JP2012502099A - C型肝炎の治療のための化合物 - Google Patents
C型肝炎の治療のための化合物 Download PDFInfo
- Publication number
- JP2012502099A JP2012502099A JP2011526911A JP2011526911A JP2012502099A JP 2012502099 A JP2012502099 A JP 2012502099A JP 2011526911 A JP2011526911 A JP 2011526911A JP 2011526911 A JP2011526911 A JP 2011526911A JP 2012502099 A JP2012502099 A JP 2012502099A
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- alkyl
- phenyl
- hydrogen
- fluorophenyl
- 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.)
- Pending
Links
- 0 *C([C@@]1C=CC=C)=C(*)OC1N Chemical compound *C([C@@]1C=CC=C)=C(*)OC1N 0.000 description 1
- VTGBINOKFZLCJS-UHFFFAOYSA-N CC(C)(C)OC(N(C)C(c1c(cc(cc2F)-c3cc(C(NC4(CC4)c4ccccc4)=O)ccc3C)[n]2nc1-c(cc1)ccc1F)=O)=O Chemical compound CC(C)(C)OC(N(C)C(c1c(cc(cc2F)-c3cc(C(NC4(CC4)c4ccccc4)=O)ccc3C)[n]2nc1-c(cc1)ccc1F)=O)=O VTGBINOKFZLCJS-UHFFFAOYSA-N 0.000 description 1
- QRNYKQCRXWPCHA-UHFFFAOYSA-N CC(C)(c1ccccc1)NC(c1cc(-c2cc3c(C(NC)=O)c(-c(cc4)ccc4F)n[n]3cc2)ccc1)=O Chemical compound CC(C)(c1ccccc1)NC(c1cc(-c2cc3c(C(NC)=O)c(-c(cc4)ccc4F)n[n]3cc2)ccc1)=O QRNYKQCRXWPCHA-UHFFFAOYSA-N 0.000 description 1
- WTDWVLJJJOTABN-UHFFFAOYSA-N CNC(c1c(-c(cc2)ccc2F)[o]c2cc(N(CCO)S(C)(=O)=O)c(C3CC3)cc12)=O Chemical compound CNC(c1c(-c(cc2)ccc2F)[o]c2cc(N(CCO)S(C)(=O)=O)c(C3CC3)cc12)=O WTDWVLJJJOTABN-UHFFFAOYSA-N 0.000 description 1
- IQSYNOOLRSWYAI-UHFFFAOYSA-N CNC(c1c(-c(cc2)ccc2F)nc(cc2)[n]1cc2Br)=O Chemical compound CNC(c1c(-c(cc2)ccc2F)nc(cc2)[n]1cc2Br)=O IQSYNOOLRSWYAI-UHFFFAOYSA-N 0.000 description 1
- LHWMPGPGIQHVJQ-UHFFFAOYSA-N CNC(c1c(cc(C2CC2)c(N(CCO)S(C)(=O)=O)c2)[n]2nc1-c(cc1)ccc1F)=O Chemical compound CNC(c1c(cc(C2CC2)c(N(CCO)S(C)(=O)=O)c2)[n]2nc1-c(cc1)ccc1F)=O LHWMPGPGIQHVJQ-UHFFFAOYSA-N 0.000 description 1
- WSTBDZAIIROPEG-UHFFFAOYSA-N Cc(c(F)cc(C(NC1(CC1)c1ccccc1)=O)c1)c1-c(cc[n](c1c2C(NC)=O)nc2-c(cc2)ccc2F)c1F Chemical compound Cc(c(F)cc(C(NC1(CC1)c1ccccc1)=O)c1)c1-c(cc[n](c1c2C(NC)=O)nc2-c(cc2)ccc2F)c1F WSTBDZAIIROPEG-UHFFFAOYSA-N 0.000 description 1
- WOTRDFJSZNXCEF-UHFFFAOYSA-N Fc(cc1)ccc1-c1cc(cc(cn2)Br)c2[o]1 Chemical compound Fc(cc1)ccc1-c1cc(cc(cn2)Br)c2[o]1 WOTRDFJSZNXCEF-UHFFFAOYSA-N 0.000 description 1
- WSMGCHYPHRQNEG-UHFFFAOYSA-N Nc1cnccc1OCc1ccccc1 Chemical compound Nc1cnccc1OCc1ccccc1 WSMGCHYPHRQNEG-UHFFFAOYSA-N 0.000 description 1
- VSKUDEANWWGRES-UHFFFAOYSA-N OC(c1c(-c(cc2)ccc2F)nc(cc2)[n]1cc2Br)=O Chemical compound OC(c1c(-c(cc2)ccc2F)nc(cc2)[n]1cc2Br)=O VSKUDEANWWGRES-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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P31/04—Antibacterial agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes 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 carbon atoms of the hetero ring
- C07D333/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Gastroenterology & Hepatology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9600408P | 2008-09-11 | 2008-09-11 | |
| US61/096,004 | 2008-09-11 | ||
| PCT/US2009/055648 WO2010030538A2 (en) | 2008-09-11 | 2009-09-02 | Compounds for the treatment of hepatitis c |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012502099A true JP2012502099A (ja) | 2012-01-26 |
| JP2012502099A5 JP2012502099A5 (cg-RX-API-DMAC7.html) | 2012-10-11 |
