MXPA03002998A - Fenilacetamidas sustituidas con aminopiridinilo, aminoguanidinilo y alcoxiguanidinilo como inhibidores de proteasas. - Google Patents
Fenilacetamidas sustituidas con aminopiridinilo, aminoguanidinilo y alcoxiguanidinilo como inhibidores de proteasas.Info
- Publication number
- MXPA03002998A MXPA03002998A MXPA03002998A MXPA03002998A MXPA03002998A MX PA03002998 A MXPA03002998 A MX PA03002998A MX PA03002998 A MXPA03002998 A MX PA03002998A MX PA03002998 A MXPA03002998 A MX PA03002998A MX PA03002998 A MXPA03002998 A MX PA03002998A
- Authority
- MX
- Mexico
- Prior art keywords
- blood
- sup
- compounds
- inhibiting
- formation
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino 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
- A61K31/13—Amines
- A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- 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
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- 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
- A61P9/08—Vasodilators for multiple indications
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/73—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
- C07C311/13—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US23813200P | 2000-10-06 | 2000-10-06 | |
PCT/US2001/031249 WO2002028825A2 (en) | 2000-10-06 | 2001-10-05 | Aminopyridinyl-, aminoguanidinyl- and alkoxyguanidinyl- substituted phenyl acetamides as protease inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA03002998A true MXPA03002998A (es) | 2004-02-12 |
Family
ID=22896640
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MXPA03002998A MXPA03002998A (es) | 2000-10-06 | 2001-10-05 | Fenilacetamidas sustituidas con aminopiridinilo, aminoguanidinilo y alcoxiguanidinilo como inhibidores de proteasas. |
Country Status (26)
Country | Link |
---|---|
US (3) | US6521663B2 (es) |
EP (1) | EP1324981B1 (es) |
JP (1) | JP4256160B2 (es) |
KR (1) | KR20030045103A (es) |
CN (1) | CN1315803C (es) |
AT (1) | ATE337299T1 (es) |
AU (2) | AU2002211464B2 (es) |
BR (1) | BR0114263A (es) |
CA (1) | CA2423883A1 (es) |
CY (1) | CY1106243T1 (es) |
DE (1) | DE60122546T2 (es) |
DK (1) | DK1324981T3 (es) |
ES (1) | ES2269474T3 (es) |
HK (1) | HK1058032A1 (es) |
HR (1) | HRP20030252A2 (es) |
HU (1) | HUP0303149A3 (es) |
IL (1) | IL155160A0 (es) |
MX (1) | MXPA03002998A (es) |
NO (1) | NO20031390L (es) |
NZ (1) | NZ525438A (es) |
PL (1) | PL361185A1 (es) |
PT (1) | PT1324981E (es) |
RU (1) | RU2003113205A (es) |
UA (1) | UA75093C2 (es) |
WO (1) | WO2002028825A2 (es) |
ZA (1) | ZA200303091B (es) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA75093C2 (en) * | 2000-10-06 | 2006-03-15 | Dimensional Pharm Inc | Aminopyridinyl-,aminoguanidinyl-, and alkoxyguanidinesubstituted phenylsubstituted phenylacetamides as protease inhibitors |
US6610701B2 (en) * | 2001-02-09 | 2003-08-26 | Merck & Co., Inc. | Thrombin inhibitors |
EP1443919A4 (en) * | 2001-11-16 | 2006-03-22 | Bristol Myers Squibb Co | DOUBLE INHIBITORS OF THE FATTY ACID BINDING PROTEIN OF THE ADIPOCYTES AND THE FATTY ACID BINDING PROTEIN OF KERATINOCYTES |
US7759513B2 (en) * | 2003-02-21 | 2010-07-20 | Nigu Chemie Gmbh | Photolabile protective groups for improved processes to prepare oligonucleotide arrays |
US7550474B2 (en) | 2003-04-10 | 2009-06-23 | Johnson & Johnson Pharmaceuticals Research & Development, L.L.C. | Substituted phenyl acetamides and their use as protease inhibitors |
