LU91220I2 - Tipranavir ou un de ses sels pharmaceutiques (aptivus) - Google Patents
Tipranavir ou un de ses sels pharmaceutiques (aptivus)Info
- Publication number
- LU91220I2 LU91220I2 LU91220C LU91220C LU91220I2 LU 91220 I2 LU91220 I2 LU 91220I2 LU 91220 C LU91220 C LU 91220C LU 91220 C LU91220 C LU 91220C LU 91220 I2 LU91220 I2 LU 91220I2
- Authority
- LU
- Luxembourg
- Prior art keywords
- aptivus
- tipranavir
- ones
- pharmaceutical salt
- pyran
- Prior art date
Links
- SUJUHGSWHZTSEU-FYBSXPHGSA-N tipranavir Chemical compound C([C@@]1(CCC)OC(=O)C([C@H](CC)C=2C=C(NS(=O)(=O)C=3N=CC(=CC=3)C(F)(F)F)C=CC=2)=C(O)C1)CC1=CC=CC=C1 SUJUHGSWHZTSEU-FYBSXPHGSA-N 0.000 title 2
- SUJUHGSWHZTSEU-UHFFFAOYSA-N Tipranavir Natural products C1C(O)=C(C(CC)C=2C=C(NS(=O)(=O)C=3N=CC(=CC=3)C(F)(F)F)C=CC=2)C(=O)OC1(CCC)CCC1=CC=CC=C1 SUJUHGSWHZTSEU-UHFFFAOYSA-N 0.000 title 1
- 229940030139 aptivus Drugs 0.000 title 1
- 150000003839 salts Chemical class 0.000 title 1
- 229960000838 tipranavir Drugs 0.000 title 1
- 241001430294 unidentified retrovirus Species 0.000 abstract 2
- QBDAFARLDLCWAT-UHFFFAOYSA-N 2,3-dihydropyran-6-one Chemical class O=C1OCCC=C1 QBDAFARLDLCWAT-UHFFFAOYSA-N 0.000 abstract 1
- ZPSJGADGUYYRKE-UHFFFAOYSA-N 2H-pyran-2-one Chemical class O=C1C=CC=CO1 ZPSJGADGUYYRKE-UHFFFAOYSA-N 0.000 abstract 1
- VXIXUWQIVKSKSA-UHFFFAOYSA-N 4-hydroxycoumarin Chemical class C1=CC=CC2=C1OC(=O)C=C2O VXIXUWQIVKSKSA-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 210000004962 mammalian cell Anatomy 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/32—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/34—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D309/36—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
- C07D309/38—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms one oxygen atom in position 2 or 4, e.g. pyrones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/74—Benzo[b]pyrans, hydrogenated in the carbocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Molecular Biology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrane Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23881794A | 1994-05-06 | 1994-05-06 | |
| US34936194A | 1994-12-02 | 1994-12-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU91220I2 true LU91220I2 (fr) | 2006-04-10 |
Family
ID=26931995
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU91220C LU91220I2 (fr) | 1994-05-06 | 2006-02-08 | Tipranavir ou un de ses sels pharmaceutiques (aptivus) |
Country Status (32)
| Country | Link |
|---|---|
| US (2) | US5852195A (fr) |
| EP (1) | EP0758327B1 (fr) |
| JP (1) | JP3883206B2 (fr) |
| KR (1) | KR100445929B1 (fr) |
| CN (2) | CN1154642C (fr) |
| AT (1) | ATE236894T1 (fr) |
| AU (2) | AU701965B2 (fr) |
| BR (1) | BR9507615A (fr) |
| CA (2) | CA2560489C (fr) |
| CO (1) | CO4810313A1 (fr) |
| CZ (1) | CZ296515B6 (fr) |
| DE (2) | DE69530294T2 (fr) |
| DK (1) | DK0758327T3 (fr) |
| ES (1) | ES2192201T3 (fr) |
| FI (1) | FI117387B (fr) |
| FR (1) | FR05C0047I2 (fr) |
| HU (1) | HU228057B1 (fr) |
| IL (3) | IL129871A (fr) |
| LU (1) | LU91220I2 (fr) |
| MX (1) | MX9605391A (fr) |
| MY (2) | MY127701A (fr) |
| NL (1) | NL300216I2 (fr) |
| NO (2) | NO315799B1 (fr) |
| NZ (1) | NZ285510A (fr) |
| PE (1) | PE23196A1 (fr) |
| PL (1) | PL190540B1 (fr) |
| PT (1) | PT758327E (fr) |
| RU (1) | RU2139284C1 (fr) |
| SI (1) | SI0758327T1 (fr) |
| SK (1) | SK284407B6 (fr) |
| TW (1) | TW504507B (fr) |
| WO (1) | WO1995030670A2 (fr) |
