BR9810955A - "4-5-diaril imidazóis 2-substituìdo" - Google Patents
"4-5-diaril imidazóis 2-substituìdo"Info
- Publication number
- BR9810955A BR9810955A BR9810955-3A BR9810955A BR9810955A BR 9810955 A BR9810955 A BR 9810955A BR 9810955 A BR9810955 A BR 9810955A BR 9810955 A BR9810955 A BR 9810955A
- Authority
- BR
- Brazil
- Prior art keywords
- replaced
- substituent
- ring
- diseases
- compounds
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
-
- 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
-
- 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
-
- 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
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
Abstract
Patente de Invenção: <B>"4,5-DIARIL IMIDAZóIS 2-SUBSTITUìDO"<D>. Novos 4,5-diarilimidazóis 2-substituído em que: i) o átomo de nitrogênio na posição 1 é substituído por um substituente contendo trialquilsilila, ou ii) o substituente na posição 2 é arilalquila, arilsulfonila, arilseleno de ariltio, arilteluro, cicloalquila, cicloalquenila, alquilcicloalquila, alquilcicloalquenila, amino ou hidrazino, ou N-heterociclila mono ou bicíclica em que o anel contendo N tenha seis membros no anel, são fornecidos, em particular compostos da fórmula I onde R~ 1~,R~ 2~, R~ 3~, e R~ 4~ são conforme definidos, em forma de sal ácido de adição farmaceuticamente aceitável ou de éster fisiologicamente clivável, que têm atividade inibidora da quinase p38 MAP (Quinase de Proteína Ativada por Mitógeno). Os compostos são usados como remédios para o tramento de doenças mediadas or TNF<244> e IL-1, como atrite reumatóide e doenças do metabolismo ósseo, por exemplo, osteoporose.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9713726.9A GB9713726D0 (en) | 1997-06-30 | 1997-06-30 | Organic compounds |
PCT/EP1998/003930 WO1999001449A1 (en) | 1997-06-30 | 1998-06-26 | 2-substituted 4,5-diaryl imidazoles |
Publications (1)
Publication Number | Publication Date |
---|---|
BR9810955A true BR9810955A (pt) | 2000-09-26 |
Family
ID=10815101
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR9810955-3A BR9810955A (pt) | 1997-06-30 | 1998-06-26 | "4-5-diaril imidazóis 2-substituìdo" |
Country Status (28)
Country | Link |
---|---|
US (1) | US6300347B1 (pt) |
EP (2) | EP1396491A3 (pt) |
JP (1) | JP3704362B2 (pt) |
KR (1) | KR20010013215A (pt) |
CN (1) | CN1261885A (pt) |
AR (1) | AR014886A1 (pt) |
AT (1) | ATE275557T1 (pt) |
AU (1) | AU744411B2 (pt) |
BR (1) | BR9810955A (pt) |
CA (1) | CA2291758A1 (pt) |
CO (1) | CO4940462A1 (pt) |
DE (1) | DE69826127T2 (pt) |
ES (1) | ES2226164T3 (pt) |
GB (1) | GB9713726D0 (pt) |
HU (1) | HUP0003351A3 (pt) |
ID (1) | ID23385A (pt) |
IL (1) | IL133034A0 (pt) |
NO (1) | NO996429L (pt) |
NZ (1) | NZ501275A (pt) |
PE (1) | PE99999A1 (pt) |
PL (1) | PL337057A1 (pt) |
PT (1) | PT993456E (pt) |
RU (1) | RU2214408C2 (pt) |
SK (1) | SK186599A3 (pt) |
TR (1) | TR199903278T2 (pt) |
TW (1) | TW429258B (pt) |
WO (1) | WO1999001449A1 (pt) |
ZA (1) | ZA985656B (pt) |
