DE69318136T2 - Sulfonsaeurederivate zur behandlung von viruserkrankungen - Google Patents
Sulfonsaeurederivate zur behandlung von viruserkrankungenInfo
- Publication number
- DE69318136T2 DE69318136T2 DE69318136T DE69318136T DE69318136T2 DE 69318136 T2 DE69318136 T2 DE 69318136T2 DE 69318136 T DE69318136 T DE 69318136T DE 69318136 T DE69318136 T DE 69318136T DE 69318136 T2 DE69318136 T2 DE 69318136T2
- Authority
- DE
- Germany
- Prior art keywords
- formula
- compound according
- amino
- group
- defined above
- 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 - Lifetime
Links
- 201000010099 disease Diseases 0.000 title description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title description 10
- 241000700605 Viruses Species 0.000 title description 7
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 title 1
- -1 Sulfonic acid stilbenes Chemical class 0.000 claims abstract description 34
- 208000015181 infectious disease Diseases 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims description 90
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 42
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 30
- 229910052717 sulfur Inorganic materials 0.000 claims description 26
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 25
- 229940092714 benzenesulfonic acid Drugs 0.000 claims description 25
- 125000004434 sulfur atom Chemical group 0.000 claims description 22
- 150000003839 salts Chemical class 0.000 claims description 16
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 12
- 239000003960 organic solvent Substances 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 10
- 239000003814 drug Substances 0.000 claims description 9
- 238000011282 treatment Methods 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 7
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 claims description 6
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
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- 230000009385 viral infection Effects 0.000 claims description 5
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
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- 239000003937 drug carrier Substances 0.000 claims description 3
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 2
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims description 2
- LRYSUGTXBIPBGB-UHFFFAOYSA-N chloromethanedithioic acid Chemical class SC(Cl)=S LRYSUGTXBIPBGB-UHFFFAOYSA-N 0.000 claims description 2
- KTRFZWJCHOQHMN-UHFFFAOYSA-N chloromethanethioic s-acid Chemical class SC(Cl)=O KTRFZWJCHOQHMN-UHFFFAOYSA-N 0.000 claims description 2
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 10
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- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 2
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- 150000001629 stilbenes Chemical class 0.000 description 10
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- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 8
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000003599 detergent Substances 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
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- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 210000004027 cell Anatomy 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 239000012528 membrane Substances 0.000 description 5
- 125000001624 naphthyl group Chemical group 0.000 description 5
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 5
- 241001430294 unidentified retrovirus Species 0.000 description 5
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 4
- 229920002261 Corn starch Polymers 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 239000008120 corn starch Substances 0.000 description 4
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 4
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 4
- QKFJKGMPGYROCL-UHFFFAOYSA-N phenyl isothiocyanate Chemical compound S=C=NC1=CC=CC=C1 QKFJKGMPGYROCL-UHFFFAOYSA-N 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 108090000623 proteins and genes Proteins 0.000 description 4
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- XBEMMSWALFCZNW-UHFFFAOYSA-N 2-nitro-5-[2-(4-nitro-3-sulfophenyl)ethenyl]benzenesulfonic acid Chemical compound C1=C([N+]([O-])=O)C(S(=O)(=O)O)=CC(C=CC=2C=C(C(=CC=2)[N+]([O-])=O)S(O)(=O)=O)=C1 XBEMMSWALFCZNW-UHFFFAOYSA-N 0.000 description 3
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- 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 3
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/41—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
- C07C309/42—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton having the sulfo groups bound to carbon atoms of non-condensed six-membered aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/51—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/38—Amides of thiocarboxylic acids
