JP2009543867A - 抗hiv剤としての1−ヒドロキシナフチリジン化合物 - Google Patents
抗hiv剤としての1−ヒドロキシナフチリジン化合物 Download PDFInfo
- Publication number
- JP2009543867A JP2009543867A JP2009520780A JP2009520780A JP2009543867A JP 2009543867 A JP2009543867 A JP 2009543867A JP 2009520780 A JP2009520780 A JP 2009520780A JP 2009520780 A JP2009520780 A JP 2009520780A JP 2009543867 A JP2009543867 A JP 2009543867A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkylene
- phenyl
- substituted
- optionally
- 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.)
- Withdrawn
Links
- 0 **C(C(N1O)=O)=C(*)c2c1nc(*)c(*)c2* Chemical compound **C(C(N1O)=O)=C(*)c2c1nc(*)c(*)c2* 0.000 description 12
- NZTXHOBIMFXDEK-UHFFFAOYSA-N CCOC(C(C(N1O)=O)=C(c2cccc(-c3ccc(CN)cc3)c2)c2c1ncc(-c(cccc1)c1OC)c2)=O Chemical compound CCOC(C(C(N1O)=O)=C(c2cccc(-c3ccc(CN)cc3)c2)c2c1ncc(-c(cccc1)c1OC)c2)=O NZTXHOBIMFXDEK-UHFFFAOYSA-N 0.000 description 1
- UUYPZAIMTIWMAW-UHFFFAOYSA-N CN(C1CNCC1)C(C(C(N(c1c2cccn1)O)=O)=C2O)=O Chemical compound CN(C1CNCC1)C(C(C(N(c1c2cccn1)O)=O)=C2O)=O UUYPZAIMTIWMAW-UHFFFAOYSA-N 0.000 description 1
- NEELGKCJSWYRLI-UHFFFAOYSA-N CN1C(CC2)CCC2C1 Chemical compound CN1C(CC2)CCC2C1 NEELGKCJSWYRLI-UHFFFAOYSA-N 0.000 description 1
- WQQSNMVOPWWPOW-UHFFFAOYSA-N IN(CC(C1)C2)C1CC2NN(CC1[IH]N2CC(C3)C3C2)C2C1NCC2 Chemical compound IN(CC(C1)C2)C1CC2NN(CC1[IH]N2CC(C3)C3C2)C2C1NCC2 WQQSNMVOPWWPOW-UHFFFAOYSA-N 0.000 description 1
- KHFDDRGLYDEEQC-UHFFFAOYSA-N NCc(cc1)ccc1-c(cc1)ccc1C(c1c(N2O)ncc(F)c1)=C(c1ccccc1)C2=O Chemical compound NCc(cc1)ccc1-c(cc1)ccc1C(c1c(N2O)ncc(F)c1)=C(c1ccccc1)C2=O KHFDDRGLYDEEQC-UHFFFAOYSA-N 0.000 description 1
- ZQFQSEQXTVJHJO-UHFFFAOYSA-N NN1C(C2)COC2C1 Chemical compound NN1C(C2)COC2C1 ZQFQSEQXTVJHJO-UHFFFAOYSA-N 0.000 description 1
- NYIDBIWYWWPALZ-UHFFFAOYSA-N NN1CC(CC2)C2C1 Chemical compound NN1CC(CC2)C2C1 NYIDBIWYWWPALZ-UHFFFAOYSA-N 0.000 description 1
- KSRIHSGNEDIHGB-URHBZAFASA-N NN1[C@H](C2)C[C@@H]2C1 Chemical compound NN1[C@H](C2)C[C@@H]2C1 KSRIHSGNEDIHGB-URHBZAFASA-N 0.000 description 1
- ZCNIYTBWFZPYHX-UHFFFAOYSA-N OC(c1c(N2O)ncc(F)c1)=C(c1ccccc1)C2=O Chemical compound OC(c1c(N2O)ncc(F)c1)=C(c1ccccc1)C2=O ZCNIYTBWFZPYHX-UHFFFAOYSA-N 0.000 description 1
- RQVPJTRZRGQVEE-UHFFFAOYSA-N ON1c(nccc2)c2C(N(CC2)Cc(cc3)c2cc3C(NCc2ccccc2)=O)=CC1=O Chemical compound ON1c(nccc2)c2C(N(CC2)Cc(cc3)c2cc3C(NCc2ccccc2)=O)=CC1=O RQVPJTRZRGQVEE-UHFFFAOYSA-N 0.000 description 1
- QWXYKYKTZXLYHG-UHFFFAOYSA-N ON1c(nccc2)c2C(Nc2ccccc2)=CC1=O Chemical compound ON1c(nccc2)c2C(Nc2ccccc2)=CC1=O QWXYKYKTZXLYHG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- AIDS & HIV (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83141506P | 2006-07-17 | 2006-07-17 | |
| PCT/US2007/016052 WO2008010964A1 (en) | 2006-07-17 | 2007-07-13 | 1-hydroxy naphthyridine compounds as anti-hiv agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009543867A true JP2009543867A (ja) | 2009-12-10 |
| JP2009543867A5 JP2009543867A5 (https=) | 2010-08-12 |
Family
ID=38957074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009520780A Withdrawn JP2009543867A (ja) | 2006-07-17 | 2007-07-13 | 抗hiv剤としての1−ヒドロキシナフチリジン化合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20100056516A1 (https=) |
| EP (1) | EP2044068A4 (https=) |
