NO317060B1 - Fluor-holdig prostaglandinderivat, anvendelse derav samt medisiner inneholdende derivatet - Google Patents
Fluor-holdig prostaglandinderivat, anvendelse derav samt medisiner inneholdende derivatet Download PDFInfo
- Publication number
- NO317060B1 NO317060B1 NO19976085A NO976085A NO317060B1 NO 317060 B1 NO317060 B1 NO 317060B1 NO 19976085 A NO19976085 A NO 19976085A NO 976085 A NO976085 A NO 976085A NO 317060 B1 NO317060 B1 NO 317060B1
- Authority
- NO
- Norway
- Prior art keywords
- group
- difluoro
- deoxy
- compound according
- tetranorprostaglandin
- Prior art date
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- 150000003180 prostaglandins Chemical class 0.000 title claims description 29
- 229910052731 fluorine Inorganic materials 0.000 title claims description 28
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- 239000011737 fluorine Substances 0.000 title claims description 26
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- 238000004519 manufacturing process Methods 0.000 claims description 3
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PXGPLTODNUVGFL-YNNPMVKQSA-N prostaglandin F2alpha Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O PXGPLTODNUVGFL-YNNPMVKQSA-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
- GRJJQCWNZGRKAU-UHFFFAOYSA-N pyridin-1-ium;fluoride Chemical compound F.C1=CC=NC=C1 GRJJQCWNZGRKAU-UHFFFAOYSA-N 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- ABTOQLMXBSRXSM-UHFFFAOYSA-N silicon tetrafluoride Chemical compound F[Si](F)(F)F ABTOQLMXBSRXSM-UHFFFAOYSA-N 0.000 description 1
- 229940096017 silver fluoride Drugs 0.000 description 1
- REYHXKZHIMGNSE-UHFFFAOYSA-M silver monofluoride Chemical compound [F-].[Ag+] REYHXKZHIMGNSE-UHFFFAOYSA-M 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229960001790 sodium citrate Drugs 0.000 description 1
- 229940037001 sodium edetate Drugs 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003890 succinate salts Chemical class 0.000 description 1
- 230000006103 sulfonylation Effects 0.000 description 1
- 238000005694 sulfonylation reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- QHMQWEPBXSHHLH-UHFFFAOYSA-N sulfur tetrafluoride Chemical compound FS(F)(F)F QHMQWEPBXSHHLH-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- HJBZFPLBRXFZNE-UHFFFAOYSA-M tetrabutylphosphanium fluoride hydrofluoride Chemical compound F.[F-].CCCC[P+](CCCC)(CCCC)CCCC HJBZFPLBRXFZNE-UHFFFAOYSA-M 0.000 description 1
- QSUJAUYJBJRLKV-UHFFFAOYSA-M tetraethylazanium;fluoride Chemical compound [F-].CC[N+](CC)(CC)CC QSUJAUYJBJRLKV-UHFFFAOYSA-M 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 150000003555 thioacetals Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- KRVIQSHPVVXYIT-UHFFFAOYSA-N trifluoro(piperidin-1-yl)-$l^{4}-sulfane Chemical compound FS(F)(F)N1CCCCC1 KRVIQSHPVVXYIT-UHFFFAOYSA-N 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 125000004360 trifluorophenyl group Chemical group 0.000 description 1
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 description 1