Families Citing this family (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998007425A1 (en) | 1996-08-21 | 1998-02-26 | Smithkline Beecham Corporation | Imidazole compounds, compositions and use |
US7301021B2 (en) | 1997-07-02 | 2007-11-27 | Smithkline Beecham Corporation | Substituted imidazole compounds |
EP1119254A4 (en) | 1998-10-07 | 2004-05-12 | Smithkline Beecham Corp | STROKE TREATMENT |
EP1143957A3 (en) * | 1998-12-16 | 2002-02-27 | Warner-Lambert Company | Treatment of arthritis with mek inhibitors |
DE60033028T2 (de) * | 1999-04-23 | 2007-11-15 | Takeda Pharmaceutical Co. Ltd. | 5-pyridyl-1,3-azol-derivate, verfahren zu ihrer herstellung und ihre verwendung |
WO2000064872A1 (en) * | 1999-04-23 | 2000-11-02 | Vertex Pharmaceuticals Incorporated | INHIBITORS OF c-JUN N-TERMINAL KINASES (JNK) |
US6291457B1 (en) * | 1999-07-01 | 2001-09-18 | Merck & Co., Inc. | Compounds having cytokine inhibitory activity |
US7122666B2 (en) | 1999-07-21 | 2006-10-17 | Sankyo Company, Limited | Heteroaryl-substituted pyrrole derivatives, their preparation and their therapeutic uses |
DE60024480T2 (de) * | 1999-10-27 | 2006-07-27 | Novartis Ag | Thiazol und imidazo[4,5-b]pyridin verbindungen und ihre verwendung als pharmazeutika |
JP2003513977A (ja) | 1999-11-10 | 2003-04-15 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | 置換2−アリール−3−(ヘテロアリール)−イミダゾ[1,2−α]ピリミジン類および関連薬剤組成物および方法 |
US6808902B1 (en) | 1999-11-12 | 2004-10-26 | Amgen Inc. | Process for correction of a disulfide misfold in IL-1Ra Fc fusion molecules |
US7026336B1 (en) * | 1999-11-22 | 2006-04-11 | Smithkline Beecham P.L.C. | Compounds |
US7053099B1 (en) | 1999-11-23 | 2006-05-30 | Smithkline Beecham Corporation | 3,4-dihydro-(1H)quinazolin-2-one compounds as CSBP/p38 kinase inhibitors |
US7612065B2 (en) | 2000-04-21 | 2009-11-03 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-JUN N-terminal kinases (JNK) |
OA12552A (en) | 2001-03-09 | 2006-06-06 | Pfizer Prod Inc | Triazolopyridines as anti-inflammatory agents. |
CA2440211A1 (en) | 2001-03-09 | 2002-09-19 | Pfizer Products Inc. | Benzimidazole anti-inflammatory compounds |
ATE304009T1 (de) | 2001-04-04 | 2005-09-15 | Pfizer Prod Inc | Neue benzotriazole mit entzündungshemmender wirkung |
ES2907826T3 (es) | 2001-06-26 | 2022-04-26 | Amgen Inc | Anticuerpos para OPGL |
EP1439174B1 (en) * | 2001-10-22 | 2012-03-21 | Mitsubishi Tanabe Pharma Corporation | 4-IMIDAZOLIN-2-ONE COMPOUNDS AS p38 MAP KINASE INHIBITORS |
AR039241A1 (es) | 2002-04-04 | 2005-02-16 | Biogen Inc | Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos |
DE10222103A1 (de) * | 2002-05-17 | 2003-11-27 | Merckle Gmbh Chem Pharm Fabrik | 2-Thio-substituierte Imidazolderivate und ihre Verwendung in der Pharmazie |
ATE349210T1 (de) | 2002-07-09 | 2007-01-15 | Boehringer Ingelheim Pharma | Pharazeutische zusammensetzungen aus anticholinergica und p38 kinase hemmern zur behandlung von erkrankungen der atemwege |
US7037923B2 (en) | 2002-08-30 | 2006-05-02 | Pfizer, Inc. | Alkyl-[4-(trifluorophenyl)-oxazol-5-yl]-triazolo-pyridines |