US7790724B2 (en) | 2003-04-25 | 2010-09-07 | Janssen Pharmaceutica N.V. | c-fms kinase inhibitors |
US7427683B2 (en) * | 2003-04-25 | 2008-09-23 | Ortho-Mcneil Pharmaceutical, Inc. | c-fms kinase inhibitors |
JP2007525460A (ja) | 2003-04-25 | 2007-09-06 | 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 | c−fmsキナーゼ阻害剤 |
US7914705B2 (en) * | 2005-01-10 | 2011-03-29 | Robert Eliot Sisson | Flowable electrical conductive liquid |
HU0500126D0 (en) * | 2005-01-26 | 2005-04-28 | Sanofi Aventis | New compounds and process for their preparation |
CN101243069A (zh) * | 2005-06-17 | 2008-08-13 | 阿斯利康(瑞典)有限公司 | 凝血酶抑制剂2-氧代-1,2,5,6-四氢吡啶衍生物 |
RU2008144571A (ru) | 2006-04-12 | 2010-05-20 | Мерк энд Ко., Инк. (US) | Пиридиламидные антагонисты кальциевых каналов т-типа |
RU2353619C2 (ru) * | 2007-06-28 | 2009-04-27 | Общество С Ограниченной Ответственностью "Бионика" | Новые соединения, обладающие функцией антикоагулянтов, фармацевтические композиции на их основе для лечения тромботических состояний и плазмозамещающий раствор для коррекции гиперкоагуляционных нарушений при гемодилюции |
RU2354647C2 (ru) * | 2007-06-28 | 2009-05-10 | Общество С Ограниченной Ответственностью "Бионика" | Новые соединения, обладающие функцией ингибиторов тромбина, и фармацевтические композиции на их основе |
CN101665465B (zh) * | 2007-09-19 | 2011-09-07 | 复旦大学 | 一种含胍基杂环化合物凝血酶抑制剂及其制备方法 |
RU2010120671A (ru) * | 2007-10-24 | 2011-11-27 | Мерк Шарп Энд Домэ Корп. (Us) | Гетероциклические фениламидные антагонисты кальциевых каналов т-типа |
US10299714B2 (en) | 2010-12-02 | 2019-05-28 | Becton, Dickinson And Company | Blood collection devices containing blood stabilization agent including variegin or analog thereof and/or a polysulfated disaccharide |
EP2658580A4 (en) | 2010-12-31 | 2014-07-23 | Corridor Pharmaceuticals Inc | ARGINE STARTER AND USE METHOD |
EP2709446A2 (en) | 2011-05-17 | 2014-03-26 | Velico Medical, Inc. | Platelet storage using a sialidase inhibitor |
US9788539B2 (en) | 2011-05-17 | 2017-10-17 | Velico Medical, Inc. | Platelet protection solution having beta-galactosidase and sialidase inhibitors |
EP2903430A1 (en) | 2012-10-05 | 2015-08-12 | Velico Medical, Inc. | Platelet additive solution having a beta-galactosidase inhibitor |
RU2524647C1 (ru) * | 2012-12-25 | 2014-07-27 | Государственное Бюджетное Учреждение Санкт-Петербургский Научно-Исследовательский Институт Скорой Помощи Им. И.И. Джанелидзе" | Способ лечения синдрома эндогенной интоксикации, обусловленного гиперпротеолизом |
WO2014120886A1 (en) | 2013-01-30 | 2014-08-07 | Velico Medical, Inc. | Platelet additive solution having a self-assembling hydrogel-forming peptide |
WO2015143376A1 (en) * | 2014-03-21 | 2015-09-24 | Nivalis Therapeutics, Inc. | Novel compounds for the treatment of cystic fibrosis |
CN108026103B (zh) | 2015-07-21 | 2021-04-16 | 伊缪诺金公司 | 制备细胞毒性苯并二氮杂䓬衍生物的方法 |
ES2963606T3 (es) * | 2017-05-24 | 2024-04-01 | Univ Ramot | Sondas quimioluminiscentes para la obtención de imagen/detección de proteasas |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
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US5084466A (en) | 1989-01-31 | 1992-01-28 | Hoffmann-La Roche Inc. | Novel carboxamide pyridine compounds which have useful pharmaceutical utility |