- C07C327/40—Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C327/42—Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C329/00—Thiocarbonic acids; Halides, esters or anhydrides thereof
- C07C329/02—Monothiocarbonic acids; Derivatives thereof
- C07C329/04—Esters of monothiocarbonic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C329/00—Thiocarbonic acids; Halides, esters or anhydrides thereof
- C07C329/12—Dithiocarbonic acids; Derivatives thereof
- C07C329/14—Esters of dithiocarbonic acids
- C07C329/20—Esters of dithiocarbonic acids having sulfur atoms of dithiocarbonic groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/02—Monothiocarbamic acids; Derivatives thereof
- C07C333/08—Monothiocarbamic acids; Derivatives thereof having nitrogen atoms of thiocarbamic groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/14—Dithiocarbamic acids; Derivatives thereof
- C07C333/18—Esters of dithiocarbamic acids
- C07C333/24—Esters of dithiocarbamic acids having nitrogen atoms of dithiocarbamate groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/04—Derivatives of thiourea
- C07C335/16—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C335/20—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (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)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83863992A | 1992-02-20 | 1992-02-20 | |
| PCT/US1993/000564 WO1993016992A1 (en) | 1992-02-20 | 1993-01-22 | Sulfonic acid derivatives in the treatment of viral diseases |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69318136D1 DE69318136D1 (de) | 1998-05-28 |
| DE69318136T2 true DE69318136T2 (de) | 1998-10-22 |
Family
ID=25277670
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69318136T Expired - Lifetime DE69318136T2 (de) | 1992-02-20 | 1993-01-22 | Sulfonsaeurederivate zur behandlung von viruserkrankungen |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US5359131A (enExample) |
| EP (1) | EP0626945B1 (enExample) |
| JP (1) | JP3309104B2 (enExample) |
| KR (1) | KR100275843B1 (enExample) |
| AT (1) | ATE165345T1 (enExample) |
| AU (1) | AU663925B2 (enExample) |
| CA (1) | CA2130360C (enExample) |
| DE (1) | DE69318136T2 (enExample) |
| ES (1) | ES2115756T3 (enExample) |
| IL (1) | IL104780A (enExample) |
| MX (1) | MX9300836A (enExample) |
| NZ (1) | NZ249032A (enExample) |
| TW (1) | TW224968B (enExample) |
| WO (1) | WO1993016992A1 (enExample) |
| ZA (1) | ZA931035B (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5276182A (en) * | 1990-07-09 | 1994-01-04 | The Dow Chemical Company | Process for preparing polyurea oligomers |
| US5670144A (en) * | 1990-07-09 | 1997-09-23 | Merrell Pharmaceuticals Inc. | Anti-herpes virus and cytomegalovirus polyester oligomers |
| US5424063A (en) * | 1992-01-09 | 1995-06-13 | The Dow Chemical Company | Narrow poly- and mono-dispersed anionic oligomers, and their uses, formulations and process |
| IL112174A (en) * | 1994-01-03 | 1999-05-09 | Merrell Dow Pharma | Oligomers of polythioureas pharmaceutical compositions containing them and a process for their preparation |
| US5681832A (en) * | 1995-02-17 | 1997-10-28 | The United States Of America As Represented By The Department Of Health And Human Services | Aroylaniline compounds, pharmaceutical compositions, and methods of using same to inhibit viral activity |
| WO1996025157A1 (en) * | 1995-02-17 | 1996-08-22 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
| JP2000515115A (ja) * | 1995-12-15 | 2000-11-14 | クライオプリザベーション テクノロジーズ シーシー | ウイルス感染及び細菌感染症治療用および臓器冷凍保存用組成物 |
| US5852015A (en) * | 1997-01-27 | 1998-12-22 | American Cyanamid Company | Triazine containing anionic compounds useful as antiviral agents |
| CN1163401A (zh) * | 1996-02-13 | 1997-10-29 | 李占元 | 全自动血球计数仪试剂及配制方法 |
| US6262113B1 (en) | 1996-03-20 | 2001-07-17 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
| US6211373B1 (en) | 1996-03-20 | 2001-04-03 | Smithkline Beecham Corporation | Phenyl urea antagonists of the IL-8 receptor |
| BR9709938A (pt) | 1996-06-27 | 1999-08-10 | Smithkline Beecham Corp | Antagonistas dos receptores de il-8 |
| EP0912505A4 (en) * | 1996-06-27 | 2001-10-24 | Smithkline Beecham Corp | IL-8 RECEPTOR ANTAGONISTS |
| ZA984649B (en) * | 1997-06-13 | 1999-12-17 | Cryopreservation Tech Cc | "Drug delivery devices and methods for treatment of viral and microbial infections and wasting syndromes". |
| GB9928418D0 (en) * | 1999-12-01 | 2000-01-26 | Novartis Ag | Organic compounds |
| WO2002062769A2 (en) * | 2001-02-02 | 2002-08-15 | Wyeth | Preparation and purification of antiviral disulfonic acid disodium salt |
| EP1711175A1 (en) * | 2004-02-04 | 2006-10-18 | Active Biotech AB | Diurea derivatives |
| WO2008001368A2 (en) * | 2006-06-27 | 2008-01-03 | Hadasit Medical Research Services And Development Ltd. | Use of stilbene derivatives for treatment and prevention of aquatic mold infections |
