AR078307A1 - Composicion farmaceutica para el tratamiento de enfermedades inflamatorias medidas por mcp-1 - Google Patents
Composicion farmaceutica para el tratamiento de enfermedades inflamatorias medidas por mcp-1Info
- Publication number
- AR078307A1 AR078307A1 ARP100103447A ARP100103447A AR078307A1 AR 078307 A1 AR078307 A1 AR 078307A1 AR P100103447 A ARP100103447 A AR P100103447A AR P100103447 A ARP100103447 A AR P100103447A AR 078307 A1 AR078307 A1 AR 078307A1
- Authority
- AR
- Argentina
- Prior art keywords
- phosphopyric
- captopril
- group
- pharmaceutical composition
- hydrogen atom
- 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
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
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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
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
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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
- A61K31/33—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
-
- 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
- A61K31/403—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 carbocyclic rings, e.g. carbazole
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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
- A61K31/33—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
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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
- A61K31/33—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
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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
- A61K31/33—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
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Obesity (AREA)
- Child & Adolescent Psychology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
La combinacion presento actividad aditiva y sinérgica en la reduccion de los niveles de MCP-1, mejorando así significativamente la inhibicion de la respuesta inflamatoria y por lo tanto reduciendo las complicaciones que se producen en pacientes que padecen enfermedades inflamatorias. Reivindicacion 1: Composicion farmacéutica que comprende: (a) un 1-bencil-3-hidroximetilindazol representado por la formula (1) siguiente: en la que: R1 y R2, iguales o diferentes entre sí, son un átomo de hidrogeno o un grupo alquilo C1-6, R3, R4 y R8, iguales o diferentes entre sí, son un átomo de hidrogeno o un grupo alquilo C1-5, un grupo alcoxi C1-3 o un átomo de halogeno, R5, es un átomo de hidrogeno o un grupo alquilo C1-5, un grupo alcoxi C1-3, un átomo de halogeno o R5 forma, junto con uno de entre R6 y R7, un ciclo que presenta cinco o seis átomos de carbono, R6 y R7, iguales o diferentes entre sí, son un átomo de hidrogeno o un grupo alquilo C1-5, o uno de entre R6 y R7 forma, junto con R5, un ciclo que presenta cinco o seis átomos de carbono, R10 y R11, iguales o diferentes entre sí, son un átomo de hidrogeno o un grupo alquilo C1-5, y R12, es un átomo de hidrogeno o un grupo alquilo C1-4. (b) por lo menos uno de entre (i) un agente reductor de la presion seleccionado de entre inhibidores de la ACE, inhibidores de la renina, BRA y BCC, y/o (ii) un agente reductor del colesterol seleccionado de entre derivados de Ia estatina, o cualquier sal y éster farmaceuticamente aceptables de los mismos, y (c) por lo menos un vehículo farmacéuticamente aceptable. Reivindicacion 3: Composicion farmacéutica segun la reivindicacion 1, en la que dicho inhibidor de ACE se selecciona de entre el grupo constituido por alacepril, alatriopril, altiopril cálcico, ancovenina, hidrocloruro de benazepril, benazeprilat, benzazepril, benzoilcaptopril, captopril, captopril-cisteína, captopril-glutation, ceranapril, ceranopril, ceronapril, cilazapril, cilazaprilat, converstatina, delapril, delapril-diácido, enalapril, enalaprilat, enalkiren, enapril, epicaptopril, foroximitina, fosfenopril, fosenopril, fosenopril sodico, fosinopril, fosinopril sodico, fosinoprilat, ácido