CA2075154A1 (en) * | 1991-08-06 | 1993-02-07 | Neelakantan Balasubramanian | Peptide aldehydes as antithrombotic agents |
DE4208051A1 (de) | 1992-03-13 | 1993-09-16 | Bayer Ag | Substituierte phenylessigsaeureamide |
DE4319887A1 (de) | 1993-06-16 | 1994-12-22 | Hoechst Schering Agrevo Gmbh | Arylacetamide, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Fungizide |
US5807885A (en) | 1993-08-12 | 1998-09-15 | Astra Aktiebolag | Amidine derivatives with nitric oxide synthetase activities |
US5885967A (en) | 1994-03-04 | 1999-03-23 | Eli Lilly And Company | Antithrombotic agents |
JPH0892224A (ja) | 1994-09-16 | 1996-04-09 | Kumiai Chem Ind Co Ltd | 3,5−置換フェニルトリアゾール誘導体および殺虫、殺ダニ剤 |
JP3570752B2 (ja) | 1994-09-22 | 2004-09-29 | 三井化学株式会社 | 4−置換カルボニルクマリン誘導体、およびこれを用いた可視光感光性組成物 |
DE19507822B4 (de) | 1995-02-21 | 2006-07-20 | Schering Ag | Substituierte DTPA-Monoamide der zentralen Carbonsäure und deren Metallkomplexe, diese Komplexe enthaltende pharmazeutische Mittel, deren Verwendung in der Diagnostik und Therapie sowie Verfahren zur Herstellung der Komplexe und Mittel |
US5741819A (en) * | 1995-06-07 | 1998-04-21 | 3-Dimensional Pharmaceuticals, Inc. | Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors |
US5721214A (en) | 1995-06-07 | 1998-02-24 | Cor Therapeutics, Inc. | Inhibitors of factor Xa |
AU703744B2 (en) * | 1995-06-27 | 1999-04-01 | Merck & Co., Inc. | Pyridinone-thrombin inhibitors |
JPH11512722A (ja) | 1995-09-29 | 1999-11-02 | 3−ディメンショナル ファーマシューティカルズ,インコーポレイテッド | グアニジノプロテアーゼインヒビター |
DE69717268T2 (de) | 1996-02-22 | 2003-09-04 | Bristol Myers Squibb Pharma Co | M-amidinophenyl-analoga als faktor-xa-inhibitoren |
DE19615262A1 (de) | 1996-04-18 | 1997-10-23 | Bayer Ag | Heteroverknüpfte Phenylglycinolamide |
AU3496297A (en) | 1996-06-25 | 1998-01-14 | Eli Lilly And Company | Anticoagulant agents |
US6174905B1 (en) | 1996-09-30 | 2001-01-16 | Mitsui Chemicals, Inc. | Cell differentiation inducer |
DE19642863A1 (de) | 1996-10-17 | 1998-04-23 | Bayer Ag | Amide |
TW499412B (en) * | 1996-11-26 | 2002-08-21 | Dimensional Pharm Inc | Aminoguanidines and alkoxyguanidines as protease inhibitors |
GB9703201D0 (en) | 1997-02-15 | 1997-04-02 | Zeneca Ltd | Chemical compounds |
SI0966436T1 (en) | 1997-02-21 | 2003-04-30 | Bayer Aktiengesellschaft | Aryl sulfonamides and analogues thereof and their use in the treatment of neurodegenerative diseases |
US6034272A (en) | 1997-06-16 | 2000-03-07 | American Home Products Corporation | Elevation of HDL cholesterol by N-[4-[(aminothioxomethyl) hydrazono]-4-arylbutyl]amides |
US6049006A (en) | 1997-06-16 | 2000-04-11 | American Home Products Corp. | Elevation of HDL cholesterol by N-[2-[(aminothioxomethyl) hydrazono]-2-arylethyl]amides |
AU7498298A (en) | 1997-06-16 | 1999-01-04 | American Home Products Corporation | Elevation of hdl cholesterol by n-{2-{ (aminothioxomethyl)hydrazono} -2-arylethyl}amides |
AU7691298A (en) | 1997-06-16 | 1999-01-04 | American Home Products Corporation | Elevation of hdl cholesterol by n-{4-{ (aminothioxomethyl) hydrazono} -4-arylbutyl}amides |
DE69836346T2 (de) * | 1997-11-26 | 2007-05-24 | Ortho-Mcneil Pharmaceutical, Inc. | Heteroaryl aminoguanidin- und alkoxyguanidinderivate und ihre verwendung als proteasehemmer |
CA2260499A1 (en) | 1998-01-29 | 1999-07-29 | Sumitomo Pharmaceuticals Company Limited | Pharmaceutical compositions for the treatment of ischemic brain damage |
