AU2010299A - Prodrugs os aspartyl protease inhibitors - Google Patents
Prodrugs os aspartyl protease inhibitorsInfo
- Publication number
- AU2010299A AU2010299A AU20102/99A AU2010299A AU2010299A AU 2010299 A AU2010299 A AU 2010299A AU 20102/99 A AU20102/99 A AU 20102/99A AU 2010299 A AU2010299 A AU 2010299A AU 2010299 A AU2010299 A AU 2010299A
- Authority
- AU
- Australia
- Prior art keywords
- prodrugs
- protease inhibitors
- aspartyl protease
- aspartyl
- inhibitors
- 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.)
- Abandoned
Links
- 239000003696 aspartic proteinase inhibitor Substances 0.000 title 1
- 229940002612 prodrug Drugs 0.000 title 1
- 239000000651 prodrug Substances 0.000 title 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
- C07C311/18—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms, not being part of nitro or nitroso groups
-
- 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
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no 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
- C07D307/20—Oxygen atoms
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/6584—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms having one phosphorus atom as ring hetero atom
- C07F9/65842—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring
- C07F9/65844—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring the phosphorus atom being part of a five-membered ring which may be condensed with another ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6880697P | 1997-12-24 | 1997-12-24 | |
| US60068806 | 1997-12-24 | ||
| PCT/US1998/027403 WO1999033792A2 (en) | 1997-12-24 | 1998-12-23 | Prodrugs os aspartyl protease inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2010299A true AU2010299A (en) | 1999-07-19 |
Family
ID=22084811
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU20102/99A Abandoned AU2010299A (en) | 1997-12-24 | 1998-12-23 | Prodrugs os aspartyl protease inhibitors |
Country Status (2)
| Country | Link |
|---|---|
| AU (1) | AU2010299A (en) |
| WO (1) | WO1999033792A2 (en) |
Families Citing this family (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5968942A (en) | 1992-08-25 | 1999-10-19 | G. D. Searle & Co. | α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
| US7141609B2 (en) | 1992-08-25 | 2006-11-28 | G.D. Searle & Co. | α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
| JP3657002B2 (en) | 1992-08-25 | 2005-06-08 | ジー．ディー．サール アンド カンパニー | Alpha- and beta-amino acid hydroxyethylaminosulfonamides useful as retroviral protease inhibitors |
| GB9815567D0 (en) | 1998-07-18 | 1998-09-16 | Glaxo Group Ltd | Antiviral compound |
| US6617310B2 (en) | 2000-07-19 | 2003-09-09 | Bristol-Myers Squibb Pharma Company | Phosphate esters of bis-amino acid sulfonamides containing substituted benzyl amines |
| BR0207862A (en) | 2001-02-14 | 2004-06-22 | Tibotec Pharm Ltd | Broad spectrum 2- (amino-substituted) -benzothiazole sulfonamide hiv protease inhibitors |
| OA12464A (en) | 2001-04-09 | 2006-05-24 | Tibotec Pharm Ltd | Broadspectrum 2-(substituted-amino)-benzoxazole sulfonamide HIV protease inhibitors. |
| EE05307B1 (en) | 2001-05-11 | 2010-06-15 | Tibotec Pharmaceuticals Ltd. | Broad-spectrum 2-aminobenzoxazole sulfonamides as HIV protease inhibitors, their use, pharmaceutical composition and method for inhibiting retroviral replication |
| CN100448444C (en) | 2001-12-21 | 2009-01-07 | 泰博特克药品有限公司 | Sulfonamide Broad-spectrum HIV Protease Inhibitors Containing Heterocyclic Substituted Phenyl |
| MY142238A (en) | 2002-03-12 | 2010-11-15 | Tibotec Pharm Ltd | Broadspectrum substituted benzimidazole sulfonamide hiv protease inhibitors |
| ATE371652T1 (en) | 2002-05-17 | 2007-09-15 | Tibotec Pharm Ltd | SUBSTITUTED BENZISOXAZOLE SULFONAMIDE WITH BROAD-BAND HIV PROTEASE INHIBITING EFFECT |