Families Citing this family (74)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL129871A (en) * | 1994-05-06 | 2003-11-23 | Pharmacia & Upjohn Inc | Process for preparing 4-phenyl-substituted octanoyl-oxazolidin-2-one intermediates that are useful for preparing pyran-2-ones useful for treating retroviral infections |
| US5914332A (en) | 1995-12-13 | 1999-06-22 | Abbott Laboratories | Retroviral protease inhibiting compounds |
| DE69724964T2 (de) * | 1996-07-03 | 2004-07-22 | Pharmacia & Upjohn Co., Kalamazoo | Zielgerichte arzneimittel abgabe für zulphonamide-derivate |
| US5834506A (en) * | 1996-11-01 | 1998-11-10 | Warner-Lambert Company | Dihydropyrones with improved antiviral activity |
| US6232333B1 (en) | 1996-11-21 | 2001-05-15 | Abbott Laboratories | Pharmaceutical composition |
| DK0999838T3 (da) * | 1997-07-29 | 2002-07-08 | Upjohn Co | Selv-emulgerende formulering for lipofile forbindelser |
| JP4524367B2 (ja) | 1997-07-29 | 2010-08-18 | ファルマシア・アンド・アップジョン・カンパニー・エルエルシー | 自己乳化性処方形態の酸性親油性化合物用の医薬組成物 |
| SI0999826T1 (en) * | 1997-07-29 | 2004-12-31 | Pharmacia & Upjohn Company | Self-emulsifying formulation for lipophilic compounds |
| DK1015441T3 (da) * | 1997-09-11 | 2004-07-26 | Upjohn Co | Fremgangsmåde til fremstilling af 4-hydroxy-2-oxo-pyranderivater, der er nyttige som proteaseinhibitorer |
| ATE226579T1 (de) * | 1999-03-18 | 2002-11-15 | Upjohn Co | Verbesserte verfahren fur assymmetrische hydrogenation |
| US6956048B2 (en) * | 1999-03-31 | 2005-10-18 | Pharmacia & Upjohn Company | Pharmaceutical emulsions for retroviral protease inhibitors |
| ES2676151T3 (es) | 2000-01-19 | 2018-07-17 | Abbvie Inc. | Formulaciones farmacéuticas mejoradas |
| FI113942B (fi) * | 2000-08-18 | 2004-07-15 | Control Ox Oy | Kasviperäisten fenolisten yhdisteiden käyttö valmistettaessa klamydiainfektion hoidossa ja ennaltaehkäisyssä käyttökelpoista farmaseuttista valmistetta, terveyteen myönteisesti vaikuttavaa ravintoainekoostumusta tai koostumusta lisättäväksi tällaisiin elintarvikkeisiin |
| DE10108470A1 (de) * | 2001-02-22 | 2002-09-05 | Boehringer Ingelheim Pharma | Verfahren zur Herstellung optisch aktiver Dihydropyrone |
| US6500963B2 (en) | 2001-02-22 | 2002-12-31 | Boehringer Ingelheim Pharma Kg | Process for preparing optically active dihydropyrones |
| MXPA04007809A (es) * | 2002-02-25 | 2004-10-15 | Kudos Pharm Ltd | Piranonas utiles como inhibidores de ataxia-telangetaxia mutada. |
| AU2003215826A1 (en) * | 2002-04-01 | 2003-10-13 | Pfizer Inc. | Pyranon and pyrandion inhibitors of hepatitis c virus rna-dependent rna polymerase |
| RU2234535C2 (ru) * | 2002-10-03 | 2004-08-20 | Государственный научный центр вирусологии и биотехнологии "Вектор" | Субстрат для определения активности интегразы вируса иммунодефицита человека |
| US8025899B2 (en) | 2003-08-28 | 2011-09-27 | Abbott Laboratories | Solid pharmaceutical dosage form |
| US8377952B2 (en) | 2003-08-28 | 2013-02-19 | Abbott Laboratories | Solid pharmaceutical dosage formulation |
| US8841326B2 (en) | 2004-02-12 | 2014-09-23 | Stc.Unm | Therapeutic curcumin derivatives |
| IL161586A (en) * | 2004-04-22 | 2015-02-26 | Rafael Advanced Defense Sys | Irreplaceable energetic material and reactive shielding that uses it |
| EP1812069A2 (fr) * | 2004-11-08 | 2007-08-01 | Boehringer Ingelheim International GmbH | Methode de traitement d'infection vih par coadministration de tipranavir et etravirine |
| US20060135562A1 (en) * | 2004-11-16 | 2006-06-22 | Boehringer Ingelheim International Gmbh | Method for treating HIV infection through co-administration of tipranavir and darunavir |
