NO982950L - Fenyltiazolderivater med inti-herpesvirus-egenskaper - Google Patents
Fenyltiazolderivater med inti-herpesvirus-egenskaperInfo
- Publication number
- NO982950L NO982950L NO982950A NO982950A NO982950L NO 982950 L NO982950 L NO 982950L NO 982950 A NO982950 A NO 982950A NO 982950 A NO982950 A NO 982950A NO 982950 L NO982950 L NO 982950L
- Authority
- NO
- Norway
- Prior art keywords
- inti
- herpes
- methods
- derivatives
- phenylthiazole derivatives
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/28—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/38—Nitrogen atoms
- C07D277/40—Unsubstituted amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/38—Nitrogen atoms
- C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/48—Acylated amino or imino radicals by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof, e.g. carbonylguanidines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Foreliggende oppfinnelse angår metoder for hemning av herpes- replikasjon og for behandling av herpes-infeksjon hos et pattedyr ved hemning av herpes-helicase-primase-enzymkomplekset. Foreliggende oppfinnelse angår også tiazolylfenyl-derivater med formel (G) som hemmer herpes- helicase-primase og farmasøytiske preparater omfattende tiazolylfenyl- derivatene, metoder for anvendelse av og metoder for fremstilling av tiazolylfenyl-derivatene. l formel (G) er R og Z som definert i beskrivelsen, hvor Z er det karakteriserende trekk.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US943395P | 1995-12-29 | 1995-12-29 | |
US2320996P | 1996-08-02 | 1996-08-02 | |
PCT/US1996/019131 WO1997024343A1 (en) | 1995-12-29 | 1996-12-04 | Phenyl thiazole derivatives with anti herpes virus properties |
Publications (2)
Publication Number | Publication Date |
---|---|
NO982950D0 NO982950D0 (no) | 1998-06-25 |
NO982950L true NO982950L (no) | 1998-06-25 |
Family
ID=26679472
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO982950A NO982950L (no) | 1995-12-29 | 1998-06-25 | Fenyltiazolderivater med inti-herpesvirus-egenskaper |
Country Status (26)
Country | Link |
---|---|
US (3) | US6057451A (no) |
EP (1) | EP0871619B1 (no) |
JP (1) | JP4327249B2 (no) |
KR (1) | KR19990076964A (no) |
AR (1) | AR037060A1 (no) |
AT (1) | ATE227279T1 (no) |
AU (1) | AU1682897A (no) |
BG (1) | BG102583A (no) |
BR (1) | BR9612435A (no) |
CA (1) | CA2192433C (no) |
CZ (1) | CZ207298A3 (no) |
DE (1) | DE69624728T2 (no) |
DK (1) | DK0871619T3 (no) |
EA (1) | EA199800611A1 (no) |
EE (1) | EE9800154A (no) |
ES (1) | ES2186811T3 (no) |
HU (1) | HUP9902341A2 (no) |
IL (1) | IL124436A0 (no) |
MX (1) | MX9805291A (no) |
NO (1) | NO982950L (no) |
NZ (1) | NZ331104A (no) |
PL (1) | PL327582A1 (no) |
PT (1) | PT871619E (no) |
SK (1) | SK89398A3 (no) |
TR (1) | TR199801244T2 (no) |
WO (1) | WO1997024343A1 (no) |
