CA1175431A - Tri-substituted imidazole derivatives, processes for their manufacture, pharmaceutical preparations containing them, and their use - Google Patents
Tri-substituted imidazole derivatives, processes for their manufacture, pharmaceutical preparations containing them, and their useInfo
- Publication number
- CA1175431A CA1175431A CA000382377A CA382377A CA1175431A CA 1175431 A CA1175431 A CA 1175431A CA 000382377 A CA000382377 A CA 000382377A CA 382377 A CA382377 A CA 382377A CA 1175431 A CA1175431 A CA 1175431A
- Authority
- CA
- Canada
- Prior art keywords
- phenyl
- substituted
- lower alkoxy
- pyridyl
- carbon atoms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- 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
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
-
- 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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/53—Nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
- C07D213/50—Ketonic radicals
-
- 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
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/20—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/26—Radicals substituted by carbon atoms having three bonds to hetero atoms
-
- 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
- C07D233/64—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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Ophthalmology & Optometry (AREA)
- Virology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Cosmetics (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA000451683A CA1185976A (en) | 1980-07-25 | 1984-04-10 | Process for the manufacture of novel tri-substituted imidazole derivatives |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH5715/80-5 | 1980-07-25 | ||
CH571580 | 1980-07-25 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000451683A Division CA1185976A (en) | 1980-07-25 | 1984-04-10 | Process for the manufacture of novel tri-substituted imidazole derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1175431A true CA1175431A (en) | 1984-10-02 |
Family
ID=4298165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000382377A Expired CA1175431A (en) | 1980-07-25 | 1981-07-23 | Tri-substituted imidazole derivatives, processes for their manufacture, pharmaceutical preparations containing them, and their use |
Country Status (23)
Country | Link |
---|---|
US (1) | US4447431A (en:Method) |
EP (1) | EP0045081B1 (en:Method) |
JP (1) | JPS5756466A (en:Method) |
KR (13) | KR850000883B1 (en:Method) |
AR (1) | AR230269A1 (en:Method) |
AT (1) | ATE17349T1 (en:Method) |
AU (2) | AU7340481A (en:Method) |
CA (1) | CA1175431A (en:Method) |
DD (2) | DD201677A5 (en:Method) |
DE (1) | DE3173434D1 (en:Method) |
DK (1) | DK331881A (en:Method) |
ES (8) | ES504257A0 (en:Method) |
FI (1) | FI812326A7 (en:Method) |
GB (1) | GB2080805B (en:Method) |
GR (1) | GR75287B (en:Method) |
IE (1) | IE52071B1 (en:Method) |
IL (1) | IL63410A (en:Method) |
NO (1) | NO812542L (en:Method) |
NZ (1) | NZ197828A (en:Method) |
PL (8) | PL135822B1 (en:Method) |
PT (1) | PT73424B (en:Method) |
SU (8) | SU1235454A3 (en:Method) |
ZA (1) | ZA815078B (en:Method) |
Families Citing this family (57)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1983002613A1 (en) * | 1981-07-20 | 1983-08-04 | Sallmann, Alfred | Trisubstituted oxazo compounds |
EP0084756A1 (de) * | 1982-01-22 | 1983-08-03 | Ciba-Geigy Ag | Trisubstituierte Oxazaverbindungen |
FR2633291B1 (fr) * | 1988-06-27 | 1990-09-07 | Oreal | Derives d'hydroxy-4 isoxazoles, leur procede de preparation et compositions cosmetiques et pharmaceutiques les contenant |
US5252322A (en) * | 1989-09-22 | 1993-10-12 | The Gillette Company | Skin tanning compositions containing imidazoles |
NZ239161A (en) * | 1990-07-31 | 1994-01-26 | Smithkline Beecham Corp | Substituted [1h-imidazol-5-yl] alkanoic acid derivatives; medicaments, |
US5916891A (en) | 1992-01-13 | 1999-06-29 | Smithkline Beecham Corporation | Pyrimidinyl imidazoles |
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. |
US5593992A (en) * | 1993-07-16 | 1997-01-14 | Smithkline Beecham Corporation | Compounds |
US5670527A (en) * | 1993-07-16 | 1997-09-23 | Smithkline Beecham Corporation | Pyridyl imidazole compounds and compositions |
US5593991A (en) * | 1993-07-16 | 1997-01-14 | Adams; Jerry L. | Imidazole compounds, use and process of making |
EP1306377A3 (en) * | 1993-11-08 | 2003-05-07 | Smithkline Beecham Corporation | Pyridyl-oxazoles and their use as cytokines inhibitors |
US5723477A (en) * | 1994-11-10 | 1998-03-03 | Sibia Neurosciences, Inc. | Modulators of acetylcholine receptors |
US5739143A (en) * | 1995-06-07 | 1998-04-14 | Smithkline Beecham Corporation | Imidazole compounds and compositions |
US6369068B1 (en) | 1995-06-07 | 2002-04-09 | Smithkline Beecham Corporation | Amino substituted pyrimidine containing compounds |
IL118544A (en) | 1995-06-07 | 2001-08-08 | Smithkline Beecham Corp | History of imidazole, the process for their preparation and the pharmaceutical preparations containing them |
ZA9610687B (en) * | 1995-12-22 | 1997-09-29 | Smithkline Beecham Corp | Novel synthesis. |
ZA97175B (en) * | 1996-01-11 | 1997-11-04 | Smithkline Beecham Corp | Novel substituted imidazole compounds. |
US6046208A (en) * | 1996-01-11 | 2000-04-04 | Smithkline Beecham Corporation | Substituted imidazole compounds |
AP9700912A0 (en) | 1996-01-11 | 1997-01-31 | Smithkline Beecham Corp | Novel cycloalkyl substituted imidazoles |
ES2205167T3 (es) * | 1996-01-11 | 2004-05-01 | Smithkline Beecham Corporation | Nuevos compuestos de imidazol sustituidos. |
WO1997035856A1 (en) * | 1996-03-25 | 1997-10-02 | Smithkline Beecham Corporation | Novel treatment for cns injuries |
WO1998007425A1 (en) | 1996-08-21 | 1998-02-26 | Smithkline Beecham Corporation | Imidazole compounds, compositions and use |
US5929076A (en) * | 1997-01-10 | 1999-07-27 | Smithkline Beecham Corporation | Cycloalkyl substituted imidazoles |
DK1028954T3 (da) * | 1997-04-24 | 2003-10-27 | Ortho Mcneil Pharm Inc | Substituerede imidazoler egnede til behandling af inflammatoriske sygdomme |
EP1023066A4 (en) | 1997-06-13 | 2001-05-23 | Smithkline Beecham Corp | NEW PYRAZOLE AND PYRAZOLINE SUBSTITUTED COMPOUND |
AU8154998A (en) | 1997-06-19 | 1999-01-04 | Smithkline Beecham Corporation | Novel aryloxy substituted pyrimidine imidazole compounds |
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 |
US7301021B2 (en) * | 1997-07-02 | 2007-11-27 | Smithkline Beecham Corporation | Substituted imidazole compounds |
TW517055B (en) | 1997-07-02 | 2003-01-11 | Smithkline Beecham Corp | Novel substituted imidazole compounds |
US6562832B1 (en) | 1997-07-02 | 2003-05-13 | Smithkline Beecham Corporation | Substituted imidazole compounds |
US6251914B1 (en) | 1997-07-02 | 2001-06-26 | Smithkline Beecham Corporation | Cycloalkyl substituted imidazoles |
US6489325B1 (en) | 1998-07-01 | 2002-12-03 | Smithkline Beecham Corporation | Substituted imidazole compounds |
EP1041989A4 (en) | 1997-10-08 | 2002-11-20 | Smithkline Beecham Corp | NEW SUBSTITUTED CYCLOALCENYL COMPOUNDS |
EP1037639A4 (en) | 1997-12-19 | 2002-04-17 | Smithkline Beecham Corp | HETEROARYL-SUBSTITUTED IMIDAZOLE COMPOUNDS, THEIR PHARMACEUTICAL COMPOSITIONS AND USES |