- CMSYDJVRTHCWFP-UHFFFAOYSA-N triphenylphosphane;hydrobromide Chemical compound Br.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 CMSYDJVRTHCWFP-UHFFFAOYSA-N 0.000 description 1
- NFHRNKANAAGQOH-UHFFFAOYSA-N triphenylstannane Chemical compound C1=CC=CC=C1[SnH](C=1C=CC=CC=1)C1=CC=CC=C1 NFHRNKANAAGQOH-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical class OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C405/00—Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins ; Analogues or derivatives thereof
-
- 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
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C405/00—Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins ; Analogues or derivatives thereof
- C07C405/0008—Analogues having the carboxyl group in the side-chains replaced by other functional groups
- C07C405/0016—Analogues having the carboxyl group in the side-chains replaced by other functional groups containing only hydroxy, etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C405/00—Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins ; Analogues or derivatives thereof
- C07C405/0008—Analogues having the carboxyl group in the side-chains replaced by other functional groups
- C07C405/0033—Analogues having the carboxyl group in the side-chains replaced by other functional groups containing sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Ophthalmology & Optometry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34861496 | 1996-12-26 | ||
| JP7405497 | 1997-03-26 | ||
| JP17247797 | 1997-06-27 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO976085D0 NO976085D0 (no) | 1997-12-23 |
| NO976085L NO976085L (no) | 1998-06-29 |
| NO317060B1 true NO317060B1 (no) | 2004-08-02 |
Family
ID=27301396
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19976085A NO317060B1 (no) | 1996-12-26 | 1997-12-23 | Fluor-holdig prostaglandinderivat, anvendelse derav samt medisiner inneholdende derivatet |
| NO2009006C NO2009006I2 (no) | 1996-12-26 | 2009-03-06 | isopropyl(5Z)-7{(1R, 2R, 3R, 5S)-2-[(IE)-3,3-difluor-4-fenoksybut-l-enyl]-3,5-dihydroksycyklopentyl}hept-5-enoat eller 16-fenoksy-15-deoksy-15,15-difluor-17,18,19,20-tetranorprostaglandin F2a isopropyl ester |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO2009006C NO2009006I2 (no) | 1996-12-26 | 2009-03-06 | isopropyl(5Z)-7{(1R, 2R, 3R, 5S)-2-[(IE)-3,3-difluor-4-fenoksybut-l-enyl]-3,5-dihydroksycyklopentyl}hept-5-enoat eller 16-fenoksy-15-deoksy-15,15-difluor-17,18,19,20-tetranorprostaglandin F2a isopropyl ester |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US5886035A (fr) |
| EP (1) | EP0850926B1 (fr) |
| JP (2) | JP3480549B2 (fr) |
| KR (1) | KR100526282B1 (fr) |
| CN (1) | CN1108289C (fr) |
| AT (1) | ATE225770T1 (fr) |
| CA (1) | CA2225761C (fr) |
| DE (2) | DE122008000050I2 (fr) |
| DK (1) | DK0850926T3 (fr) |
| ES (1) | ES2187719T3 (fr) |
| FR (1) | FR11C0020I2 (fr) |
| LU (1) | LU91943I2 (fr) |
| NL (1) | NL300407I2 (fr) |
| NO (2) | NO317060B1 (fr) |
| PT (1) | PT850926E (fr) |
| TW (1) | TW536534B (fr) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE221048T1 (de) * | 1996-09-17 | 2002-08-15 | Asahi Glass Co Ltd | Fluorierte prostaglandinderivate und medikamente |
