un vehículo farmacéuticamente aceptable y una cantidad farmacéuticamente efectiva de un inhibidor de la síntesis de citocinas seleccionado entre el grupo que consiste en inhibidores de lascinasas activadas por mitógenos, inhibidores de la cinasa C-jun N terminal e inhibidores de la cinasa I-kappa, inhibidores de la síntesis de IL-1beta, inhibidores de la síntesis de TNFalfa, inhibidores de la tirosina cinasa de la familia Janus,inhibidores de transductores de senal y activadores de la transcripción y ligandos de los receptores de retinoides X para la elaboración de un medicamento para el tratamiento del ojo seco y otros trastornos que requieren la humectación el ojo en unmamífero. Reivindicación 3: El uso de acuerdo con la reivindicación 1, en el cual el inhibidor de la síntesis de citocinas es seleccionado entre el grupo que consiste en (5-(2-amino-4-pirimidinil)-4-(4-fluofenil)-1-(4-piperidinil)imidazol),antra[1,9-cd]pirazol-6-(2H)-ona, (D)Arginil-(D)Norleucil-(D)Norleucil-(D)Arginil-(D)Norleucil-(D)Norleucil-(D)Norleucil-Glicina-(D)Tirosina-amida, sal de acetato, 2-cloro-N-[3,5-di(trifluometil)fenil]-4-(trifluometil)pirimidin-5-carboxamida,trifusal y bexaroteno.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41246302P | 2002-09-20 | 2002-09-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR041262A1 true AR041262A1 (es) | 2005-05-11 |
Family
ID=32030872
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030103339A AR041262A1 (es) | 2002-09-20 | 2003-09-15 | Metodos para tratar los trastornos de ojo seco |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US7026296B2 (es) |
| EP (1) | EP1542768A1 (es) |
| JP (1) | JP2006502183A (es) |
| KR (1) | KR20050057175A (es) |
| CN (1) | CN1684738A (es) |
| AR (1) | AR041262A1 (es) |
| AU (1) | AU2003278727A1 (es) |
| BR (1) | BR0314603A (es) |
| CA (1) | CA2497977A1 (es) |
| MX (1) | MXPA05003063A (es) |
| PL (1) | PL374700A1 (es) |
| TW (1) | TW200404534A (es) |
| WO (1) | WO2004026406A1 (es) |
| ZA (1) | ZA200502119B (es) |
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| US7803824B2 (en) * | 2004-10-29 | 2010-09-28 | Alcon, Inc. | Use of inhibitors of Jun N-terminal kinases to treat glaucoma |
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| US8080562B2 (en) | 2008-04-15 | 2011-12-20 | Sarcode Bioscience Inc. | Crystalline pharmaceutical and methods of preparation and use thereof |
| WO2009143865A1 (en) | 2008-05-30 | 2009-12-03 | Xigen S.A. | Use of cell-permeable peptide inhibitors of the jnk signal transduction pathway for the treatment of various diseases |
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| CL2009001884A1 (es) * | 2008-10-02 | 2010-05-14 | Incyte Holdings Corp | Uso de 3-ciclopentil-3-[4-(7h-pirrolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il)propanonitrilo, inhibidor de janus quinasa, y uso de una composición que lo comprende para el tratamiento del ojo seco. |
| WO2010072228A1 (en) | 2008-12-22 | 2010-07-01 | Xigen S.A. | Novel transporter constructs and transporter cargo conjugate molecules |
| HRP20192203T1 (hr) | 2009-05-22 | 2020-03-06 | Incyte Holdings Corporation | 3-[4-(7h-pirolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il]oktan- ili heptan-nitril kao jak inhibitori |
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| ES2136581B1 (es) | 1998-05-27 | 2000-09-16 | Uriach & Cia Sa J | Uso de derivados del acido-2-hidroxi-4-trifluorometilbenzoico para la preparacion de medicamentos utiles para inhibir el factor de transcripcion nuclear nf-kb. |
| ATE203668T1 (de) * | 1998-07-14 | 2001-08-15 | Alcon Lab Inc | Verwendung von 11-(3-dimethylaminopropyliden)-6, 11-dihydrodibenz(b,e)oxepin-2-essigsäure und deren pharmazeutisch annehmbaren salzen zur herstellung eines medikaments zur behandlung nicht-allergisch-bedingten augenentzündungen und zur prevention der okularen neovaskularisation |
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-
2003
- 2003-08-26 PL PL03374700A patent/PL374700A1/xx not_active Application Discontinuation
- 2003-08-26 US US10/650,006 patent/US7026296B2/en not_active Expired - Fee Related
- 2003-08-26 CN CNA03822514XA patent/CN1684738A/zh active Pending
- 2003-08-26 WO PCT/US2003/026689 patent/WO2004026406A1/en not_active Ceased
- 2003-08-26 EP EP03770254A patent/EP1542768A1/en not_active Withdrawn
- 2003-08-26 MX MXPA05003063A patent/MXPA05003063A/es not_active Application Discontinuation
- 2003-08-26 BR BR0314603-0A patent/BR0314603A/pt not_active IP Right Cessation
- 2003-08-26 JP JP2004537690A patent/JP2006502183A/ja active Pending
- 2003-08-26 CA CA002497977A patent/CA2497977A1/en not_active Abandoned
- 2003-08-26 AU AU2003278727A patent/AU2003278727A1/en not_active Abandoned
- 2003-08-26 KR KR1020057003759A patent/KR20050057175A/ko not_active Withdrawn
- 2003-09-04 TW TW092124459A patent/TW200404534A/zh unknown
- 2003-09-15 AR ARP030103339A patent/AR041262A1/es not_active Application Discontinuation
-
2005
- 2005-03-14 ZA ZA200502119A patent/ZA200502119B/en unknown
-
2006
- 2006-03-28 US US11/390,874 patent/US20060189541A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| PL374700A1 (pl) | 2005-10-31 |
| WO2004026406A1 (en) | 2004-04-01 |
| MXPA05003063A (es) | 2005-05-27 |
| US20060189541A1 (en) | 2006-08-24 |
| KR20050057175A (ko) | 2005-06-16 |
| US7026296B2 (en) | 2006-04-11 |
| US20040058875A1 (en) | 2004-03-25 |
| AU2003278727A1 (en) | 2004-04-08 |
| BR0314603A (pt) | 2005-07-26 |
| CN1684738A (zh) | 2005-10-19 |
| CA2497977A1 (en) | 2004-04-01 |
| JP2006502183A (ja) | 2006-01-19 |
| ZA200502119B (en) | 2006-09-27 |
| EP1542768A1 (en) | 2005-06-22 |
| TW200404534A (en) | 2004-04-01 |
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| Date | Code | Title | Description |
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| FA | Abandonment or withdrawal |