Families Citing this family (54)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6100282A (en) * | 1998-01-02 | 2000-08-08 | Hoffman-La Roche Inc. | Thiazole derivatives |
SI0928790T1 (en) * | 1998-01-02 | 2003-06-30 | F. Hoffmann-La Roche Ag | Thiazole derivatives |
AU1707700A (en) | 1998-10-29 | 2000-05-22 | Bristol-Myers Squibb Company | Novel inhibitors of impdh enzyme |
WO2000029399A1 (en) * | 1998-11-12 | 2000-05-25 | Boehringer Ingelheim (Canada) Ltd. | Antiherpes compounds |
US6166028A (en) | 1998-12-09 | 2000-12-26 | American Home Products Corporation | Diaminopuridine-containing thiourea inhibitors of herpes viruses |
US6395897B1 (en) | 1999-03-02 | 2002-05-28 | Boehringer Ingelheim Pharmaceuticals, Inc. | Nitrile compounds useful as reversible inhibitors of #9 cathepsin 5 |
US6500817B1 (en) | 1999-03-08 | 2002-12-31 | Bayer Aktiengesellschaft | Thiazolyl urea derivatives and their utilization as antiviral agents |
DE19927415A1 (de) * | 1999-06-16 | 2000-12-21 | Bayer Ag | Indolinylharnstoffderivate |
EP1193255A4 (en) * | 1999-07-01 | 2002-08-07 | Ajinomoto Kk | HETEROCYCLIC COMPOUNDS AND THEIR APPLICATIONS IN MEDICINE |
US6420364B1 (en) | 1999-09-13 | 2002-07-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compound useful as reversible inhibitors of cysteine proteases |
DOP2000000109A (es) * | 1999-12-23 | 2002-08-30 | Gerald Kleymann | Derivados de tiazolilamida |
US6867299B2 (en) * | 2000-02-24 | 2005-03-15 | Hoffmann-La Roche Inc. | Oxamide IMPDH inhibitors |
CA2412720A1 (en) * | 2000-06-15 | 2001-12-20 | Bayer Aktiengesellschaft | Method for identifying compounds with anti-herpes activity |
DE10038022A1 (de) * | 2000-08-04 | 2002-02-14 | Bayer Ag | Inverse Thiazolylamid-Derivate |
KR100453080B1 (ko) * | 2000-08-21 | 2004-10-15 | 주식회사 태평양 | 신규 티오카르밤산 유도체 및 이를 함유하는 약제학적조성물 |
CN100439332C (zh) * | 2000-08-21 | 2008-12-03 | 株式会社太平洋 | 硫脲衍生物以及包含该衍生物的药物组合物 |
ATE328868T1 (de) * | 2000-08-21 | 2006-06-15 | Pacific Corp | Neue (thio)harnstoffverbindungen und arzneimittelkompositionen, die diese enthalten |
AU2002212734A1 (en) * | 2000-11-10 | 2002-05-21 | Rational Drug Design Laboratories | Amide derivatives |
DE10129714A1 (de) | 2001-06-22 | 2003-01-02 | Bayer Ag | Topische Anwendung von Thiazolylamiden |
CA2479928A1 (en) * | 2002-03-28 | 2003-10-09 | Neurogen Corporation | Substituted biaryl amides as c5a receptor modulators |
US6858637B2 (en) | 2002-03-28 | 2005-02-22 | Neurogen Corporation | Substituted biaryl amides as C5a receptor modulators |
WO2003095435A1 (fr) * | 2002-05-09 | 2003-11-20 | Yamanouchi Pharmaceutical Co., Ltd. | Derives d'amides |
CA2503844A1 (en) * | 2002-10-30 | 2004-05-21 | Merck & Co., Inc. | Piperidinyl-alpha-aminoamide modulators of chemokine receptor activity |
DE10254336A1 (de) * | 2002-11-21 | 2004-06-03 | Merck Patent Gmbh | Carbonsäureamide |
CA2514573A1 (en) * | 2003-01-27 | 2004-08-12 | Astellas Pharma Inc. | Thiazole derivatives and their use as vap-1 inhibitors |
