HRP20010454B1 - 1,2-annelated quinoline derivatives - Google Patents
1,2-annelated quinoline derivativesInfo
- Publication number
- HRP20010454B1 HRP20010454B1 HR20010454A HRP20010454A HRP20010454B1 HR P20010454 B1 HRP20010454 B1 HR P20010454B1 HR 20010454 A HR20010454 A HR 20010454A HR P20010454 A HRP20010454 A HR P20010454A HR P20010454 B1 HRP20010454 B1 HR P20010454B1
- Authority
- HR
- Croatia
- Prior art keywords
- quinoline derivatives
- annelated quinoline
- annelated
- derivatives
- quinoline
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- A61K31/435—Heterocyclic 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
-
- 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)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Quinoline Compounds (AREA)
- Information Retrieval, Db Structures And Fs Structures Therefor (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98204444 | 1998-12-23 | ||
| PCT/EP1999/010214 WO2000039082A2 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HRP20010454A2 HRP20010454A2 (en) | 2002-06-30 |
| HRP20010454B1 true HRP20010454B1 (en) | 2004-06-30 |
Family
ID=8234557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20010454A HRP20010454B1 (en) | 1998-12-23 | 2001-06-15 | 1,2-annelated quinoline derivatives |
Country Status (32)
| Country | Link |
|---|---|
| US (2) | US6458800B1 (de) |
| EP (1) | EP1140935B1 (de) |
| JP (1) | JP4725940B2 (de) |
| KR (2) | KR100712226B1 (de) |
| CN (1) | CN1178938C (de) |
| AR (1) | AR021995A1 (de) |
| AT (1) | ATE240327T1 (de) |
| AU (1) | AU765437B2 (de) |
| BG (1) | BG65124B1 (de) |
| BR (1) | BR9916827A (de) |
| CA (1) | CA2355717C (de) |
| CZ (1) | CZ302374B6 (de) |
| DE (1) | DE69907964T2 (de) |
| DK (1) | DK1140935T3 (de) |
| EA (1) | EA004542B1 (de) |
| EE (1) | EE04962B1 (de) |
| ES (1) | ES2200591T3 (de) |
| HK (1) | HK1038746B (de) |
| HR (1) | HRP20010454B1 (de) |
| HU (1) | HU229404B1 (de) |
| ID (1) | ID29241A (de) |
| IL (2) | IL143859A0 (de) |
| NO (1) | NO318922B1 (de) |
| PL (1) | PL199080B1 (de) |
| PT (1) | PT1140935E (de) |
| SI (1) | SI1140935T1 (de) |
| SK (1) | SK286072B6 (de) |
| TR (1) | TR200101961T2 (de) |
| TW (1) | TW531533B (de) |
| UA (1) | UA71592C2 (de) |
| WO (1) | WO2000039082A2 (de) |
| ZA (1) | ZA200105136B (de) |
Families Citing this family (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60118889T2 (de) * | 2000-02-04 | 2006-11-30 | Janssen Pharmaceutica N.V. | Farnesyl protein transferase inhibitoren zur behandlung von brustkrebs |
| CA2397558A1 (en) | 2000-02-24 | 2001-08-30 | Janssen Pharmaceutica N.V. | Dosing regimen |
| EP1267871A2 (de) * | 2000-02-29 | 2003-01-02 | Janssen Pharmaceutica N.V. | Kombination von farnesyl proteintransferase inhibitoren mit antitumor wirksamen podophyllotoxin-derivaten |
| AU2001244166A1 (en) * | 2000-02-29 | 2001-09-12 | Janssen Pharmaceutica N.V. | Farnesyl protein transferase inhibitor combinations with further anti-cancer agents |
| EP1261343A2 (de) * | 2000-02-29 | 2002-12-04 | Janssen Pharmaceutica N.V. | Kombination von farnesyl proteintransferase inhibitoren mit antitumor wirksamen nukleosid-derivaten |