Family
ID=41203516
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011526911A Pending JP2012502099A (ja) | 2008-09-11 | 2009-09-02 | C型肝炎の治療のための化合物 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US8198449B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2331502B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2012502099A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20110056537A (cg-RX-API-DMAC7.html) |
| CN (2) | CN103864783A (cg-RX-API-DMAC7.html) |
| AR (1) | AR073586A1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU2009291993A1 (cg-RX-API-DMAC7.html) |
| MX (1) | MX2011002471A (cg-RX-API-DMAC7.html) |
| TW (1) | TW201014855A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2010030538A2 (cg-RX-API-DMAC7.html) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016500705A (ja) * | 2012-11-05 | 2016-01-14 | バイエル・ファルマ・アクティエンゲゼルシャフト | アミノ置換イミダゾ[1,2−a]ピリジンカルボキサミドおよびその使用 |
| JP2016540745A (ja) * | 2013-11-12 | 2016-12-28 | ダウ アグロサイエンシィズ エルエルシー | 化合物をフッ素化するための方法 |
| JP2017529401A (ja) * | 2014-09-26 | 2017-10-05 | チャーンジョウ インシュヨン ファーマシューティカル カンパニー,リミティド | Ns4b阻害剤としてのベンゾフラン類似体 |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101774035B1 (ko) | 2009-10-30 | 2017-09-01 | 얀센 파마슈티카 엔.브이. | 이미다조[1,2―b]피리다진 유도체 및 PDE10 저해제로서의 그의 용도 |
| EP3257854A1 (en) * | 2009-11-05 | 2017-12-20 | University of Notre Dame du Lac | Imidazo[1,2-a]pyridine compounds, synthesis thereof, and methods of using same |
| FR2953520B1 (fr) * | 2009-12-04 | 2011-11-25 | Sanofi Aventis | Derives de diphenyl-pyrazolopyridines, leur preparation et leur application en therapeutique |
| US8324212B2 (en) * | 2010-02-25 | 2012-12-04 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| WO2011112186A1 (en) * | 2010-03-10 | 2011-09-15 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis c |
| US8354410B2 (en) | 2010-03-11 | 2013-01-15 | Bristol-Meyers Squibb Company | Compounds for the treatment of hepatitis C |
| US8324239B2 (en) * | 2010-04-21 | 2012-12-04 | Novartis Ag | Furopyridine compounds and uses thereof |
| US8445497B2 (en) | 2010-06-30 | 2013-05-21 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| WO2012051659A1 (en) * | 2010-10-20 | 2012-04-26 | Biota Scientific Management Pty Ltd | Viral polymerase inhibitors |
| CN103269586B (zh) | 2010-10-26 | 2015-07-15 | 普雷西迪奥制药公司 | 丙型肝炎病毒抑制剂 |
| JP5918264B2 (ja) * | 2010-12-22 | 2016-05-18 | アッヴィ・インコーポレイテッド | C型肝炎阻害剤およびその使用 |
| EA027418B1 (ru) | 2011-06-27 | 2017-07-31 | Янссен Фармацевтика Нв | ПРОИЗВОДНЫЕ 1-АРИЛ-4-МЕТИЛ[1,2,4]ТРИАЗОЛО[4,3-a]ХИНОКСАЛИНА, ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ НА ИХ ОСНОВЕ, СПОСОБЫ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ ИХ, ПРОМЕЖУТОЧНЫЕ СОЕДИНЕНИЯ |
| WO2013030750A1 (en) | 2011-09-01 | 2013-03-07 | Lupin Limited | Antiviral compounds |
| US9303020B2 (en) | 2012-02-08 | 2016-04-05 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| NZ628515A (en) | 2012-02-10 | 2016-06-24 | Lupin Ltd | Antiviral compounds with a dibenzooxaheterocycle moiety |
| EP2831066B1 (en) | 2012-03-27 | 2016-10-05 | Bristol-Myers Squibb Company | Benzofuran derivatives for the treatment of hepatitis c |
| US8785478B2 (en) | 2012-04-11 | 2014-07-22 | Biota Scientific Management Pty Ltd. | Viral polymerase inhibitors |