CA2520957C (en) * | 2003-03-31 | 2013-08-06 | Sucampo Ag | Method for treating vascular hyperpermeable disease |
TW200505894A (en) * | 2003-08-08 | 2005-02-16 | Yamanouchi Pharma Co Ltd | Tetrahydro-2H-thiopyran-4-carboxamide derivative |
FR2860514A1 (fr) | 2003-10-03 | 2005-04-08 | Sanofi Synthelabo | Derives d'arylalkylcarbamates, leur preparation et leur application en therapeutique |
KR20050039573A (ko) * | 2003-10-23 | 2005-04-29 | 주식회사 태평양 | 티오우레아계 유도체의 용해성과 생체이용률이 개선된약제학적 조성물 |
EP1686949A2 (en) * | 2003-11-24 | 2006-08-09 | Viropharma Incorporated | Compounds, compositions and methods for treatment and prophylaxis of hepatitis c viral infections and associated diseases |
WO2005090406A2 (en) | 2004-03-12 | 2005-09-29 | Vasgene Therapeutics, Inc. | Antibodies binding to ephb4 for inhibiting angiogenesis and tumor growth |
JP5011739B2 (ja) * | 2005-02-03 | 2012-08-29 | アステラス製薬株式会社 | テトラヒドロ−2h−チオピラン−4−カルボキサミド誘導体を含有する医薬組成物 |
DE102005014248A1 (de) | 2005-03-30 | 2006-10-05 | Aicuris Gmbh & Co. Kg | Pharmazeutische Zubereitung von N-[5-(Aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamid |
KR20080019213A (ko) | 2005-05-09 | 2008-03-03 | 아칠리온 파르마세우티칼스 인코포레이티드 | 티아졸 화합물 및 그 사용방법 |
US20070021434A1 (en) * | 2005-06-24 | 2007-01-25 | Migenix Inc. | Non-nucleoside anti-hepacivirus agents and uses thereof |
BRPI0706610A2 (pt) * | 2006-01-18 | 2011-04-05 | Siena Biotech Spa | moduladores de receptores alfa 7 nicotìnico acetilcolina e usos terapêuticos destes |
WO2008025694A1 (en) * | 2006-08-30 | 2008-03-06 | F. Hoffmann-La Roche Ag | Inhibitors for glyt-1 |
TW200906826A (en) * | 2007-06-12 | 2009-02-16 | Genelabs Tech Inc | Anti-viral inhibitors and methods of use |
US20110201659A1 (en) | 2008-10-20 | 2011-08-18 | Astellas Pharma Inc. | Agent for preventing or treating zoster-associated pain |
EP2384320B1 (en) * | 2009-01-05 | 2015-03-04 | Boehringer Ingelheim International GmbH | Pyrrolidine compounds which modulate the cb2 receptor |
WO2011047390A2 (en) | 2009-10-16 | 2011-04-21 | University Of Maryland, Baltimore County | Heterocyclic benzoxazole compositions as inhibitors of hepatitis c virus |
WO2012113920A1 (en) | 2011-02-24 | 2012-08-30 | Katholieke Universiteit Leuven | Arylsulfone derivatives with activity against human betaherpesviruses |
KR101399484B1 (ko) * | 2011-07-14 | 2014-05-29 | 한국화학연구원 | 허피스바이러스 엑소뉴클리에이즈 활성 억제 물질을 유효성분으로 함유하는 항허피스바이러스용 약학적 조성물 |
UY35772A (es) | 2013-10-14 | 2015-05-29 | Bayer Cropscience Ag | Nuevos compuestos plaguicidas |
MX2017006043A (es) | 2014-11-10 | 2018-02-13 | Forge Life Science Llc | Metodo y composiciones de anti-hcmv. |
JP6749344B2 (ja) * | 2015-02-13 | 2020-09-02 | アジエンダ・オスペダリエラ・ウニベルシタリア・セネーゼ | 治療剤としてのヒトヘリカーゼddx3阻害剤 |
AU2017245679B2 (en) | 2016-04-06 | 2021-07-01 | Innovative Molecules Gmbh | Aminothiazole derivatives useful as antiviral agents |