| WO2001064197A2 (en) * | 2000-02-29 | 2001-09-07 | Janssen Pharmaceutica N.V. | Farnesyl protein transferase inhibitor combinations with anti-tumor anthracycline derivatives |
| WO2001064194A2 (en) * | 2000-02-29 | 2001-09-07 | Janssen Pharmaceutica N.V. | Farnesyl protein transferase inhibitor combinations with camptothecin compounds |
| CA2397475A1 (en) * | 2000-02-29 | 2001-09-07 | Janssen Pharmaceutica N.V. | Farnesyl protein transferase inhibitor combinations with vinca alkaloids |
| CA2397657A1 (en) * | 2000-02-29 | 2001-09-07 | Janssen Pharmaceutica Inc. | Farnesyl protein transferase inhibitor combinations with platinum compounds |
| US20030078281A1 (en) * | 2000-02-29 | 2003-04-24 | Rybak Mary Ellen Margaret | Farnesyl protein transferase inhibitor combinations with anti-tumor alkylating agents |
| US20030181473A1 (en) * | 2000-02-29 | 2003-09-25 | Palmer Peter Albert | Farnesyl protein transferase inhibitor combinations with taxane compounds |
| JP2003525252A (ja) * | 2000-02-29 | 2003-08-26 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Ｈｅｒ２抗体とのファルネシルタンパク質トランスフェラーゼ阻害剤組み合わせ剤 |
| EP1261342A2 (de) * | 2000-02-29 | 2002-12-04 | Janssen Pharmaceutica N.V. | Kombination von farnesyl proteintransferase inhibitoren |
| JO2361B1 (en) * | 2000-06-22 | 2006-12-12 | جانسين فارماسيوتيكا ان. في | Enaniumer 1,2-anylated quinoline inhibitor for the transporter - farnesyl |
| JP4974439B2 (ja) * | 2000-09-25 | 2012-07-11 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | ファルネシルトランスフェラーゼを阻害する６−ヘテロシクリルメチルキノリノン誘導体 |
| JP4974437B2 (ja) * | 2000-09-25 | 2012-07-11 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | ファルネシルトランスフェラーゼを阻害する６−［（置換フェニル）メチル］−キノリンおよびキナゾリン誘導体 |
| EP1322650B1 (de) * | 2000-09-25 | 2008-09-24 | Janssen Pharmaceutica N.V. | Farnesyl transferase-hemmende 6-heterocyclylmethyl-chinolin und chinazol-derivate |
| DE60118225T2 (de) * | 2000-09-25 | 2007-05-03 | Janssen Pharmaceutica N.V. | Chinolin- und chinazolinderivate und deren verwendung als farnesyl transferase inhibitoren |
| AU2001293847B2 (en) | 2000-10-02 | 2007-05-24 | Janssen Pharmaceutica N.V. | Metabotropic glutamate receptor antagonists |
| DE60139080D1 (de) | 2000-11-21 | 2009-08-06 | Janssen Pharmaceutica Nv | Farnesyltransferase hemmende benzoheterocyclische derivate |
| ATE323490T1 (de) * | 2000-11-28 | 2006-05-15 | Janssen Pharmaceutica Nv | Farnesyl-protein-transferasehemmer zur behandlung der entzündlichen darmerkrankung |
| EP1347966B1 (de) | 2000-12-27 | 2006-03-08 | Janssen Pharmaceutica N.V. | Farnesyltransferase hemmende, in der 4-stellung substituierte chinolin- und chinazolinderivate |
| DE60230017D1 (de) * | 2001-02-15 | 2009-01-08 | Janssen Pharmaceutica Nv | Farnesyl-protein-transferase hemmer in kombination mit antiöstrogenen |
| EP1390033A1 (de) * | 2001-04-25 | 2004-02-25 | Janssen Pharmaceutica N.V. | Farnesyl protein transferase inhibitoren für die behandlung von cachexie |