| AU2003262574B2 (en) | 2002-08-14 | 2009-07-09 | Tibotec Pharmaceuticals Ltd. | Broadspectrum substituted oxindole sulfonamide HIV protease inhibitors |
| US8193227B2 (en) | 2003-12-11 | 2012-06-05 | Abbott Laboratories | HIV protease inhibiting compounds |
| US20050131042A1 (en) * | 2003-12-11 | 2005-06-16 | Flentge Charles A. | HIV protease inhibiting compounds |
| DE602004012891T2 (en) | 2003-12-18 | 2009-04-09 | Janssen Pharmaceutica N.V. | PYRIDO AND PYRIMIDOPYRIMIDIN DERIVATIVES AS ANTI-PROLIFERATIVE AGENTS |
| WO2006024491A1 (en) | 2004-08-30 | 2006-03-09 | Interstitial Therapeutics | Methods and compositions for the treatment of cell proliferation |
| CA2588517A1 (en) | 2004-12-01 | 2006-06-08 | Devgen N.V. | 5-carboxamido substituted thiazole derivatives that interact with ion channels, in particular with ion channels from the kv family |
| NI200700147A (en) | 2004-12-08 | 2019-05-10 | Janssen Pharmaceutica Nv | QUINAZOLINE DERIVATIVES KINE INHIBITORS TARGETING MULTIP |
| MX2007006534A (en) | 2004-12-17 | 2007-07-25 | Devgen Nv | Nematicidal compositions. |
| JP2008533017A (en) * | 2005-03-11 | 2008-08-21 | スミスクライン ビーチャム コーポレーション | HIV protease inhibitor |
| AR053845A1 (en) | 2005-04-15 | 2007-05-23 | Tibotec Pharm Ltd | 5-TIAZOLILMETIL [(1S, 2R) -3 - [[(2-AMINO-6-BENZOXAZOLIL) SULFONIL)] (2-METHYLPROPIL) AMINO] -2-HYDROXY-1- (PHENYLMETIL) PROPIL] CARBAMATE AS A PHARMACY IMPROVER METABOLIZED BY THE CYCROCHROME P450 |
| WO2007045496A1 (en) | 2005-10-21 | 2007-04-26 | Universiteit Antwerpen | Novel urokinase inhibitors |
| TWI385173B (en) | 2005-11-28 | 2013-02-11 | Tibotec Pharm Ltd | Substituted aminophenylsulfonamide compounds as hiv protease inhibitor |
| AR058238A1 (en) | 2005-11-28 | 2008-01-23 | Tibotec Pharm Ltd | COMPOUNDS AND DERIVATIVES OF AMINOPHENYL SULFONAMIDE REPLACED AS HIV PROTEASE INHIBITORS |
| SI2049506T2 (en) | 2006-07-07 | 2024-07-31 | Gilead Sciences, Inc. | Modulators of pharmacokinetic properties of therapeutics |
| DK2044084T3 (en) | 2006-07-13 | 2016-05-09 | Janssen Pharmaceutica Nv | MTKI-quinazoline derivatives |
| AU2007294124A1 (en) | 2006-09-08 | 2008-03-13 | Bayer Schering Pharma Aktiengesellschaft | Compounds and methods for 18F labeled agents |
| EP4403221A3 (en) * | 2007-02-23 | 2024-10-09 | Gilead Sciences, Inc. | Modulators of pharmacokinetic properties of therapeutics |
| DK2185562T3 (en) | 2007-07-27 | 2016-02-22 | Janssen Pharmaceutica Nv | PYRROLOPYRIMIDINES SUITABLE FOR TREATING PROLIFERATIVE DISEASES |
| EP2053033A1 (en) | 2007-10-26 | 2009-04-29 | Bayer Schering Pharma AG | Compounds for use in imaging, diagnosing and/or treatment of diseases of the central nervous system or of tumors |
| EP2100900A1 (en) | 2008-03-07 | 2009-09-16 | Universitätsspital Basel | Bombesin analog peptide antagonist conjugates |
| DK2283024T3 (en) | 2008-03-10 | 2013-08-05 | Janssen Pharmaceutica Nv | 4-aryl-2-aniline pyrimidines as PLK kinase inhibitors |
| EP2116236A1 (en) | 2008-04-21 | 2009-11-11 | Université de Mons-Hainaut | Bisbenzamidine derivatives for use as antioxidant |
| EP2501431B1 (en) | 2009-11-19 | 2020-01-08 | Wellinq Medical B.V. | Narrow profile composition-releasing expandable medical balloon catheter |
| WO2011141515A1 (en) | 2010-05-14 | 2011-11-17 | Bayer Pharma Aktiengesellschaft | Diagnostic agents for amyloid beta imaging |
| US8785648B1 (en) | 2010-08-10 | 2014-07-22 | The Regents Of The University Of California | PKC-epsilon inhibitors |
| GB201019043D0 (en) | 2010-11-10 | 2010-12-22 | Protea Biopharma N V | Use of 2',5'-oligoadenylate derivative compounds |
| EP2700396A3 (en) | 2012-06-20 | 2015-04-29 | Sylphar Nv | Strip for the delivery of oral care compositions |
| WO2014059034A2 (en) | 2012-10-09 | 2014-04-17 | President And Fellows Of Harvard College | Nad biosynthesis and precursors for the treatment and prevention of cancer and proliferation |
