NO20013072L - Nitrogenholdige heterocykler som faktor Xa-inhibitorer - Google Patents
Nitrogenholdige heterocykler som faktor Xa-inhibitorerInfo
- Publication number
- NO20013072L NO20013072L NO20013072A NO20013072A NO20013072L NO 20013072 L NO20013072 L NO 20013072L NO 20013072 A NO20013072 A NO 20013072A NO 20013072 A NO20013072 A NO 20013072A NO 20013072 L NO20013072 L NO 20013072L
- Authority
- NO
- Norway
- Prior art keywords
- inhibitors
- nitrogen
- factor
- containing heterocycles
- heterocycles
- Prior art date
Links
Classifications
-
- 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
- C07D471/02—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 two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11362898P | 1998-12-23 | 1998-12-23 | |
US12763399P | 1999-04-02 | 1999-04-02 | |
PCT/US1999/030316 WO2000039131A1 (en) | 1998-12-23 | 1999-12-17 | Nitrogen containing heterobicycles as factor xa inhibitors |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20013072D0 NO20013072D0 (no) | 2001-06-20 |
NO20013072L true NO20013072L (no) | 2001-06-20 |
NO319816B1 NO319816B1 (no) | 2005-09-19 |
Family
ID=26811284
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20013072A NO319816B1 (no) | 1998-12-23 | 2001-06-20 | Nitrogenholdige heterocykler,anvendelse av disse for fremstilling av medikamenter samt farmasoytiske preparater. |
Country Status (26)
Country | Link |
---|---|
US (2) | US6413980B1 (no) |
EP (1) | EP1140941B1 (no) |
JP (1) | JP2002533465A (no) |
KR (1) | KR100628407B1 (no) |
CN (1) | CN100340559C (no) |
AR (1) | AR024242A1 (no) |
AT (1) | ATE280171T1 (no) |
AU (1) | AU759711B2 (no) |
BR (1) | BR9917080A (no) |
CA (1) | CA2349330C (no) |
DE (1) | DE69921358T2 (no) |
DK (1) | DK1140941T3 (no) |
EA (1) | EA004515B1 (no) |
ES (1) | ES2232202T3 (no) |
HK (1) | HK1052508B (no) |
HR (1) | HRP990396A2 (no) |
IL (2) | IL142959A0 (no) |
MX (1) | MXPA01006502A (no) |
MY (1) | MY138239A (no) |
NO (1) | NO319816B1 (no) |
NZ (1) | NZ511674A (no) |
PT (1) | PT1140941E (no) |
SI (1) | SI1140941T1 (no) |
TW (1) | TWI225862B (no) |
WO (1) | WO2000039131A1 (no) |
ZA (1) | ZA200103795B (no) |
Families Citing this family (66)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE373655T1 (de) * | 2000-06-23 | 2007-10-15 | Bristol Myers Squibb Pharma Co | 1-(heteroaryl-phenyl)-kondensierte pyrazol- derivate als factor xa inhibitoren |
US20040077605A1 (en) * | 2001-06-20 | 2004-04-22 | Salvati Mark E. | Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function |
EP1854798A3 (en) | 2000-09-19 | 2007-11-28 | Bristol-Myers Squibb Company | Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function |
US20040087548A1 (en) | 2001-02-27 | 2004-05-06 | Salvati Mark E. | Fused cyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function |
US6960595B2 (en) * | 2001-03-23 | 2005-11-01 | Bristol-Myers Squibb Pharma Company | 5-6 to 5-7 Heterobicycles as factor Xa inhibitors |
US6706730B2 (en) | 2001-04-18 | 2004-03-16 | Bristol-Myers Squibb Pharma Company | 1,4,5,6-tetrahydropyrazolo-[3,4-c]-pyridin-7-ones as factor Xa inhibitors |
US6750225B2 (en) | 2001-04-18 | 2004-06-15 | Bristol-Myers Squibb Pharms Company | 1,4,5,6-tetrahydropyrazolo-[3,4,-c]-pyridin-7-ones useful as factor Xa inhibitors |
EP1414449A4 (en) * | 2001-05-22 | 2005-04-06 | Bristol Myers Squibb Co | FACTOR XA BICYCLIC INHIBITORS |
TWI320039B (en) | 2001-09-21 | 2010-02-01 | Lactam-containing compounds and derivatives thereof as factor xa inhibitors | |
MXPA04002526A (es) | 2001-09-21 | 2004-05-31 | Bristol Myers Squibb Co | Compuestos que contienen lactama y sus derivados como inhibidores del factor xa. |
TW200302225A (en) | 2001-12-04 | 2003-08-01 | Bristol Myers Squibb Co | Substituted amino methyl factor Xa inhibitors |
WO2003048081A2 (en) * | 2001-12-04 | 2003-06-12 | Bristol-Myers Squibb Company | Glycinamides as factor xa inhibitors |
TW200738672A (en) * | 2001-12-10 | 2007-10-16 | Bristol Myers Squibb Co | Intermediated for the preparation of 4,5-dihydro-pyrazolo [3,4-c] pyrid-2-ones |
PL206962B1 (pl) * | 2001-12-19 | 2010-10-29 | Bristol Myers Squibb Co | Związek heterocykliczny o budowie skondensowanej |
ES2373875T3 (es) * | 2002-03-05 | 2012-02-09 | Transtech Pharma, Inc. | Derivados de azol mono y bicíclicos que inhiben la interacción de ligandos con rage. |
US7312214B2 (en) | 2002-05-10 | 2007-12-25 | Bristol-Myers Squibb Company | 1, 1-disubstituted cycloalkyl derivatives as factor Xa inhibitors |
PT1569912E (pt) | 2002-12-03 | 2015-09-15 | Pharmacyclics Llc | Derivados 2-(2-hidroxibifenil-3-il)-1h-benzoimidazole-5- carboxamidina como inibidores do fator viia |
EP1479678A1 (en) * | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Pyrazole-derivatives as factor xa inhibitors |
BR0317659A (pt) * | 2002-12-23 | 2005-12-06 | Aventis Pharma Gmbh | Derivados de pirazol como inibidores de fator xa |
US7429581B2 (en) | 2002-12-23 | 2008-09-30 | Sanofi-Aventis Deutschland Gmbh | Pyrazole-derivatives as factor Xa inhibitors |
US7122557B2 (en) * | 2003-03-18 | 2006-10-17 | Bristol-Myers Squibb Company | Sulfonyl-amidino-containing and tetrahydropyrimidino-containing compounds as factor Xa inhibitors |
US7135469B2 (en) * | 2003-03-18 | 2006-11-14 | Bristol Myers Squibb, Co. | Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors |
EP1479675A1 (en) * | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Indazole-derivatives as factor Xa inhibitors |
AU2004251599A1 (en) * | 2003-05-20 | 2005-01-06 | Transtech Pharma, Inc. | Rage antagonists as agents to reverse amyloidosis and diseases associated therewith |
US7022850B2 (en) | 2003-05-22 | 2006-04-04 | Bristol-Myers Squibb Co. | Bicyclicpyrimidones and their use to treat diseases |
EP1668013B1 (en) | 2003-09-23 | 2012-02-22 | Vertex Pharmaceuticals Incorporated | Pyrazolopyrrole derivatives as protein kinase inhibitors |
ES2538587T3 (es) | 2004-02-24 | 2015-06-22 | Sumitomo Chemical Co., Ltd | Composiciones insecticidas |
BRPI0514390A (pt) | 2004-08-18 | 2008-06-10 | Astrazeneca Ab | enanciÈmero de um composto ou um sal farmacêuticamente aceitável ou um éster hidrolisável in vivo do mesmo, uso do mesmo, métodos para o tratamento de cáncer, para produzir um efeito inibidor de eg5 em um animal de sangue quente e para tratar doenças, e, composição farmacêutica |