| US6740757B2 (en) * | 2001-08-29 | 2004-05-25 | Pfizer Inc | Enantiomers of 6-[(4-chloro-phenyl)-hydroxy-(3-methyl-3h-imidazol-4-yl)-methyl]-4-[3-(3-hydroxy-3-methyl-but-1-ynyl)-phenyl]-1-methyl-1h-quinolin-2-one and salts thereof, useful in the treatment of cancer |
| AU2002352878B2 (en) * | 2001-11-27 | 2007-11-22 | Merck Sharp & Dohme Corp. | 2-Aminoquinoline compounds |
| DE60231646D1 (de) | 2001-12-19 | 2009-04-30 | Janssen Pharmaceutica Nv | Durch c-verbundene imidazole substituierte 1,8-annellierten chinolon-derivate als farnesyl transferase inhibitoren |
| US7241777B2 (en) | 2002-03-22 | 2007-07-10 | Janssen Pharmaceutica N.V. | Benzylimidazolyl substituted 2-quinoline and quinazoline derivatives for use as farnesyl transferase inhibitors |
| NZ535438A (en) * | 2002-03-29 | 2006-08-31 | Janssen Pharmaceutica Nv | Radiolabelled quinoline and quinolinone derivatives and their use as metabotropic glutamate receptor ligands |
| AU2003229688B2 (en) * | 2002-04-15 | 2009-07-30 | Janssen Pharmaceutica N.V. | Farnesyl transferase inhibiting tricyclic quinazoline derivatives substituted with carbon-linked imidazoles or triazoles |
| US20030125268A1 (en) * | 2002-08-28 | 2003-07-03 | Rybak Mary Ellen Margaret | Farnesyl protein transferase inhibitor combinations with anti-tumor anthracycline derivatives |
| US7358259B2 (en) | 2003-09-26 | 2008-04-15 | Rigel Pharmaceuticals, Inc. | HCV inhibitors and methods of using them |
| WO2005089518A2 (en) * | 2004-03-18 | 2005-09-29 | The Brigham And Women's Hospital, Inc. | Uch-l1 expression and cancer therapy |
| PL2362218T3 (pl) | 2004-11-05 | 2015-02-27 | Janssen Pharmaceutica Nv | Sposoby kontroli skuteczności inhibitorów transferazy farnezylowej |
| US20060194821A1 (en) * | 2005-02-18 | 2006-08-31 | The Brigham And Women's Hospital, Inc. | Compounds inhibiting the aggregation of superoxide dismutase-1 |
| US20060281769A1 (en) * | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using thienopyrimidine and thienopyridine kinase modulators |
| US20060281755A1 (en) * | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using aminopyrimidines kinase modulators |
| US20060281788A1 (en) * | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor |
| EP1968591A4 (de) | 2005-12-23 | 2010-02-17 | Link Medicine Corp | Behandlung von synucleinopathien |
| DE102006012545A1 (de) * | 2006-03-18 | 2007-09-27 | Sanofi-Aventis | Substituierte 2-Amino-4-phenyl-dihydrochinoline, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament, sowie sie enthaltendes Medikament |
| US8697716B2 (en) | 2006-04-20 | 2014-04-15 | Janssen Pharmaceutica Nv | Method of inhibiting C-KIT kinase |
| EP2021335B1 (de) | 2006-04-20 | 2011-05-25 | Janssen Pharmaceutica N.V. | Heterocyclische verbindungen als c-fms-kinasehemmer |
| UA93085C2 (en) | 2006-04-20 | 2011-01-10 | Янссен Фармацевтика Н.В. | Inhibitors of c-fms kinase |
| JO3240B1 (ar) | 2007-10-17 | 2018-03-08 | Janssen Pharmaceutica Nv | c-fms مثبطات كيناز |
| US8232402B2 (en) | 2008-03-12 | 2012-07-31 | Link Medicine Corporation | Quinolinone farnesyl transferase inhibitors for the treatment of synucleinopathies and other indications |
