RU2005136864A - Применение соединений оксикама - Google Patents

Применение соединений оксикама Download PDF

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Publication number
RU2005136864A
RU2005136864A RU2005136864/15A RU2005136864A RU2005136864A RU 2005136864 A RU2005136864 A RU 2005136864A RU 2005136864/15 A RU2005136864/15 A RU 2005136864/15A RU 2005136864 A RU2005136864 A RU 2005136864A RU 2005136864 A RU2005136864 A RU 2005136864A
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RU
Russia
Prior art keywords
lornoxicam
cox
induction
thiazine
thieno
Prior art date
Application number
RU2005136864/15A
Other languages
English (en)
Other versions
RU2366425C2 (ru
Inventor
Дитер БИНДЕР (умер)
Original Assignee
БИНДЕР Ева (AT)
БИНДЕР Ева
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.)
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Publication date
Application filed by БИНДЕР Ева (AT), БИНДЕР Ева filed Critical БИНДЕР Ева (AT)
Publication of RU2005136864A publication Critical patent/RU2005136864A/ru
Application granted granted Critical
Publication of RU2366425C2 publication Critical patent/RU2366425C2/ru

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Classifications

    • 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
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Urology & Nephrology (AREA)
  • Hospice & Palliative Care (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Psychiatry (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Saccharide Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Claims (3)

1. Применение лорноксикама или аналогов лорноксикама, которые ингибируют циклооксигеназу 1 и циклооксигеназу 2 (СОХ 1 и СОХ 2), не могут преодолевать гематоэнцефалический барьер при физиологических условиях, и сокращают индуцированную простогландином Е2 индукцию белка-предшественника амилоидов (АРР), для получения фармацевтической композиции для лечения или предотвращения болезни Альцгеймера (БА) или артериосклероза.
2. Применение по п.1, отличающееся тем, что введение вещества сопровождается тяжелыми нежелательными побочными действиями на уровне ниже 1%, предпочтительно ниже 0,5%, более предпочтительно ниже 0,1%, в особенности ниже 0,05% пациентов.
3. Применение по п.1 или 2, отличающееся тем, что аналог лорноксикама выбран из группы включающей 6-хлор-4-(1-(этоксикарбамоилокси)этокси)-2-метил-N-(2-пиридил)-2Н-тиено-(2,3-е)-1,2-тиазин-3-карбоновой кислоты амид-1,1-диоксид, 6-хлор-4-гидрокси-2-метил-3-(2-пиридил-карбамоил)-2Н-тиено[3,2-е]1,2-тиазин-1,1-диоксид.
RU2005136864/15A 2003-05-27 2004-05-27 Применение соединений оксикама RU2366425C2 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ATA819/2003 2003-05-27
AT0081903A AT413944B (de) 2003-05-27 2003-05-27 Verwendung von oxicam-verbindungen

Publications (2)

Publication Number Publication Date
RU2005136864A true RU2005136864A (ru) 2006-06-10
RU2366425C2 RU2366425C2 (ru) 2009-09-10

Family

ID=33479909

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2005136864/15A RU2366425C2 (ru) 2003-05-27 2004-05-27 Применение соединений оксикама

Country Status (13)

Country Link
US (2) US8129370B2 (ru)
EP (1) EP1626726B1 (ru)
JP (1) JP5597339B2 (ru)
KR (1) KR101134244B1 (ru)
CN (3) CN102218067A (ru)
AT (2) AT413944B (ru)
CA (1) CA2526816C (ru)
DE (1) DE502004001499D1 (ru)
DK (1) DK1626726T3 (ru)
ES (1) ES2271893T3 (ru)
PL (1) PL1626726T3 (ru)
RU (1) RU2366425C2 (ru)
WO (1) WO2004105766A2 (ru)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2563575C (en) * 2004-04-29 2012-12-18 Binder, Eva Enantiomerically pure hexahydropyrrolocyclopentapyridine derivatives
WO2010057020A2 (en) * 2008-11-13 2010-05-20 Modgene, Llc Modification of amyloid-beta load in non-brain tissue
EP2776035B1 (en) 2011-11-01 2016-08-10 Modgene, Llc Compositions and methods for reduction of amyloid-beta load
CN115227655A (zh) * 2022-08-17 2022-10-25 海南锦瑞制药有限公司 注射用氯诺昔康的制备方法

