TR200102958T2 - Siklooksijenaz-2 inhibitörleri olarak 4,5-diaril-3(2H)-furanon türevleri. - Google Patents
Siklooksijenaz-2 inhibitörleri olarak 4,5-diaril-3(2H)-furanon türevleri.Info
- Publication number
- TR200102958T2 TR200102958T2 TR2001/02958T TR200102958T TR200102958T2 TR 200102958 T2 TR200102958 T2 TR 200102958T2 TR 2001/02958 T TR2001/02958 T TR 2001/02958T TR 200102958 T TR200102958 T TR 200102958T TR 200102958 T2 TR200102958 T2 TR 200102958T2
- Authority
- TR
- Turkey
- Prior art keywords
- diaryl
- cyclooxygenase
- inhibitors
- furanone derivatives
- cox
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
-
- 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
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- 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
- A61P9/10—Drugs 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/58—One oxygen atom, e.g. butenolide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/64—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/94—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom spiro-condensed with carbocyclic rings or ring systems, e.g. griseofulvins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Ophthalmology & Optometry (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Mevcut bulus yeni bir 4,5-diaril-3(2H)-furanon türevi sinifini saglamakta olup, bu bilesikler güçlü bir sekilde ve selektif olarak COX-2'yi COX-1'e karsi inhibe etmektedir. Bu bilesikler enflamasyon, enflamasyona bagli rahatsizliklarin ve COX-kaynakli hastaliklarin tedavi edilmesinde kullanislidir.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019990013170A KR20000066223A (ko) | 1999-04-14 | 1999-04-14 | 디아릴-3(2h)퓨라논 유도체 및 이를 함유하는 시클로옥시게네이즈-2 저해제 조성물 |
KR1019990029779A KR20010010728A (ko) | 1999-07-22 | 1999-07-22 | 2,2-디알킬-4,5-디아릴-3(2h)퓨라논의 유도체 및 이를 함유하는 시클로옥시게네이즈-2 저해제 조성물 |
KR1019990039043A KR20010027342A (ko) | 1999-09-13 | 1999-09-13 | 2,2-디알킬-4,5-디아릴-3(2h)퓨라논의 술폰아마이드 유도체 및 이를 함유하는 시클로옥시게네이즈-2 저해제 조성물 |
KR1020000016866A KR20010094519A (ko) | 2000-03-31 | 2000-03-31 | 2,2,4,5-사중 치환된 3(2h)-퓨라논 유도체의 제조 방법 |
KR1020000017647A KR20010094161A (ko) | 2000-04-04 | 2000-04-04 | 2,2-디메틸-4,5-디아릴-3(2h)퓨라논의 유도체 및 이를함유하는 선택적인 시클로옥시게네이즈-2 저해제로서약제학적 조성물 |
Publications (1)
Publication Number | Publication Date |
---|---|
TR200102958T2 true TR200102958T2 (tr) | 2002-05-21 |
Family
ID=27532305
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TR2001/02958T TR200102958T2 (tr) | 1999-04-14 | 2000-04-12 | Siklooksijenaz-2 inhibitörleri olarak 4,5-diaril-3(2H)-furanon türevleri. |
Country Status (26)
Country | Link |
---|---|
US (1) | US6492416B1 (tr) |
EP (1) | EP1109799B1 (tr) |
JP (1) | JP3844657B2 (tr) |
KR (1) | KR20010111584A (tr) |
CN (1) | CN1166658C (tr) |
AT (1) | ATE256672T1 (tr) |
AU (1) | AU767811B2 (tr) |
BR (1) | BRPI0011172B8 (tr) |
CA (1) | CA2369979C (tr) |
CZ (1) | CZ300766B6 (tr) |
DE (1) | DE60007267T2 (tr) |
DZ (1) | DZ3265A1 (tr) |
EA (1) | EA004432B1 (tr) |
ES (1) | ES2213007T3 (tr) |
HK (1) | HK1046413B (tr) |
HU (1) | HU227863B1 (tr) |
IL (2) | IL145305A0 (tr) |
MA (1) | MA25406A1 (tr) |
MX (1) | MXPA01010312A (tr) |
NO (1) | NO327814B1 (tr) |
NZ (1) | NZ514101A (tr) |
PL (1) | PL204249B1 (tr) |
PT (1) | PT1109799E (tr) |
SK (1) | SK286314B6 (tr) |
TR (1) | TR200102958T2 (tr) |
WO (1) | WO2000061571A1 (tr) |
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010010728A (ko) * | 1999-07-22 | 2001-02-15 | 서경배 | 2,2-디알킬-4,5-디아릴-3(2h)퓨라논의 유도체 및 이를 함유하는 시클로옥시게네이즈-2 저해제 조성물 |
KR20010094161A (ko) * | 2000-04-04 | 2001-10-31 | 서경배 | 2,2-디메틸-4,5-디아릴-3(2h)퓨라논의 유도체 및 이를함유하는 선택적인 시클로옥시게네이즈-2 저해제로서약제학적 조성물 |
