EA200000398A1 - Химические соединения - Google Patents
Химические соединенияInfo
- Publication number
- EA200000398A1 EA200000398A1 EA200000398A EA200000398A EA200000398A1 EA 200000398 A1 EA200000398 A1 EA 200000398A1 EA 200000398 A EA200000398 A EA 200000398A EA 200000398 A EA200000398 A EA 200000398A EA 200000398 A1 EA200000398 A1 EA 200000398A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- alkyl
- sor
- cor
- halogen
- salts
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/167—Purine radicals with ribosyl as the saccharide radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
-
- 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
- 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
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Molecular Biology (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
Соединение формулы (I), где Rпредставляет собой Cалкил, галоген или водород; Rпредставляет собой алкильную группу с прямой или разветвленной цепью, состоящую из 1-6 атомов углерода; при условии, что когда Rпредставляет собой Cалкил, Rявляется Cалкилом, Rне может представлять собой фенил, возможно замещенный одним или более чем одним заместителем, выбранным из галогена, Cалкила, трифторметила, нитро, циано, -COR, -CONRR, -COR, -SOR, -SOR, -SOH, -SONRR, -OR, -NHSOR, -NHCORи -NRR; и его соли и сольваты, в частности его физиологически приемлемые сольваты и соли. Эти соединения являются агонистами к аденозиновому A1-рецептору.Отчет о международном поиске был опубликован 1999.08.19.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9723590.7A GB9723590D0 (en) | 1997-11-08 | 1997-11-08 | Chemical compounds |
PCT/EP1998/007023 WO1999024451A2 (en) | 1997-11-08 | 1998-11-06 | Adenosine a1 receptor agonists |
Publications (2)
Publication Number | Publication Date |
---|---|
EA200000398A1 true EA200000398A1 (ru) | 2000-12-25 |
EA003087B1 EA003087B1 (ru) | 2002-12-26 |
Family
ID=10821761
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200000398A EA003087B1 (ru) | 1997-11-08 | 1998-11-06 | Производные аденозина |
Country Status (27)
Country | Link |
---|---|
US (2) | US6544960B1 (ru) |
EP (1) | EP1030856B1 (ru) |
JP (1) | JP2001522859A (ru) |
KR (1) | KR20010031878A (ru) |
CN (1) | CN1217952C (ru) |
AP (1) | AP2000001804A0 (ru) |
AT (1) | ATE273989T1 (ru) |
AU (1) | AU763414B2 (ru) |
BR (1) | BR9813989A (ru) |
CA (1) | CA2309202C (ru) |
DE (1) | DE69825779T2 (ru) |
EA (1) | EA003087B1 (ru) |
EE (1) | EE04499B1 (ru) |
ES (1) | ES2222619T3 (ru) |
GB (1) | GB9723590D0 (ru) |
HR (1) | HRP20000277A2 (ru) |
HU (1) | HUP0004102A3 (ru) |
ID (1) | ID24758A (ru) |
IL (2) | IL135966A0 (ru) |
IS (1) | IS5479A (ru) |
NO (1) | NO20002359L (ru) |
NZ (1) | NZ504336A (ru) |
PL (1) | PL340873A1 (ru) |
SK (1) | SK6702000A3 (ru) |
TR (1) | TR200001937T2 (ru) |
WO (1) | WO1999024451A2 (ru) |
YU (1) | YU26800A (ru) |