| EP1814549A2 (fr) * | 2004-11-19 | 2007-08-08 | Boehringer Ingelheim International GmbH | Traitement de l'infection a vih par co-administration de tipranavir et d'uk-427, 857 |
| US20060128733A1 (en) * | 2004-11-19 | 2006-06-15 | Boehringer Ingelheim International Gmbh | Method for treating HIV infection through co-administration of tipranavir and reverset |
| WO2006060177A1 (fr) * | 2004-12-01 | 2006-06-08 | Boehringer Ingelheim International Gmbh | Methode de traitement de l'infection a vih par co-administration de tipranavir et de gw873140 |
| JP2008521896A (ja) * | 2004-12-01 | 2008-06-26 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | チプラナビル及びgw695634を共に投与することを含むhiv感染症の治療方法 |
| WO2006060175A1 (fr) * | 2004-12-01 | 2006-06-08 | Boehringer Ingelheim International Gmbh | Procede de traitement d'une infection par le vih par co-administration de tipranavir et de sch-417690 |
| WO2008112289A2 (fr) | 2007-03-12 | 2008-09-18 | Nektar Therapeutics | Conjugués d'oligomère-inhibiteur de protéase |
| US20090062346A1 (en) * | 2007-08-29 | 2009-03-05 | Protia, Llc | Deuterium-enriched tipranavir |
| EP2203420A1 (fr) * | 2007-09-25 | 2010-07-07 | Merck Sharp & Dohme Corp. | Inhibiteurs de la protease du vih |
| KR101076680B1 (ko) * | 2007-11-01 | 2011-10-26 | 한미홀딩스 주식회사 | (6r)-3-헥실-4-히드록시-6-운데실-5,6-다이히드로피란-2-온의 제조방법 및 이에 사용되는 중간체 |
| EP2262498A2 (fr) * | 2008-03-10 | 2010-12-22 | Vertex Pharmceuticals Incorporated | Pyrimidines et pyridines utiles comme inhibiteurs des protéines kinases |
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| CL2009002206A1 (es) | 2008-12-23 | 2011-08-26 | Gilead Pharmasset Llc | Compuestos derivados de pirrolo -(2-3-d]-pirimidin-7(6h)-tetrahidrofuran-2-il fosfonamidato, composicion farmaceutica; y su uso en el tratamiento de enfermedades virales. |
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| GEP20207129B (en) | 2009-06-17 | 2020-07-10 | Vertex Pharma | Inhibitors of influenza viruses replication |
| KR101466245B1 (ko) * | 2010-01-15 | 2014-12-01 | 한미사이언스 주식회사 | 테트라졸 메탄설폰산 염의 제조방법 및 이에 사용되는 신규 화합물 |
| AP2012006535A0 (en) | 2010-03-31 | 2012-10-31 | Gilead Pharmasset Llc | Stereoselective synthesis of phosphorous containing actives |
| WO2012033846A1 (fr) | 2010-09-09 | 2012-03-15 | Rutgers, The State University Of New Jersey | Agents antibactériens à base d'arylpropionyl-tricétone |
| WO2012033815A1 (fr) * | 2010-09-09 | 2012-03-15 | Rutgers, The State University Of New Jersey | Agents anti-bactériens à base d'arylpropionyl-alpha-pyrone |
| WO2012037508A2 (fr) | 2010-09-17 | 2012-03-22 | Rutgers, The State University Of New Jersey | Agents antibactériens : dérivés de myxopyronine de puissance élevée |
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| RU2013132681A (ru) | 2010-12-16 | 2015-01-27 | Вертекс Фармасьютикалз Инкорпорейтед | Ингибиторы репликации вирусов гриппа |
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| WO2013103969A1 (fr) | 2012-01-05 | 2013-07-11 | Rutgers, The State University Of New Jersey | Agents antibactériens : dérivés du phloroglucinol |
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| US10450292B2 (en) | 2015-12-10 | 2019-10-22 | Rutgers, The State University of New Jersesy | Inhibitors of bacterial RNA polymerase: arylpropanoyl, arylpropenoyl, and arylcyclopropanecarboxyl phloroglucinols |
