AU2002212598A1 - Pyridinone and pyridinethione derivatives having hiv inhibiting properties - Google Patents
Pyridinone and pyridinethione derivatives having hiv inhibiting propertiesInfo
- Publication number
- AU2002212598A1 AU2002212598A1 AU2002212598A AU1259802A AU2002212598A1 AU 2002212598 A1 AU2002212598 A1 AU 2002212598A1 AU 2002212598 A AU2002212598 A AU 2002212598A AU 1259802 A AU1259802 A AU 1259802A AU 2002212598 A1 AU2002212598 A1 AU 2002212598A1
- Authority
- AU
- Australia
- Prior art keywords
- sub
- sup
- inhibiting properties
- pyridinone
- alkyl
- 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
- 230000002401 inhibitory effect Effects 0.000 title abstract 2
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 title 1
- WHMDPDGBKYUEMW-UHFFFAOYSA-N pyridine-2-thiol Chemical class SC1=CC=CC=N1 WHMDPDGBKYUEMW-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 2
- 125000001475 halogen functional group Chemical group 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
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- 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
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- AIDS & HIV (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Molecular Biology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Abstract
The present invention is concerned among others with compounds of formula (1), the N-oxides, the pharmaceutically acceptable addition salts, the quaternary amines and stereochemically isomeric forms thereof, wherein Q is halo, C<SUB>1-6 </SUB>alkyl or C<SUB>2-6 </SUB>alkenyl; X is (a-2) with q and r being O and Z being O, S or SO; R<SUB>1 </SUB>is aryl; R<SUB>2 </SUB>is selected from formyl; C<SUB>1-6</SUB>alkyloxycarbonylalkyl; Het<SUP>2</SUP>; Het<SUP>2</SUP>C<SUB>1-6</SUB>alkyl, C<SUB>1-6</SUB>alkylthio; C<SUB>1-6</SUB>alkyl optionally substituted with one or two substituents each independently selected from hydroxy, and halo; R<SUB>3 </SUB>is selected from formyl; C<SUB>1-6</SUB>alkyl optionally substituted with one or two C<SUB>1-6</SUB>alkyloxy; R<SUB>4 </SUB>is hydrogen, with HTV inhibiting properties
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00402583.9 | 2000-09-19 | ||
| EP00402583 | 2000-09-19 | ||
| PCT/IB2001/002082 WO2002024650A2 (en) | 2000-09-19 | 2001-09-18 | Pyridinone and pyridinethione derivatives having hiv inhibiting properties |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2002212598A1 true AU2002212598A1 (en) | 2002-04-02 |
Family
ID=8173871
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2002212598A Abandoned AU2002212598A1 (en) | 2000-09-19 | 2001-09-18 | Pyridinone and pyridinethione derivatives having hiv inhibiting properties |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7115608B2 (en) |
| EP (1) | EP1318995B1 (en) |
| JP (1) | JP2004509867A (en) |
| AT (1) | ATE319706T1 (en) |
| AU (1) | AU2002212598A1 (en) |
| DE (1) | DE60117839T2 (en) |
| WO (1) | WO2002024650A2 (en) |
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| US20040235761A1 (en) * | 2001-08-14 | 2004-11-25 | Yousuke Furuta | Novel virus proliferaton inhibition/virucidal method and novel pyradine nucleotide/pyradine nucleoside analogue |
| CA2824106A1 (en) * | 2003-08-29 | 2005-03-10 | Ono Pharmaceutical Co., Ltd. | Compound capable of binding s1p receptor and pharmaceutical use thereof |
| EP1516873A1 (en) * | 2003-09-22 | 2005-03-23 | Facultés Universitaires Notre-Dame de la Paix | 2-pyridinone derivatives, having HIV inhibiting properties |