US6949652B2 (en) | 2002-08-30 | 2005-09-27 | Pfizer, Inc. | Crystalline forms of 3-isopropyl-6-[4-(2,5-difluoro-phenyl)-oxazol-5-yl]-[1,2,4]triazolo-[4,3-A]pyridine |
US7012143B2 (en) | 2002-08-30 | 2006-03-14 | Dombroski Mark A | Cycloalkyl-[4-(difluorophenyl)-oxazol-5-yl]-triazolo-pyridines |
US7005523B2 (en) | 2002-08-30 | 2006-02-28 | Pfizer Inc. | Cycloalkyl-[4-(trifluorophenyl)-oxazol-5yl]-triazolo-pyridines |
PA8579601A1 (es) | 2002-08-30 | 2004-05-07 | Pfizer Prod Inc | Compuestos antiinflamatorios de di y trifloruro-triazolo-piridinas |
UA80295C2 (en) | 2002-09-06 | 2007-09-10 | Biogen Inc | Pyrazolopyridines and using the same |
WO2004053107A2 (en) * | 2002-12-06 | 2004-06-24 | Scios Inc. | Methods for treating diabetes |
JP2006516548A (ja) | 2002-12-30 | 2006-07-06 | アンジオテック インターナショナル アクツィエン ゲゼルシャフト | 迅速ゲル化ポリマー組成物からの薬物送達法 |
CN100422175C (zh) * | 2003-04-03 | 2008-10-01 | 麦克公司 | 作为代谢型谷氨酸受体-5调制剂的四环咪唑衍生物 |
US20040229878A1 (en) * | 2003-05-13 | 2004-11-18 | Depuy Spine, Inc. | Transdiscal administration of specific inhibitors of P38 kinase |
US8273347B2 (en) * | 2003-05-13 | 2012-09-25 | Depuy Spine, Inc. | Autologous treatment of degenerated disc with cells |
US7553827B2 (en) * | 2003-08-13 | 2009-06-30 | Depuy Spine, Inc. | Transdiscal administration of cycline compounds |
US7344716B2 (en) * | 2003-05-13 | 2008-03-18 | Depuy Spine, Inc. | Transdiscal administration of specific inhibitors of pro-inflammatory cytokines |
US8361467B2 (en) | 2003-07-30 | 2013-01-29 | Depuy Spine, Inc. | Trans-capsular administration of high specificity cytokine inhibitors into orthopedic joints |
MXPA06001081A (es) * | 2003-07-31 | 2006-04-24 | Irm Llc | Compuestos biciclicos y composiciones como inhibidores de pdf. |
CN100455579C (zh) * | 2003-10-02 | 2009-01-28 | Irm责任有限公司 | 作为蛋白激酶抑制剂的化合物和组合物 |
US8895540B2 (en) * | 2003-11-26 | 2014-11-25 | DePuy Synthes Products, LLC | Local intraosseous administration of bone forming agents and anti-resorptive agents, and devices therefor |
WO2005063716A1 (en) | 2003-12-22 | 2005-07-14 | Janssen Pharmaceutica, N.V. | Imidazoles and their use cck-1 receptor modulators |
US20060035893A1 (en) | 2004-08-07 | 2006-02-16 | Boehringer Ingelheim International Gmbh | Pharmaceutical compositions for treatment of respiratory and gastrointestinal disorders |
US7713998B2 (en) | 2004-11-10 | 2010-05-11 | Ono Pharmaceutical Co., Ltd. | Nitrogenous heterocyclic compound and pharmaceutical use thereof |
PE20060777A1 (es) | 2004-12-24 | 2006-10-06 | Boehringer Ingelheim Int | Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas |
ES2351308T3 (es) * | 2005-02-28 | 2011-02-02 | Merckle Gmbh | Derivados de imidazol 2-sulfinil- y 2-sulfonil-sustituidos y su uso como inhibidores de citocina. |
BRPI0616655A2 (pt) * | 2005-10-03 | 2011-06-28 | Ono Pharmaceutical Co | composto heterocìclico contendo nitrogênio e aplicação farmacêutica do mesmo |
ES2380236T3 (es) | 2005-10-28 | 2012-05-09 | Takeda Pharmaceutical Company Limited | Compuesto de amida heterocíclica y uso del mismo |