Families Citing this family (65)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9723590D0 (en) * | 1997-11-08 | 1998-01-07 | Glaxo Group Ltd | Chemical compounds |
US6576619B2 (en) * | 1999-05-24 | 2003-06-10 | Cv Therapeutics, Inc. | Orally active A1 adenosine receptor agonists |
AU4138601A (en) * | 1999-12-03 | 2001-06-12 | Cv Therapeutics, Inc. | Method of identifying partial adenosine a1 receptor agonists and their use in the treatment of arrhythmias |
US6605597B1 (en) * | 1999-12-03 | 2003-08-12 | Cv Therapeutics, Inc. | Partial or full A1agonists-N-6 heterocyclic 5′-thio substituted adenosine derivatives |
GB9930085D0 (en) * | 1999-12-20 | 2000-02-09 | Glaxo Group Ltd | Medicaments |
US6921753B2 (en) | 2000-06-27 | 2005-07-26 | Pfizer Inc | Purine derivatives |
GB0015727D0 (en) * | 2000-06-27 | 2000-08-16 | Pfizer Ltd | Purine derivatives |
GB0022695D0 (en) | 2000-09-15 | 2000-11-01 | Pfizer Ltd | Purine Derivatives |
GB0106867D0 (en) | 2001-03-20 | 2001-05-09 | Glaxo Group Ltd | Process |
EP1258247A1 (en) * | 2001-05-14 | 2002-11-20 | Aventis Pharma Deutschland GmbH | Adenosine analogues for the treatment of insulin resistance syndrome and diabetes |
US6946449B2 (en) | 2001-07-13 | 2005-09-20 | Cv Therapeutics, Inc. | Partial and full agonists of A1 adenosine receptors |
US7713946B2 (en) | 2002-07-11 | 2010-05-11 | Cv Therapeutics, Inc. | Partial and full agonists A1 adenosine receptors |
US7157440B2 (en) | 2001-07-13 | 2007-01-02 | Cv Therapeutics, Inc. | Partial and full agonists of A1 adenosine receptors |
GB0221694D0 (en) * | 2002-09-18 | 2002-10-30 | Glaxo Group Ltd | Compounds |
GB0228723D0 (en) * | 2002-12-09 | 2003-01-15 | Cambridge Biotechnology Ltd | Treatment of pain |
US7163928B2 (en) | 2003-02-03 | 2007-01-16 | Cv Therapeutics, Inc. | Partial and full agonists of A1 adenosine receptors |
GB0305153D0 (en) * | 2003-03-07 | 2003-04-09 | Cambridge Biotechnology Ltd | Identification of therapeutic compounds |
AR044519A1 (es) | 2003-05-02 | 2005-09-14 | Novartis Ag | Derivados de piridin-tiazol amina y de pirimidin-tiazol amina |
ES2574918T3 (es) * | 2003-06-02 | 2016-06-23 | Isis Innovation Limited | Tratamiento de la fatiga muscular |
WO2004108740A2 (en) | 2003-06-03 | 2004-12-16 | The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Nutritional supplements and therapeutic compositions comprising (r)-3-hydroxybutyrate derivatives |
FR2862873A1 (fr) * | 2003-12-01 | 2005-06-03 | Pf Medicament | Utilisation des acides gras polyinsatures omega 3 dans l'apnee du sommeil |
GB0401334D0 (en) | 2004-01-21 | 2004-02-25 | Novartis Ag | Organic compounds |
GB0411056D0 (en) | 2004-05-18 | 2004-06-23 | Novartis Ag | Organic compounds |
GB0424284D0 (en) | 2004-11-02 | 2004-12-01 | Novartis Ag | Organic compounds |
GB0426164D0 (en) | 2004-11-29 | 2004-12-29 | Novartis Ag | Organic compounds |
GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