| EP2370436A1 (de) | 2008-11-13 | 2011-10-05 | Link Medicine Corporation | Azachinolinonderivate und deren verwendungen |
| TW201329025A (zh) | 2011-11-01 | 2013-07-16 | Astex Therapeutics Ltd | 醫藥化合物 |
| CA2860099A1 (en) * | 2012-02-13 | 2013-08-22 | Johannes Aebi | Imidazolylketone derivatives asd aldosterone synthase inhibitors |
| JP6359537B2 (ja) | 2012-08-07 | 2018-07-18 | ヤンセン ファーマシューティカ エヌ．ベー． | 複素環エステル誘導体の調製プロセス |
| JOP20180012A1 (ar) | 2012-08-07 | 2019-01-30 | Janssen Pharmaceutica Nv | عملية السلفنة باستخدام نونافلوروبوتانيسولفونيل فلوريد |
| WO2014062658A1 (en) | 2012-10-16 | 2014-04-24 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of ror-gamma-t |
| EP2909189B8 (de) | 2012-10-16 | 2017-04-19 | Janssen Pharmaceutica NV | Heteroarylverknüpfte chinolinyl-modulatoren von ror-gamma-t |
| EP2909193B1 (de) | 2012-10-16 | 2017-04-19 | Janssen Pharmaceutica NV | Phenylgebundene chinolinylmodulatoren von ror-gamma-t |
| US9328095B2 (en) | 2013-10-15 | 2016-05-03 | Janssen Pharmaceutica Nv | Heteroaryl linked quinolinyl modulators of RORgammat |
| US10555941B2 (en) | 2013-10-15 | 2020-02-11 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
| US9284308B2 (en) | 2013-10-15 | 2016-03-15 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
| US9221804B2 (en) | 2013-10-15 | 2015-12-29 | Janssen Pharmaceutica Nv | Secondary alcohol quinolinyl modulators of RORγt |
| US9346782B2 (en) | 2013-10-15 | 2016-05-24 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
| US9403816B2 (en) | 2013-10-15 | 2016-08-02 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| AU2014334616A1 (en) | 2013-10-15 | 2016-04-28 | Janssen Pharmaceutica Nv | Quinolinyl modulators of RORyt |
| US10076512B2 (en) | 2014-05-01 | 2018-09-18 | Eiger Biopharmaceuticals, Inc. | Treatment of hepatitis delta virus infection |
| US11311519B2 (en) | 2014-05-01 | 2022-04-26 | Eiger Biopharmaceuticals, Inc. | Treatment of hepatitis delta virus infection |
| US20180338993A1 (en) * | 2014-12-04 | 2018-11-29 | Eiger Biopharmaceuticals, Inc. | Treatment of hepatitis delta virus infection |
| DK3285768T3 (da) | 2015-04-21 | 2021-01-25 | Eiger Biopharmaceuticals Inc | Farmaceutiske sammensætninger omfattende lonafarnib og ritonavir |
| EP3385395B9 (de) | 2015-08-17 | 2020-05-20 | Kura Oncology, Inc. | Verfahren zur behandlung von krebspatienten mit farnesyl-transferase-inhibitoren |
| WO2017162122A1 (en) * | 2016-03-23 | 2017-09-28 | Yu-Jen Chen | Farnesyl transferase inhibitors and uses thereof |
| WO2018085518A2 (en) | 2016-11-03 | 2018-05-11 | Kura Oncology, Inc. | Methods of treating cancer patients with farnesyltransferase inhibitors |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2002864C (en) | 1988-11-29 | 1999-11-16 | Eddy J. E. Freyne | (1h-azol-1-ylmethyl) substituted quinoline, quinazoline or quinoxaline derivatives |
| TW349948B (en) * | 1995-10-31 | 1999-01-11 | Janssen Pharmaceutica Nv | Farnesyl transferase inhibiting 2-quinolone derivatives |