WO2018132372A1 (en) | 2017-01-10 | 2018-07-19 | Sanford Burnham Prebys Medical Discovery Institute | Small molecule activators of nicotinamide phosphoribosyltransferase (nampt) and uses thereof |
HUE061307T2 (hu) | 2017-10-05 | 2023-06-28 | Innovative Molecules Gmbh | Szubsztituált tiazolok enantiomerei mint vírusellenes vegyületek |
CN112654608B (zh) | 2018-07-05 | 2024-05-07 | 桑福德伯纳姆普利斯医学发现研究所 | 具有脲结构的稠环化合物 |
CN112996789A (zh) | 2018-09-12 | 2021-06-18 | 诺华股份有限公司 | 抗病毒吡啶并吡嗪二酮化合物 |
SG11202106444WA (en) | 2018-12-19 | 2021-07-29 | Leo Pharma As | Amino-acid anilides as small molecule modulators of il-17 |
KR20220070005A (ko) | 2019-09-26 | 2022-05-27 | 노파르티스 아게 | 항바이러스성 피라졸로피리디논 화합물 |
WO2024047508A1 (en) | 2022-08-29 | 2024-03-07 | Assembly Biosciences, Inc. | Pharmaceutical compositions for herpes virus |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3629247A (en) * | 1969-06-06 | 1971-12-21 | Pfizer | Thiazoline and 5 6-dihydro-4h-1 3-thiazine antiviral agents |
US4746669A (en) * | 1985-12-23 | 1988-05-24 | Merck & Co., Inc. | Substituted thiazoles as immunoregulants |
JPH075579B2 (ja) * | 1986-09-01 | 1995-01-25 | 吉富製薬株式会社 | アミノチアゾ−ル化合物 |
MX174210B (es) * | 1987-02-17 | 1994-04-28 | Pfizer | Procedimiento para la preparacion de compuestos arilpiperazinil-alquilenfenil-p-heterociclicos |
US5153206A (en) * | 1988-12-02 | 1992-10-06 | Pfizer Inc. | Arylpiperidine derivatives |
FR2656610B1 (fr) * | 1989-12-29 | 1992-05-07 | Sanofi Sa | Derives d'amino-2 phenyl-4 thiazole, leur procede de preparation et leur application therapeutique. |
US5077409A (en) * | 1990-05-04 | 1991-12-31 | American Cyanamid Company | Method of preparing bis-aryl amide and urea antagonists of platelet activating factor |
US5128351A (en) * | 1990-05-04 | 1992-07-07 | American Cyanamid Company | Bis-aryl amide and urea antagonists of platelet activating factor |
AU1347292A (en) * | 1991-01-18 | 1992-08-27 | Oncogene Science, Inc. | Methods of transcriptionally modulating gene expression of viral genes and other genes |
GB9125970D0 (en) * | 1991-12-06 | 1992-02-05 | Fujisawa Pharmaceutical Co | New compounds |
TW288010B (no) * | 1992-03-05 | 1996-10-11 | Pfizer | |
US5342851A (en) * | 1992-10-07 | 1994-08-30 | Mcneil-Ppc, Inc. | Substituted thiazole derivatives useful as platelet aggregation inhibitors |
GB2276164A (en) * | 1993-03-17 | 1994-09-21 | Glaxo Group Ltd | Aniline and benzanilide derivatives |
IT1266582B1 (it) * | 1993-07-30 | 1997-01-09 | Recordati Chem Pharm | Derivati (di)azacicloesanici e diazacicloeptanici |
CA2190870A1 (en) * | 1994-05-27 | 1995-12-07 | George D. Hartman | Compounds for inhibiting osteoclast-mediated bone resorption |
AU3289299A (en) * | 1998-02-19 | 1999-09-06 | Tularik Inc. | Antiviral agents |
-
1996
- 1996-12-04 SK SK893-98A patent/SK89398A3/sk unknown
- 1996-12-04 DE DE69624728T patent/DE69624728T2/de not_active Expired - Lifetime
