NO163583B - Koplingsanordning for maaleinstrumenter. - Google Patents
Koplingsanordning for maaleinstrumenter. Download PDFInfo
- Publication number
- NO163583B NO163583B NO86862260A NO862260A NO163583B NO 163583 B NO163583 B NO 163583B NO 86862260 A NO86862260 A NO 86862260A NO 862260 A NO862260 A NO 862260A NO 163583 B NO163583 B NO 163583B
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- compound
- measuring
- acid
- phenyl
- Prior art date
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 9
- -1 N-substituted-l-phenyl-2-aminopropanes Chemical class 0.000 claims description 6
- 230000001975 sympathomimetic effect Effects 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- KWTSXDURSIMDCE-UHFFFAOYSA-N 1-phenylpropan-2-amine Chemical compound CC(N)CC1=CC=CC=C1 KWTSXDURSIMDCE-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 238000006683 Mannich reaction Methods 0.000 claims description 2
- 239000000150 Sympathomimetic Substances 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- 229940126062 Compound A Drugs 0.000 description 4
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- FLDRLXJNISEWNZ-UHFFFAOYSA-N 9-methylacridine Chemical compound C1=CC=C2C(C)=C(C=CC=C3)C3=NC2=C1 FLDRLXJNISEWNZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 230000036772 blood pressure Effects 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000010412 perfusion Effects 0.000 description 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical class CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000000219 Sympatholytic Substances 0.000 description 1
- 206010062119 Sympathomimetic effect Diseases 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001251 acridines Chemical class 0.000 description 1
- 229940027998 antiseptic and disinfectant acridine derivative Drugs 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- PBKVEOSEPXMKDN-LZHUFOCISA-N chembl2311030 Chemical compound CS(O)(=O)=O.CS(O)(=O)=O.CS(O)(=O)=O.CS(O)(=O)=O.C1=CC([C@H]2C[C@H](CN(C)[C@@H]2C2)C(=O)N[C@]3(C(=O)N4[C@H](C(N5CCC[C@H]5[C@]4(O)O3)=O)C(C)C)C(C)C)=C3C2=CNC3=C1.C1=CC([C@H]2C[C@H](CN(C)[C@@H]2C2)C(=O)N[C@]3(C(=O)N4[C@H](C(N5CCC[C@H]5[C@]4(O)O3)=O)C(C)CC)C(C)C)=C3C2=CNC3=C1.C1=CC([C@H]2C[C@H](CN(C)[C@@H]2C2)C(=O)N[C@]3(C(=O)N4[C@H](C(N5CCC[C@H]5[C@]4(O)O3)=O)CC(C)C)C(C)C)=C3C2=CNC3=C1.C([C@H]1C(=O)N2CCC[C@H]2[C@]2(O)O[C@](C(N21)=O)(NC(=O)[C@H]1CN(C)[C@H]2[C@@H](C=3C=CC=C4NC=C(C=34)C2)C1)C(C)C)C1=CC=CC=C1 PBKVEOSEPXMKDN-LZHUFOCISA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000036543 hypotension Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- WLJNZVDCPSBLRP-UHFFFAOYSA-N pamoic acid Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=C(C=3O)C(=O)O)=C(O)C(C(O)=O)=CC2=C1 WLJNZVDCPSBLRP-UHFFFAOYSA-N 0.000 description 1
- MRBDMNSDAVCSSF-UHFFFAOYSA-N phentolamine Chemical compound C1=CC(C)=CC=C1N(C=1C=C(O)C=CC=1)CC1=NCCN1 MRBDMNSDAVCSSF-UHFFFAOYSA-N 0.000 description 1
- 229960001999 phentolamine Drugs 0.000 description 1
- 235000013849 propane Nutrition 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical class CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000000304 vasodilatating effect Effects 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01D—MEASURING NOT SPECIALLY ADAPTED FOR A SPECIFIC VARIABLE; ARRANGEMENTS FOR MEASURING TWO OR MORE VARIABLES NOT COVERED IN A SINGLE OTHER SUBCLASS; TARIFF METERING APPARATUS; MEASURING OR TESTING NOT OTHERWISE PROVIDED FOR
- G01D11/00—Component parts of measuring arrangements not specially adapted for a specific variable
- G01D11/24—Housings ; Casings for instruments
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01L—MEASURING FORCE, STRESS, TORQUE, WORK, MECHANICAL POWER, MECHANICAL EFFICIENCY, OR FLUID PRESSURE
- G01L19/00—Details of, or accessories for, apparatus for measuring steady or quasi-steady pressure of a fluent medium insofar as such details or accessories are not special to particular types of pressure gauges
- G01L19/14—Housings
-
- G—PHYSICS
- G12—INSTRUMENT DETAILS
- G12B—CONSTRUCTIONAL DETAILS OF INSTRUMENTS, OR COMPARABLE DETAILS OF OTHER APPARATUS, NOT OTHERWISE PROVIDED FOR
- G12B9/00—Housing or supporting of instruments or other apparatus
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Measuring Fluid Pressure (AREA)
- Testing Or Calibration Of Command Recording Devices (AREA)
- Length Measuring Devices With Unspecified Measuring Means (AREA)
- Measurement Of Radiation (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
- Measurement Of Length, Angles, Or The Like Using Electric Or Magnetic Means (AREA)
- Arrangements For Transmission Of Measured Signals (AREA)
Description
Analogifremgangsmåte til fremstilling av sympati-
komimetisk aktive N-substituerte-l-fenyl-2-amino-
propaner.
Foreliggende oppfinnelse vedrorer en analogifremgangsmåte
til fremstilling av sympatikomimetisk aktive N-substituerte-l-fenyl-2-aminopropaner. Oppfinnelsen er en modifikasjon av det som læres i norsk patentsøknad nr. 150 $ 00 som omhandler forbindelser med koronar vasodilaterende egenskaper, og slike forbindelser er også beskrevet i belgisk patent nr. 638 839* Det skal også nevnes at forbindelser som er strukturelt beslektede med de som fremstilles ifolge foreliggende oppfinnelse, er beskrevet i norsk patent nr. 107 826.
Det er nå funnet at forbindelser som ligner de i nevnte nors-ke patentsøknad også har egenskaper av sammei art, spesielt bevirker de en okning i koronar perfusjon, men har dessuten en sympatikomimetisk virkning som ikke innehas av de tidligere kjente forbindelser.
Ifolge foreliggende oppfinnelse er det tilveiebragt en ana-logif remgangsmåte til fremstilling av sympatikomimetisk aktive N-sub-stituerte-l-f enyl-2-aminopropaner med formelen:
hvor R-^ er et hydrogen- eller halogenatom eller en alkylgruppe inne-holdende hoyst 6 karbonatomer samt syreaddisjonssalter derav. Den foretrukne forbindelse er den med formel II hvor R-^ er et hydrogen-atom.
De fremstilte nye aminopropaner kan til terapeutiske formål anvendes som sådanne eller i form av ikke-toksiske syreaddisjonssalter, dvs. salter som ikke er skadelige på dyreorganismen når de anvendes i terapeutiske doser, avledet fra uorganiske syrer slik som hydro-halogensyrene (f.eks. saltsyre og hydrobromsyre), og organiske syrer slik som sitronsyre, maleinsyre, fumarsyre, vinsyre, eddiksyre, rav-syre, melkesyre og pamoinsyre.
Ifolge oppfinnelsen fremstilles forbindelsene med formel II ved å omsette en 9-metylakridinforbindelse med formelen:
hvor R-^ har den samme betydning som angitt ovenfor, med oc-metylfenetylamin og formaldehyd under Mannich-reaksjonens betingelser.
Folgende eksempel illustrerer oppfinnelsen.
Eksempel
Til en opplosning av 3 «8 g 9-metylakridin i 5 ml konsentrert saltsyreopplosning tilsettes 3 g a-metylfenetylamin, 3.5 ml av en 4-0 volumprosent opplosning av formaldehyd i vann og 5 ml etylalkohol. Blandingen kokes under tilbakelop i 2 timer, gjores alkalisk etter avkjoling og behandles med dietyleter. Den eteriske opplosning vaskes 3 ganger med vann, for å fjerne overskudd a-metylfenetylamin, og torkes. Melkesyre tilsettes for å fjerne overskudd 9-me'tylakridin.
Det dannes et oljeaktig lag som opploses i vann, opplosningen gjores
alkalisk og behandles igjen med dietyleter. Den eteriske opplosning torkes, surgjores med maleinsyre og det utfelte maleat filtreres fra. Det tilveiebringes således 2.5 g N-/~2-(akridin-9-yl)etyl/-l-fenyl-2-aminopropanmaleat, som smelter ved 151°-152°C etter krystallisering fra en blanding av metylalkohol og dietyleter.