| ATE321757T1 (de) * | 1995-12-08 | 2006-04-15 | Janssen Pharmaceutica Nv | (imidazol-5-yl)methyl-2-chinolinonderivate als farnesyl protein transferase inhibitoren |
| TW591030B (en) * | 1997-03-10 | 2004-06-11 | Janssen Pharmaceutica Nv | Farnesyl transferase inhibiting 1,8-annelated quinolinone derivatives substituted with N- or C-linked imidazoles |
| KR100520401B1 (ko) * | 1997-04-25 | 2005-10-12 | 얀센 파마슈티카 엔.브이. | 파네실 트랜스퍼라제 억제작용을 갖는 퀴나졸리논 |
| CN1231215C (zh) * | 1997-06-02 | 2005-12-14 | 詹森药业有限公司 | (咪唑－5－基)甲基－2－喹啉酮衍生物用作平滑肌细胞增殖抑制剂 |
-
1999
- 1999-12-17 SI SI9930350T patent/SI1140935T1/xx unknown
- 1999-12-17 EP EP99969220A patent/EP1140935B1/de not_active Expired - Lifetime
- 1999-12-17 PT PT99969220T patent/PT1140935E/pt unknown
- 1999-12-17 EA EA200100708A patent/EA004542B1/ru not_active IP Right Cessation
- 1999-12-17 AT AT99969220T patent/ATE240327T1/de active
- 1999-12-17 JP JP2000590995A patent/JP4725940B2/ja not_active Expired - Lifetime
- 1999-12-17 CZ CZ20012142A patent/CZ302374B6/cs not_active IP Right Cessation
- 1999-12-17 BR BR9916827-8A patent/BR9916827A/pt not_active Application Discontinuation
- 1999-12-17 ES ES99969220T patent/ES2200591T3/es not_active Expired - Lifetime
- 1999-12-17 EE EEP200100318A patent/EE04962B1/xx unknown
- 1999-12-17 US US09/868,992 patent/US6458800B1/en not_active Expired - Lifetime
- 1999-12-17 WO PCT/EP1999/010214 patent/WO2000039082A2/en not_active Application Discontinuation
- 1999-12-17 SK SK873-2001A patent/SK286072B6/sk not_active IP Right Cessation
- 1999-12-17 PL PL349504A patent/PL199080B1/pl unknown
- 1999-12-17 TW TW088122193A patent/TW531533B/zh not_active IP Right Cessation
- 1999-12-17 CA CA2355717A patent/CA2355717C/en not_active Expired - Lifetime
- 1999-12-17 DE DE69907964T patent/DE69907964T2/de not_active Expired - Lifetime
- 1999-12-17 TR TR2001/01961T patent/TR200101961T2/xx unknown
- 1999-12-17 KR KR1020017006140A patent/KR100712226B1/ko active IP Right Grant
- 1999-12-17 HU HU0104582A patent/HU229404B1/hu unknown
- 1999-12-17 UA UA2001064401A patent/UA71592C2/uk unknown
- 1999-12-17 ID IDW00200101373A patent/ID29241A/id unknown
- 1999-12-17 DK DK99969220T patent/DK1140935T3/da active
- 1999-12-17 IL IL14385999A patent/IL143859A0/xx active IP Right Grant
- 1999-12-17 KR KR1020067021243A patent/KR100818541B1/ko active IP Right Grant
- 1999-12-17 AU AU27953/00A patent/AU765437B2/en not_active Expired
- 1999-12-17 CN CNB99814763XA patent/CN1178938C/zh not_active Expired - Lifetime
- 1999-12-22 AR ARP990106687A patent/AR021995A1/es active IP Right Grant
-
2001
- 2001-06-15 HR HR20010454A patent/HRP20010454B1/xx not_active IP Right Cessation
- 2001-06-20 IL IL143859A patent/IL143859A/en not_active IP Right Cessation
- 2001-06-20 BG BG105631A patent/BG65124B1/bg unknown
- 2001-06-21 ZA ZA200105136A patent/ZA200105136B/en unknown
- 2001-06-21 NO NO20013088A patent/NO318922B1/no not_active IP Right Cessation
-
2002
- 2002-01-10 HK HK02100160.2A patent/HK1038746B/zh not_active IP Right Cessation
- 2002-06-24 US US10/179,444 patent/US6914066B2/en not_active Expired - Lifetime
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