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)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (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)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (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 (33)
Country | Link |
---|---|
US (2) | US5852195A (fr) |
EP (1) | EP0758327B1 (fr) |
JP (1) | JP3883206B2 (fr) |
KR (1) | KR100445929B1 (fr) |
CN (2) | CN1329378C (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) |
HK (2) | HK1066796A1 (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 (70)
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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 |
EP0909184B1 (fr) * | 1996-07-03 | 2003-09-17 | PHARMACIA & UPJOHN COMPANY | Distribution ciblee de medicaments a l'aide de derives de sulfonamides |
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 |
RU2202346C2 (ru) * | 1997-07-29 | 2003-04-20 | Фармация Энд Апджон Компани | Фармацевтическая композиция для кислотных липофильных соединений в форме самоэмульгирующейся композиции |
ATE215370T1 (de) * | 1997-07-29 | 2002-04-15 | Upjohn Co | Selbstemulgierende formulierung enthaltend lipophile verbindungen |
RU2211021C2 (ru) * | 1997-07-29 | 2003-08-27 | Фармация Энд Апджон Компани | Фармацевтическая самоэмульгирующая композиция и ее носитель для липофильных фармацевтически активных агентов |
ATE266654T1 (de) | 1997-09-11 | 2004-05-15 | Upjohn Co | Verfahren zur herstellung von als protease inhibitoren wervollen 4-hydroxy-2-oxo-pyran- derivaten |
JP3610014B2 (ja) | 1999-03-18 | 2005-01-12 | ファルマシア アンド アップジョン カンパニー リミティド ライアビリティー カンパニー | 不斉水素化のための改良された製法 |
US6956048B2 (en) * | 1999-03-31 | 2005-10-18 | Pharmacia & Upjohn Company | Pharmaceutical emulsions for retroviral protease inhibitors |
CZ304118B6 (cs) | 2000-01-19 | 2013-11-06 | Abbott Laboratories | Farmaceutická kompozice |
US6500963B2 (en) | 2001-02-22 | 2002-12-31 | Boehringer Ingelheim Pharma Kg | Process for preparing optically active dihydropyrones |
DE10108470A1 (de) * | 2001-02-22 | 2002-09-05 | Boehringer Ingelheim Pharma | Verfahren zur Herstellung optisch aktiver Dihydropyrone |
GB2401606B (en) * | 2002-02-25 | 2005-08-31 | Kudos Pharm Ltd | Pyranones useful as ATM inhibitors |
ES2268394T3 (es) * | 2002-04-01 | 2007-03-16 | Pfizer Inc. | Inhibidores de piranona y pirandiona de la arn polimerasa dependiente del arn del virus de la hepatitis c. |
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 |
JP2008519073A (ja) * | 2004-11-08 | 2008-06-05 | 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 | チプラナビル及びエトラビリンの同時投与によるhiv感染症の治療法 |
JP2008520672A (ja) * | 2004-11-16 | 2008-06-19 | 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 | チプラナビルとダルナビルの共投与によるhiv感染症の治療方法 |
US20060128733A1 (en) * | 2004-11-19 | 2006-06-15 | Boehringer Ingelheim International Gmbh | Method for treating HIV infection through co-administration of tipranavir and reverset |
WO2006055660A2 (fr) * | 2004-11-19 | 2006-05-26 | Boehringer Ingelheim International Gmbh | Traitement de l'infection a vih par co-administration de tipranavir et d'uk-427, 857 |
US20060135563A1 (en) * | 2004-12-01 | 2006-06-22 | Boehringer Ingelheim International Gmbh | Method for treating HIV infection through co-administration of tipranavir and SCH-417690 |
WO2006060159A1 (fr) * | 2004-12-01 | 2006-06-08 | Boehringer Ingelheim International Gmbh | Procede de traitement des infections a vih par administration conjointe de tipranavir et de gw695634 |
JP2008521898A (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gw873140を共に投与することを含むhiv感染症の治療方法 |
JP5448854B2 (ja) | 2007-03-12 | 2014-03-19 | ウェルズ ファーゴ バンク ナショナル アソシエイション | オリゴマー−プロテアーゼ阻害剤複合体 |
US20090062346A1 (en) * | 2007-08-29 | 2009-03-05 | Protia, Llc | Deuterium-enriched tipranavir |
WO2009042093A1 (fr) * | 2007-09-25 | 2009-04-02 | Merck & Co., Inc. | Inhibiteurs de la protéase du vih |
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US8772332B2 (en) * | 2010-09-09 | 2014-07-08 | Richard H. Ebright | Arylpropionyl-alpha-pyrone antibacterial agents |
US10800725B2 (en) | 2010-09-09 | 2020-10-13 | Richard H. Ebright | Arylpropionyl-triketone antibacterial agents |
WO2012037508A2 (fr) | 2010-09-17 | 2012-03-22 | Rutgers, The State University Of New Jersey | Agents antibactériens : dérivés de myxopyronine de puissance élevée |
US9079834B2 (en) | 2010-10-28 | 2015-07-14 | Merck Canada Inc. | HIV protease inhibitors |
WO2012083117A1 (fr) | 2010-12-16 | 2012-06-21 | Vertex Pharmaceuticals Incorporated | Inhibiteurs de la réplication des virus de la grippe |
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WO2017156458A1 (fr) | 2016-03-11 | 2017-09-14 | University Of South Florida | Inhibiteurs de bêta-lactamases, formulations et utilisations correspondantes |
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WO2019160875A1 (fr) | 2018-02-13 | 2019-08-22 | Rutgers, The State University Of New Jersey | Agents antibactériens : sels solubles et formulations aqueuses de pyronines |
WO2019160873A1 (fr) | 2018-02-13 | 2019-08-22 | Rutgers, The State University Of New Jersey | Agents antibactériens : pyronines o-alkyl-deutérés |
US11572337B2 (en) | 2018-03-06 | 2023-02-07 | Rutgers, The State University Of New Jersey | Antibacterial agents: arylalkylcarboxamido phloroglucinols |
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1995
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- 1995-05-04 HU HU9603074A patent/HU228057B1/hu active Protection Beyond IP Right Term
- 1995-05-04 PT PT95918864T patent/PT758327E/pt unknown
- 1995-05-04 CZ CZ0317296A patent/CZ296515B6/cs not_active IP Right Cessation
- 1995-05-04 MX MX9605391A patent/MX9605391A/es active IP Right Grant
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- 1995-05-04 CN CNB2004100346805A patent/CN1329378C/zh not_active Expired - Lifetime
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- 1995-05-04 CA CA002560489A patent/CA2560489C/fr not_active Expired - Lifetime
- 1995-05-04 DE DE1995630294 patent/DE122006000014I2/de active Active
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- 1995-05-04 CA CA002187523A patent/CA2187523C/fr not_active Expired - Lifetime
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- 1995-05-04 BR BR9507615A patent/BR9507615A/pt active Search and Examination
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- 1995-05-04 AT AT95918864T patent/ATE236894T1/de active
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- 1995-05-04 WO PCT/US1995/005219 patent/WO1995030670A2/fr active IP Right Grant
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