| WO2013163466A1 (en) * | 2012-04-25 | 2013-10-31 | Presidio Pharmaceuticals, Inc. | Inhibitors of hepatitis c virus |
| CN102690264B (zh) * | 2012-06-20 | 2014-07-02 | 泰山医学院 | 2-苯基-3-取代咪唑并[1,2-a]吡啶类衍生物及其制备方法 |
| ES2855575T3 (es) | 2012-06-26 | 2021-09-23 | Janssen Pharmaceutica Nv | Combinaciones que comprenden compuestos de 4-metil-[1,2,4]triazolo[4,3-a]quinoxalina como inhibidores de PDE2 e inhibidores de PDE10 para su uso en el tratamiento de trastornos neurológicos o metabólicos |
| KR102171706B1 (ko) | 2012-07-09 | 2020-10-30 | 얀센 파마슈티카 엔.브이. | 포스포디에스테라아제 10 효소의 억제제 |
| US8796305B2 (en) | 2012-11-05 | 2014-08-05 | Bayer Pharma Aktiengesellschaft | Carboxy-substituted imidazo[1,2-a]pyridinecarboxamides and their use |
| US9126998B2 (en) | 2012-11-05 | 2015-09-08 | Bayer Pharma AG | Amino-substituted imidazo[1,2-a]pyridinecarboxamides and their use |
| US8778964B2 (en) | 2012-11-05 | 2014-07-15 | Bayer Pharma Aktiengesellschaft | Hydroxy-substituted imidazo[1,2-a]-pyridinecarboxamides and their use |
| PT2925757T (pt) | 2012-11-19 | 2018-01-09 | Novartis Ag | Compostos e composições para o tratamento de doenças parasitárias |
| US8871754B2 (en) | 2012-11-19 | 2014-10-28 | Irm Llc | Compounds and compositions for the treatment of parasitic diseases |
| US8962651B2 (en) * | 2013-03-13 | 2015-02-24 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US9776997B2 (en) | 2013-06-04 | 2017-10-03 | Bayer Pharma Aktiengesellschaft | 3-aryl-substituted imidazo[1,2-A]pyridines and their use |
| CA2939793A1 (en) | 2014-02-19 | 2015-08-27 | Bayer Pharma Aktiengesellschaft | 3-(pyrimidine-2-yl)imidazo[1,2-a]pyridines |
| KR20160126085A (ko) * | 2014-03-21 | 2016-11-01 | 브리스톨-마이어스 스큅 컴퍼니 | C형 간염의 치료를 위한 시아노 함유 아자벤조푸란 화합물 |
| US9771360B2 (en) | 2014-03-21 | 2017-09-26 | Bayer Pharma Aktiengesellschaft | Cyano-substituted imidazo[1,2-A]pyridinecarboxamides and their use |
| WO2015143256A1 (en) * | 2014-03-21 | 2015-09-24 | Bristol-Myers Squibb Company | Cyanoamino (aza)benzofuran compounds for the treatment of hepatitis c |
| CN106459037A (zh) | 2014-05-02 | 2017-02-22 | 拜耳医药股份有限公司 | 用于治疗心血管疾病的N‑(2‑氨基‑5‑氟‑2‑甲基戊基)‑8‑[(2,6‑二氟苄基)氧基]‑2‑甲基咪唑并[1,2‑a]吡啶‑3‑甲酰胺的对映异构体及其二‑和三氟衍生物的对映异构体 |
| US9957278B2 (en) * | 2014-08-05 | 2018-05-01 | Bristol-Myers Squibb Company | Furopyridine compounds for the treatment of hepatitis C |
| EP3227287B1 (de) | 2014-12-02 | 2019-08-07 | Bayer Pharma Aktiengesellschaft | Heteroaryl-substituierte imidazo[1,2-a]pyridine und ihre verwendung |
| PE20181352A1 (es) | 2015-09-17 | 2018-08-22 | Marvin J Miller | Compuestos heterociclicos que contienen bencilamina y composiciones utiles contra infeccion por micobacterias |
| WO2018184976A1 (de) | 2017-04-05 | 2018-10-11 | Bayer Pharma Aktiengesellschaft | Substituierte imidazo[1,2-a]pyridincarboxamide und ihre verwendung |
| RU2019123849A (ru) | 2019-07-29 | 2021-02-01 | Дзе Брихэм Энд Уимен`З Хоспитал, Инк. | Ингибиторы фактора ингибирования миграции макрофагов |
| WO2024102699A1 (en) * | 2022-11-07 | 2024-05-16 | ELANCO US, Inc. | Guanylate cyclase (gc) stimulator formulations and uses thereof |