| WO2006012624A2 (en) * | 2004-07-21 | 2006-02-02 | The Regents Of The University Of California | Mechanism-based crosslinkers |
| CN103102303B (en) * | 2004-12-31 | 2015-10-28 | 雷迪博士实验室有限公司 | As the benzyl amine derivative of CETP inhibitor |
| US7728013B2 (en) | 2005-05-10 | 2010-06-01 | Intermune, Inc. | Method of modulating stress-activated protein kinase system |
| DE602006020293D1 (en) * | 2005-08-29 | 2011-04-07 | Vertex Pharma | 3,5-DISUBSTITUTED PYRID-2-ONE, WHICH ARE USES AS INHIBITORS OF THE TEC FAMILY OF NON-RECEPTOR TYROSINE KINASES |
| JP5539216B2 (en) * | 2007-11-20 | 2014-07-02 | メルク・シャープ・アンド・ドーム・コーポレーション | Non-nucleoside reverse transcriptase inhibitors |
| CL2009000949A1 (en) * | 2008-04-21 | 2010-12-24 | Novartis Ag | Compounds derived from 1,2,3,5-tetrahydro-indolizine, 6,7,8,9-tetrahydro-4h-quinolizine substituted, inhibitors of mek kinase activity; its pharmaceutical composition; its use for the treatment of hyperproliferative diseases, such as cancer and inflammation. |
| CA2722159C (en) | 2008-04-24 | 2016-04-05 | Newlink Genetics Corporation | Substituted phenylimidazole compounds and their use as ido inhibitors |
| ES2567283T3 (en) | 2008-06-03 | 2016-04-21 | Intermune, Inc. | Compounds and methods to treat inflammatory and fibrotic disorders |
| WO2010026075A1 (en) * | 2008-09-04 | 2010-03-11 | F. Hoffmann-La Roche Ag | Pyridine derivatives as inhibitors of hiv-i reverse transcriptase |
| CN103288719A (en) * | 2012-03-05 | 2013-09-11 | 苏州欧凯医药技术有限公司 | Synthesis of non-nucleoside HIV (human immunodeficiency virus) inhibitor pyridone lead |
| WO2014043252A2 (en) | 2012-09-11 | 2014-03-20 | Rutgers, The State University Of New Jersey | Therapeutic hydroxypyridinones, hydroxypyrimidinones and hydroxypyridazinones |
| AR092742A1 (en) | 2012-10-02 | 2015-04-29 | Intermune Inc | ANTIFIBROTIC PYRIDINONES |
| TW201441193A (en) | 2012-12-06 | 2014-11-01 | Kyowa Hakko Kirin Co Ltd | Pyridone compound |
| JP6466461B2 (en) | 2014-02-03 | 2019-02-06 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | Dihydropyrrolopyridine inhibitors of ROR gamma |
| CA2943363A1 (en) | 2014-04-02 | 2015-10-08 | Intermune, Inc. | Anti-fibrotic pyridinones |
| EP3180335B1 (en) | 2014-08-11 | 2021-05-05 | Angion Biomedica Corporation | Cytochrome p450 inhibitors and uses thereof |
| AU2015333610B2 (en) | 2014-10-14 | 2019-11-07 | Vitae Pharmaceuticals, Llc | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| US9663515B2 (en) | 2014-11-05 | 2017-05-30 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| US9845308B2 (en) | 2014-11-05 | 2017-12-19 | Vitae Pharmaceuticals, Inc. | Isoindoline inhibitors of ROR-gamma |
| US10287282B2 (en) | 2014-12-31 | 2019-05-14 | Angion Biomedica Corp. | Methods and agents for treating disease |
| WO2016185026A1 (en) * | 2015-05-20 | 2016-11-24 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical composition for modulation polarization and activation of macrophages |
| ES2856931T3 (en) | 2015-08-05 | 2021-09-28 | Vitae Pharmaceuticals Llc | ROR-gamma modulators |
| BR112018010018A2 (en) | 2015-11-20 | 2018-11-21 | Vitae Pharmaceuticals Inc | ror-gamma modulators |
| US9481674B1 (en) | 2016-06-10 | 2016-11-01 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| CN106279011A (en) * | 2016-08-16 | 2017-01-04 | 成都百事兴科技实业有限公司 | A kind of preparation method of 2,4 dihydroxy 6 methylnicotinic acid ethyl esters |