EP2532677A1 (en) | 2005-10-21 | 2012-12-12 | Novartis AG | Human antibodies against il13 and therapeutic uses |
CA2627319A1 (en) * | 2005-11-30 | 2007-06-07 | Prakash Jagtap | Purine derivatives and methods of use thereof |
GB0601951D0 (en) | 2006-01-31 | 2006-03-15 | Novartis Ag | Organic compounds |
JP5349306B2 (ja) | 2006-08-21 | 2013-11-20 | ジェネンテック, インコーポレイテッド | アザベンゾチオフェニル化合物および使用方法 |
BRPI0717564A2 (pt) | 2006-09-29 | 2013-10-22 | Novartis Ag | Pirazolopirimidinas como inibidores de pi3k lipídeo cinase |
CA2667962A1 (en) | 2006-10-30 | 2008-05-08 | Novartis Ag | Heterocyclic compounds as antiinflammatory agents |
CN101969769A (zh) | 2008-01-04 | 2011-02-09 | 伊希斯创新有限公司 | 用作降低血脂药剂的酮体和酮体酯 |
KR20100113557A (ko) | 2008-01-11 | 2010-10-21 | 노파르티스 아게 | 키나제 억제제로서의 피리미딘 |
CN101602786B (zh) * | 2008-06-10 | 2014-04-30 | 中国医学科学院药物研究所 | N6-取代腺苷衍生物、其制法以及药物组合物与用途 |
US8642654B2 (en) | 2009-04-16 | 2014-02-04 | Isis Innovation Limited | Hydroxybutyrate ester and medical use thereof |
ES2396023T3 (es) | 2009-01-29 | 2013-02-18 | Novartis Ag | Bencimidazoles sustituidos para el tratamiento de astrocitomas |
CN101857622B (zh) * | 2009-04-07 | 2014-12-03 | 中国医学科学院药物研究所 | 一种腺苷衍生物及其制备方法和应用 |
US8389526B2 (en) | 2009-08-07 | 2013-03-05 | Novartis Ag | 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives |
JP5781510B2 (ja) | 2009-08-12 | 2015-09-24 | ノバルティス アーゲー | ヘテロ環式ヒドラゾン化合物および癌および炎症の処置のためのそれらの使用 |
JP5819831B2 (ja) | 2009-08-17 | 2015-11-24 | インテリカイン, エルエルシー | 複素環式化合物およびそれらの使用 |
WO2011020861A1 (en) | 2009-08-20 | 2011-02-24 | Novartis Ag | Heterocyclic oxime compounds |
US10174033B2 (en) | 2009-12-10 | 2019-01-08 | Institute Of Materia Medica, Chinese Academy Of Medical Sciences | N6-substituted adenosine derivatives and N6-substituted adenine derivatives and uses thereof |
CN104382924B (zh) * | 2009-12-10 | 2017-12-22 | 中国医学科学院药物研究所 | N6‑取代腺苷衍生物和n6‑取代腺嘌呤衍生物及其用途 |
US8877732B2 (en) | 2010-01-11 | 2014-11-04 | Inotek Pharmaceuticals Corporation | Combination, kit and method of reducing intraocular pressure |
GB201002983D0 (en) | 2010-02-22 | 2010-04-07 | Tdeltas Ltd | Nutritinal composition |
MX2012010724A (es) | 2010-03-26 | 2012-11-12 | Inotek Pharmaceuticals Corp | Metodo para reducir la presion intraocular en seres humanos empleando n6-ciclopentiladenosina (cpa), derivados de cpa o profarmacos de los mismos. |
US8637516B2 (en) | 2010-09-09 | 2014-01-28 | Irm Llc | Compounds and compositions as TRK inhibitors |
WO2012034095A1 (en) | 2010-09-09 | 2012-03-15 | Irm Llc | Compounds and compositions as trk inhibitors |
JP2014505088A (ja) | 2011-02-10 | 2014-02-27 | ノバルティス アーゲー | C−METチロシンキナーゼ阻害剤としての[1,2,4]トリアゾロ[4,3−b]ピリダジン化合物 |
WO2012116237A2 (en) | 2011-02-23 | 2012-08-30 | Intellikine, Llc | Heterocyclic compounds and uses thereof |
US9102671B2 (en) | 2011-02-25 | 2015-08-11 | Novartis Ag | Compounds and compositions as TRK inhibitors |