KR20000066223A (ko) * | 1999-04-14 | 2000-11-15 | 서경배 | 디아릴-3(2h)퓨라논 유도체 및 이를 함유하는 시클로옥시게네이즈-2 저해제 조성물 |
US6686390B2 (en) * | 2000-05-22 | 2004-02-03 | Dr. Reddy's Laboratories Limited | Compounds having antiinflamatory activity: process for their preparation and pharmaceutical compositions containing them |
CA2411960C (en) | 2000-06-13 | 2010-10-12 | Wyeth | Analgesic and anti-inflammatory compositions containing cox-2 inhibitors |
US20030105144A1 (en) | 2001-04-17 | 2003-06-05 | Ping Gao | Stabilized oral pharmaceutical composition |
US6858592B2 (en) | 2001-06-29 | 2005-02-22 | Genzyme Corporation | Aryl boronic acids for treating obesity |
US7041280B2 (en) | 2001-06-29 | 2006-05-09 | Genzyme Corporation | Aryl boronate functionalized polymers for treating obesity |
WO2003018575A1 (en) * | 2001-08-24 | 2003-03-06 | Wyeth Holdings Corporation | 5-substituted-3(2h)-furanones useful for inhibition of farnesyl-protein transferase |
US6667330B2 (en) * | 2002-01-31 | 2003-12-23 | Galileo Pharmaceuticals, Inc. | Furanone derivatives |
ES2214129B1 (es) * | 2003-02-13 | 2005-12-01 | Almirall Prodesfarma, S.A. | 3-fenilfuran-2-onas. |
ES2214130B1 (es) * | 2003-02-13 | 2005-12-01 | Almirall Prodesfarma, S.A. | 2-3'-bipiridinas. |
ES2213485B1 (es) * | 2003-02-13 | 2005-12-16 | Almirall Prodesfarma, S.A. | Derivados de la 2-fenilpiran-4-ona. |
US20040220155A1 (en) * | 2003-03-28 | 2004-11-04 | Pharmacia Corporation | Method of providing a steroid-sparing benefit with a cyclooxygenase-2 inhibitor and compositions therewith |
US20050014729A1 (en) * | 2003-07-16 | 2005-01-20 | Pharmacia Corporation | Method for the treatment or prevention of dermatological disorders with a cyclooxygenase-2 inhibitor alone and in combination with a dermatological treatment agent and compositions therewith |
US20050119262A1 (en) * | 2003-08-21 | 2005-06-02 | Pharmacia Corporation | Method for preventing or treating an optic neuropathy with a cox-2 inhibitor and an intraocular pressure reducing agent |
WO2005023189A2 (en) * | 2003-09-03 | 2005-03-17 | Pharmacia Corporation | Method of cox-2 selective inhibitor and nitric oxide-donating agent |
JP4641772B2 (ja) * | 2003-10-23 | 2011-03-02 | 長谷川香料株式会社 | フラノンの製造方法 |
WO2005094815A1 (en) * | 2004-03-30 | 2005-10-13 | Amorepacific Corporation | Dual inhibition of cyclooxygenase-2 and carbonic anhydrase |
US20080306146A1 (en) * | 2005-11-02 | 2008-12-11 | Amorepacific Corporation | Dosing Regimens for Cox-2 Inhibitor |
EP2032147A4 (en) * | 2006-04-28 | 2011-02-02 | Cambridge Scient Pty Ltd | INHIBITOR OF COX-2 ENZYME |
EP2121669A2 (en) * | 2007-01-30 | 2009-11-25 | Biogen Idec MA, Inc. | Furanone compounds and methods of making and using the same |
TWI634114B (zh) * | 2013-05-08 | 2018-09-01 | 永恒生物科技公司 | 作為激酶抑制劑之呋喃酮化合物 |
WO2015080435A1 (ko) * | 2013-11-26 | 2015-06-04 | 화일약품주식회사 | 4-(3-(3-플루오로페닐)-5,5-디메틸-4-옥소-4,5-디하이드로푸란-2-일)벤젠설폰아마이드의 제조 방법 |
US10413520B2 (en) | 2014-01-29 | 2019-09-17 | Crystalgenomics, Inc. | Oral pharmacological composition including 5-{4-(amino sulfonyl)phenyl}-2,2-dimethyl-4-(3-fluorophenyl)-3(2H)-furanone having crystalline structure with excellent stability |
KR101446601B1 (ko) * | 2014-01-29 | 2014-10-07 | 크리스탈지노믹스(주) | 5-(4-(아미노설포닐)페닐)-2,2-디메틸-4-(3-플루오로페닐)-3(2h)-퓨라논을 포함하는 약학적 조성물 및 캡슐 제형 |
CN104926797B (zh) * | 2014-06-10 | 2019-04-16 | 北京元博方医药科技有限公司 | 呋喃酮衍生物、制备方法及用途 |
CN104098535A (zh) * | 2014-07-25 | 2014-10-15 | 南通市华峰化工有限责任公司 | 一种4-(3-氟苯基)-2,2-二甲基-5-(4-(甲硫基)苯基)呋喃-3(2h)-酮的制备方法 |
