PH27141A - 1-phenyl-3-naphthalenyloxy-propanamines - Google Patents
1-phenyl-3-naphthalenyloxy-propanamines Download PDFInfo
- Publication number
- PH27141A PH27141A PH36759A PH36759A PH27141A PH 27141 A PH27141 A PH 27141A PH 36759 A PH36759 A PH 36759A PH 36759 A PH36759 A PH 36759A PH 27141 A PH27141 A PH 27141A
- Authority
- PH
- Philippines
- Prior art keywords
- propanamine
- compound
- phenyl
- mixture
- naphthalenyloxy
- Prior art date
Links
- LLJKLSASLJIYAO-UHFFFAOYSA-N 3-naphthalen-1-yloxy-1-phenylpropan-1-amine Chemical class C=1C=CC2=CC=CC=C2C=1OCCC(N)C1=CC=CC=C1 LLJKLSASLJIYAO-UHFFFAOYSA-N 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 94
- 239000002253 acid Substances 0.000 claims abstract description 25
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 22
- 239000001257 hydrogen Substances 0.000 claims abstract description 16
- 150000003839 salts Chemical class 0.000 claims abstract description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 4
- 125000001475 halogen functional group Chemical group 0.000 claims abstract 4
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims description 53
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 9
- 229940095064 tartrate Drugs 0.000 claims description 8
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 101100491335 Caenorhabditis elegans mat-2 gene Proteins 0.000 claims 1
- 229940117229 cialis Drugs 0.000 claims 1
- WOXKDUGGOYFFRN-IIBYNOLFSA-N tadalafil Chemical compound C1=C2OCOC2=CC([C@@H]2C3=C(C4=CC=CC=C4N3)C[C@H]3N2C(=O)CN(C3=O)C)=C1 WOXKDUGGOYFFRN-IIBYNOLFSA-N 0.000 claims 1
- -1 methylenedioxy Chemical group 0.000 abstract description 29
- 230000013275 serotonin uptake Effects 0.000 abstract description 4
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 72
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 55
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 39
- 238000004458 analytical method Methods 0.000 description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 37
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 35
- 239000000243 solution Substances 0.000 description 33
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- 238000006243 chemical reaction Methods 0.000 description 18
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- 229910052757 nitrogen Inorganic materials 0.000 description 16
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- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
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- 125000001207 fluorophenyl group Chemical group 0.000 description 8
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- 239000000284 extract Substances 0.000 description 7
- QYWYGVROYHZRFV-UHFFFAOYSA-N oxalic acid;propan-1-amine Chemical compound CCCN.OC(=O)C(O)=O QYWYGVROYHZRFV-UHFFFAOYSA-N 0.000 description 7
- 229940076279 serotonin Drugs 0.000 description 7
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
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- 150000001412 amines Chemical class 0.000 description 6
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
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- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 6
- 239000012074 organic phase Substances 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
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- 241000518994 Conta Species 0.000 description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 125000005843 halogen group Chemical group 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
- 150000007524 organic acids Chemical class 0.000 description 5
- 235000005985 organic acids Nutrition 0.000 description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
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- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 4
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- 238000010561 standard procedure Methods 0.000 description 4
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- 238000003828 vacuum filtration Methods 0.000 description 4
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- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 description 3
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- GRRVXJBAUSPWCB-UHFFFAOYSA-N 1-naphthalen-1-yloxypropan-1-amine Chemical compound C1=CC=C2C(OC(N)CC)=CC=CC2=C1 GRRVXJBAUSPWCB-UHFFFAOYSA-N 0.000 description 2