JP5957526B2 (ja) | 2011-09-15 | 2016-07-27 | ノバルティス アーゲー | チロシンキナーゼとしての6−置換3−(キノリン−6−イルチオ)−[1,2,4]トリアゾロ[4,3−a]ピラジン |
EP2793893A4 (en) | 2011-11-23 | 2015-07-08 | Intellikine Llc | IMPROVED TREATMENT REGIMES USING MTOR INHIBITORS |
DK2807178T3 (en) | 2012-01-26 | 2017-09-04 | Inotek Pharmaceuticals Corp | Anhydrous polymorphs of (2R, 3S, 4R, 5R) -5- (6- (cyclopentylamino) -9H-purin-9-yl) -3,4-dihydroxytetrahydrofuran-2-yl) methyl nitrate and processes for their preparation |
EP3964513A1 (en) | 2012-04-03 | 2022-03-09 | Novartis AG | Combination products with tyrosine kinase inhibitors and their use |
EP3659595A1 (en) | 2012-11-05 | 2020-06-03 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Ketone bodies to protect tissues from damage by ionizing radiation |
GB201304467D0 (en) | 2013-03-12 | 2013-04-24 | Tdeltas Ltd | Compound for use in protecting skin |
GB2515603B (en) | 2013-03-14 | 2015-10-14 | Isis Innovation | Process for producing (R)-3-Hydroxybutyl (R)-3-Hydroxybutyrate |
SG11201506882YA (en) | 2013-03-15 | 2015-09-29 | Inotek Pharmaceuticals Corp | Ophthalmic formulations |
CN105246482A (zh) | 2013-03-15 | 2016-01-13 | 因特利凯有限责任公司 | 激酶抑制剂的组合及其用途 |
TW201605450A (zh) | 2013-12-03 | 2016-02-16 | 諾華公司 | Mdm2抑制劑與BRAF抑制劑之組合及其用途 |
WO2016011658A1 (en) | 2014-07-25 | 2016-01-28 | Novartis Ag | Combination therapy |
US10195208B2 (en) | 2014-07-31 | 2019-02-05 | Novartis Ag | Combination therapy |
TW202140550A (zh) | 2020-01-29 | 2021-11-01 | 瑞士商諾華公司 | 使用抗tslp抗體治療炎性或阻塞性氣道疾病之方法 |
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US4868160A (en) * | 1985-11-06 | 1989-09-19 | Warner-Lambert Company | Method of treating psychosis using N6 -substituted -5'-oxidized adenosine analogs |
US4738954A (en) * | 1985-11-06 | 1988-04-19 | Warner-Lambert Company | Novel N6 -substituted-5'-oxidized adenosine analogs |
US4843066A (en) * | 1986-11-27 | 1989-06-27 | Nippon Zoki Pharmaceutical Co., Ltd. | Novel adenosine derivatives and pharmaceutical composition containing them as an active ingredient |
US5652366A (en) * | 1990-09-25 | 1997-07-29 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | DI (1R)-(-)camphosulfonic acid) salt, preparation thereof and use thereof |
US5561134A (en) * | 1990-09-25 | 1996-10-01 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties |
WO1992005177A1 (en) * | 1990-09-25 | 1992-04-02 | Rhone-Poulenc Rorer International (Holdings) Inc. | Compounds having antihypertensive and anti-ischemic properties |
DK62592D0 (ru) * | 1992-05-14 | 1992-05-14 | Novo Nordisk As | |
EP0601322A3 (en) * | 1992-10-27 | 1994-10-12 | Nippon Zoki Pharmaceutical Co | Adenosine deaminase inhibitor. |
US5589467A (en) * | 1993-09-17 | 1996-12-31 | Novo Nordisk A/S | 2,5',N6-trisubstituted adenosine derivatives |
JPH07118156A (ja) * | 1993-10-26 | 1995-05-09 | Nippon Zoki Pharmaceut Co Ltd | アデノシンデアミナーゼ阻害剤 |
JPH08269083A (ja) * | 1995-04-03 | 1996-10-15 | Banyu Pharmaceut Co Ltd | N6−置換アデノシン誘導体 |