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU518216B2 (en) 1977-09-06 1981-09-17 Hafslund Nycomed Pharma Aktiengesellschaft Thienothiazine derivatives
JPS58146040A (ja) * 1982-02-24 1983-08-31 Pioneer Video Kk 光学式情報記録原盤
ATE26720T1 (de) 1982-09-09 1987-05-15 Hoffmann La Roche Thieno(2,3-e)-1,2-thiazin-derivate.
IL87951A (en) 1987-10-29 1992-03-29 Chem Pharm Forsch Gmbh Carbonic acid esters of 6-chloro-4-(1-hydroxyethoxy)-2-methyl-n-(2-pyridyl)-2h-thieno(2,3-e)-1,2-thiazine-3-carboxamide 1,1-dioxide,their preparation and pharmaceutical compositions containing them
US5192753A (en) * 1991-04-23 1993-03-09 Mcgeer Patrick L Anti-rheumatoid arthritic drugs in the treatment of dementia
AT400437B (de) * 1993-12-14 1995-12-27 Chem Pharm Forsch Gmbh Neue n-heterocyclische thienothiazincarboxamide, verfahren zu ihrer herstellung und ihre verwendung
US5643960A (en) * 1994-04-15 1997-07-01 Duke University Method of delaying onset of alzheimer's disease symptoms
US6043224A (en) 1996-09-05 2000-03-28 The Massachusetts Institute Of Technology Compositions and methods for treatment of neurological disorders and neurodegenerative diseases
US6184248B1 (en) * 1996-09-05 2001-02-06 Robert K. K. Lee Compositions and methods for treatment of neurological disorders and neurodegenerative diseases
AU3885901A (en) * 1999-09-21 2001-04-24 Emory University Methods and compositions for treating platelet-related disorders
AU2001257022B2 (en) * 2000-04-13 2005-02-03 Mayo Foundation For Medical Education And Research Abeta 42 lowering agents
US6429223B1 (en) 2000-06-23 2002-08-06 Medinox, Inc. Modified forms of pharmacologically active agents and uses therefor
TWI256305B (en) * 2000-08-18 2006-06-11 Pharmacia Corp Oral fast-melt pharmaceutical composition of a cyclooxygenase-2 inhibitor and process for preparing the same
JP2002363104A (ja) 2001-04-04 2002-12-18 Sankyo Co Ltd 炎症性サイトカイン産生抑制剤の新規医薬用途
US7008614B2 (en) * 2001-08-20 2006-03-07 Fuji Photo Film Co., Ltd. Liposome containing hydrophobic iodine compound and X-ray contrast medium for radiograph comprising the liposome
US20030225054A1 (en) * 2002-06-03 2003-12-04 Jingwu Duan Combined use of tace inhibitors and COX2 inhibitors as anti-inflammatory agents

Also Published As

Publication number Publication date
ES2271893T3 (es) 2007-04-16
ATE339206T1 (de) 2006-10-15
CA2526816C (en) 2012-11-27
CN102218067A (zh) 2011-10-19
KR101134244B1 (ko) 2012-04-09
CA2526816A1 (en) 2004-12-09
EP1626726A2 (de) 2006-02-22
KR20060017618A (ko) 2006-02-24
JP5597339B2 (ja) 2014-10-01
CN101450057A (zh) 2009-06-10
US8129370B2 (en) 2012-03-06
US20070275958A1 (en) 2007-11-29
EP1626726B1 (de) 2006-09-13
PL1626726T3 (pl) 2007-02-28
WO2004105766A3 (de) 2005-03-03
WO2004105766A2 (de) 2004-12-09
JP2006528206A (ja) 2006-12-14
DE502004001499D1 (de) 2006-10-26
CN1842338A (zh) 2006-10-04
US20090239852A1 (en) 2009-09-24
ATA8192003A (de) 2005-11-15
AT413944B (de) 2006-07-15
RU2366425C2 (ru) 2009-09-10
DK1626726T3 (da) 2006-12-27

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PC41 Official registration of the transfer of exclusive right

Effective date: 20110928

PC41 Official registration of the transfer of exclusive right

Effective date: 20131122

MM4A The patent is invalid due to non-payment of fees

Effective date: 20200528