NO942864L - Benzo-condensed 5-ring heterocycles, process for their preparation, their use as a drug, their use as a diagnostic, and drug containing these - Google Patents
Benzo-condensed 5-ring heterocycles, process for their preparation, their use as a drug, their use as a diagnostic, and drug containing theseInfo
- Publication number
- NO942864L NO942864L NO942864A NO942864A NO942864L NO 942864 L NO942864 L NO 942864L NO 942864 A NO942864 A NO 942864A NO 942864 A NO942864 A NO 942864A NO 942864 L NO942864 L NO 942864L
- Authority
- NO
- Norway
- Prior art keywords
- drug
- benzo
- diagnostic
- condensed
- preparation
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- A61P9/06—Antiarrhythmics
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
- C07D235/32—Benzimidazole-2-carbamic acids, unsubstituted or substituted; Esters thereof; Thio-analogues thereof
-
- 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
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans 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 carbon atoms of the hetero ring
- C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D307/85—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/86—Benzo [b] furans; Hydrogenated benzo [b] furans with an oxygen atom directly attached in position 7
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes 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 carbon atoms of the hetero ring
- C07D333/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D333/70—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4326005A DE4326005A1 (en) | 1993-08-03 | 1993-08-03 | Benzo-fused 5-membered ring heterocycles, processes for their preparation, their use as a medicament, their use as a diagnostic, and medicament containing them |
DE19944414316 DE4414316A1 (en) | 1994-04-25 | 1994-04-25 | New benzo-fused heterocyclyl-carbonyl-guanidine derivs. |
Publications (3)
Publication Number | Publication Date |
---|---|
NO942864D0 NO942864D0 (en) | 1994-08-02 |
NO942864L true NO942864L (en) | 1995-02-06 |
NO301584B1 NO301584B1 (en) | 1997-11-17 |
Family
ID=25928286
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO942864A NO301584B1 (en) | 1993-08-03 | 1994-08-02 | Benzo-condensed 5-ring heterocycles, their use in the manufacture of drugs and diagnostics, as well as drugs containing these |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0639573A1 (en) |
JP (1) | JPH07145149A (en) |
KR (2) | KR950005817A (en) |
CN (1) | CN1118347A (en) |
AU (1) | AU682371B2 (en) |
CA (1) | CA2129301A1 (en) |
FI (1) | FI943579A (en) |
HU (1) | HU218790B (en) |
IL (1) | IL110503A (en) |
NO (1) | NO301584B1 (en) |
NZ (1) | NZ264130A (en) |
Families Citing this family (76)
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CA2121391A1 (en) * | 1993-04-28 | 1994-10-29 | Atsuyuki Kojima | Indoloylguanidine derivatives |
US6169107B1 (en) | 1993-04-28 | 2001-01-02 | Sumitomo Pharmaceutical Co., Ltd. | Indoloylguanidine derivatives |
AU683552B2 (en) * | 1994-04-11 | 1997-11-13 | Chugai Seiyaku Kabushiki Kaisha | 4,6-DI-t-butyl-2,3-dihydrobenzothiophene derivative |
DE4412334A1 (en) * | 1994-04-11 | 1995-10-19 | Hoechst Ag | Substituted N-heteroaroylguanidines, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them |
CA2160600A1 (en) * | 1994-10-18 | 1996-04-19 | Masahumi Kitano | Indoloylguanidine derivatives |
US5834466A (en) * | 1994-12-22 | 1998-11-10 | The Regents Of The University Of California | Method for protecting of heart by limiting metabolic and ionic abnormalities developed during ischemia, following ischemia or resulting from ischemia |
ATE183498T1 (en) * | 1995-04-18 | 1999-09-15 | Hoechst Ag | SUBSTITUTED INDENOYLGUANIDINES WITH ANTIARRHYTHMIC AND CARDIOPROTECTIVE EFFECTS |