| US6225348B1 (en) | 1998-08-20 | 2001-05-01 | Alfred W. Paulsen | Method of treating macular degeneration with a prostaglandin derivative |
| IL134241A (en) | 2000-01-27 | 2006-06-11 | Finetech Pharmaceutical Ltd | Process for the preparation of latanoprost |
| IL143477A (en) | 2001-05-31 | 2009-07-20 | Finetech Pharmaceutical Ltd | Process for the preparation of 17-phenyl-18,19,20-trinor-pgf2?? and its derivatives |
| AU2001228836A1 (en) * | 2000-01-28 | 2001-08-07 | Santen Pharmaceutical Co., Ltd. | Novel difluoroprostaglandin derivative |
| ES2357551T3 (es) * | 2000-09-13 | 2011-04-27 | Santen Pharmaceutical Co., Ltd. | Colirio. |
| CN100361661C (zh) * | 2002-08-23 | 2008-01-16 | 参天制药株式会社 | 以拉坦前列素为有效成分的稳定的滴眼液 |
| CA2707067C (fr) * | 2002-09-09 | 2013-07-16 | Santen Pharmaceutical Co., Ltd. | Solution ophtalmique transparente contenant du latonoprost comme principe actif |
| WO2005011704A1 (fr) * | 2003-07-31 | 2005-02-10 | Santen Pharmaceutical Co., Ltd. | Produit contenant de la prostaglandine |
| MXPA06006452A (es) * | 2003-12-08 | 2006-08-31 | Qualcomm Inc | Interfase de tasa alta de datos con sincronizacion de enlace mejorada. |
| JP2006187602A (ja) * | 2004-12-09 | 2006-07-20 | Santen Pharmaceut Co Ltd | 分子内にフッ素原子を有するプロスタグランジン含有製品 |
| JP4753178B2 (ja) * | 2004-12-24 | 2011-08-24 | 参天製薬株式会社 | プロスタグランジンＦ２α誘導体含有製品 |
| JP5100025B2 (ja) * | 2005-03-31 | 2012-12-19 | 旭硝子株式会社 | プロスタグランジンＦ２α誘導体を有効成分として含む網膜神経細胞保護剤 |
| WO2006106915A1 (fr) | 2005-03-31 | 2006-10-12 | Asahi Glass Company, Limited | AGENT PROTECTEUR POUR LA CELLULE NEURONALE RETINIENNE CONTENANT UN DERIVE DE PROSTAGLANDINE F2α COMME INGREDIENT ACTIF |
| CN101160128B (zh) | 2005-04-13 | 2010-08-18 | 宇部兴产株式会社 | 含有吲唑衍生物作为有效成分的视网膜神经细胞保护剂 |
| WO2007000642A1 (fr) * | 2005-06-29 | 2007-01-04 | Pfizer Inc. | Derives nitres de fluoroprostaglandines |
| HUE034571T2 (en) * | 2006-02-07 | 2018-02-28 | Sucampo Pharma Llc | A method for preparing a prostaglandin derivative |
| US7666912B2 (en) | 2006-03-23 | 2010-02-23 | Massachusetts Eye And Ear Infirmary | Compositions and methods for reducing body fat |
| FR2918891B1 (fr) * | 2007-07-20 | 2009-09-25 | Thea Sa Lab | Solution ophtalmique a base de prostaglandines sans conservateur |
| EP2127638A1 (fr) * | 2008-05-30 | 2009-12-02 | Santen Pharmaceutical Co., Ltd | Procédé et composition pour traiter l'hypertension oculaire et le glaucome |
| CN102143753B (zh) * | 2008-09-04 | 2013-07-03 | 参天制药株式会社 | 含有15,15-二氟前列腺素F2α衍生物作为有效成分的毛发生长促进剂 |
| US20110293549A1 (en) | 2009-02-03 | 2011-12-01 | Athena Cosmetics, Inc. | Composition, method and kit for enhancing hair |
| BR112013002584A2 (pt) | 2010-08-02 | 2016-06-07 | Pharma Patent Holding Inc | composição, processo de kit para aperfeiçoamento de cabelo |
| US9089579B2 (en) | 2011-01-19 | 2015-07-28 | Topokine Therapeutics, Inc. | Methods and compositions for treating metabolic syndrome |
| TW201906614A (zh) | 2011-02-04 | 2019-02-16 | 日商興和股份有限公司 | 青光眼或高眼壓症之預防或治療用之點眼藥 |