fosinoprílico, glicopril, hemorfina-4, idapril, imidapril, indolapril, indolaprilat, libenzapril, lisinopril, liciumina A, liciumina B, mixanpril, moexipril, moexiprilat, moveltipril, muraceína A, muraceína B, muraceína C, pentopril, perindopril, perindoprilat, pivalopril, pivopril, quinapril, hidrocloruro de quinapril, quinaprilat, ramipril, ramiprilat, espirapril, hidrocloruro de espirapril, espiraprilat, espiropril, hidrocloruro de espiropril, temocapril, hidrocloruro de temocapril, teprotido, trandolapril, trandolaprilat, utibapril, zabicipril, zabiciprilat, zofenopril, zofenoprilat, las sales farmacéuticamente aceptables de los mismos y la mezcla de los mismos. Reivindicacion 6: Composicion farmacéutica segun la reivindicacion 1, en la que dicho BRA se selecciona de entre el grupo constituido por candesartán, cilexetil, eprosartán, irbesartán, losartán, olmesartán, tasosartán, telmisartán, valsartán y pratosartán. Reivindicacion 9: Composicion farmacéutica segun la reivindicacion 1, en la que dicho inhibidor de renina se selecciona de entre el grupo constituido por aliskiren, ditekiren, enalkiren, remikiren, terlakiren, ciprokiren y zankiren. Reivindicacion 11: Composicion farmacéutica segun la reivindicacion 1, en la que dicho BCC es seleccionado de entre el grupo constituido por amlodipina, aranidipina, barnidipina, benidipina, cilnidipina, efonidipina, elgodipina, felodipina, isradipina, lacidipina, lercanidipina, manidipina, nicardipina, nifedipina, nilvadipina, nimodipina, nisoldipina, nitrendipina, diltiacem, clentiacem, bepridilo, benciclano, etafenona, flunaricina, lidoflacina, lomericina, mibefradilo, fendilina, prenilamina, semotiadilo, terodilina, galopamilo, y verapamilo. Reivindicacion 14: Composicion farmacéutica segun la reivindicacion 1, en la que dicho en derivado de estatina se selecciona de entre el grupo constituido por atorvastatina, cerivastatina, fluvastatina, lovastatina, mevastatina, pitavastatina, pravastatina, rosuvastatina y simvastatina.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09425368 | 2009-09-23 |
Publications (1)
Publication Number | Publication Date |
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AR078307A1 true AR078307A1 (es) | 2011-10-26 |
Family
ID=41722750
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP100103447A AR078307A1 (es) | 2009-09-23 | 2010-09-22 | Composicion farmaceutica para el tratamiento de enfermedades inflamatorias medidas por mcp-1 |
Country Status (25)
Country | Link |
---|---|
US (1) | US9492542B2 (es) |
EP (1) | EP2480224B1 (es) |
JP (2) | JP2013505278A (es) |
KR (1) | KR101774402B1 (es) |
CN (1) | CN102573827B (es) |
AR (1) | AR078307A1 (es) |
AU (1) | AU2010297405B2 (es) |
BR (1) | BR112012006149A2 (es) |
CA (1) | CA2760180C (es) |
CY (1) | CY1119125T1 (es) |
DK (1) | DK2480224T3 (es) |
EA (1) | EA021485B1 (es) |
ES (1) | ES2637024T3 (es) |
GE (1) | GEP20146067B (es) |
HR (1) | HRP20171209T1 (es) |
HU (1) | HUE033102T2 (es) |
IL (1) | IL218001A (es) |
LT (1) | LT2480224T (es) |
MX (1) | MX347957B (es) |
PL (1) | PL2480224T3 (es) |
PT (1) | PT2480224T (es) |
SG (2) | SG10201405408YA (es) |
SI (1) | SI2480224T1 (es) |
UA (1) | UA108742C2 (es) |
WO (1) | WO2011036047A1 (es) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT2262778T (pt) | 2008-03-07 | 2019-11-19 | Acraf | Derivados de 1-benzil-3-hidroximetilindazolo e utilização dos mesmos no tratamento de doenças baseadas na expressão de mcp-1, cxcr1 e p40 |
JP5509102B2 (ja) | 2008-03-07 | 2014-06-04 | アジェンデ・キミケ・リウニテ・アンジェリニ・フランチェスコ・ア・チ・エレ・ア・エフェ・ソシエタ・ペル・アチオニ | 新規な1−ベンジル−3−ヒドロキシメチルインダゾール誘導体およびそのmcp−1およびcx3cr1の発現に基づく疾患の治療への使用 |
US8999292B2 (en) | 2012-05-01 | 2015-04-07 | Translatum Medicus Inc. | Methods for treating and diagnosing blinding eye diseases |
US11221321B2 (en) * | 2019-05-29 | 2022-01-11 | Imam Abdulrahman Bin Faisal University | Liquid chromatographic method for the simultaneous analysis of antihypertensive and antilipidemic agents and interactions thereof |