DE19540995A1 (en) * | 1995-11-03 | 1997-05-07 | Hoechst Ag | Substituted sulfonimidamides, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them |
DE19542306A1 (en) * | 1995-11-14 | 1997-05-15 | Hoechst Ag | Sulfonylamino-substituted benzoylguanidines, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them |
PL316439A1 (en) * | 1995-11-20 | 1997-05-26 | Hoechst Ag | Novel substituted derivatives of benzoyloguanidine, method of obtaining them, their application in production of pharmaceutic and diagnostic agents and pharmaceutic agent as such |
DE19546736A1 (en) * | 1995-12-14 | 1997-06-19 | Hoechst Ag | Substituted chromanylsulfonyl (thio) ureas, process for their preparation and their use in the manufacture of pharmaceutical preparations |
DE19548708A1 (en) * | 1995-12-23 | 1997-06-26 | Merck Patent Gmbh | Cyclic sulfones |
DE19548812A1 (en) * | 1995-12-27 | 1997-07-03 | Hoechst Ag | Use of inhibitors of the cellular Na · + · / H · + · exchanger (NHE) for the manufacture of a medicament for respiratory stimulation |
CA2195697A1 (en) * | 1996-02-02 | 1997-08-03 | Masahumi Kitano | Novel substituted guanidine derivatives, process for production thereof, and pharmaceutical uses thereof |
EP0886524A2 (en) * | 1996-03-01 | 1998-12-30 | Chiron Corporation | Delivery of therapeutic agents to the prostate |
WO1998055475A1 (en) * | 1997-06-02 | 1998-12-10 | Fujisawa Pharmaceutical Co., Ltd. | Guanidine deriviatives as inhibitors of na+/h+ exchange in cells |
GB9716657D0 (en) * | 1997-08-07 | 1997-10-15 | Zeneca Ltd | Chemical compounds |
US6160134A (en) * | 1997-12-24 | 2000-12-12 | Bristol-Myers Squibb Co. | Process for preparing chiral cyclopropane carboxylic acids and acyl guanidines |
US6011059A (en) * | 1997-12-24 | 2000-01-04 | Bristol-Myers Squibb Company | Acyl guanidine sodium/proton exchange inhibitors and method |
CA2260499A1 (en) * | 1998-01-29 | 1999-07-29 | Sumitomo Pharmaceuticals Company Limited | Pharmaceutical compositions for the treatment of ischemic brain damage |
GB9803226D0 (en) | 1998-02-17 | 1998-04-08 | Zeneca Ltd | Chemical compounds |
EP1056729B1 (en) * | 1998-02-27 | 2004-12-29 | Pfizer Products Inc. | N-[(substituted five-membered di- or triaza diunsaturated ring)carbonyl]guanidine derivatives for the treatment of ischemia |
US7314888B1 (en) | 1998-11-05 | 2008-01-01 | Toyama Chemical Co., Ltd. | Compounds and medicinal use thereof |
GB9902459D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
GB9902461D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
GB9902453D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
GB9902455D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
GB9902452D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
CA2370607A1 (en) | 1999-04-23 | 2000-11-02 | Bristol-Myers Squibb Company | Bicyclic acyl guanidine sodium/proton exchange inhibitors and method |
AU1733701A (en) * | 1999-12-16 | 2001-06-25 | Sumitomo Pharmaceuticals Company, Limited | Substituted guanidine derivatives |
GB0000625D0 (en) | 2000-01-13 | 2000-03-01 | Zeneca Ltd | Chemical compounds |
WO2002051805A1 (en) | 2000-12-27 | 2002-07-04 | Bayer Aktiengesellschaft | Indole derivatives as ligands of thyroid receptors |
DE10163239A1 (en) * | 2001-12-21 | 2003-07-10 | Aventis Pharma Gmbh | Substituted imidazolidines, process for their preparation, their use as medicaments or diagnostic agents, and medicaments containing them |
SG148857A1 (en) | 2002-03-13 | 2009-01-29 | Array Biopharma Inc | N3 alkylated benzimidazole derivatives as mek inhibitors |
FR2842525B1 (en) * | 2002-07-16 | 2005-05-13 | Aventis Pharma Sa | 3-GUANIDINOCARBONYL-1-HETEROARYL-INDOLE DERIVATIVES, PROCESS FOR THE PREPARATION AS MEDICAMENTS AND PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME |
FR2842526B1 (en) * | 2002-07-16 | 2007-07-13 | Aventis Pharma Sa | PHARMACEUTICAL COMPOSITIONS COMPRISING A 3-GUANIDINOCARBONYL-1-HETEROARYL-INDOLE DERIVATIVE, PROCESS FOR THE PREPARATION AS MEDICAMENTS |
US7141600B2 (en) | 2003-04-15 | 2006-11-28 | The Regents Of The University Of California | Small molecule inhibition of a PDZ-domain interaction |
FR2856062B1 (en) * | 2003-06-12 | 2005-11-11 | Aventis Pharma Sa | 3-GUANIDINOCARBONYL-HETEROCYCLE DERIVATIVES, PREPARATION METHOD AND INTERMEDIATES THEREOF AS MEDICAMENTS AND PHARMACEUTICAL COMPOSITIONS COMPRISING SAME |
AU2005254782A1 (en) | 2004-06-18 | 2005-12-29 | Biolipox Ab | Indoles useful in the treatment of inflammation |
WO2006007542A1 (en) | 2004-07-01 | 2006-01-19 | The Regents Of The University Of California | Small molecule inhibition of a pdz-domain interaction |
US7868037B2 (en) | 2004-07-14 | 2011-01-11 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
US7781478B2 (en) | 2004-07-14 | 2010-08-24 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
US7772271B2 (en) | 2004-07-14 | 2010-08-10 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
JP2008507518A (en) | 2004-07-22 | 2008-03-13 | ピーティーシー セラピューティクス,インコーポレーテッド | Thienopyridine for treating hepatitis C |
EP1831192B1 (en) * | 2004-12-27 | 2011-08-24 | Korea Research Institute Of Chemical Technology | Benzothiophen-2-carbonylguanidine derivatives, preparation thereof, and pharmaceutical composition containing the same |
DE602005026867D1 (en) | 2005-01-19 | 2011-04-21 | Biolipox Ab | INFLAMMATORY INDOL DERIVATIVES |
KR100644385B1 (en) * | 2005-02-25 | 2006-11-10 | 동양수기산업(주) | Suction-type sludge collecting device |
CN101243046A (en) | 2005-08-08 | 2008-08-13 | 安斯泰来制药有限公司 | Acylguanidine derivative or salt thereof |
TW200804345A (en) | 2005-08-30 | 2008-01-16 | Novartis Ag | Substituted benzimidazoles and methods of preparation |
CN101321761A (en) | 2005-12-09 | 2008-12-10 | 霍夫曼-拉罗奇有限公司 | Tricyclic amide derivatives useful for treating obesity |
UA95788C2 (en) | 2005-12-15 | 2011-09-12 | Ф. Хоффманн-Ля Рош Аг | Fused pyrrole derivatives |
CA2636007A1 (en) | 2006-01-13 | 2007-07-26 | Wyeth | Sulfonyl substituted 1h-indoles as ligands for the 5-hydroxytryptamine receptors |
CN101384549B (en) | 2006-02-20 | 2011-04-13 | 安斯泰来制药株式会社 | Pyrrole derivative or salt thereof |
JP5157892B2 (en) | 2006-02-20 | 2013-03-06 | アステラス製薬株式会社 | Amide derivatives or salts thereof |
CN110003079A (en) * | 2006-12-26 | 2019-07-12 | 兰休斯医疗成像公司 | For making the ligand of imaging cardiac innervation |
AU2011210765A1 (en) | 2010-01-28 | 2012-09-13 | President And Fellows Of Harvard College | Compositions and methods for enhancing proteasome activity |
US8759535B2 (en) | 2010-02-18 | 2014-06-24 | High Point Pharmaceuticals, Llc | Substituted fused imidazole derivatives, pharmaceutical compositions, and methods of use thereof |
CN103635230B (en) | 2011-05-12 | 2017-10-31 | 普罗蒂斯特斯治疗公司 | Albumen homeostasis conditioning agent |
US8889730B2 (en) | 2012-04-10 | 2014-11-18 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
WO2014047427A2 (en) | 2012-09-21 | 2014-03-27 | Vanderbilt University | Substituted benzofuran, benzothiophene and indole mcl-1 inhibitors |
WO2014116228A1 (en) | 2013-01-25 | 2014-07-31 | President And Fellows Of Harvard College | Usp14 inhibitors for treating or preventing viral infections |
US9394285B2 (en) | 2013-03-15 | 2016-07-19 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
CA2922341C (en) | 2013-08-28 | 2022-06-07 | Vanderbilt University | Substituted indole mcl-1 inhibitors |
WO2015073528A1 (en) | 2013-11-12 | 2015-05-21 | Proteostasis Therapeutics, Inc. | Proteasome activity enhancing compounds |