US20060069085A1 (en) * | 2004-09-28 | 2006-03-30 | Rulin Zhao | Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones |
US7381732B2 (en) * | 2004-10-26 | 2008-06-03 | Bristol-Myers Squibb Company | Pyrazolobenzamides and derivatives as factor Xa inhibitors |
BRPI0606476A2 (pt) | 2005-01-07 | 2009-06-30 | Synta Pharmaceuticals Corp | compostos para inflamação e usos imuno-relacionados e suas composições farmacêuticas |
KR20090064478A (ko) * | 2006-11-13 | 2009-06-18 | 화이자 프로덕츠 인크. | 디아릴, 디피리디닐 및 아릴-피리디닐 유도체, 및 이들의 용도 |
EP2145889A4 (en) | 2007-04-18 | 2012-04-18 | Kissei Pharmaceutical | HETEROCYCLIC FUSED CORE DERIVATIVE, PHARMACEUTICAL COMPOSITION COMPRISING THE DERIVATIVE, AND USE OF THE COMPOSITION FOR MEDICAL PURPOSES |
US8426427B2 (en) | 2007-04-18 | 2013-04-23 | Kissei Pharmaceutical Co., Ltd. | Fused heterocyclic derivative, pharmaceutical composition comprising the derivative, and use of the composition for medical purposes |
CA2772797C (en) | 2009-09-30 | 2018-09-25 | Transtech Pharma, Inc. | Substituted imidazole derivatives |
PL3246021T3 (pl) | 2010-02-25 | 2020-04-30 | Bristol-Myers Squibb Holdings Ireland Unlimited Company | Formulacje apiksabanu |
WO2012168364A1 (en) | 2011-06-10 | 2012-12-13 | Dipharma Francis S.R.L. | Apixaban preparation process |
CN104109165A (zh) * | 2013-04-19 | 2014-10-22 | 四川海思科制药有限公司 | 4,5-二氢-吡唑并[3,4-c]吡啶-2-酮衍生物、其制备方法以及应用 |
CN103992310B (zh) * | 2013-05-14 | 2016-07-06 | 中国医学科学院医药生物技术研究所 | 一组取代苯并杂环胺衍生物及其制备方法和作为impdh抑制剂的相关应用 |
CN104395312B (zh) * | 2013-06-21 | 2016-04-27 | 四川海思科制药有限公司 | 4,5-二氢吡唑并[3,4-c]吡啶-2-酮的螺环衍生物、其制备方法以及应用 |
WO2015004028A1 (de) | 2013-07-08 | 2015-01-15 | Bayer Cropscience Ag | Sechsgliedrige c-n-verknüpfte arylsulfid- und arylsulfoxid- derivate als schädlingsbekämpfungsmittel |
WO2015081901A1 (zh) * | 2013-12-06 | 2015-06-11 | 四川海思科制药有限公司 | 取代的4,5-二氢吡唑并[3,4-c]吡啶-2-酮的螺环衍生物及应用 |
WO2015162551A1 (en) | 2014-04-21 | 2015-10-29 | Mylan Laboratories Ltd | Process for the preparation of apixaban |
KR102412045B1 (ko) * | 2014-05-22 | 2022-06-22 | 놀스 차이나 파마수티칼 컴퍼니., 엘티디. | 혈액응고인자 Xa 억제제로서의 히드라지드 화합물 |
CN105085515B (zh) * | 2014-05-22 | 2019-02-01 | 华北制药股份有限公司 | 作为凝血因子Xa抑制剂的酰肼类化合物 |
US9975893B2 (en) | 2014-09-02 | 2018-05-22 | Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. | Pyrazolo[3,4-c]pyridine derivatives |
EP3189053B1 (en) | 2014-09-05 | 2021-05-05 | Unichem Laboratories Limited | An improved process for the preparation of apixaban and intermediates thereof |
CN104311556B (zh) * | 2014-09-19 | 2016-06-01 | 广东东阳光药业有限公司 | 含有环氧烷基取代基的吡唑并哌啶酮类化合物及其组合物及用途 |
CN104311555B (zh) * | 2014-09-19 | 2016-04-20 | 广东东阳光药业有限公司 | 吡唑并哌啶酮类化合物及其组合物及用途 |
CN104311575B (zh) * | 2014-09-19 | 2016-04-20 | 广东东阳光药业有限公司 | 含有稠环的吡唑并哌啶酮类化合物及其组合物及用途 |
CN104311557B (zh) * | 2014-09-19 | 2016-01-06 | 广东东阳光药业有限公司 | 含有二酮取代基的吡唑并哌啶酮类化合物及其组合物及用途 |
CN104311574B (zh) * | 2014-09-19 | 2016-04-20 | 广东东阳光药业有限公司 | 含有噻唑的吡唑并哌啶酮类化合物及其组合物及用途 |