EP3990433A4 (en) | 2019-06-25 | 2023-07-26 | Translatum Medicus Inc. | METHODS FOR THE MANUFACTURE OF 2-((1-BENZYL-1H-INDAZOL-3-YL)METHOXY)-2-METHYLPROPANOIC ACID AND ITS DERIVATIVES |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FI88400C (fi) | 1984-08-06 | 1993-05-10 | Upjohn Co | Foerfarande foer framstaellning av renin inhiberande peptider |
MY103189A (en) | 1986-10-31 | 1993-05-29 | Pfizer | Nor-statine and nor-cyclostatine polypeptides |
US4927807A (en) | 1987-10-06 | 1990-05-22 | Abbott Laboratories | Glaucoma treatment |
IT1230441B (it) | 1989-02-07 | 1991-10-23 | Acraf | Eteri della serie dell'indazolo |
CA2023099A1 (en) | 1989-09-04 | 1991-03-05 | Quirico Branca | Amino acid derivatives |
US5209933A (en) | 1990-01-10 | 1993-05-11 | Syntex (U.S.A.) Inc. | Long acting calcium channel blocker composition |
IE68045B1 (en) | 1990-05-11 | 1996-05-15 | Abbott Lab | Renin inhibitors |
TW198712B (es) | 1991-04-17 | 1993-01-21 | Hoffmann La Roche | |
IT1253703B (it) | 1991-04-22 | 1995-08-23 | Angelini Francesco Ist Ricerca | Uso di acidi metossi alcanoici dell'indazolo per preparare un farmaco attivo nel trattamento di malattie autoimmunitarie |
MY119161A (en) | 1994-04-18 | 2005-04-30 | Novartis Ag | Delta-amino-gamma-hydroxy-omega-aryl-alkanoic acid amides with enzyme especially renin inhibiting activities |
US5994348A (en) * | 1995-06-07 | 1999-11-30 | Sanofi | Pharmaceutical compositions containing irbesartan |
IT1276031B1 (it) | 1995-10-31 | 1997-10-24 | Angelini Ricerche Spa | Composizione farmaceutica per il trattamento delle malattie autoimmuni |
SE9600120D0 (sv) | 1996-01-15 | 1996-01-15 | Astra Ab | Novel medical use |
IT1293795B1 (it) * | 1997-07-28 | 1999-03-10 | Angelini Ricerche Spa | Farmaco attivo nel ridurre la produzione di proteina mcp-1 |
US6268377B1 (en) | 1998-09-28 | 2001-07-31 | Merck & Co., Inc. | Method for treating androgen-related conditions |
GB0111077D0 (en) | 2001-05-04 | 2001-06-27 | Biochemie Gmbh | Organic compounds |
US20030073705A1 (en) | 2001-05-14 | 2003-04-17 | Shahnaz Shahinfar | Method of treatment |
US20030060501A1 (en) | 2001-09-19 | 2003-03-27 | Francois Mach | Facilitating tissue grafts with statins (HMG-COa reductase inhibitors) |
US7183285B2 (en) | 2004-04-29 | 2007-02-27 | Pharmix Corp. | Compositions and treatments for inhibiting kinase and/or HMG-CoA reductase |
US20070060549A1 (en) | 2004-08-10 | 2007-03-15 | Friesen Albert D | Combination therapies employing ace inhibitors and uses thereof for the treatment of diabetic disorders |
US20060046996A1 (en) | 2004-08-31 | 2006-03-02 | Kowa Co., Ltd. | Method for treating hyperlipidemia |
CN101052402A (zh) | 2004-10-29 | 2007-10-10 | 兴和株式会社 | 肾小球疾病治疗剂 |
CN101365438A (zh) | 2006-02-07 | 2009-02-11 | 持田制药株式会社 | 预防中风复发的组合物 |
WO2008084504A2 (en) | 2007-01-12 | 2008-07-17 | Rubicon Research Private Limited | Pharmaceutical compositions of angiotensin ii receptor blockers |
CA2679446C (en) * | 2007-03-01 | 2016-05-17 | Probiodrug Ag | New use of glutaminyl cyclase inhibitors |
JP5509102B2 (ja) | 2008-03-07 | 2014-06-04 | アジェンデ・キミケ・リウニテ・アンジェリニ・フランチェスコ・ア・チ・エレ・ア・エフェ・ソシエタ・ペル・アチオニ | 新規な1−ベンジル−3−ヒドロキシメチルインダゾール誘導体およびそのmcp−1およびcx3cr1の発現に基づく疾患の治療への使用 |
PL2254870T3 (pl) * | 2008-03-07 | 2016-07-29 | Acraf | Pochodne 1-benzylo-3-hydroksymetyloindazolu i ich zastosowanie w leczeniu chorób opartych na ekspresji MCP-1, CX3CR1 |
PT2262778T (pt) | 2008-03-07 | 2019-11-19 | Acraf | Derivados de 1-benzil-3-hidroximetilindazolo e utilização dos mesmos no tratamento de doenças baseadas na expressão de mcp-1, cxcr1 e p40 |
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2010
- 2010-03-09 UA UAA201203482A patent/UA108742C2/uk unknown
- 2010-09-03 SI SI201031512T patent/SI2480224T1/sl unknown
- 2010-09-03 BR BR112012006149A patent/BR112012006149A2/pt not_active Application Discontinuation
- 2010-09-03 PL PL10747897T patent/PL2480224T3/pl unknown
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- 2010-09-03 CN CN201080042390.9A patent/CN102573827B/zh not_active Expired - Fee Related
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