| US8426471B1 (en) | 2011-12-19 | 2013-04-23 | Topokine Therapeutics, Inc. | Methods and compositions for reducing body fat and adipocytes |
| US20150011755A1 (en) * | 2012-02-07 | 2015-01-08 | Dr. Reddys Laboratories Limited | Amine salts of prostaglandin analogs |
| EP2857002A4 (fr) | 2012-05-30 | 2015-12-09 | Asahi Glass Co Ltd | Composition pour la croissance capillaire |
| EP2922542A4 (fr) | 2012-11-21 | 2016-10-05 | Topokine Therapeutics Inc | Méthodes et compositions pour augmenter localement la graisse corporelle |
| NO2753788T3 (fr) | 2013-05-10 | 2018-06-16 | ||
| WO2014186504A1 (fr) | 2013-05-15 | 2014-11-20 | Topokine Therapeutics, Inc. | Procédés et compositions pour l'administration topique de prostaglandines à la graisse sous-cutanée |
| CN103570549B (zh) * | 2013-10-11 | 2016-01-27 | 天泽恩源（天津）制药有限公司 | 一种合成他氟前列素的方法 |
| CN103804195B (zh) * | 2014-01-26 | 2016-06-15 | 天泽恩源（天津）制药有限公司 | 一种合成他氟前列素的方法 |
| CN103819436A (zh) * | 2014-02-21 | 2014-05-28 | 天泽恩源（天津）医药技术有限公司 | (3aR,4R,5R,6aS)-4-((E)-3,3-二氟-4-苯氧基丁-1-烯-1-基)-2-氧代六氢-2H-环戊烷[b]呋喃-5-基苯甲酸酯的一种晶型及相应晶体的制备方法 |
| WO2015200425A1 (fr) | 2014-06-27 | 2015-12-30 | Topokine Therapeutics, Inc. | Forme posologique à usage topique |
| KR20160116402A (ko) | 2015-03-30 | 2016-10-10 | 연성정밀화학(주) | 타플루프로스트의 제조방법 |
| JP2018536017A (ja) | 2015-09-22 | 2018-12-06 | グレイバグ ビジョン インコーポレイテッド | 眼障害の治療のための化合物及び組成物 |
| CN107226790A (zh) * | 2016-03-25 | 2017-10-03 | 苏州朗科生物技术有限公司 | 一种高纯度他氟前列素及其类似化合物的制备方法及中间体化合物 |
| GR1009040B (el) | 2016-04-19 | 2017-05-19 | Φαρματεν Ανωνυμος Βιομηχανικη Και Εμπορικη Εταιρεια Φαρμακευτικων Ιατρικων Και Καλλυντικων Προϊοντων | Φαρμακευτικο οφθαλμικο σκευασμα ελευθερο συντηρητικου |
| WO2018033854A1 (fr) | 2016-08-15 | 2018-02-22 | Santen Pharmaceutical Co., Ltd. | Composition ophtalmique et procédé de traitement de l'hypertension oculaire et du glaucome |
| CN108299192A (zh) * | 2017-01-10 | 2018-07-20 | 江苏恒瑞医药股份有限公司 | 一种他氟前列素酸的金属盐化合物结晶形式及其制备方法 |
| CN106986766B (zh) * | 2017-05-08 | 2021-01-12 | 扬子江药业集团有限公司 | 他氟前列素的制备方法 |
| CN112457277B (zh) * | 2020-12-16 | 2022-06-28 | 西安国康瑞金制药有限公司 | 一种他氟前列腺素的制备方法 |
| CN115385793A (zh) * | 2021-01-27 | 2022-11-25 | Ａｇｃ株式会社 | 他氟前列素的纯化方法 |
| CN112832150B (zh) * | 2021-01-27 | 2022-06-24 | 中交第三公路工程局有限公司 | 一种涵洞通道等立面垂直凿毛装置 |
| CN116120268A (zh) * | 2023-03-06 | 2023-05-16 | 南京华威医药科技集团有限公司 | 一种他氟前列素中间体杂质及其制备方法 |
| CN116425707A (zh) * | 2023-03-31 | 2023-07-14 | 南京华威医药科技集团有限公司 | 一种他氟前列素中间体异构体杂质及其制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5166178B1 (en) * | 1987-09-18 | 1998-07-21 | R Tech Ueno Ltd | Ocular hypotensive agents |
| US5510383A (en) * | 1993-08-03 | 1996-04-23 | Alcon Laboratories, Inc. | Use of cloprostenol, fluprostenol and their salts and esters to treat glaucoma and ocular hypertension |
| JPH0770054A (ja) * | 1993-08-30 | 1995-03-14 | R Tec Ueno:Kk | 生化学的拮抗および疾患処置剤 |
| ATE221048T1 (de) * | 1996-09-17 | 2002-08-15 | Asahi Glass Co Ltd | Fluorierte prostaglandinderivate und medikamente |
| CA2269855A1 (fr) * | 1996-11-12 | 1998-05-22 | Alcon Laboratories, Inc. | 15-fluoro prostaglandines utilisees en tant qu'hypotenseurs oculaires |
-
1997