AU2022597A (en) * | 1996-03-13 | 1997-10-01 | Novo Nordisk A/S | A method of treating disorders related to cytokines in mammals |
AU2022497A (en) * | 1996-03-13 | 1997-10-01 | Novo Nordisk A/S | A method of treating disorders related to cytokines in mammals |
GB9610031D0 (en) * | 1996-05-14 | 1996-07-17 | Glaxo Group Ltd | Chemical compounds |
UA51716C2 (ru) | 1996-07-08 | 2002-12-16 | Авентіс Фармасьютікалз Продактс Інк. | СОЕДИНЕНИЯ, ИМЕЮЩИЕ ГИПОТЕНЗИВНОЕ, КАРДИОПРОТЕКТОРНОЕ, АНТИ-ИШЕМИЧЕСКОЕ И АНТИЛИПОЛИТИЧЕСКОЕ СВОЙСТВА, фармацевтическая композиция и способЫ лечения |
GB9723590D0 (en) * | 1997-11-08 | 1998-01-07 | Glaxo Group Ltd | Chemical compounds |
-
1997
- 1997-11-08 GB GBGB9723590.7A patent/GB9723590D0/en not_active Ceased
-
1998
- 1998-11-06 AU AU16665/99A patent/AU763414B2/en not_active Ceased
- 1998-11-06 AP APAP/P/2000/001804A patent/AP2000001804A0/en unknown
- 1998-11-06 US US09/530,575 patent/US6544960B1/en not_active Expired - Fee Related
- 1998-11-06 NZ NZ504336A patent/NZ504336A/xx unknown
- 1998-11-06 KR KR1020007004962A patent/KR20010031878A/ko not_active Application Discontinuation
- 1998-11-06 DE DE69825779T patent/DE69825779T2/de not_active Expired - Lifetime
- 1998-11-06 ES ES98961132T patent/ES2222619T3/es not_active Expired - Lifetime
- 1998-11-06 EA EA200000398A patent/EA003087B1/ru not_active IP Right Cessation
- 1998-11-06 BR BR9813989-4A patent/BR9813989A/pt not_active Application Discontinuation
- 1998-11-06 CA CA002309202A patent/CA2309202C/en not_active Expired - Fee Related
- 1998-11-06 PL PL98340873A patent/PL340873A1/xx unknown
- 1998-11-06 JP JP2000520459A patent/JP2001522859A/ja active Pending
- 1998-11-06 EP EP98961132A patent/EP1030856B1/en not_active Expired - Lifetime
- 1998-11-06 TR TR2000/01937T patent/TR200001937T2/xx unknown
- 1998-11-06 ID IDW20001088A patent/ID24758A/id unknown
- 1998-11-06 WO PCT/EP1998/007023 patent/WO1999024451A2/en not_active Application Discontinuation
- 1998-11-06 SK SK670-2000A patent/SK6702000A3/sk unknown
- 1998-11-06 AT AT98961132T patent/ATE273989T1/de not_active IP Right Cessation
- 1998-11-06 YU YU26800A patent/YU26800A/sh unknown
- 1998-11-06 EE EEP200000283A patent/EE04499B1/xx not_active IP Right Cessation
- 1998-11-06 CN CN988129779A patent/CN1217952C/zh not_active Expired - Fee Related
- 1998-11-06 IL IL13596698A patent/IL135966A0/xx not_active IP Right Cessation
- 1998-11-06 HU HU0004102A patent/HUP0004102A3/hu unknown
-
2000
- 2000-05-03 IL IL135966A patent/IL135966A/en unknown
- 2000-05-03 IS IS5479A patent/IS5479A/is unknown
- 2000-05-05 NO NO20002359A patent/NO20002359L/no not_active Application Discontinuation
- 2000-05-08 HR HR20000277A patent/HRP20000277A2/xx not_active Application Discontinuation
-
2003
- 2003-02-26 US US10/373,064 patent/US6740644B2/en not_active Expired - Fee Related
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