- 1996-12-04 KR KR1019980705092A patent/KR19990076964A/ko not_active Application Discontinuation
- 1996-12-04 JP JP52432597A patent/JP4327249B2/ja not_active Expired - Fee Related
- 1996-12-04 EE EE9800154A patent/EE9800154A/xx unknown
- 1996-12-04 TR TR1998/01244T patent/TR199801244T2/xx unknown
- 1996-12-04 PL PL96327582A patent/PL327582A1/xx unknown
- 1996-12-04 US US08/759,201 patent/US6057451A/en not_active Expired - Lifetime
- 1996-12-04 IL IL12443696A patent/IL124436A0/xx unknown
- 1996-12-04 BR BR9612435A patent/BR9612435A/pt unknown
- 1996-12-04 HU HU9902341A patent/HUP9902341A2/hu unknown
- 1996-12-04 AU AU16828/97A patent/AU1682897A/en not_active Abandoned
- 1996-12-04 AT AT96945567T patent/ATE227279T1/de active
- 1996-12-04 NZ NZ331104A patent/NZ331104A/xx unknown
- 1996-12-04 ES ES96945567T patent/ES2186811T3/es not_active Expired - Lifetime
- 1996-12-04 WO PCT/US1996/019131 patent/WO1997024343A1/en active IP Right Grant
- 1996-12-04 CZ CZ982072A patent/CZ207298A3/cs unknown
- 1996-12-04 EP EP96945567A patent/EP0871619B1/en not_active Expired - Lifetime
- 1996-12-04 EA EA199800611A patent/EA199800611A1/ru unknown
- 1996-12-04 PT PT96945567T patent/PT871619E/pt unknown
- 1996-12-04 DK DK96945567T patent/DK0871619T3/da active
- 1996-12-09 CA CA002192433A patent/CA2192433C/en not_active Expired - Fee Related
- 1996-12-30 AR ARP960105968A patent/AR037060A1/es not_active Withdrawn
-
1998
- 1998-06-25 NO NO982950A patent/NO982950L/no not_active Application Discontinuation
- 1998-06-26 BG BG102583A patent/BG102583A/xx active Pending
- 1998-06-29 MX MX9805291A patent/MX9805291A/es not_active IP Right Cessation
-
1999
- 1999-12-08 US US09/456,857 patent/US6348477B1/en not_active Expired - Lifetime
-
2000
- 2000-10-10 US US09/685,686 patent/US6458959B1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US6057451A (en) | 2000-05-02 |
WO1997024343A1 (en) | 1997-07-10 |
MX9805291A (es) | 1998-10-31 |
EP0871619A1 (en) | 1998-10-21 |
AU1682897A (en) | 1997-07-28 |
EE9800154A (et) | 1998-12-15 |
DE69624728T2 (de) | 2003-07-10 |
IL124436A0 (en) | 1998-12-06 |
ES2186811T3 (es) | 2003-05-16 |
KR19990076964A (ko) | 1999-10-25 |
AR037060A1 (es) | 2004-10-20 |
CZ207298A3 (cs) | 1998-11-11 |
BR9612435A (pt) | 1999-07-13 |
NO982950D0 (no) | 1998-06-25 |
DE69624728D1 (de) | 2002-12-12 |
SK89398A3 (en) | 1998-11-04 |
EA199800611A1 (ru) | 1999-04-29 |
NZ331104A (en) | 2000-03-27 |
CA2192433A1 (en) | 1997-06-30 |
TR199801244T2 (xx) | 1998-12-21 |
PL327582A1 (en) | 1998-12-21 |
JP2000502702A (ja) | 2000-03-07 |
HUP9902341A2 (hu) | 1999-10-28 |
PT871619E (pt) | 2003-03-31 |
EP0871619B1 (en) | 2002-11-06 |
US6458959B1 (en) | 2002-10-01 |
US6348477B1 (en) | 2002-02-19 |
CA2192433C (en) | 2008-01-08 |
JP4327249B2 (ja) | 2009-09-09 |
ATE227279T1 (de) | 2002-11-15 |
DK0871619T3 (da) | 2003-03-03 |
BG102583A (en) | 1999-06-30 |
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