| JP (1) | JP2009543867A (https=) |
| AU (1) | AU2007275816A1 (https=) |
| CA (1) | CA2657287A1 (https=) |
| WO (1) | WO2008010964A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013115265A1 (ja) * | 2012-01-31 | 2013-08-08 | 富山化学工業株式会社 | 抗hiv活性を有する複素環化合物 |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO2985B1 (ar) | 2006-12-20 | 2016-09-05 | Takeda Pharmaceuticals Co | مثبطات كينازmapk/erk |
| WO2011057989A1 (en) * | 2009-11-11 | 2011-05-19 | Basf Se | Heterocyclic compounds having herbicidal action |
| EP2632454A1 (en) * | 2010-10-29 | 2013-09-04 | Merck Sharp & Dohme Corp. | Hiv integrase inhibitors |
| FR2970967B1 (fr) | 2011-01-27 | 2013-02-15 | Pf Medicament | Derives de type azaindazole ou diazaindazole comme medicament |
| US20140369934A1 (en) | 2011-06-02 | 2014-12-18 | Massachusetts Institute Of Technology | dsRNA/DNA Hybrid Genome Replication Intermediate Of Metakaryotic Stem Cells |
| WO2013049332A1 (en) * | 2011-09-29 | 2013-04-04 | Infinity Pharmaceuticals, Inc. | Inhibitors of monoacylglycerol lipase and methods of their use |
| WO2013165898A2 (en) * | 2012-05-01 | 2013-11-07 | The Trustees Of The University Of Pennsylvania | Compositions and methods for inhibiting resolvases |
| EP2689779A1 (en) | 2012-07-27 | 2014-01-29 | Pierre Fabre Medicament | Derivatives of azaindazole or diazaindazole type for treating a cancer overexpressing trk |
| EP2689778A1 (en) | 2012-07-27 | 2014-01-29 | Pierre Fabre Medicament | Derivatives of azaindoles or diazaindoles for treating pain |
| WO2014102818A1 (en) * | 2012-12-24 | 2014-07-03 | Cadila Healthcare Limited | Novel quinolone derivatives |
| JP2016524607A (ja) * | 2013-05-16 | 2016-08-18 | ザ ユナイテッド ステイツ オブ アメリカ, アズ リプレゼンテッド バイ ザ セクレタリー, デパートメント オブ ヘルス アンド ヒューマン サービシーズ | Hiv−1インテグラーゼの薬物耐性株を阻害するための化合物 |
| EP3102576B8 (en) | 2014-02-03 | 2019-06-19 | Vitae Pharmaceuticals, LLC | Dihydropyrrolopyridine inhibitors of ror-gamma |
| ES2768694T3 (es) | 2014-09-19 | 2020-06-23 | Forma Therapeutics Inc | Composiciones de quinolinona pirimidinas como inhibidores de isocitrato dehidrogenasa mutante |
| WO2016044789A1 (en) | 2014-09-19 | 2016-03-24 | Forma Therapeutics, Inc. | Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors |
| US11008340B2 (en) | 2015-11-20 | 2021-05-18 | Vitae Pharmaceuticals, Llc | Modulators of ROR-gamma |
| CN105418609B (zh) * | 2015-12-31 | 2017-06-23 | 山东大学 | 4‑(1,2,3‑三氮唑取代苯胺基)‑吡啶骈嘧啶酮衍生物及其制备方法与应用 |
| TW202220968A (zh) | 2016-01-29 | 2022-06-01 | 美商維它藥物有限責任公司 | ROR-γ調節劑 |
| JP2020528904A (ja) | 2017-07-24 | 2020-10-01 | ヴァイティー ファーマシューティカルズ,エルエルシー | RORγの阻害剤 |
| WO2019018975A1 (en) | 2017-07-24 | 2019-01-31 | Vitae Pharmaceuticals, Inc. | INHIBITORS OF ROR GAMMA |
| US11013734B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation |
| US11013733B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1) |
| US10532047B2 (en) | 2018-05-16 | 2020-01-14 | Forma Therapeutics, Inc. | Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile |
| US11311527B2 (en) | 2018-05-16 | 2022-04-26 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1) |
| WO2019222553A1 (en) | 2018-05-16 | 2019-11-21 | Forma Therapeutics, Inc. | Inhibiting mutant idh-1 |