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- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229940071104 xylenesulfonate Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/48—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/58—Radicals substituted by nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical 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)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Child & Adolescent Psychology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Addiction (AREA)
- Anesthesiology (AREA)
- Hospice & Palliative Care (AREA)
- Nutrition Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3653487A | 1987-04-09 | 1987-04-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PH27141A true PH27141A (en) | 1993-04-02 |
Family
ID=21889125
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PH36759A PH27141A (en) | 1987-04-09 | 1988-04-07 | 1-phenyl-3-naphthalenyloxy-propanamines |
Country Status (23)
| Country | Link |
|---|---|
| EP (1) | EP0288188B1 (ko) |
| JP (1) | JPH0637443B2 (ko) |
| KR (1) | KR960007723B1 (ko) |
| CN (1) | CN1020093C (ko) |
| AT (1) | ATE68473T1 (ko) |
| AU (1) | AU602971B2 (ko) |
| CA (1) | CA1329937C (ko) |
| CY (1) | CY1658A (ko) |
| DE (1) | DE3865504D1 (ko) |
| DK (1) | DK170637B1 (ko) |
| EG (1) | EG18584A (ko) |
| ES (1) | ES2045109T3 (ko) |
| GR (1) | GR3003267T3 (ko) |
| HK (1) | HK63992A (ko) |
| HU (1) | HU204767B (ko) |
| IL (1) | IL85988A (ko) |
| MX (1) | MX11031A (ko) |
| NZ (1) | NZ224161A (ko) |
| PH (1) | PH27141A (ko) |
| PT (1) | PT87163B (ko) |
| SG (1) | SG67092G (ko) |
| SU (1) | SU1568886A3 (ko) |
| ZA (1) | ZA882418B (ko) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK258389D0 (da) * | 1989-05-26 | 1989-05-26 | Ferrosan As | Aryloxyphenylpropylaminer, deres fremstilling og anvendelse |
| PH30083A (en) * | 1991-02-25 | 1996-12-27 | Lilly Co Eli | Treatment of lower urinary tract disorders |
| WO1993013049A1 (fr) * | 1991-12-20 | 1993-07-08 | Karin Elisabeth Peuschel | Emploi de l'effet immunoactivant de 3-naphthyloxy-2-hydroxy-propylamines, interessant specialement pour l'immunite cellulaire, par exemple contre infections virales |
| TW344661B (en) * | 1993-11-24 | 1998-11-11 | Lilly Co Eli | Pharmaceutical composition for treatment of incontinence |
| US5948820A (en) | 1994-08-22 | 1999-09-07 | Yoshitomi Pharmaceutical Industries, Ltd. | Benzene compound and pharmaceutical use thereof |
| ES2171191T3 (es) * | 1994-08-22 | 2002-09-01 | Mitsubishi Pharma Corp | Compuesto de benceno y uso medicinal del mismo. |
| DE19956786A1 (de) * | 1999-11-25 | 2001-05-31 | Basf Ag | Verfahren zur Herstellung optisch aktiver Amine |
| CN100402488C (zh) * | 2006-03-15 | 2008-07-16 | 上海玛耀化学技术有限公司 | 一种达泊西汀的合成方法 |
| WO2008035358A2 (en) * | 2006-06-05 | 2008-03-27 | Cadila Healthcare Limited | Process for preparing dapoxetine |
| CN101367739B (zh) * | 2008-09-24 | 2013-02-13 | 台州职业技术学院 | N,n-二甲基-1-苯基-3-(1-萘氧基)丙胺制备工艺 |
| DE102009015702A1 (de) | 2009-03-31 | 2010-10-07 | Ratiopharm Gmbh | Tabletten enthaltend Dapoxetin und Trockenverarbeitungsverfahren zu deren Herstellung |
| EP2513042A4 (en) | 2009-11-13 | 2013-06-26 | Symed Labs Ltd | DAPOXETIN SOLID |
| DE102009058321A1 (de) | 2009-12-15 | 2011-06-16 | Ratiopharm Gmbh | Schmelztablette, enthaltend Dapoxetin |
| WO2011161690A1 (en) * | 2010-06-23 | 2011-12-29 | Symed Labs Limited | Processes for the preparation of (+)-n,n-dimethyl-2-[1-(naphthalenyloxy) ethyl] benzene methanamine and intermediates thereof |
| CN102229538B (zh) * | 2011-05-11 | 2013-11-13 | 中南大学 | 一种达泊西汀的合成方法 |
| CN102850318A (zh) * | 2011-07-01 | 2013-01-02 | 中国人民解放军军事医学科学院毒物药物研究所 | 新的选择性5-羟色胺重摄取抑制剂及其医药用途 |
| CN103130660B (zh) * | 2011-11-25 | 2014-09-17 | 厦门福满药业有限公司 | 一类达泊西汀的酸式盐及其晶体,以及晶体的制备方法 |
| WO2013180675A1 (en) | 2012-05-28 | 2013-12-05 | Mahmut Bilgic | Tablet formulation comprising dapoxetine |
| CN102746170A (zh) * | 2012-07-28 | 2012-10-24 | 湖南尔文生物科技有限公司 | 一种达泊西汀的制备方法 |
| WO2014027981A2 (en) | 2012-08-17 | 2014-02-20 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Effervescent tablet formulations of dapoxetine and a pde5 inhibitor |
| US20150202168A1 (en) | 2012-08-17 | 2015-07-23 | Sanovel llac Sanayi Ve Ticaret Anonim Sirketi | Oral film formulations comprising dapoxetine and tadalafil |