| WO2008079897A2 (en) * | 2006-12-22 | 2008-07-03 | The Regents Of The University Of California | Macromolecular conjugates of cystic fibrosis transmembrane conductance regulator protein inhibitors and uses thereof |
| WO2010148177A2 (en) * | 2009-06-17 | 2010-12-23 | The Board Of Trustees Of The Leland Stanford Junior University | Compounds, compositions, methods of synthesis, and methods of treatment |
| TW201702218A (zh) * | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法 |
| JP7611824B2 (ja) * | 2018-11-22 | 2025-01-10 | ナント ユニベルシテ | 増殖性疾患の処置で使用するためのジスルホナートスチルベン |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD39717A (enExample) * | ||||
| US2676982A (en) * | 1951-06-08 | 1954-04-27 | Gen Aniline & Film Corp | Fluorescent agents |
| BE660945A (enExample) * | 1964-03-12 | 1965-07-01 | ||
| US4107202A (en) * | 1977-03-28 | 1978-08-15 | American Cyanamid Company | Substituted 4,4'-biphenylylene bis(2-thioureylene)di-naphthalenetrisulfonic acids and salts thereof |
| FR2429782A1 (fr) | 1978-06-27 | 1980-01-25 | American Cyanamid Co | Acides naphtalene-trisulfoniques substitues et leurs sels, leur preparation et leurs utilisations therapeutiques |
| US4328244A (en) * | 1980-05-21 | 1982-05-04 | The Dow Chemical Company | Novel (((substituted-phenyl)methyl)amino)benzenesulfonic acids and pharmaceutically-acceptable salts thereof |
| US4349568A (en) * | 1980-06-12 | 1982-09-14 | The Dow Chemical Company | Sulfur-substituted diphenyl ethers having antiviral activity |
| US4435394A (en) * | 1981-12-17 | 1984-03-06 | Shionogi & Co., Ltd. | 3-Sulfonamido-benzophenonimine derivatives useful for treating virus infections |
| DE3600046A1 (de) * | 1985-08-13 | 1987-07-09 | Barthell Eduard | Sulfonamidderivate, verfahren zu ihrer herstellung und verwendung |
| DE3528992A1 (de) * | 1985-08-13 | 1987-02-26 | Barthell Eduard | Sulfonamidderivate, verfahren zu ihrer herstellung und verwendung |
| DE3530718A1 (de) * | 1985-08-28 | 1987-03-12 | Madaus & Co Dr | Methylendioxyphenanthren- und -stilbenderivate, verfahren zur herstellung derselben und arzneimittel, die diese enthalten |
| EP0221021B1 (en) * | 1985-10-16 | 1989-11-08 | Ciba-Geigy Ag | Bechamp reduction of dns to das using h2so4 and trace of hoac |
| DE3626309A1 (de) * | 1986-08-02 | 1988-02-18 | Stockhausen Chem Fab Gmbh | Antivirusmittel |
| US5276182A (en) * | 1990-07-09 | 1994-01-04 | The Dow Chemical Company | Process for preparing polyurea oligomers |
| DK0498095T3 (da) * | 1991-02-05 | 1995-06-19 | Merrell Dow Pharma | Sulfoniske stilbenderivater til behandling af virussygdomme |
-
1993
- 1993-01-22 NZ NZ249032A patent/NZ249032A/en unknown
- 1993-01-22 ES ES93903629T patent/ES2115756T3/es not_active Expired - Lifetime
- 1993-01-22 DE DE69318136T patent/DE69318136T2/de not_active Expired - Lifetime
- 1993-01-22 JP JP51484393A patent/JP3309104B2/ja not_active Expired - Lifetime
- 1993-01-22 AU AU34818/93A patent/AU663925B2/en not_active Expired
- 1993-01-22 KR KR1019940702899A patent/KR100275843B1/ko not_active Expired - Fee Related
- 1993-01-22 CA CA002130360A patent/CA2130360C/en not_active Expired - Lifetime
- 1993-01-22 EP EP93903629A patent/EP0626945B1/en not_active Expired - Lifetime
- 1993-01-22 WO PCT/US1993/000564 patent/WO1993016992A1/en not_active Ceased
- 1993-01-22 AT AT93903629T patent/ATE165345T1/de active
- 1993-02-15 ZA ZA931035A patent/ZA931035B/xx unknown
- 1993-02-16 TW TW082101064A patent/TW224968B/zh active
- 1993-02-17 MX MX9300836A patent/MX9300836A/es not_active IP Right Cessation
- 1993-02-18 IL IL10478093A patent/IL104780A/en not_active IP Right Cessation
- 1993-08-13 US US08/106,311 patent/US5359131A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| NZ249032A (en) | 1996-09-25 |
| WO1993016992A1 (en) | 1993-09-02 |
| ZA931035B (en) | 1993-09-17 |
| IL104780A0 (en) | 1993-06-10 |
| MX9300836A (es) | 1993-09-01 |
| KR950700245A (ko) | 1995-01-16 |
| KR100275843B1 (ko) | 2000-12-15 |
| AU3481893A (en) | 1993-09-13 |
| EP0626945B1 (en) | 1998-04-22 |
| AU663925B2 (en) | 1995-10-26 |
| CA2130360C (en) | 1998-06-09 |
| CA2130360A1 (en) | 1993-08-21 |
| ATE165345T1 (de) | 1998-05-15 |
| IL104780A (en) | 1998-10-30 |
| EP0626945A1 (en) | 1994-12-07 |
| TW224968B (enExample) | 1994-06-11 |
| JPH07504190A (ja) | 1995-05-11 |
| DE69318136D1 (de) | 1998-05-28 |
| JP3309104B2 (ja) | 2002-07-29 |
| US5359131A (en) | 1994-10-25 |
| ES2115756T3 (es) | 1998-07-01 |
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| 8364 | No opposition during term of opposition | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: AVENTIS INC. (N.D.GES.D. STAATES PENNSYLVANIA), GR |
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| 8327 | Change in the person/name/address of the patent owner |
Owner name: AVENTISUB II INC., GREENVILLE, DEL., US |
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