ES2301380B1 (es) | 2006-08-09 | 2009-06-08 | Laboratorios Almirall S.A. | Nuevos derivados de 1,7-naftiridina. |
ES2320955B1 (es) | 2007-03-02 | 2010-03-16 | Laboratorios Almirall S.A. | Nuevos derivados de 3-((1,2,4)triazolo(4,3-a)piridin-7-il)benzamida. |
ES2329639B1 (es) | 2007-04-26 | 2010-09-23 | Laboratorios Almirall S.A. | Nuevos derivados de 4,8-difenilpoliazanaftaleno. |
EP1992344A1 (en) | 2007-05-18 | 2008-11-19 | Institut Curie | P38 alpha as a therapeutic target in pathologies linked to FGFR3 mutation |
US20100168210A1 (en) * | 2007-06-05 | 2010-07-01 | Edwards Iii Carl Keith | T-Cell Cytokine-Inducing Surface Molecules and Methods of Use |
US20090162351A1 (en) * | 2007-12-21 | 2009-06-25 | Depuy Spine, Inc. | Transdiscal administration of inhibitors of p38 MAP kinase |
US8986696B2 (en) * | 2007-12-21 | 2015-03-24 | Depuy Mitek, Inc. | Trans-capsular administration of p38 map kinase inhibitors into orthopedic joints |
EP2108641A1 (en) | 2008-04-11 | 2009-10-14 | Laboratorios Almirall, S.A. | New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors |
EP2113503A1 (en) | 2008-04-28 | 2009-11-04 | Laboratorios Almirall, S.A. | New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors |
TWI435874B (zh) | 2008-10-31 | 2014-05-01 | Toray Industries | 環己烷衍生物及其醫藥用途 |
EP2322176A1 (en) | 2009-11-11 | 2011-05-18 | Almirall, S.A. | New 7-phenyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one derivatives |
EP2516668B1 (en) * | 2009-12-22 | 2016-04-06 | Csir | Inhibition of the activity of kinase and synthetase enzymes |
JP2013523766A (ja) * | 2010-03-31 | 2013-06-17 | グラクソ グループ リミテッド | キナーゼ阻害剤としてのイミダゾリル‐イミダゾール |
WO2017151409A1 (en) | 2016-02-29 | 2017-09-08 | University Of Florida Research Foundation, Incorporated | Chemotherapeutic methods |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69322254T2 (de) * | 1992-01-13 | 1999-04-29 | Smithkline Beecham Corp | Pyridyl-substituierte imidazole |
MX9300141A (es) * | 1992-01-13 | 1994-07-29 | Smithkline Beecham Corp | Compuestos de imidazol novedosos, procedimiento para su preparacion y composiciones farmaceuticas que lo contienen. |
US5916891A (en) | 1992-01-13 | 1999-06-29 | Smithkline Beecham Corporation | Pyrimidinyl imidazoles |
ZA945363B (en) * | 1993-07-21 | 1995-03-14 | Smithkline Beecham Corp | Novel compounds |
US5620999A (en) * | 1994-07-28 | 1997-04-15 | Weier; Richard M. | Benzenesulfonamide subtituted imidazolyl compounds for the treatment of inflammation |
US5717100A (en) * | 1995-10-06 | 1998-02-10 | Merck & Co., Inc. | Substituted imidazoles having anti-cancer and cytokine inhibitory activity |
IL123950A (en) * | 1995-10-06 | 2001-04-30 | Merck & Co Inc | Transformed imidazoles with anti-cancer and cytokine-inhibiting activity and pharmaceutical preparations containing them |
DE69816109T2 (de) | 1997-04-24 | 2004-04-22 | Ortho-Mcneil Pharmaceutical, Inc. | Substituierte imidazole zur behandlung von entzündlichen krankheiten |
AU742293B2 (en) | 1997-06-12 | 2001-12-20 | Aventis Pharma Limited | Imidazolyl-cyclic acetals |