CZ20004339A3 (cs) | 1998-05-22 | 2001-10-17 | Smithkline Beecham Corporation | Nové 2-alkylem substituované imidazolové sloučeniny |
US6858617B2 (en) | 1998-05-26 | 2005-02-22 | Smithkline Beecham Corporation | Substituted imidazole compounds |
DE69917296T2 (de) * | 1998-08-20 | 2005-05-25 | Smithkline Beecham Corp. | Neue substituierte triazolverbindungen |
ATE258055T1 (de) * | 1998-11-04 | 2004-02-15 | Smithkline Beecham Corp | Pyridin-4-yl oder pyrimidin-4-yl substituierte pyrazine |
WO2000029399A1 (en) * | 1998-11-12 | 2000-05-25 | Boehringer Ingelheim (Canada) Ltd. | Antiherpes compounds |
US6239279B1 (en) | 1998-12-16 | 2001-05-29 | Smithkline Beecham Corporation | Synthesis for 4-aryl-5-pyrimidine imidazole substituted derivatives |
CN1543346A (zh) | 1999-11-22 | 2004-11-03 | ʷ��˿�������ȳ�ķ����˾ | 新化合物 |
US6759410B1 (en) | 1999-11-23 | 2004-07-06 | Smithline Beecham Corporation | 3,4-dihydro-(1H)-quinazolin-2-ones and their use as CSBP/p38 kinase inhibitors |
WO2001038312A1 (en) | 1999-11-23 | 2001-05-31 | Smithkline Beecham Corporation | 3,4-DIHYDRO-(1H)QUINAZOLIN-2-ONE COMPOUNDS AS CSBP/p38 KINASE INHIBITORS |
JP2003528043A (ja) | 1999-11-23 | 2003-09-24 | スミスクライン・ビーチャム・コーポレイション | CSBP/p38キナーゼ阻害剤としての3,4‐ジヒドロ−(1H)キナゾリン−2−オン化合物 |
US7053098B1 (en) | 1999-11-23 | 2006-05-30 | Smithkline Beecham Corporation | 3,4-Dihydro-(1H) quinazolin-2-one compounds as CSBP/P38 kinase inhibitors |
US7235551B2 (en) * | 2000-03-02 | 2007-06-26 | Smithkline Beecham Corporation | 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases |
GB0005357D0 (en) | 2000-03-06 | 2000-04-26 | Smithkline Beecham Plc | Compounds |
US7235658B2 (en) * | 2000-03-06 | 2007-06-26 | Smithkline Beecham P.L.C. | Imidazol derivatives as Raf kinase inhibitors |
HU229471B1 (en) * | 2000-10-23 | 2014-01-28 | Smithkline Beecham Corp | 2,4,8-trisubstituted-8h-pyrido[2,3d]pyrimidine-7-one compounds, for the treatment of diseases mediated by csbp/p38 kinase |
GB0112348D0 (en) * | 2001-05-19 | 2001-07-11 | Smithkline Beecham Plc | Compounds |
JP2005504793A (ja) * | 2001-09-05 | 2005-02-17 | スミスクライン ビーチャム パブリック リミテッド カンパニー | Rafキナーゼ阻害剤としてのヘテロサイクルカルボキサミド誘導体 |
MXPA04005880A (es) * | 2001-12-18 | 2004-09-13 | Hoffmann La Roche | Cis-imidazolinas como inhibidores de la mdm2. |
TW200505446A (en) * | 2003-01-17 | 2005-02-16 | Fuj Isawa Pharmaceutical Co Ltd | Inhibitor of cox |
KR20060007008A (ko) * | 2003-05-08 | 2006-01-23 | 아스텔라스세이야쿠 가부시키가이샤 | Cox 저해제 |
PE20061351A1 (es) * | 2005-03-25 | 2007-01-14 | Glaxo Group Ltd | COMPUESTOS 8H-PIRIDO[2,3-d]PIRIMIDIN-7-ONA 2,4,8-TRISUSTITUIDOS COMO INHIBIDORES DE LA QUINASA CSBP/RK/p38 |
US20080096905A1 (en) * | 2005-03-25 | 2008-04-24 | Glaxo Group Limited | Process For Preparing Pyrido[2,3-D]Pyrimidin-7-One And 3,4-Dihydropyrimido{4,5-D}Pyrimidin-2(1H)-One Derivatives |
WO2013049272A2 (en) | 2011-09-29 | 2013-04-04 | Theraceutix, Llc | Composition and method for treatment of symptoms associated with various skin conditions |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3558645A (en) * | 1968-07-08 | 1971-01-26 | Sandoz Ag | 2-(4-(4',5-diphenyl - 2 - imidazolyl)-phenoxy) lower aliphatic monocarboxylic acids |
CH561202A5 (en:Method) * | 1971-05-10 | 1975-04-30 | Ciba Geigy Ag | |
GB1469532A (en) * | 1973-06-28 | 1977-04-06 | Dumex Ltd As | Imimdazolyl-alkanoic acid derivatives |
US4372964A (en) * | 1980-10-30 | 1983-02-08 | E. I. Du Pont De Nemours And Company | Antiinflammatory 4,5-diaryl-1H-imidazole-2-methanols |
-
1981
- 1981-07-23 GR GR65613A patent/GR75287B/el unknown
- 1981-07-23 CA CA000382377A patent/CA1175431A/en not_active Expired
- 1981-07-23 DD DD81232030A patent/DD201677A5/de unknown
- 1981-07-24 GB GB8122920A patent/GB2080805B/en not_active Expired