Analyse: Beregnet for C2gH2gN20^: C 73.66$; H 6. 18% ; N 6.13$
Funnet: C 73.2 % ; H 6.2 % ; N 6.1 % En sammenligning mellom en ny forbindelse fremstilt ifolge foreliggende oppfinnelse nemlig N-/~2-(akridin-9-yl)-etyl/-l-fenyl-2-aminopropanmaleat (forbindelse A) og de i fra nevnte belgiske patent kjente forbindelser N-/~-(9,10-dihydro-10-metylakridin-9-yl)-etyl/-l-fenyl-2-aminopropanhydroklorid (forbindelse B) og N-/~2-(5H-dibenzo-/~a,d/-cyklohepten-5-yl)-etyl/-l-fenyl-2-aminopropanhydroklorid (forbindelse C), ga folgende resultater:
Fra disse resultater er det tydelig at forbindelse A ikke
har en så sterk innvirkning på den koronare perfusjon som forbindelsene B og C. Virkningen av forbindelsen A på blodtrykket er overraskende nok motsatt til den som vises av forbindelsene B og C. Virkningen av forbindelse A på blodtrykket motvirkes av de sympatikolytiske midler fentolamin og hydergin R. Dette demonstrerer den sympatikomimetiske aktivitet til de nye akridinderivater. Denne aktivitet vises ikke av forbindelsene B og C, og vites heller ikke å være tilstede i de strukturelt beslektede forbindelser som beskrives i norsk patent nr. IO7826. Den sympatikomimetiske aktivitet gjor de nye forbindelser fremstilt ifolge foreliggende oppfinnelse nyttige ved behandling av hypotensjon og forskjellige former for sjokk.
Claims (1)
- Analogifremgangsmåte til fremstilling av sympatikomimetisk aktive N-substituerte-l-fenyl-2-aminopropaner med formelen:hvor R-^ er et hydrogen- eller halogenatom eller en alkylgruppe inne-holdende hoyst 6 karbonatomer, samt syreaddisjonssalter derav, karakterisert ved at en 9_metylakridinforbindelse med formelen:hvor R^ har den samme betydning som angitt ovenfor, omsettes med a-metylfenetylamin og formaldehyd under Mannich-reaksjonens betingelser.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI843985A FI71838C (fi) | 1984-10-11 | 1984-10-11 | Maetstuts. |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| NO862260D0 NO862260D0 (no) | 1986-06-06 |
| NO862260L NO862260L (no) | 1986-06-06 |
| NO163583B true NO163583B (no) | 1990-03-12 |
| NO163583C NO163583C (no) | 1990-06-20 |
Family
ID=8519720
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO86862260A NO163583C (no) | 1984-10-11 | 1986-06-06 | Koplingsanordning for maaleinstrumenter. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4628732A (no) |
| EP (1) | EP0197077B1 (no) |
| JP (2) | JPS61501797A (no) |
| KR (1) | KR930007769B1 (no) |
| DE (1) | DE3566577D1 (no) |
| ES (1) | ES296278Y (no) |
| FI (1) | FI71838C (no) |
| IN (1) | IN162388B (no) |
| NO (1) | NO163583C (no) |
| WO (1) | WO1986002442A1 (no) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5379658A (en) * | 1992-11-16 | 1995-01-10 | Simmonds Precision Products, Inc. | Intrusive acoustic sensor mounting arrangement |
| US5591907A (en) * | 1995-07-13 | 1997-01-07 | Scientific Solutions, Inc. | Weatherproof sensing apparatus with rotatable sensor |
| EP0959371A3 (de) * | 1998-05-22 | 2002-04-17 | INES Elektronik-Systementwicklung-Produktions GmbH | Lichtgitterprofil |
| US5905213A (en) * | 1998-07-14 | 1999-05-18 | Jaeger; Ben E. | Liquid sampler having connecting device |
| KR100651759B1 (ko) * | 2000-08-18 | 2006-11-30 | 두산중공업 주식회사 | 연소로의 누설방지용 이중플랜지 |
| US6854328B2 (en) * | 2001-06-14 | 2005-02-15 | Custom Spec Engineering, Inc. | Cover structure for marine instrument |
| US6792818B2 (en) | 2002-04-08 | 2004-09-21 | Ben E. Jaeger | Liquid sampler having an in-line valve |