CN104277037B (zh) * | 2014-09-19 | 2015-12-09 | 广东东阳光药业有限公司 | 含有螺环的吡唑并哌啶酮类化合物及其组合物及用途 |
CN104277039B (zh) * | 2014-09-19 | 2016-06-01 | 广东东阳光药业有限公司 | 含有取代丁炔基的吡唑并哌啶酮类化合物及其组合物及用途 |
CN104530029B (zh) * | 2014-12-09 | 2017-04-12 | 广东东阳光药业有限公司 | 作为Xa因子抑制剂的杂环化合物及其使用方法和用途 |
CN104513239B (zh) * | 2014-12-10 | 2017-08-22 | 沈阳药科大学 | 吡唑并[3,4‑c]吡啶‑7‑酮类化合物及其应用 |
US10077263B2 (en) | 2016-04-29 | 2018-09-18 | Optimus Drugs Private Limited | Process for the preparation of Apixaban |
EP3582777A4 (en) | 2017-02-17 | 2020-12-23 | Unichem Laboratories Ltd | PHARMACEUTICAL COMPOSITION OF APIXABAN |
CN107235986B (zh) * | 2017-05-27 | 2019-04-12 | 华南师范大学 | 一种合成氮氧杂桥联唑啉化合物的方法 |
GB201807014D0 (en) | 2018-04-30 | 2018-06-13 | Univ Leeds Innovations Ltd | Factor xlla inhibitors |
TWI838401B (zh) | 2018-09-12 | 2024-04-11 | 瑞士商諾華公司 | 抗病毒性吡啶并吡𠯤二酮化合物 |
KR102128509B1 (ko) * | 2018-12-19 | 2020-07-01 | 한국과학기술연구원 | 말단 아민기에 아릴 또는 헤테로아릴기가 치환된 신규한 히드라존 유도체 및 이의 용도 |
AU2020353055B2 (en) | 2019-09-26 | 2024-03-07 | Gilead Sciences, Inc. | Antiviral pyrazolopyridinone compounds |
GB202107722D0 (en) | 2021-05-28 | 2021-07-14 | Lunac Therapeutics Ltd | Factor XIIA Inhibitors |
CN113956248B (zh) * | 2021-11-12 | 2023-07-04 | 贵州中医药大学 | 一种具有抗炎作用的化合物衍生物及其制备方法和应用 |
AU2022386486A1 (en) | 2021-11-12 | 2024-05-09 | Insilico Medicine Ip Limited | Small molecule inhibitors of ubiquitin specific protease 1 (usp1) and uses thereof |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3365459A (en) * | 1964-09-08 | 1968-01-23 | Ciba Geigy Corp | Certain tetrahydro pyrazolo-pyridine and pyrazolo-piperidine derivatives |
US3340269A (en) * | 1964-09-08 | 1967-09-05 | Ciba Geigy Corp | 1-substituted 4-acyl-2, 3-dioxo-piperidine |
US3423414A (en) * | 1966-01-13 | 1969-01-21 | Ciba Geigy Corp | Pyrazolopyridines |
US3939161A (en) * | 1973-10-29 | 1976-02-17 | Abbott Laboratories | 1,3-Dimethyl- 1H-pyrazolo(4,3-D) pyrimidine-7 (6H)-ones |
JPS5721388A (en) * | 1980-07-11 | 1982-02-04 | Nippon Nohyaku Co Ltd | Condensed pyrazole derivative |
JPS63145282A (ja) * | 1986-12-08 | 1988-06-17 | Taiyo Yakuhin Kogyo Kk | ピリダジン誘導体 |
GB9114760D0 (en) * | 1991-07-09 | 1991-08-28 | Pfizer Ltd | Therapeutic agents |
ES2196000T3 (es) * | 1991-08-07 | 2003-12-16 | Daiichi Suntory Pharma Co Ltd | Compuesto de pirroloazepina. |
WO1994020460A1 (en) | 1993-03-11 | 1994-09-15 | Smithkline Beecham Corporation | Chemical compounds |
CN1048015C (zh) * | 1993-07-06 | 2000-01-05 | 美国辉瑞有限公司 | 双环四氢吡唑并吡啶类化合物 |
NZ292991A (en) * | 1994-10-20 | 1999-02-25 | Pfizer | Bicyclic tetrahydropyrazolopyridines that are selective inhibitors of phosphodiesterase (pde) type iv or the production of tnf and pharmaceutical compositions containing them |
US6323201B1 (en) * | 1994-12-29 | 2001-11-27 | The Regents Of The University Of California | Compounds for inhibition of ceramide-mediated signal transduction |
WO1997023480A1 (en) * | 1995-12-22 | 1997-07-03 | The Du Pont Merck Pharmaceutical Company | Novel integrin receptor antagonists |