CN106456602B (en) | 2014-03-27 | 2020-11-24 | 范德比尔特大学 | Substituted indole MCL-1 inhibitors |
JP6578349B2 (en) | 2014-08-11 | 2019-09-18 | アンジオン バイオメディカ コーポレーション | Cytochrome P450 inhibitors and uses thereof |
CN105884675A (en) * | 2014-09-24 | 2016-08-24 | 中国药科大学 | N-substituted indole carboxylic acid derivative and its preparation method and medical use |
US9949965B2 (en) | 2014-10-17 | 2018-04-24 | Vanderbilt University | Tricyclic indole Mcl-1 inhibitors and uses thereof |
WO2016089648A1 (en) | 2014-12-01 | 2016-06-09 | Vtv Therapeutics Llc | Bach 1 inhibitors in combination with nrf2 activators and pharmaceutical compositions thereof |
EP3240778A4 (en) | 2014-12-31 | 2018-07-11 | Angion Biomedica Corp. | Methods and agents for treating disease |
US11596639B2 (en) | 2016-03-04 | 2023-03-07 | Vanderbilt University | Substituted indole Mcl-1 inhibitors |
CN105968059B (en) * | 2016-05-12 | 2018-11-13 | 广西师范大学 | N- alkenyl benzotriazole nitrogen oxygen derivatives and its preparation method and application |
CN105820132B (en) * | 2016-05-12 | 2018-11-13 | 广西师范大学 | N- aryl benzotriazole nitrogen oxygen derivatives and its synthetic method |
CN111960985A (en) * | 2018-08-08 | 2020-11-20 | 中国人民解放军总医院 | Antitumor compounds |
WO2021226261A1 (en) | 2020-05-06 | 2021-11-11 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
CN113967210A (en) * | 2020-07-24 | 2022-01-25 | 上海交通大学医学院附属瑞金医院 | Application of compound interfering integrin beta 3/Src interaction |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US4544670A (en) * | 1982-08-24 | 1985-10-01 | William H. Rorer, Inc. | Method of treating coccidiosis with acyl guanidines |
DE3304019A1 (en) * | 1983-02-07 | 1984-08-09 | Kali-Chemie Pharma Gmbh, 3000 Hannover | 3-ACYLOXY-1-PHENYL-2-AMINOCARBONYLINDOL COMPOUNDS AND METHOD FOR THE PRODUCTION THEREOF, AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS |
DE3929582A1 (en) * | 1989-09-06 | 1991-03-07 | Hoechst Ag | BENZOYLGUANIDINE, METHOD FOR THE PRODUCTION THEREOF, THEIR USE AS A MEDICINE AND THE MEDICINE CONTAINING IT |
DE4127026A1 (en) * | 1991-08-16 | 1993-02-18 | Boehringer Ingelheim Kg | New 3-amino-6-chloro:pyrazine 2-carboxamide derivs. - useful as hypotensive, mucolytic, diuretic and antitumoural drugs |
-
1994
- 1994-07-28 EP EP94111765A patent/EP0639573A1/en not_active Withdrawn
- 1994-07-29 IL IL11050394A patent/IL110503A/en not_active IP Right Cessation
- 1994-07-29 NZ NZ264130A patent/NZ264130A/en unknown
- 1994-08-01 FI FI943579A patent/FI943579A/en unknown
- 1994-08-01 AU AU68844/94A patent/AU682371B2/en not_active Ceased
- 1994-08-02 CA CA002129301A patent/CA2129301A1/en not_active Abandoned
- 1994-08-02 KR KR1019940019071A patent/KR950005817A/en not_active Application Discontinuation
- 1994-08-02 KR KR1019940019259A patent/KR100343292B1/en not_active IP Right Cessation
- 1994-08-02 JP JP6198940A patent/JPH07145149A/en active Pending
- 1994-08-02 CN CN94109516A patent/CN1118347A/en active Pending
- 1994-08-02 NO NO942864A patent/NO301584B1/en not_active IP Right Cessation
- 1994-08-03 HU HU9402271A patent/HU218790B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CA2129301A1 (en) | 1995-02-04 |
AU682371B2 (en) | 1997-10-02 |
KR950005817A (en) | 1995-03-20 |
NZ264130A (en) | 1995-12-21 |
EP0639573A1 (en) | 1995-02-22 |
AU6884494A (en) | 1995-02-16 |
FI943579A (en) | 1995-02-04 |
FI943579A0 (en) | 1994-08-01 |
KR950005512A (en) | 1995-03-20 |
NO942864D0 (en) | 1994-08-02 |
JPH07145149A (en) | 1995-06-06 |
IL110503A (en) | 2000-06-29 |
HU9402271D0 (en) | 1994-09-28 |
NO301584B1 (en) | 1997-11-17 |
KR100343292B1 (en) | 2002-12-26 |
CN1118347A (en) | 1996-03-13 |
HUT70547A (en) | 1995-10-30 |
IL110503A0 (en) | 1994-10-21 |
HU218790B (en) | 2000-12-28 |
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