- 1981-07-24 PT PT73424A patent/PT73424B/pt unknown
- 1981-07-24 ES ES504257A patent/ES504257A0/es active Granted
- 1981-07-24 NO NO812542A patent/NO812542L/no unknown
- 1981-07-24 IE IE1680/81A patent/IE52071B1/en unknown
- 1981-07-24 ZA ZA815078A patent/ZA815078B/xx unknown
- 1981-07-24 AU AU73404/81A patent/AU7340481A/en not_active Abandoned
- 1981-07-24 FI FI812326A patent/FI812326A7/fi not_active Application Discontinuation
- 1981-07-24 SU SU813317053A patent/SU1235454A3/ru active
- 1981-07-24 NZ NZ197828A patent/NZ197828A/en unknown
- 1981-07-24 IL IL63410A patent/IL63410A/xx unknown
- 1981-07-24 DK DK331881A patent/DK331881A/da not_active Application Discontinuation
- 1981-07-25 JP JP56115896A patent/JPS5756466A/ja active Pending
- 1981-07-25 PL PL1981232352A patent/PL135822B1/pl unknown
- 1981-07-25 PL PL23700081A patent/PL237000A1/xx unknown
- 1981-07-25 PL PL23700281A patent/PL237002A1/xx unknown
- 1981-07-25 PL PL23699781A patent/PL236997A1/xx unknown
- 1981-07-25 PL PL23700381A patent/PL237003A1/xx unknown
- 1981-07-25 KR KR1019810002709A patent/KR850000883B1/ko not_active Expired
- 1981-07-25 PL PL23700181A patent/PL237001A1/xx unknown
- 1981-07-25 PL PL23700481A patent/PL237004A1/xx unknown
- 1981-07-25 PL PL23700581A patent/PL237005A1/xx unknown
- 1981-07-27 EP EP81105914A patent/EP0045081B1/de not_active Expired
- 1981-07-27 AT AT81105914T patent/ATE17349T1/de not_active IP Right Cessation
- 1981-07-27 DE DE8181105914T patent/DE3173434D1/de not_active Expired
-
1982
- 1982-07-21 SU SU823465351A patent/SU1138023A3/ru active
- 1982-07-21 SU SU823465356A patent/SU1205764A3/ru active
- 1982-07-21 SU SU823466067A patent/SU1227112A3/ru active
- 1982-07-21 SU SU823466066A patent/SU1145928A3/ru active
- 1982-07-30 ES ES514580A patent/ES514580A0/es active Granted
- 1982-07-30 SU SU823468675A patent/SU1169534A3/ru active
- 1982-07-30 ES ES514585A patent/ES8307245A1/es not_active Expired
- 1982-07-30 ES ES514581A patent/ES514581A0/es active Granted
- 1982-07-30 DD DD82242110A patent/DD202554A5/de unknown
- 1982-07-30 ES ES514584A patent/ES8306124A1/es not_active Expired
- 1982-07-30 ES ES514583A patent/ES514583A0/es active Granted
- 1982-07-30 SU SU823469534A patent/SU1152520A3/ru active
- 1982-07-30 ES ES514582A patent/ES8306122A1/es not_active Expired
- 1982-07-30 ES ES514579A patent/ES8306119A1/es not_active Expired
- 1982-09-28 US US06/425,603 patent/US4447431A/en not_active Expired - Fee Related
- 1982-11-22 AR AR291374A patent/AR230269A1/es active
-
1983
- 1983-07-19 SU SU833618708A patent/SU1205763A3/ru active
-
1984
- 1984-09-27 KR KR1019840005965A patent/KR850000888B1/ko not_active Expired
- 1984-09-27 KR KR1019840005970A patent/KR850000911B1/ko not_active Expired
- 1984-09-27 KR KR1019840005962A patent/KR850000885B1/ko not_active Expired
- 1984-09-27 KR KR1019840005966A patent/KR850000889B1/ko not_active Expired
- 1984-09-27 KR KR1019840005961A patent/KR850000884B1/ko not_active Expired
- 1984-09-27 KR KR1019840005960A patent/KR850000873B1/ko not_active Expired
- 1984-09-27 KR KR1019840005964A patent/KR850000887B1/ko not_active Expired
- 1984-09-27 KR KR1019840005971A patent/KR850000892B1/ko not_active Expired
- 1984-09-27 KR KR1019840005968A patent/KR850000890B1/ko not_active Expired
- 1984-09-27 KR KR1019840005969A patent/KR850000891B1/ko not_active Expired
- 1984-09-27 KR KR1019840005972A patent/KR850001064B1/ko not_active Expired
- 1984-09-27 KR KR1019840005963A patent/KR850000886B1/ko not_active Expired
-
1986
- 1986-04-23 AU AU56555/86A patent/AU5655586A/en not_active Abandoned
Also Published As
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