| WO2014027975A2 (en) | 2012-08-17 | 2014-02-20 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Novel orally administered pharmaceutical formulations |
| WO2014027979A2 (en) | 2012-08-17 | 2014-02-20 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Tablet formulations comprising tadalafil and dapoxetine |
| WO2014027982A2 (en) | 2012-08-17 | 2014-02-20 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Novel effervescent sachet formulations of dapoxetine and a pde5 inhibitor |
| TR201309037A2 (tr) | 2012-08-17 | 2014-03-21 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Dapoksetin ve bir pde5 inhibitörü içeren yeni efervesan saşe formülasyonları. |
| CN102942496B (zh) * | 2012-11-28 | 2014-06-11 | 扬州工业职业技术学院 | (s)-n,n-二甲基-3-(萘酚-1-氧基)-1-苯基丙基-1-胺的制备方法 |
| EP2749553A1 (en) | 2012-12-31 | 2014-07-02 | Deva Holding Anonim Sirketi | Process for preparation of enantiomerically pure S-(+)-N, N-dimethyl-a-[2-(naphthalenyloxy)ethyl] benzenemethanamine |
| CN106748825A (zh) * | 2016-11-29 | 2017-05-31 | 聊城大学 | 一种达泊西汀的合成、拆分纯化和成盐方法 |
| CN108853072A (zh) * | 2018-08-03 | 2018-11-23 | 安徽省金楠医疗科技有限公司 | 一种盐酸达泊西汀片及其制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4018895A (en) * | 1974-01-10 | 1977-04-19 | Eli Lilly And Company | Aryloxyphenylpropylamines in treating depression |
| US4207343A (en) * | 1978-06-22 | 1980-06-10 | Eli Lilly And Company | 1-Phenyl-3-(substituted phenoxy)propylamines |
| NZ213651A (en) * | 1984-10-11 | 1989-07-27 | Hoffmann La Roche | Tetrahydronapthalene derivatives and medicaments |
-
1988
- 1988-04-06 IL IL85988A patent/IL85988A/xx not_active IP Right Cessation
- 1988-04-06 CA CA000563374A patent/CA1329937C/en not_active Expired - Fee Related
- 1988-04-06 PT PT87163A patent/PT87163B/pt not_active IP Right Cessation
- 1988-04-07 MX MX1103188A patent/MX11031A/es unknown
- 1988-04-07 DK DK188288A patent/DK170637B1/da not_active IP Right Cessation
- 1988-04-07 EG EG19888A patent/EG18584A/xx active
- 1988-04-07 AU AU14335/88A patent/AU602971B2/en not_active Ceased
- 1988-04-07 JP JP63088025A patent/JPH0637443B2/ja not_active Expired - Lifetime
- 1988-04-07 ZA ZA882418A patent/ZA882418B/xx unknown
- 1988-04-07 NZ NZ224161A patent/NZ224161A/en unknown
- 1988-04-07 PH PH36759A patent/PH27141A/en unknown
- 1988-04-08 EP EP88303177A patent/EP0288188B1/en not_active Expired - Lifetime
- 1988-04-08 AT AT88303177T patent/ATE68473T1/de not_active IP Right Cessation
- 1988-04-08 KR KR1019880003954A patent/KR960007723B1/ko not_active IP Right Cessation
- 1988-04-08 HU HU881790A patent/HU204767B/hu not_active IP Right Cessation
- 1988-04-08 CN CN88102018A patent/CN1020093C/zh not_active Expired - Fee Related
- 1988-04-08 DE DE8888303177T patent/DE3865504D1/de not_active Expired - Lifetime
- 1988-04-08 ES ES88303177T patent/ES2045109T3/es not_active Expired - Lifetime
- 1988-04-08 SU SU884355511A patent/SU1568886A3/ru active
-
1991
- 1991-12-04 GR GR91401895T patent/GR3003267T3/el unknown
-
1992
- 1992-07-01 SG SG670/92A patent/SG67092G/en unknown
- 1992-08-20 HK HK639/92A patent/HK63992A/xx not_active IP Right Cessation
-
1993
- 1993-05-14 CY CY1658A patent/CY1658A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU602971B2 (en) | 1990-11-01 |
| ATE68473T1 (de) | 1991-11-15 |
| SU1568886A3 (ru) | 1990-05-30 |
| ZA882418B (en) | 1989-12-27 |
| NZ224161A (en) | 1990-04-26 |
| SG67092G (en) | 1992-09-04 |
| HU204767B (en) | 1992-02-28 |
| DE3865504D1 (de) | 1991-11-21 |
| HUT50316A (en) | 1990-01-29 |
| IL85988A0 (en) | 1988-09-30 |
| MX11031A (es) | 1993-11-01 |
| EP0288188B1 (en) | 1991-10-16 |
| ES2045109T3 (es) | 1994-01-16 |
| HK63992A (en) | 1992-08-28 |
| CY1658A (en) | 1993-05-14 |
| PT87163A (pt) | 1988-05-01 |
| JPH0637443B2 (ja) | 1994-05-18 |
| GR3003267T3 (en) | 1993-02-17 |
| KR880012526A (ko) | 1988-11-28 |
| AU1433588A (en) | 1988-10-13 |
| EP0288188A1 (en) | 1988-10-26 |
| DK170637B1 (da) | 1995-11-20 |
| EG18584A (en) | 1994-07-30 |
| DK188288A (da) | 1989-01-12 |
| DK188288D0 (da) | 1988-04-07 |
| CA1329937C (en) | 1994-05-31 |
| CN1020093C (zh) | 1993-03-17 |
| KR960007723B1 (ko) | 1996-06-11 |
| PT87163B (pt) | 1992-07-31 |
| IL85988A (en) | 1992-08-18 |
| JPS63258837A (ja) | 1988-10-26 |
| CN88102018A (zh) | 1988-10-26 |
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