DK171597B1 - Substituerede phenyleddikesyreamidforbindelser og farmaceutisk acceptable salte heraf samt farmaceutisk sammensætning med anti-inflammatorisk og analgetisk virkning indeholdende disse - Google Patents
Substituerede phenyleddikesyreamidforbindelser og farmaceutisk acceptable salte heraf samt farmaceutisk sammensætning med anti-inflammatorisk og analgetisk virkning indeholdende disse Download PDFInfo
- Publication number
- DK171597B1 DK171597B1 DK274086A DK274086A DK171597B1 DK 171597 B1 DK171597 B1 DK 171597B1 DK 274086 A DK274086 A DK 274086A DK 274086 A DK274086 A DK 274086A DK 171597 B1 DK171597 B1 DK 171597B1
- Authority
- DK
- Denmark
- Prior art keywords
- phenylacetic acid
- acid amide
- substituted phenylacetic
- pharmaceutically acceptable
- hydroxy
- Prior art date
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- -1 phenylacetic acid amide compound Chemical class 0.000 claims description 35
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- PCZMUTQYZKAXBW-ZHACJKMWSA-N 2-(4-hydroxy-3-methoxyphenyl)-n-[(e)-octadec-9-enyl]acetamide Chemical compound CCCCCCCC\C=C\CCCCCCCCNC(=O)CC1=CC=C(O)C(OC)=C1 PCZMUTQYZKAXBW-ZHACJKMWSA-N 0.000 claims 2
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- VSVWVWUICFMZLJ-UHFFFAOYSA-N n-cyclooctyl-2-(4-hydroxy-3-methoxyphenyl)acetamide Chemical compound C1=C(O)C(OC)=CC(CC(=O)NC2CCCCCCC2)=C1 VSVWVWUICFMZLJ-UHFFFAOYSA-N 0.000 description 1
- OKVZSDSHRCJXLQ-UHFFFAOYSA-N n-dec-9-enyl-2-(4-hydroxy-3-methoxyphenyl)acetamide Chemical compound COC1=CC(CC(=O)NCCCCCCCCC=C)=CC=C1O OKVZSDSHRCJXLQ-UHFFFAOYSA-N 0.000 description 1
- PBZXLTBSXBKDMU-UHFFFAOYSA-N n-decyl-2-(4-hydroxy-3-methoxyphenyl)acetamide Chemical compound CCCCCCCCCCNC(=O)CC1=CC=C(O)C(OC)=C1 PBZXLTBSXBKDMU-UHFFFAOYSA-N 0.000 description 1
- RKJUCUQACSSXQI-UHFFFAOYSA-N n-dodecyl-2-(4-hydroxy-3-methoxyphenyl)acetamide Chemical compound CCCCCCCCCCCCNC(=O)CC1=CC=C(O)C(OC)=C1 RKJUCUQACSSXQI-UHFFFAOYSA-N 0.000 description 1
- JEZORZPZXADHPR-UHFFFAOYSA-N n-heptyl-2-(4-hydroxy-3-methoxyphenyl)acetamide Chemical compound CCCCCCCNC(=O)CC1=CC=C(O)C(OC)=C1 JEZORZPZXADHPR-UHFFFAOYSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 239000004081 narcotic agent Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 210000001640 nerve ending Anatomy 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- RGOVYLWUIBMPGK-UHFFFAOYSA-N nonivamide Chemical compound CCCCCCCCC(=O)NCC1=CC=C(O)C(OC)=C1 RGOVYLWUIBMPGK-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- NKBWPOSQERPBFI-UHFFFAOYSA-N octadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC NKBWPOSQERPBFI-UHFFFAOYSA-N 0.000 description 1
- HBXNJMZWGSCKPW-UHFFFAOYSA-N octan-2-amine Chemical compound CCCCCCC(C)N HBXNJMZWGSCKPW-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 238000001543 one-way ANOVA Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- QUANRIQJNFHVEU-UHFFFAOYSA-N oxirane;propane-1,2,3-triol Chemical compound C1CO1.OCC(O)CO QUANRIQJNFHVEU-UHFFFAOYSA-N 0.000 description 1
- 229940124641 pain reliever Drugs 0.000 description 1
- 230000008058 pain sensation Effects 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 230000037368 penetrate the skin Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 210000001428 peripheral nervous system Anatomy 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229960003893 phenacetin Drugs 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229960002895 phenylbutazone Drugs 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000008389 polyethoxylated castor oil Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000002390 rotary evaporation Methods 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000007909 solid dosage form Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000012453 sprague-dawley rat model Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000000528 statistical test Methods 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000002511 suppository base Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 238000007910 systemic administration Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 229940072651 tylenol Drugs 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 230000008728 vascular permeability Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 210000001835 viscera Anatomy 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 235000019386 wax ester Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/12—Esters of phosphoric acids with hydroxyaryl compounds