CA2294137A1 (en) | 1997-06-19 | 1998-12-23 | Smithkline Beecham Corporation | Novel aryloxy substituted pyrimidine imidazole compounds |
IL133766A0 (en) | 1997-06-30 | 2001-04-30 | Ortho Mcneil Pharm Inc | 2-substituted imidazoles useful in the treatment of inflammatory diseases |
TW517055B (en) | 1997-07-02 | 2003-01-11 | Smithkline Beecham Corp | Novel substituted imidazole compounds |
WO1999001452A1 (en) | 1997-07-02 | 1999-01-14 | Smithkline Beecham Corporation | Novel cycloalkyl substituted imidazoles |
AR016294A1 (es) | 1997-07-02 | 2001-07-04 | Smithkline Beecham Corp | Compuesto de imidazol sustituido, composicion farmaceutica que la contiene, su uso en la fabricacion de un medicamento y procedimiento para supreparacion |
FR2772377B1 (fr) | 1997-12-12 | 2000-01-07 | Synthelabo | Derives de 1-(1-h-imidazol-2-yl)pyrrolidines et 1-(1-h-imidazol-2-ylpiperidines), leur preparation et leur application en therapeutique |
-
1997
- 1997-06-30 GB GBGB9713726.9A patent/GB9713726D0/en active Pending
-
1998
- 1998-06-11 TW TW087109301A patent/TW429258B/zh active
- 1998-06-25 CO CO98036362A patent/CO4940462A1/es unknown
- 1998-06-26 KR KR19997011203A patent/KR20010013215A/ko not_active Application Discontinuation
- 1998-06-26 US US09/446,885 patent/US6300347B1/en not_active Expired - Fee Related
- 1998-06-26 AT AT98939541T patent/ATE275557T1/de not_active IP Right Cessation
- 1998-06-26 AR ARP980103093A patent/AR014886A1/es unknown
- 1998-06-26 EP EP03026996A patent/EP1396491A3/en not_active Withdrawn
- 1998-06-26 HU HU0003351A patent/HUP0003351A3/hu unknown
- 1998-06-26 PT PT98939541T patent/PT993456E/pt unknown
- 1998-06-26 EP EP98939541A patent/EP0993456B1/en not_active Expired - Lifetime
- 1998-06-26 IL IL13303498A patent/IL133034A0/xx unknown
- 1998-06-26 SK SK1865-99A patent/SK186599A3/sk unknown
- 1998-06-26 CA CA002291758A patent/CA2291758A1/en not_active Abandoned
- 1998-06-26 WO PCT/EP1998/003930 patent/WO1999001449A1/en not_active Application Discontinuation
- 1998-06-26 NZ NZ501275A patent/NZ501275A/en unknown
- 1998-06-26 DE DE69826127T patent/DE69826127T2/de not_active Expired - Fee Related
- 1998-06-26 BR BR9810955-3A patent/BR9810955A/pt not_active IP Right Cessation
- 1998-06-26 AU AU88015/98A patent/AU744411B2/en not_active Ceased
- 1998-06-26 CN CN98806673A patent/CN1261885A/zh active Pending
- 1998-06-26 ID IDW991681A patent/ID23385A/id unknown
- 1998-06-26 TR TR1999/03278T patent/TR199903278T2/xx unknown
- 1998-06-26 ES ES98939541T patent/ES2226164T3/es not_active Expired - Lifetime
- 1998-06-26 PL PL98337057A patent/PL337057A1/xx unknown
- 1998-06-26 RU RU2000101820/04A patent/RU2214408C2/ru not_active IP Right Cessation
- 1998-06-26 JP JP50628899A patent/JP3704362B2/ja not_active Expired - Fee Related
- 1998-06-26 PE PE1998000569A patent/PE99999A1/es not_active Application Discontinuation
- 1998-06-29 ZA ZA985656A patent/ZA985656B/xx unknown
-
1999
- 1999-12-23 NO NO996429A patent/NO996429L/no not_active Application Discontinuation
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