| WO2020197991A1 (en) | 2019-03-22 | 2020-10-01 | Gilead Sciences, Inc. | Bridged tricyclic carbamoylpyridone compounds and their pharmaceutical use |
| TWI902729B (zh) | 2019-11-28 | 2025-11-01 | 日商鹽野義製藥股份有限公司 | 以組合整合酶阻礙劑及抗hiv藥為特徵之hiv感染症的預防及治療用醫藥 |
| IL295677B1 (en) | 2020-02-24 | 2026-04-01 | Gilead Sciences Inc | Tetracyclic compounds for the treatment of HIV infection |
| CA3192145A1 (en) | 2020-09-30 | 2022-04-07 | Gilead Sciences, Inc. | Bridged tricyclic carbamoylpyridone compounds and uses thereof |
| FI4196479T3 (fi) | 2021-01-19 | 2024-01-17 | Gilead Sciences Inc | Substituoituja pyridotriatsiiniyhdisteitä ja niiden käyttöjä |
| TWI856796B (zh) | 2022-04-06 | 2024-09-21 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
| KR20250128292A (ko) | 2022-09-26 | 2025-08-27 | 엣지와이즈 테라퓨틱스, 인크. | 1,4-디하이드로퀴나졸리논 화합물 및 이의 용도 |
| WO2024206345A1 (en) | 2023-03-27 | 2024-10-03 | Edgewise Therapeutics, Inc. | Quinazoline dione compounds and uses thereof |
| CN121194963A (zh) * | 2023-03-27 | 2025-12-23 | 艾知怀斯治疗学公司 | 喹啉酮酰胺类化合物及其用途 |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5527819A (en) * | 1991-09-06 | 1996-06-18 | Merck & Co., Inc. | Inhibitors of HIV reverse transcriptase |
| GB9420168D0 (en) * | 1994-10-06 | 1994-11-23 | Boots Co Plc | Therapeutic agents |
| US6262055B1 (en) * | 1998-06-03 | 2001-07-17 | Merck & Co., Inc. | HIV integrase inhibitors |
| US6306891B1 (en) * | 1998-06-03 | 2001-10-23 | Merck & Co., Inc. | HIV integrase inhibitors |
| US6380249B1 (en) * | 1998-06-03 | 2002-04-30 | Merck & Co., Inc. | HIV integrase inhibitors |
| JP2003503386A (ja) * | 1999-06-25 | 2003-01-28 | メルク エンド カムパニー インコーポレーテッド | 1−(芳香族またはヘテロ芳香族置換)−3−(ヘテロ芳香族置換)−1,3−プロパンジオン類およびそれの使用 |
| JP2004517860A (ja) * | 2000-10-12 | 2004-06-17 | メルク エンド カムパニー インコーポレーテッド | Hivインテグラーゼ阻害薬として有用なアザ−およびポリアザ−ナフタレニルカルボキサミド類 |
| US6919351B2 (en) * | 2000-10-12 | 2005-07-19 | Merck & Co., Inc. | Aza-and polyaza-naphthalenyl-carboxamides useful as HIV integrase inhibitors |
| CA2425440C (en) * | 2000-10-12 | 2010-04-13 | Merck & Co., Inc. | Aza- and polyaza-naphthalenyl carboxamides useful as hiv integrase inhibitors |
| JP2004513134A (ja) * | 2000-10-12 | 2004-04-30 | メルク エンド カムパニー インコーポレーテッド | Hivインテグラーゼ阻害薬として有用なアザ−およびポリアザ−ナフタレニルケトン類 |
| BR0211750A (pt) * | 2001-08-10 | 2004-10-13 | Shionogi & Co | Agente antiviral |
| NZ533057A (en) * | 2001-10-26 | 2005-11-25 | Angeletti P Ist Richerche Bio | N-substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase |
| EP1441734B1 (en) * | 2001-10-26 | 2007-02-28 | Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. | Dihydroxypyrimidine carboxamide inhibitors of hiv integrase |
| EP1467970B1 (en) * | 2002-01-17 | 2007-08-22 | Merck & Co., Inc. | Hydroxynaphthyridinone carboxamides useful as hiv integrase inhibitors |
| US7109186B2 (en) * | 2002-07-09 | 2006-09-19 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| EP1541558B1 (en) * | 2002-08-13 | 2008-08-13 | Shionogi & Co., Ltd. | Heterocyclic compounds having hiv integrase inhibitory activity |
| US7902203B2 (en) * | 2002-11-01 | 2011-03-08 | Abbott Laboratories, Inc. | Anti-infective agents |
| US20040162285A1 (en) * | 2002-11-01 | 2004-08-19 | Pratt John K. | Anti-infective agents |
| US7501503B2 (en) * | 2002-12-31 | 2009-03-10 | Mcgill University | Compositions and methods for inhibiting RNase H activity of retroid reverse transcriptase |