| WO2018125983A1 (en) | 2016-12-30 | 2018-07-05 | Mitobridge, Inc. | Oxopyridine derivatives useful as aminocarboxymuconate semialdehyde decarboxylase (acmsd) inhibitors |
| WO2019018975A1 (en) | 2017-07-24 | 2019-01-31 | Vitae Pharmaceuticals, Inc. | Inhibitors of ror gamma |
| MX2020000887A (en) | 2017-07-24 | 2020-07-22 | Vitae Pharmaceuticals Llc | Inhibitors of rorï. |
| CN113234084B (en) * | 2021-05-18 | 2023-05-05 | 云南民族大学 | Compound with anti-rotavirus activity in Meadowrue of Crane celebration and preparation method thereof |
| AU2023276599A1 (en) | 2022-05-25 | 2024-12-05 | Imagenebio, Inc. | Mek inhibitors and uses thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4017499A (en) * | 1976-04-05 | 1977-04-12 | Sandoz, Inc. | 6H(1)-Benzopyrano(3,2-c)quinolines |
| DE3406329A1 (en) * | 1984-02-22 | 1985-08-22 | Merck Patent Gmbh, 6100 Darmstadt | PYRIDONE |
| IL98526A0 (en) * | 1990-06-18 | 1992-07-15 | Merck & Co Inc | Pyridones,processes for their preparation and pharmaceutical compositions containing them |
| FR2737496B1 (en) * | 1995-07-31 | 1997-12-19 | Centre Nat Rech Scient | 4-ARYL-THIO-PYRIDIN-2 (1H) -ONES, MEDICAMENTS CONTAINING THEM, AND USES THEREOF IN THE TREATMENT OF HIV-1 AND 2-RELATED DISEASES |
| DE19544098A1 (en) * | 1995-11-27 | 1997-05-28 | Hoechst Schering Agrevo Gmbh | Cycloalkylmethyl and cycloalkylidenemethyl pyridines, processes for their preparation, compositions containing them and their use as pesticides and fungicides |
| DE19613591A1 (en) * | 1996-04-04 | 1997-10-09 | Hoechst Ag | Substituted quinoline derivatives, process for their preparation and their use |
| NZ335992A (en) * | 1996-12-05 | 2001-09-28 | Amgen Inc | Substituted pyrimidinone and pyridone compounds and methods of use |
| DE19732330C2 (en) * | 1997-07-28 | 2001-04-19 | Koenig & Bauer Ag | Drive for a printing unit |
| DE19755316C2 (en) * | 1997-12-12 | 1999-10-07 | Koenig & Bauer Ag | Drive for cylinders of a printing unit |
| US6451822B1 (en) * | 1998-04-27 | 2002-09-17 | Centre National De La Recherche Scientifique | 3-(Amino- or aminoalkyl)pyridinone derivatives and their use for the treatment of HIV related diseases |
| CA2333643A1 (en) * | 1998-06-30 | 2000-01-06 | James D. Rodgers | Substituted quinolin-2(1h)-ones useful as hiv reverse transcriptase inhibitors |
| GB9930061D0 (en) * | 1999-12-20 | 2000-02-09 | Glaxo Group Ltd | Quinolone compounds for use in treating viral infections |
| EP1318914B1 (en) * | 2000-09-20 | 2012-08-15 | Koenig & Bauer Aktiengesellschaft | Method for operating a printing unit. |
-
2001
- 2001-09-18 EP EP01980812A patent/EP1318995B1/en not_active Expired - Lifetime
- 2001-09-18 DE DE60117839T patent/DE60117839T2/en not_active Expired - Lifetime
- 2001-09-18 JP JP2002529063A patent/JP2004509867A/en active Pending
- 2001-09-18 AT AT01980812T patent/ATE319706T1/en not_active IP Right Cessation
- 2001-09-18 US US10/380,784 patent/US7115608B2/en not_active Expired - Fee Related
- 2001-09-18 WO PCT/IB2001/002082 patent/WO2002024650A2/en not_active Ceased
- 2001-09-18 AU AU2002212598A patent/AU2002212598A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1318995B1 (en) | 2006-03-08 |
| WO2002024650B1 (en) | 2002-11-14 |
| DE60117839D1 (en) | 2006-05-04 |
| WO2002024650A2 (en) | 2002-03-28 |
| US7115608B2 (en) | 2006-10-03 |
| DE60117839T2 (en) | 2006-11-23 |
| EP1318995A2 (en) | 2003-06-18 |
| WO2002024650A3 (en) | 2002-08-08 |
| JP2004509867A (en) | 2004-04-02 |
| ATE319706T1 (en) | 2006-03-15 |
| US20040229847A1 (en) | 2004-11-18 |
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