DK0807633T3 (da) * | 1996-05-15 | 2002-11-25 | Pfizer | Hidtil ukendte 2,3-disubstituerede-(5,6)-heteroarylkondenserede pyrimidin-4-oner |
FR2750862B1 (fr) * | 1996-07-12 | 1998-10-16 | Dupin Jean Pierre | Utilisation d'heterocycles diazotes fusionnes avec un systeme aromatique ou heteroaromatique pour le traitement des maladies thrombo-emboliques |
HUP0100179A3 (en) * | 1997-07-03 | 2002-12-28 | Bristol Myers Squibb Pharma Co | Imidazopyrimidine and imidazopyridine derivatives and pharmaceutical compositions thereof |
ES2230841T3 (es) * | 1998-03-27 | 2005-05-01 | Bristol-Myers Squibb Pharma Company | Pirazolinas y triazolinas disustituidas como inhibidores del factor xa. |
DE19845153A1 (de) | 1998-10-01 | 2000-04-06 | Merck Patent Gmbh | Imidazo[4,5]-pyridin-4-on-derivate |
DE19900471A1 (de) | 1999-01-08 | 2000-07-13 | Merck Patent Gmbh | Imidazo[4,5c]-pyridin-4-on-derivate |
JP2003509412A (ja) | 1999-09-17 | 2003-03-11 | シーオーアール セラピューティクス インコーポレイテッド | Xa因子阻害剤 |
-
1999
- 1999-12-17 EA EA200100688A patent/EA004515B1/ru not_active IP Right Cessation
- 1999-12-17 MX MXPA01006502A patent/MXPA01006502A/es active IP Right Grant
- 1999-12-17 JP JP2000591042A patent/JP2002533465A/ja active Pending
- 1999-12-17 IL IL14295999A patent/IL142959A0/xx unknown
- 1999-12-17 DK DK99967444T patent/DK1140941T3/da active
- 1999-12-17 KR KR1020017007991A patent/KR100628407B1/ko not_active IP Right Cessation
- 1999-12-17 BR BR9917080-9A patent/BR9917080A/pt not_active Application Discontinuation
- 1999-12-17 DE DE69921358T patent/DE69921358T2/de not_active Expired - Lifetime
- 1999-12-17 AT AT99967444T patent/ATE280171T1/de active
- 1999-12-17 CA CA002349330A patent/CA2349330C/en not_active Expired - Lifetime
- 1999-12-17 EP EP99967444A patent/EP1140941B1/en not_active Expired - Lifetime
- 1999-12-17 AU AU23717/00A patent/AU759711B2/en active Active
- 1999-12-17 PT PT99967444T patent/PT1140941E/pt unknown
- 1999-12-17 NZ NZ511674A patent/NZ511674A/en not_active IP Right Cessation
- 1999-12-17 WO PCT/US1999/030316 patent/WO2000039131A1/en active IP Right Grant
- 1999-12-17 SI SI9930721T patent/SI1140941T1/xx unknown
- 1999-12-17 ES ES99967444T patent/ES2232202T3/es not_active Expired - Lifetime
- 1999-12-17 CN CNB998147710A patent/CN100340559C/zh not_active Expired - Fee Related
- 1999-12-21 HR HR990396A patent/HRP990396A2/hr not_active Application Discontinuation
- 1999-12-22 US US09/470,326 patent/US6413980B1/en not_active Expired - Lifetime
- 1999-12-22 MY MYPI99005666A patent/MY138239A/en unknown
- 1999-12-23 AR ARP990106759A patent/AR024242A1/es active IP Right Grant
-
2000
- 2000-01-15 TW TW088122748A patent/TWI225862B/zh not_active IP Right Cessation
-
2001
- 2001-05-03 IL IL142959A patent/IL142959A/en not_active IP Right Cessation
- 2001-05-10 ZA ZA200103795A patent/ZA200103795B/en unknown
- 2001-06-20 NO NO20013072A patent/NO319816B1/no not_active IP Right Cessation
- 2001-07-03 US US09/898,279 patent/US6673810B2/en not_active Expired - Lifetime
-
2003
- 2003-07-04 HK HK03104763.4A patent/HK1052508B/zh not_active IP Right Cessation
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