| EP3180003B1 (en) | 2014-07-01 | 2022-01-12 | The Regents of the University of California | Pkc-epsilon inhibitors |
| WO2016083490A1 (en) | 2014-11-27 | 2016-06-02 | Remynd Nv | Compounds for the treatment of amyloid-associated diseases |
| JP7193232B2 (en) | 2015-04-28 | 2022-12-20 | ニューサウス イノベーションズ ピーティーワイ リミテッド | Targeting NAD+ to Treat Chemo- and Radiation-Induced Cognitive Dysfunction, Neuropathy and Inactivity |
| DK3621963T3 (en) | 2017-05-11 | 2024-04-15 | Remynd N V | Compounds for the treatment of epilepsy, neurodegenerative disorders and other CNS disorders |
| EP3634407A1 (en) | 2017-05-11 | 2020-04-15 | Remynd N.V. | Inhibitors of pde6delta for use in the prevention and/or treatment of epilepsy and/or neurodegenerative disorders |
| AU2021225333A1 (en) | 2020-02-24 | 2022-08-11 | Katholieke Universiteit Leuven | Pyrrolopyridine and imidazopyridine antiviral compounds |
| EP4267579A1 (en) | 2020-12-22 | 2023-11-01 | Luxembourg Institute of Health (LIH) | Conolidine analogues as selective ackr3 modulators for the treatment of cancer and cardiovascular diseases |
| EP4301369A1 (en) | 2021-03-04 | 2024-01-10 | Universiteit Antwerpen | Quinazolin-4-one and thieno[2,3-d]pyrimidin-4-one inhibitors of erbb4 (her4) for use in the treatment of cancer |
| CN117500772A (en) | 2021-05-31 | 2024-02-02 | 泰利克斯制药(创新)私人有限公司 | Improved prostate specific membrane antigen targeted radiopharmaceuticals and uses thereof |
| EP4387629A1 (en) | 2021-08-18 | 2024-06-26 | Katholieke Universiteit Leuven KU Leuven Research & Development | 6-substituted- and 6,7-disubstituted-7-deazapurine ribonucleoside analogues |
| EP4405357A1 (en) | 2021-09-23 | 2024-07-31 | Katholieke Universiteit Leuven KU Leuven Research & Development | Ribonucleoside analogues against -sars-cov-2 |
| WO2023241799A1 (en) | 2022-06-15 | 2023-12-21 | Université Libre de Bruxelles | Flavanols for use in the treatment of retroviral infections |
| WO2024062043A1 (en) | 2022-09-21 | 2024-03-28 | Universiteit Antwerpen | Substituted phenothiazines as ferroptosis inhibitors |
| CN121001993A (en) | 2023-02-24 | 2025-11-21 | 鲁汶天主教大学 | Nuclear transport modulator |
| WO2025104221A1 (en) | 2023-11-15 | 2025-05-22 | Université Libre de Bruxelles | Uses of protein tyrosine phosphatase receptor kappa inhibitors |
| WO2025157901A1 (en) | 2024-01-26 | 2025-07-31 | Aneurotech Bv | Piperidine carboxamide fatty acid prodrugs |
| WO2026013165A1 (en) | 2024-07-10 | 2026-01-15 | Université Libre de Bruxelles | Combination of ship2 inhibitor and plk1 inhibitor for use in the treatment of cancer |
| EP4678627A1 (en) | 2024-07-10 | 2026-01-14 | Universiteit Antwerpen | Novel ferroptosis inhibitors |
| EP4678633A1 (en) | 2024-07-10 | 2026-01-14 | Universiteit Antwerpen | Novel ferroptosis inhibitors |
| WO2026013198A1 (en) | 2024-07-10 | 2026-01-15 | Universiteit Antwerpen | Oxazole derivatives for oral administration |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5723490A (en) * | 1992-09-08 | 1998-03-03 | Vertex Pharmaceuticals Incorporated | THF-containing sulfonamide inhibitors of aspartyl protease |
| IS2334B (en) * | 1992-09-08 | 2008-02-15 | Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) | Aspartyl protease inhibitor of a new class of sulfonamides |
| AU7669794A (en) * | 1993-08-24 | 1995-03-21 | G.D. Searle & Co. | Hydroxyethylamino sulphonamides useful as retroviral protease inhibitors |
| ES2139195T3 (en) * | 1994-03-07 | 2000-02-01 | Vertex Pharma | SULFONAMID DERIVATIVES AS ASPARTIL-PROTEASE INHIBITORS. |
-
1998
- 1998-12-23 WO PCT/US1998/027403 patent/WO1999033792A2/en not_active Ceased
- 1998-12-23 AU AU20102/99A patent/AU2010299A/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO1999033792A3 (en) | 1999-09-16 |
| WO1999033792A2 (en) | 1999-07-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK6 | Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase |