ES2182890T3 - Sintesis de acidos 4-arilo-2-hidroxitetronicos opticamente puros. - Google Patents
Sintesis de acidos 4-arilo-2-hidroxitetronicos opticamente puros.Info
- Publication number
- ES2182890T3 ES2182890T3 ES95911075T ES95911075T ES2182890T3 ES 2182890 T3 ES2182890 T3 ES 2182890T3 ES 95911075 T ES95911075 T ES 95911075T ES 95911075 T ES95911075 T ES 95911075T ES 2182890 T3 ES2182890 T3 ES 2182890T3
- Authority
- ES
- Spain
- Prior art keywords
- optically pure
- hydroxythetronic
- synthesis
- acids
- treatment
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/08—Six-membered 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
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
-
- 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]
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/62—Three oxygen atoms, e.g. ascorbic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Furan Compounds (AREA)
Abstract
LA PRESENTE INVENCION SE REFIERE A UN METODO PARA LA SINTESIS DE ACIDOS 4-ARIL-2-HIDROXITETRONICOS, LABILES ESTEREOGENICAMENTE OPTICAMENTE PUROS DE UN ALDEHIDO OPTICAMENTE PURO. LA INVENCION ADEMAS SE REFIERE AL USO DE TALES COMPUESTOS OPTICAMENTE PUROS COMO POTENTES INHIBIDORES DE AGREGACION DE PLAQUETAS TRABAJANDO AL NIVEL DE LA CICLOOXIGENASA, Y ADICIONALMENTE COMO INHIBIDORES DE CICLOOXIGENASA Y 5-LIPOXIGENASA. LA INVENCION ADEMAS SE REFIERE AL USO FARMACEUTICO DE TALES COMPUESTOS EN EL TRATAMIENTO DE ENFERMEDADES ARTERIALES CORONARIAS, ESPECIALMENTE EN EL TRATAMIENTO Y/O PREVENCION DE ATEROSCLEROSIS, Y EN EL TRATAMIENTO DE DIVERSAS PATOLOGIAS INFLAMATORIAS, ESPECIALMENTE ARTRITIS.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/201,775 US5399721A (en) | 1990-01-12 | 1994-02-25 | Synthesis of optically pure 4-aryl-2-hydroxytetronic acids |
| US08/350,205 US5504108A (en) | 1990-01-12 | 1994-12-05 | Optically pure 4-aryl-2-hydroxytetronic acids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2182890T3 true ES2182890T3 (es) | 2003-03-16 |
Family
ID=26897085
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES95911075T Expired - Lifetime ES2182890T3 (es) | 1994-02-25 | 1995-02-22 | Sintesis de acidos 4-arilo-2-hidroxitetronicos opticamente puros. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5504108A (es) |
| EP (1) | EP0746551B1 (es) |
| JP (1) | JP3241735B2 (es) |
| AT (1) | ATE223395T1 (es) |
| CA (1) | CA2184068A1 (es) |
| DE (1) | DE69528044T2 (es) |
| DK (1) | DK0746551T3 (es) |
| ES (1) | ES2182890T3 (es) |
| PT (1) | PT746551E (es) |
| WO (1) | WO1995023139A1 (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6005000A (en) | 1996-08-22 | 1999-12-21 | Oxis International, Inc. | 5,5-Disubstituted-3, 4-dihydroxy-2(5H)-furanones and methods of use therefor |
| DE69913390D1 (de) * | 1999-12-29 | 2004-01-15 | Oxis Isle Of Man Ltd | Methode zur trennung von racemischen mischungen von 5-substituierten 4-hydroxy-2-furanonen |
| NZ524252A (en) | 2000-07-20 | 2004-03-26 | Lauras As | Cox-2 inhibitors for treating HIV and AIDS |
| US20040242693A1 (en) * | 2001-11-30 | 2004-12-02 | Norimasa Okuda | Optically active mandelic acid and its derivative, and method for crystallization thereof |
| WO2003053916A1 (en) * | 2001-12-21 | 2003-07-03 | Ortho-Mcneil Pharmaceutical, Inc. | Process for preparing 2-(substituted phenyl) - 2 - hydroxy-ethyl carbamates |
| KR20100134082A (ko) * | 2001-12-21 | 2010-12-22 | 오르토-맥네일 파마슈티칼, 인코퍼레이티드 | 2-(치환된 페닐)-2-하이드록시-에틸 카바메이트의 제조방법 |
| CN107233337A (zh) | 2009-04-29 | 2017-10-10 | 阿马里纳药物爱尔兰有限公司 | 含有epa和心血管剂的药物组合物以及使用其的方法 |
| GB2512863A (en) * | 2013-04-09 | 2014-10-15 | Pornthip Lattmann | Medicinal applications of arylated hydroxy-tetronic acids |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2830268B2 (ja) * | 1989-01-21 | 1998-12-02 | 武田薬品工業株式会社 | アスコルビン酸誘導体の製造法 |
| US5095126A (en) * | 1990-01-12 | 1992-03-10 | Ohio State University Research Foundation | Efficient synthesis for optically pure stereogenically labile 4-substituted-2-hydroxytetronic acids |
| US5071872A (en) * | 1990-08-14 | 1991-12-10 | The Ohio State University Research Foundation | Method for improving interleukin-2 activity using aci-reductone compounds |
-
1994
- 1994-12-05 US US08/350,205 patent/US5504108A/en not_active Expired - Fee Related
-
1995
- 1995-02-22 DE DE69528044T patent/DE69528044T2/de not_active Expired - Fee Related
- 1995-02-22 AT AT95911075T patent/ATE223395T1/de not_active IP Right Cessation
- 1995-02-22 ES ES95911075T patent/ES2182890T3/es not_active Expired - Lifetime
- 1995-02-22 JP JP52242295A patent/JP3241735B2/ja not_active Expired - Fee Related
- 1995-02-22 DK DK95911075T patent/DK0746551T3/da active
- 1995-02-22 WO PCT/US1995/002183 patent/WO1995023139A1/en not_active Ceased
- 1995-02-22 PT PT95911075T patent/PT746551E/pt unknown
- 1995-02-22 EP EP95911075A patent/EP0746551B1/en not_active Expired - Lifetime
- 1995-02-22 CA CA002184068A patent/CA2184068A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP0746551A1 (en) | 1996-12-11 |
| JP3241735B2 (ja) | 2001-12-25 |
| DE69528044D1 (de) | 2002-10-10 |
| PT746551E (pt) | 2003-01-31 |
| DE69528044T2 (de) | 2003-04-17 |
| EP0746551B1 (en) | 2002-09-04 |
| US5504108A (en) | 1996-04-02 |
| WO1995023139A1 (en) | 1995-08-31 |
| DK0746551T3 (da) | 2003-01-06 |
| ATE223395T1 (de) | 2002-09-15 |
| CA2184068A1 (en) | 1995-08-31 |
| JPH10500663A (ja) | 1998-01-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES467828A1 (es) | Un procedimiento para preparar nuevos compuestos de cefem y cefam | |
| ATE253586T1 (de) | 2-(purin-9-yl)-tetrahydrofuran-3,4-diol-derivat | |
| ATE247666T1 (de) | Wasserlöslische prodrugs von 2,6- diisopropylphenol-analoga | |
| ES2192213T3 (es) | Arilalquil-diazinonas como inhibidores de fosfodiesterasa iv. | |
| PT1309589E (pt) | Compostos de ureia e metodos de utilizacao | |
| EA200000358A1 (ru) | Способ получения диарилпиридинов, полезных в качестве ингибиторов cox-2 | |
| RU94029662A (ru) | Фосфонооксиметиловые эфиры производных таксана, фармацевтическая композиция, способы лечения | |
| ES2178291T3 (es) | Uso de acidos 3-benzoil-aceticos, esteres, o amidas para el tratamiento del glaucoma glc1a. | |
| ES2186015T3 (es) | Derivados de 2-(purin-9-il)-tetrahidrofuran-3,4-diol. | |
| MX9307779A (es) | Compuestos benzoicos fundidos. | |
| MX9404749A (es) | Heterociclos de fenilo como inhibidores de cox-2. | |
| DE60233420D1 (de) | Fumagillolderivate und verfahren zu deren herstellung | |
| ES2182161T3 (es) | Utilizacion de derivados de pirimidina para la preparacion de un medicamento para la prevencion del cancer. | |
| AR022469A1 (es) | Uso de acidos isoxazolcarboxilicos sustituidos y derivados y nuevas sustancias | |
| PA8432901A1 (es) | Compuestos de piridilpirrol | |
| MX9503529A (es) | Derivados de glicinamida, procedimiento para su preparacion y medicamentos que los contienen. | |
| PA8542901A1 (es) | Uso de (z)-2-ciano-3-hidroxi-but-2-acido enoico-(4-trifluorometilfenil)-amida para tratar la esclerosis multiple | |
| LV12291A (lv) | Savienojums un farmaceitiskas kompozicijas ar triptazes aktivitates izmainam saistitu slimibu arstesanai | |
| GT199900154A (es) | Agentes farmaceuticos para el tratamiento de la enfermedad de parkinson, adhd y microadenomas. | |
| ES2119300T3 (es) | Procedimiento para la preparacion de 5-formilvalerato. | |
| GT199900081A (es) | Compuestos de sulfonilbenceno como agentes anti-inflamatorios / analgesicos. | |
| TR200400228T4 (tr) | Psöryazinin tedavisinde kullanılacak maddeler | |
| SE9601677D0 (sv) | New use | |
| ES2190471T3 (es) | Procedimiento para producir derivados de guanidina, intermedios de dichos compuestos y su produccion. | |
| ATE281432T1 (de) | C-16 ungesätigte fp-selektive prostaglandin analoge |