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Pain & Pain Management (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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74283385A | 1985-06-10 | 1985-06-10 | |
| US74283385 | 1985-06-10 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DK274086D0 DK274086D0 (da) | 1986-06-10 |
| DK274086A DK274086A (da) | 1986-12-11 |
| DK171597B1 true DK171597B1 (da) | 1997-02-17 |
Family
ID=24986434
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK274086A DK171597B1 (da) | 1985-06-10 | 1986-06-10 | Substituerede phenyleddikesyreamidforbindelser og farmaceutisk acceptable salte heraf samt farmaceutisk sammensætning med anti-inflammatorisk og analgetisk virkning indeholdende disse |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP0206609B1 (de) |
| JP (1) | JPH0819067B2 (de) |
| AT (1) | ATE46499T1 (de) |
| AU (1) | AU605744B2 (de) |
| CA (1) | CA1273360A (de) |
| DE (1) | DE3665708D1 (de) |
| DK (1) | DK171597B1 (de) |
| GB (1) | GB2178031B (de) |
| HK (1) | HK48292A (de) |
| IE (1) | IE58664B1 (de) |
| MY (1) | MY102776A (de) |
| NZ (1) | NZ216468A (de) |
| PH (1) | PH23807A (de) |
| SG (1) | SG49692G (de) |
| ZA (1) | ZA864323B (de) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5045565A (en) * | 1987-03-09 | 1991-09-03 | The Procter & Gamble Company | Novel compounds, pharmaceutical compositions, and methods for treating inflammation and pain |
| US5099030A (en) * | 1987-03-09 | 1992-03-24 | The Procter & Gamble Company | Novel compounds, pharmaceutical compositions, and methods for treating inflammation and pain |
| ES2061624T3 (es) * | 1987-03-09 | 1994-12-16 | Procter & Gamble | Compuestos fenilicos sustituidos con amino-etilo en posicion beta, y composiciones anti-inflamatorias o analgesicas que los contienen. |
| NZ228329A (en) * | 1988-03-18 | 1991-12-23 | Mitsui Toatsu Chemicals | Catechol derivatives and pharmaceutical compositions thereof |
| ATE113205T1 (de) * | 1988-06-17 | 1994-11-15 | Procter & Gamble | Anwendung von vanillin-derivaten zur herstellung eines arzneimittels zur behandlung von herpes simplex-infektion. |
| US5461075A (en) * | 1988-06-17 | 1995-10-24 | The Procter & Gamble Company | Use of vanilloids for the prevention of lesions due to herpes simplex infections |
| GB2321455A (en) | 1997-01-24 | 1998-07-29 | Norsk Hydro As | Lipophilic derivatives of biologically active compounds |
| CA2605351A1 (en) | 2005-04-21 | 2006-11-02 | Dainippon Sumitomo Pharma Co., Ltd. | N-substituted phenylacetamide derivative and pharmaceutical composition comprising the same |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3903297A (en) | 1973-11-01 | 1975-09-02 | Upjohn Co | Method of treatment and prophylaxis of gastric hypersecretion and gastric and duodenal ulcers using prostaglandin analogs |
| US4238505A (en) | 1978-01-20 | 1980-12-09 | Fmc Corporation | Insecticidal biphenylmethyl perhaloalkylvinylcyclopropanecarboxylates |
| US4313958A (en) | 1980-10-24 | 1982-02-02 | The Procter & Gamble Company | Method of producing analgesia |
| US4460602A (en) | 1981-06-30 | 1984-07-17 | The Procter & Gamble Company | Urea derivatives |
| US4443473A (en) | 1981-06-30 | 1984-04-17 | The Procter & Gamble Company | Carbamate derivatives |
| US4401663A (en) | 1981-06-30 | 1983-08-30 | The Procter & Gamble Company | Novel sulfonamide derivatives |
| US4424205A (en) | 1982-03-18 | 1984-01-03 | The Procter & Gamble Company | Hydroxyphenylacetamides having analgesic and anti-irritant activity |
| US4855086A (en) * | 1982-10-15 | 1989-08-08 | Burroughs Wellcome Co. | Novel pesticides, preparation and use |
| US4532139A (en) | 1983-07-14 | 1985-07-30 | The Procter & Gamble Company | Compounds and compositions useful for producing analgesia |