| US20050203156A1 (en) * | 2004-03-12 | 2005-09-15 | Wyeth | Hydantoins having RNase modulatory activity |
| US7553967B2 (en) * | 2004-03-12 | 2009-06-30 | Wyeth | 1,2-Dihydroquinoline derivatives and method for using the same to treat HIV infections |
| WO2005090299A2 (en) * | 2004-03-12 | 2005-09-29 | Wyeth | Carbamates as hiv anti-viral agents |
-
2007
- 2007-07-13 US US12/373,907 patent/US20100056516A1/en not_active Abandoned
- 2007-07-13 CA CA002657287A patent/CA2657287A1/en not_active Abandoned
- 2007-07-13 JP JP2009520780A patent/JP2009543867A/ja not_active Withdrawn
- 2007-07-13 AU AU2007275816A patent/AU2007275816A1/en not_active Abandoned
- 2007-07-13 WO PCT/US2007/016052 patent/WO2008010964A1/en not_active Ceased
- 2007-07-13 EP EP07796862A patent/EP2044068A4/en not_active Withdrawn
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013115265A1 (ja) * | 2012-01-31 | 2013-08-08 | 富山化学工業株式会社 | 抗hiv活性を有する複素環化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2044068A4 (en) | 2010-07-21 |
| EP2044068A1 (en) | 2009-04-08 |
| CA2657287A1 (en) | 2008-01-24 |
| AU2007275816A1 (en) | 2008-01-24 |
| US20100056516A1 (en) | 2010-03-04 |
| WO2008010964A1 (en) | 2008-01-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2009543867A (ja) | 抗hiv剤としての1−ヒドロキシナフチリジン化合物 | |
| US7619086B2 (en) | HIV integrase inhibitors | |
| EP3414234B1 (en) | Bruton's tyrosine kinase inhibitors | |
| JP6215338B2 (ja) | キナーゼモジュレーターとして有用な二環式ヘテロ環置換ピリジル化合物 | |
| AU2014347275B2 (en) | Alkyl-amide-substituted pyridyl compounds useful as modulators of IL-12, IL-23 and/or IFNalpha responses | |
| EP2802577B1 (en) | Triazolyl-substituted pyridyl compounds useful as kinase inhibitors | |
| JP4625838B2 (ja) | Hivインテグラーゼ阻害薬 | |
| US20090099168A1 (en) | HIV Integrase inhibitors | |
| JP2006506352A (ja) | Hivインテグラーゼ阻害剤として有用なジヒドロキシピリドピラジン−1,6−ジオン化合物 | |
| JP2019508467A (ja) | 癌治療用の2−シアノイソインドリン誘導体 | |
| HUP0302367A2 (hu) | HIV Integráz inhibitorokként hasznos aza- és poliazanaftalenil-karboxamidok, ezeket tartalmazó gyógyszerkészítmények | |
| US10301306B2 (en) | Substituted dihydro-1H-pyrrolo[3,2-c]pyridin-4(5H)-ones as RIPK3 inhibitors | |
| JP2007519735A (ja) | Hivインテグラーゼ阻害剤として有用であるn−ベンジル−3,4−ジヒドロキシピリジン−2−カルボキサミド及びn−ベンジル−2,3−ジヒドロキシピリジン−4−カルボキサミド化合物 | |
| JP2008504367A (ja) | ピロロトリアジンキナーゼ阻害剤 | |
| KR20200094168A (ko) | 할로-알릴아민 ssao/vap-1 억제제 및 그의 용도 | |
| CA2607151C (en) | Hiv integrase inhibitors | |
| EP4337649A1 (en) | Substituted heterocyclic compounds | |
| CN112521386B (zh) | 具有抗病毒作用的多环吡啶酮化合物及其药物组合和用途 | |
| JP4494020B2 (ja) | Hivインテグラーゼ阻害剤として有用なn−(置換ベンジル)−8−ヒドロキシ−1,6−ナフチリジン−7−カルボキサミド | |
| CN100577663C (zh) | 稠合杂环型激酶抑制剂 | |
| JP2024545235A (ja) | 複素芳香族化合物、その製造方法及び使用 | |
| TWI870185B (zh) | 雙環類化合物及其製備方法和應用 | |
| CA3008653C (en) | Bruton's tyrosine kinase inhibitors | |
| TW202428252A (zh) | 類Cdc激酶之雜環抑制劑 | |
| HU214595B (hu) | Eljárás 5,11-dihidro-6H-dipirido [3,2-b:2',3'-e][1,4] diazepinek és ezeket tartalmazó gyógyszerkészítmények előállítására |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100623 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20100623 |
|
| A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20111205 |