| WO2017156458A1 (fr) | 2016-03-11 | 2017-09-14 | University Of South Florida | Inhibiteurs de bêta-lactamases, formulations et utilisations correspondantes |
| US11993590B2 (en) * | 2016-12-04 | 2024-05-28 | 712 North Inc. | Pyranone compounds useful to modulate OMA1 protease |
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| US12209082B2 (en) | 2018-02-13 | 2025-01-28 | Rutgers, The State University Of New Jersey | Antibacterial agents: soluble salts and aqueous formulations of pyronins |
| US11572337B2 (en) | 2018-03-06 | 2023-02-07 | Rutgers, The State University Of New Jersey | Antibacterial agents: arylalkylcarboxamido phloroglucinols |
| CN110551090B (zh) * | 2019-10-21 | 2021-06-18 | 扬州工业职业技术学院 | 一种超声波提取中药狗脊中抗肿瘤活性成分的方法 |
| WO2021209563A1 (fr) | 2020-04-16 | 2021-10-21 | Som Innovation Biotech, S.A. | Composés destinés à être utilisés dans le traitement d'infections virales par un coronavirus associé au syndrome respiratoire |
| TW202430153A (zh) * | 2022-12-16 | 2024-08-01 | 美商戴納立製藥公司 | 化合物、組成物及方法 |
| CN116730993B (zh) * | 2023-04-25 | 2026-01-23 | 浙江科技学院 | 一种替拉那韦中间体及替拉那韦的制备方法 |
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1995
- 1995-05-01 IL IL12987195A patent/IL129871A/xx not_active IP Right Cessation
- 1995-05-04 AT AT95918864T patent/ATE236894T1/de active
- 1995-05-04 BR BR9507615A patent/BR9507615A/pt active Search and Examination
- 1995-05-04 MX MX9605391A patent/MX9605391A/es active IP Right Grant
- 1995-05-04 CZ CZ0317296A patent/CZ296515B6/cs not_active IP Right Cessation
- 1995-05-04 US US08/809,224 patent/US5852195A/en not_active Expired - Lifetime
- 1995-05-04 KR KR1019960706245A patent/KR100445929B1/ko not_active Expired - Lifetime
- 1995-05-04 DK DK95918864T patent/DK0758327T3/da active
- 1995-05-04 NZ NZ285510A patent/NZ285510A/en not_active IP Right Cessation
- 1995-05-04 CN CNB951935534A patent/CN1154642C/zh not_active Expired - Lifetime
- 1995-05-04 RU RU96123286A patent/RU2139284C1/ru active
- 1995-05-04 SK SK1384-96A patent/SK284407B6/sk not_active IP Right Cessation
- 1995-05-04 ES ES95918864T patent/ES2192201T3/es not_active Expired - Lifetime
- 1995-05-04 EP EP95918864A patent/EP0758327B1/fr not_active Expired - Lifetime
- 1995-05-04 CA CA002560489A patent/CA2560489C/fr not_active Expired - Lifetime
- 1995-05-04 CA CA002187523A patent/CA2187523C/fr not_active Expired - Lifetime
- 1995-05-04 PT PT95918864T patent/PT758327E/pt unknown
- 1995-05-04 TW TW084104473A patent/TW504507B/zh not_active IP Right Cessation
- 1995-05-04 SI SI9530660T patent/SI0758327T1/xx unknown
- 1995-05-04 AU AU24626/95A patent/AU701965B2/en not_active Expired
- 1995-05-04 HU HU9603074A patent/HU228057B1/hu active Protection Beyond IP Right Term
- 1995-05-04 DE DE69530294T patent/DE69530294T2/de not_active Expired - Lifetime
- 1995-05-04 WO PCT/US1995/005219 patent/WO1995030670A2/fr not_active Ceased
- 1995-05-04 JP JP52901695A patent/JP3883206B2/ja not_active Expired - Lifetime
- 1995-05-04 CN CNB2004100346805A patent/CN1329378C/zh not_active Expired - Lifetime
- 1995-05-04 PL PL95317061A patent/PL190540B1/pl unknown
- 1995-05-04 DE DE1995630294 patent/DE122006000014I2/de active Active
- 1995-05-05 CO CO95018810A patent/CO4810313A1/es unknown
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1996
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1998
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2005
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- 2006-03-02 NO NO2006003C patent/NO2006003I2/no unknown
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