| WO2006007655A1 (en) * | 2004-07-23 | 2006-01-26 | In2Process Pty Ltd | Pipeline sampling device |
| GB2466894B (en) * | 2005-01-11 | 2010-08-25 | Parker Hannifin Plc | Connection module and connector |
| US7481124B2 (en) | 2006-05-24 | 2009-01-27 | Sentry Equipment Corp. | Positive-displacement sampling apparatus |
| SE534959C2 (sv) * | 2009-10-20 | 2012-02-28 | Somas Ventiler | Vridbar ventil för en mätanordning |
| FI122499B (fi) | 2010-01-11 | 2012-02-29 | Satron Instr Oy | Mittausyhde ja menetelmä mittausyhteeseen sijoitetun mittausvälineen mittauspään puhdistamiseksi |
| FI122118B (fi) | 2010-01-11 | 2011-08-31 | Satron Instr Oy | Mittausyhde |
| NO330935B1 (no) * | 2010-02-04 | 2011-08-22 | Mirmorax As | Anordning for stromningsprove |
| CN102797520B (zh) * | 2012-09-03 | 2016-02-03 | 中国航空动力机械研究所 | 一种燃气涡轮发动机的机匣 |
| DE202013011774U1 (de) | 2013-06-18 | 2014-06-24 | Voith Patent Gmbh | Messvorrichtung |
| US10139261B2 (en) * | 2014-03-28 | 2018-11-27 | Parker-Hannifin Corporation | Through wall installation of sensors in fuel tanks |
| KR101670762B1 (ko) * | 2014-11-26 | 2016-11-01 | (주)프론틱스 | 휴대용 시험장치 |
| US11339830B2 (en) * | 2017-12-19 | 2022-05-24 | Itt Manufacturing Enterprises Llc | Bearing housing filler plate |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2780094A (en) * | 1954-04-22 | 1957-02-05 | Standard Oil Co | Pipeline mount for thermistor installation |
| CH521657A (de) * | 1970-12-14 | 1972-04-15 | Proton Ag | Messwertgebereinrichtung mit herausnehmbarer Messwertgebersonde |
| US4091672A (en) * | 1977-06-09 | 1978-05-30 | Sarns, Inc. | Temperature probe and connector |
| US4096754A (en) * | 1977-08-26 | 1978-06-27 | E. I. Du Pont De Nemours And Company | Removable probe |
| GB2058247B (en) * | 1979-09-10 | 1983-02-16 | Redland Automation Ltd | Stuffing box |
| US4495810A (en) * | 1983-04-20 | 1985-01-29 | General Electric Company | Probe mounting system |
-
1984
- 1984-10-11 FI FI843985A patent/FI71838C/fi not_active IP Right Cessation
-
1985
- 1985-09-26 WO PCT/FI1985/000080 patent/WO1986002442A1/en active IP Right Grant
- 1985-09-26 KR KR1019860700350A patent/KR930007769B1/ko not_active IP Right Cessation
- 1985-09-26 EP EP85904820A patent/EP0197077B1/en not_active Expired
- 1985-09-26 JP JP60504260A patent/JPS61501797A/ja active Pending
- 1985-09-26 DE DE8585904820T patent/DE3566577D1/de not_active Expired
- 1985-10-01 IN IN691/CAL/85A patent/IN162388B/en unknown
- 1985-10-03 US US06/783,496 patent/US4628732A/en not_active Ceased
- 1985-10-10 ES ES1985296278U patent/ES296278Y/es not_active Expired
-
1986
- 1986-06-06 NO NO86862260A patent/NO163583C/no unknown
-
1993
- 1993-02-15 JP JP1993004483U patent/JPH0736256Y2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| FI843985A0 (fi) | 1984-10-11 |
| FI71838B (fi) | 1986-10-31 |
| ES296278U (es) | 1988-04-16 |
| FI843985L (fi) | 1986-04-12 |
| US4628732A (en) | 1986-12-16 |
| KR880700250A (ko) | 1988-02-22 |
| KR930007769B1 (ko) | 1993-08-19 |
| EP0197077B1 (en) | 1988-11-30 |
| ES296278Y (es) | 1988-12-01 |
| NO163583C (no) | 1990-06-20 |
| FI71838C (fi) | 1987-02-09 |
| IN162388B (no) | 1988-05-21 |
| NO862260D0 (no) | 1986-06-06 |
| WO1986002442A1 (en) | 1986-04-24 |
| JPS61501797A (ja) | 1986-08-21 |
| EP0197077A1 (en) | 1986-10-15 |
| NO862260L (no) | 1986-06-06 |
| JPH0720523U (ja) | 1995-04-11 |
| DE3566577D1 (en) | 1989-01-05 |
| JPH0736256Y2 (ja) | 1995-08-16 |
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