RU2563876C1 (ru) * | 2014-11-11 | 2015-09-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Санкт-Петербургский государственный университет" (СПбГУ) | Способ получения 2,2-диалкил-4,5-диарилфуран-3(2н)-онов |
CN106866558B (zh) * | 2015-08-21 | 2019-07-30 | 宁波百思佳医药科技有限公司 | 酰基三氮唑类化合物及其制备方法和应用 |
RU2631317C1 (ru) * | 2016-05-13 | 2017-09-21 | Общество с ограниченной ответственностью "Органик Эмиттерс" | Селективные ингибиторы циклооксигеназы и способ их получения |
US11583516B2 (en) | 2016-09-07 | 2023-02-21 | Trustees Of Tufts College | Dash inhibitors, and uses related thereto |
CN111303085B (zh) * | 2020-03-13 | 2022-04-01 | 西安瑞联新材料股份有限公司 | 5-溴-2,2-二甲基-5-(4-甲磺酰基苯基)呋喃-3(2h)-酮的合成方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63313719A (ja) * | 1987-06-15 | 1988-12-21 | T Hasegawa Co Ltd | 香料組成物 |
JPH0745483B2 (ja) * | 1987-09-26 | 1995-05-17 | 長谷川香料株式会社 | フラノン類の製造方法 |
JPH0825864B2 (ja) * | 1988-12-16 | 1996-03-13 | 長谷川香料株式会社 | 柴外線吸収剤 |
US5474995A (en) * | 1993-06-24 | 1995-12-12 | Merck Frosst Canada, Inc. | Phenyl heterocycles as cox-2 inhibitors |
DE69529690T2 (de) * | 1994-12-21 | 2003-11-13 | Merck Frosst Canada & Co., Halifax | Diaryl-2(5h)-fuaranone als cox-2-inhibitoren |
US5698585A (en) * | 1995-04-13 | 1997-12-16 | Kikkoman Corporation | Pharmaceutical preparation for prevention and/or treatment for cataract |
UA57002C2 (uk) * | 1995-10-13 | 2003-06-16 | Мерк Фросст Кенада Енд Ко./Мерк Фросст Кенада Енд Сі. | Похідне (метилсульфоніл)феніл-2-(5н)-фуранону, фармацевтична композиція та спосіб лікування |
-
2000
- 2000-04-12 TR TR2001/02958T patent/TR200102958T2/tr unknown
- 2000-04-12 US US09/744,762 patent/US6492416B1/en not_active Expired - Lifetime
- 2000-04-12 KR KR1020017012902A patent/KR20010111584A/ko unknown
- 2000-04-12 AU AU41480/00A patent/AU767811B2/en not_active Expired
- 2000-04-12 EA EA200100958A patent/EA004432B1/ru not_active IP Right Cessation
- 2000-04-12 PT PT00921133T patent/PT1109799E/pt unknown
- 2000-04-12 DE DE60007267T patent/DE60007267T2/de not_active Expired - Lifetime
- 2000-04-12 NZ NZ514101A patent/NZ514101A/en not_active IP Right Cessation
- 2000-04-12 JP JP2000610845A patent/JP3844657B2/ja not_active Expired - Lifetime
- 2000-04-12 IL IL14530500A patent/IL145305A0/xx active IP Right Grant
- 2000-04-12 CN CNB008062293A patent/CN1166658C/zh not_active Expired - Lifetime
- 2000-04-12 DZ DZ003265A patent/DZ3265A1/fr active
- 2000-04-12 CZ CZ20013662A patent/CZ300766B6/cs not_active IP Right Cessation
- 2000-04-12 CA CA002369979A patent/CA2369979C/en not_active Expired - Lifetime
- 2000-04-12 BR BRPI0011172A patent/BRPI0011172B8/pt not_active IP Right Cessation
- 2000-04-12 EP EP00921133A patent/EP1109799B1/en not_active Expired - Lifetime
- 2000-04-12 AT AT00921133T patent/ATE256672T1/de not_active IP Right Cessation
- 2000-04-12 ES ES00921133T patent/ES2213007T3/es not_active Expired - Lifetime
- 2000-04-12 HU HU0200623A patent/HU227863B1/hu unknown
- 2000-04-12 SK SK1451-2001A patent/SK286314B6/sk not_active IP Right Cessation
- 2000-04-12 WO PCT/KR2000/000339 patent/WO2000061571A1/en active IP Right Grant
- 2000-04-12 PL PL351125A patent/PL204249B1/pl unknown
-
2001
- 2001-09-06 IL IL145305A patent/IL145305A/en not_active IP Right Cessation
- 2001-10-12 MA MA26357A patent/MA25406A1/fr unknown
- 2001-10-12 NO NO20014986A patent/NO327814B1/no not_active IP Right Cessation
- 2001-10-12 MX MXPA01010312A patent/MXPA01010312A/es active IP Right Grant
-
2002
- 2002-11-05 HK HK02108027.8A patent/HK1046413B/zh not_active IP Right Cessation
Also Published As
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