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| US3502707A (en) * | 1967-09-11 | 1970-03-24 | Mcneilab Inc | Beta-(cyclohexyl and substituted phenyl)-alpha-(4,5-dimethoxy-2-nitro- or aminophenyl) acrylonitriles |
| JPS57123181A (en) * | 1981-01-23 | 1982-07-31 | Mitsubishi Paper Mills Ltd | Preparation of pyrazolo (1,5-a) pyridine derivative |
| JPH06234667A (ja) * | 1992-10-29 | 1994-08-23 | Hoechst Ag | 芳香族ブロモメチル化合物の製造方法 |
| JP2001526286A (ja) * | 1997-12-19 | 2001-12-18 | イーライ・リリー・アンド・カンパニー | 低血糖性イミダゾリン化合物 |
| JP2004506736A (ja) * | 2000-08-22 | 2004-03-04 | グラクソ グループ リミテッド | タンパク質キナーゼ阻害剤としての縮合ピラゾール誘導体 |
| JP2004507542A (ja) * | 2000-08-28 | 2004-03-11 | 藤沢薬品工業株式会社 | ピラゾロピリジン化合物およびその医薬 |
| JP2004525150A (ja) * | 2001-03-30 | 2004-08-19 | スミスクライン ビーチャム コーポレーション | 治療用化合物としてのピラゾロピリジン類の使用 |
| JP2005530788A (ja) * | 2002-05-13 | 2005-10-13 | メルク エンド カムパニー インコーポレーテッド | フェニル置換イミダゾピリジン類およびフェニル置換ベンズイミダゾール類 |
| JP2006510736A (ja) * | 2002-11-01 | 2006-03-30 | バイロファーマ・インコーポレイテッド | ベンゾフラン化合物、組成物およびc型肝炎感染症および関連疾患の治療または予防方法 |
| WO2008082490A2 (en) * | 2006-12-20 | 2008-07-10 | Schering Corporation | Novel jnk inhibitors |
| WO2008100867A2 (en) * | 2007-02-12 | 2008-08-21 | Intermune, Inc. | Novel inhibitors hepatitis c virus replication |
| JP2008247878A (ja) * | 2007-03-30 | 2008-10-16 | Maruishi Pharmaceutical Co Ltd | イミダゾピリジンおよびイミダゾピリミジン化合物ならびにそれを含有する麻酔または鎮静薬組成物 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
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2009
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- 2009-09-02 WO PCT/US2009/055648 patent/WO2010030538A2/en not_active Ceased
- 2009-09-02 JP JP2011526911A patent/JP2012502099A/ja active Pending
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- 2009-09-02 KR KR1020117008086A patent/KR20110056537A/ko not_active Withdrawn
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- 2009-09-11 AR ARP090103513A patent/AR073586A1/es not_active Application Discontinuation
- 2009-09-11 TW TW098130826A patent/TW201014855A/zh unknown
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2012
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| JP2016500705A (ja) * | 2012-11-05 | 2016-01-14 | バイエル・ファルマ・アクティエンゲゼルシャフト | アミノ置換イミダゾ[1,2−a]ピリジンカルボキサミドおよびその使用 |
| JP2016540745A (ja) * | 2013-11-12 | 2016-12-28 | ダウ アグロサイエンシィズ エルエルシー | 化合物をフッ素化するための方法 |
| JP2017529401A (ja) * | 2014-09-26 | 2017-10-05 | チャーンジョウ インシュヨン ファーマシューティカル カンパニー,リミティド | Ns4b阻害剤としてのベンゾフラン類似体 |
| US10100027B2 (en) | 2014-09-26 | 2018-10-16 | Changzhou Yinsheng Pharmaceutical Co., Ltd. | Benzofuran analogue as NS4B inhibitor |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102209711B (zh) | 2014-06-18 |
| AR073586A1 (es) | 2010-11-17 |
| CN103864783A (zh) | 2014-06-18 |
| EP2331502A2 (en) | 2011-06-15 |
| MX2011002471A (es) | 2011-04-05 |
| US8536338B2 (en) | 2013-09-17 |
| US8198449B2 (en) | 2012-06-12 |
| WO2010030538A3 (en) | 2010-05-06 |
| US20100063068A1 (en) | 2010-03-11 |
| AU2009291993A1 (en) | 2010-03-18 |
| WO2010030538A2 (en) | 2010-03-18 |
| CN102209711A (zh) | 2011-10-05 |
| TW201014855A (en) | 2010-04-16 |
| EP2331502B1 (en) | 2016-03-02 |
| US20120232099A1 (en) | 2012-09-13 |
| KR20110056537A (ko) | 2011-05-30 |
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