| US4564633A (en) | 1983-07-14 | 1986-01-14 | The Procter & Gamble Company | Compositions and methods useful for producing analgesia |
| US4544668A (en) | 1983-07-14 | 1985-10-01 | The Procter & Gamble Company | Compounds and compositions useful for producing analgesia |
| US4544669A (en) | 1983-07-14 | 1985-10-01 | The Procter & Gamble Company | Compounds and compositions useful for producing analgesia |
| US4493848A (en) | 1983-07-14 | 1985-01-15 | The Procter & Gamble Company | Compositions and methods useful for producing analgesia |
| US4681897A (en) * | 1984-01-16 | 1987-07-21 | The Procter & Gamble Company | Pharmaceutical products providing enhanced analgesia |
| US4579866A (en) * | 1984-05-29 | 1986-04-01 | Usv Pharmaceutical Corp. | Phenylacetamides as anti-allergy, anti-asthma and anti-inflammatory agents |
| EP0196184B1 (de) * | 1985-03-16 | 1992-09-16 | The Wellcome Foundation Limited | Aryl-Derivate |
-
1986
- 1986-06-06 GB GB8613866A patent/GB2178031B/en not_active Expired
- 1986-06-09 DE DE8686304377T patent/DE3665708D1/de not_active Expired
- 1986-06-09 IE IE152786A patent/IE58664B1/en not_active IP Right Cessation
- 1986-06-09 EP EP86304377A patent/EP0206609B1/de not_active Expired
- 1986-06-09 AT AT86304377T patent/ATE46499T1/de active
- 1986-06-09 CA CA000511134A patent/CA1273360A/en not_active Expired - Fee Related
- 1986-06-10 PH PH33874A patent/PH23807A/en unknown
- 1986-06-10 JP JP61132923A patent/JPH0819067B2/ja not_active Expired - Lifetime
- 1986-06-10 ZA ZA864323A patent/ZA864323B/xx unknown
- 1986-06-10 NZ NZ216468A patent/NZ216468A/xx unknown
- 1986-06-10 AU AU58497/86A patent/AU605744B2/en not_active Ceased
- 1986-06-10 DK DK274086A patent/DK171597B1/da not_active IP Right Cessation
-
1987
- 1987-09-30 MY MYPI87002600A patent/MY102776A/en unknown
-
1992
- 1992-04-30 SG SG49692A patent/SG49692G/en unknown
- 1992-07-02 HK HK482/92A patent/HK48292A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AU5849786A (en) | 1986-12-18 |
| EP0206609B1 (de) | 1989-09-20 |
| DE3665708D1 (en) | 1989-10-26 |
| GB2178031B (en) | 1989-07-26 |
| AU605744B2 (en) | 1991-01-24 |
| SG49692G (en) | 1992-06-12 |
| PH23807A (en) | 1989-11-23 |
| GB2178031A (en) | 1987-02-04 |
| CA1273360A (en) | 1990-08-28 |
| NZ216468A (en) | 1989-08-29 |
| GB8613866D0 (en) | 1986-07-09 |
| HK48292A (en) | 1992-07-10 |
| JPS6248657A (ja) | 1987-03-03 |
| MY102776A (en) | 1992-10-31 |
| IE58664B1 (en) | 1993-11-03 |
| JPH0819067B2 (ja) | 1996-02-28 |
| IE861527L (en) | 1986-12-10 |
| DK274086D0 (da) | 1986-06-10 |
| ZA864323B (en) | 1988-02-24 |
| DK274086A (da) | 1986-12-11 |
| EP0206609A1 (de) | 1986-12-30 |
| ATE46499T1 (de) | 1989-10-15 |
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| EP0068592B1 (de) | Carbamatderivate | |
| EP0132346B1 (de) | Verbindungen und zur Herbeiführung einer Analgesie geeignete Zusammensetzung | |
| US4564633A (en) | Compositions and methods useful for producing analgesia | |
| US5045565A (en) | Novel compounds, pharmaceutical compositions, and methods for treating inflammation and pain | |
| EP0282127B1 (de) | Beta-aminoethyl-substituierte Phenyl-Verbindungen, diese enthaltende entzündungshemmende oder analgetische Zusammensetzungen | |
| US5099030A (en) | Novel compounds, pharmaceutical compositions, and methods for treating inflammation and pain | |
| DK171597B1 (da) | Substituerede phenyleddikesyreamidforbindelser og farmaceutisk acceptable salte heraf samt farmaceutisk sammensætning med anti-inflammatorisk og analgetisk virkning indeholdende disse | |
| US5013759A (en) | Compounds and compositions having anti-inflammatory and analgesic activity | |
| CA1337117C (en) | Use of vanilloids for the treatment of herpes simplex infections | |
| EP0187009B1 (de) | Verbindungen und Zusammensetzungen mit entzündungshemmender und analgetischer Wirkung | |
| US4898887A (en) | Compounds and compositions having anti-inflammatory and analgesic activity | |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B1 | Patent granted (law 1993) | ||
| PBP | Patent lapsed |