US6344486B1 (en) * | 1998-04-03 | 2002-02-05 | 3-Dimensional Pharmaceuticals, Inc. | Benzamide and sulfonamide substituted aminoguanidines and alkoxyguanidines as protease inhibitors |
AU3459999A (en) | 1998-04-27 | 1999-11-16 | Warner-Lambert Company | Substituted diarylalkyl amides as calcium channel antagonists |
DE19824470A1 (de) | 1998-05-30 | 1999-12-02 | Boehringer Ingelheim Pharma | Neue Neurokininantagonisten, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende pharmazeutische Zusammensetzungen |
DE19937494A1 (de) * | 1999-08-07 | 2001-02-08 | Boehringer Ingelheim Pharma | Carbonsäureamide, deren Herstellung und deren Verwendung als Arzneimittel |
US6660885B2 (en) | 2000-03-13 | 2003-12-09 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted benzenes useful for selective inhibition of the coagulation cascade |
UA75093C2 (en) * | 2000-10-06 | 2006-03-15 | Dimensional Pharm Inc | Aminopyridinyl-,aminoguanidinyl-, and alkoxyguanidinesubstituted phenylsubstituted phenylacetamides as protease inhibitors |
-
2001
- 2001-05-10 UA UA2003054058A patent/UA75093C2/uk unknown
- 2001-10-05 NZ NZ525438A patent/NZ525438A/en unknown
- 2001-10-05 BR BR0114263-1A patent/BR0114263A/pt not_active IP Right Cessation
- 2001-10-05 DE DE60122546T patent/DE60122546T2/de not_active Expired - Fee Related
- 2001-10-05 HU HU0303149A patent/HUP0303149A3/hu unknown
- 2001-10-05 PL PL36118501A patent/PL361185A1/xx not_active Application Discontinuation
- 2001-10-05 CA CA002423883A patent/CA2423883A1/en not_active Abandoned
- 2001-10-05 ES ES01979513T patent/ES2269474T3/es not_active Expired - Lifetime
- 2001-10-05 DK DK01979513T patent/DK1324981T3/da active
- 2001-10-05 ZA ZA200303091A patent/ZA200303091B/en unknown
- 2001-10-05 AU AU2002211464A patent/AU2002211464B2/en not_active Ceased
- 2001-10-05 US US09/971,000 patent/US6521663B2/en not_active Expired - Lifetime
- 2001-10-05 KR KR10-2003-7004831A patent/KR20030045103A/ko not_active Application Discontinuation
- 2001-10-05 MX MXPA03002998A patent/MXPA03002998A/es active IP Right Grant
- 2001-10-05 AT AT01979513T patent/ATE337299T1/de not_active IP Right Cessation
- 2001-10-05 IL IL15516001A patent/IL155160A0/xx unknown
- 2001-10-05 PT PT01979513T patent/PT1324981E/pt unknown
- 2001-10-05 CN CNB018182542A patent/CN1315803C/zh not_active Expired - Fee Related
- 2001-10-05 EP EP01979513A patent/EP1324981B1/en not_active Expired - Lifetime
- 2001-10-05 RU RU2003113205/04A patent/RU2003113205A/ru not_active Application Discontinuation
- 2001-10-05 AU AU1146402A patent/AU1146402A/xx active Pending
- 2001-10-05 JP JP2002532411A patent/JP4256160B2/ja not_active Expired - Fee Related
- 2001-10-05 WO PCT/US2001/031249 patent/WO2002028825A2/en active Application Filing
-
2002
- 2002-10-03 US US10/262,871 patent/US6900231B2/en not_active Expired - Lifetime
-
2003
- 2003-03-26 NO NO20031390A patent/NO20031390L/no not_active Application Discontinuation
- 2003-04-03 HR HR20030252A patent/HRP20030252A2/hr not_active Application Discontinuation
-
2004
- 2004-01-02 HK HK0100042A patent/HK1058032A1/xx not_active IP Right Cessation
-
2005
- 2005-01-10 US US11/032,297 patent/US20050159457A1/en not_active Abandoned
-
2006
- 2006-11-14 CY CY20061101657T patent/CY1106243T1/el unknown
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