- 1997-12-12 JP JP34334397A patent/JP3480549B2/ja not_active Expired - Lifetime
- 1997-12-17 TW TW086119094A patent/TW536534B/zh not_active IP Right Cessation
- 1997-12-18 US US08/993,017 patent/US5886035A/en not_active Expired - Lifetime
- 1997-12-22 DK DK97122702T patent/DK0850926T3/da active
- 1997-12-22 AT AT97122702T patent/ATE225770T1/de active
- 1997-12-22 DE DE122008000050C patent/DE122008000050I2/de active Active
- 1997-12-22 EP EP97122702A patent/EP0850926B1/fr not_active Expired - Lifetime
- 1997-12-22 ES ES97122702T patent/ES2187719T3/es not_active Expired - Lifetime
- 1997-12-22 DE DE69716226T patent/DE69716226T2/de not_active Expired - Lifetime
- 1997-12-22 PT PT97122702T patent/PT850926E/pt unknown
- 1997-12-23 CA CA002225761A patent/CA2225761C/fr not_active Expired - Lifetime
- 1997-12-23 NO NO19976085A patent/NO317060B1/no not_active IP Right Cessation
- 1997-12-26 CN CN97126331A patent/CN1108289C/zh not_active Expired - Lifetime
- 1997-12-26 KR KR1019970074620A patent/KR100526282B1/ko not_active IP Right Cessation
-
1998
- 1998-08-03 US US09/127,804 patent/US5985920A/en not_active Expired - Lifetime
-
2003
- 2003-07-31 JP JP2003284134A patent/JP3994074B2/ja not_active Expired - Lifetime
-
2009
- 2009-03-06 NO NO2009006C patent/NO2009006I2/no not_active IP Right Cessation
- 2009-09-02 NL NL300407C patent/NL300407I2/nl unknown
-
2011
- 2011-06-21 FR FR11C0020C patent/FR11C0020I2/fr active Active
-
2012
- 2012-02-15 LU LU91943C patent/LU91943I2/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW536534B (en) | 2003-06-11 |
| ATE225770T1 (de) | 2002-10-15 |
| PT850926E (pt) | 2003-02-28 |
| LU91943I2 (fr) | 2012-04-16 |
| ES2187719T3 (es) | 2003-06-16 |
| DE69716226T2 (de) | 2003-06-05 |
| CN1187486A (zh) | 1998-07-15 |
| DE69716226D1 (de) | 2002-11-14 |
| KR19980064718A (ko) | 1998-10-07 |
| US5886035A (en) | 1999-03-23 |
| JP3994074B2 (ja) | 2007-10-17 |
| NL300407I1 (nl) | 2009-11-02 |
| JPH1171344A (ja) | 1999-03-16 |
| NO976085D0 (no) | 1997-12-23 |
| NO976085L (no) | 1998-06-29 |
| FR11C0020I2 (fr) | 2012-03-16 |
| CA2225761C (fr) | 2009-04-21 |
| EP0850926A3 (fr) | 1999-06-16 |
| EP0850926B1 (fr) | 2002-10-09 |
| DE122008000050I2 (de) | 2011-06-16 |
| NO2009006I1 (no) | 2009-03-16 |
| EP0850926A2 (fr) | 1998-07-01 |
| CA2225761A1 (fr) | 1998-06-26 |
| KR100526282B1 (ko) | 2006-05-17 |
| US5985920A (en) | 1999-11-16 |
| CN1108289C (zh) | 2003-05-14 |
| NL300407I2 (nl) | 2010-03-01 |
| DE122008000050I1 (de) | 2009-01-29 |
| JP2004002462A (ja) | 2004-01-08 |
| JP3480549B2 (ja) | 2003-12-22 |
| NO2009006I2 (no) | 2012-03-05 |
| DK0850926T3 (da) | 2003-02-17 |
| FR11C0020I1 (fr) | 2011-07-29 |
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| Date | Code | Title | Description |
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| SPCG | Granted supplementary protection certificate |
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| MK1K | Patent expired | ||
| SPCS | Change of name or address of the owner of a supplementary protection certificate |
Owner name: SANTEN PHARMACEUTICAL CO LTD, JP Spc suppl protection certif: 2009006 |