CN102159579B - 三环吲哚衍生物及其使用方法 - Google Patents
三环吲哚衍生物及其使用方法 Download PDFInfo
- Publication number
- CN102159579B CN102159579B CN200980131569.9A CN200980131569A CN102159579B CN 102159579 B CN102159579 B CN 102159579B CN 200980131569 A CN200980131569 A CN 200980131569A CN 102159579 B CN102159579 B CN 102159579B
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- compound
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- antiviral agent
- agent comprises
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- 0 **[n]1c2cc([Al])c(CCO3)c3c2c(C2=CC=CN(*)C2=O)c1[*+] Chemical compound **[n]1c2cc([Al])c(CCO3)c3c2c(C2=CC=CN(*)C2=O)c1[*+] 0.000 description 20
- IAYOKRHKOCDQQH-ARJAWSKDSA-N C/C=C\c(c(C)c(C=O)cc1)c1F Chemical compound C/C=C\c(c(C)c(C=O)cc1)c1F IAYOKRHKOCDQQH-ARJAWSKDSA-N 0.000 description 1
- KTWIZNDHFVZCDJ-UHFFFAOYSA-N C=Cc1nc2ccccc2cc1CCl Chemical compound C=Cc1nc2ccccc2cc1CCl KTWIZNDHFVZCDJ-UHFFFAOYSA-N 0.000 description 1
- GJGICKPORZTPRU-UHFFFAOYSA-N CC(C(F)=CC1N=CN2)=CC1C2=O Chemical compound CC(C(F)=CC1N=CN2)=CC1C2=O GJGICKPORZTPRU-UHFFFAOYSA-N 0.000 description 1
- DFVFDTMDLSHAGC-UHFFFAOYSA-N CC(C)C1=CC2NCNC2C=C1F Chemical compound CC(C)C1=CC2NCNC2C=C1F DFVFDTMDLSHAGC-UHFFFAOYSA-N 0.000 description 1
- QADLIMTUDQPESU-UHFFFAOYSA-N CC(C)C1=CC=CNC1=O Chemical compound CC(C)C1=CC=CNC1=O QADLIMTUDQPESU-UHFFFAOYSA-N 0.000 description 1
- VPOYOQMWKWPTIN-UHFFFAOYSA-N CC(C)c(c(F)c1)cc2c1NCN2 Chemical compound CC(C)c(c(F)c1)cc2c1NCN2 VPOYOQMWKWPTIN-UHFFFAOYSA-N 0.000 description 1
- WFMSCKAATPPSRL-UHFFFAOYSA-N CC(C)c(c(F)c1)cc2c1[nH]nc2 Chemical compound CC(C)c(c(F)c1)cc2c1[nH]nc2 WFMSCKAATPPSRL-UHFFFAOYSA-N 0.000 description 1
- CBICQVIAVZYAIA-UHFFFAOYSA-N CC(C)c(cc(cccc1)c1n1)c1Cl Chemical compound CC(C)c(cc(cccc1)c1n1)c1Cl CBICQVIAVZYAIA-UHFFFAOYSA-N 0.000 description 1
- UBZPALPLRJQXJV-UHFFFAOYSA-O CC([NH2+]c(cc1I)c(C=N)cc1O)=O Chemical compound CC([NH2+]c(cc1I)c(C=N)cc1O)=O UBZPALPLRJQXJV-UHFFFAOYSA-O 0.000 description 1
- ZSBKRMSHHXMYRQ-UHFFFAOYSA-N CC1(Nc2ccccc2C(CBr)=C1)Cl Chemical compound CC1(Nc2ccccc2C(CBr)=C1)Cl ZSBKRMSHHXMYRQ-UHFFFAOYSA-N 0.000 description 1
- JTBJGFSLUNISGV-UHFFFAOYSA-N CC=C=C(c(cc(C)c(Cl)c1)c1S)NC Chemical compound CC=C=C(c(cc(C)c(Cl)c1)c1S)NC JTBJGFSLUNISGV-UHFFFAOYSA-N 0.000 description 1
- PMSMTNPHJSWSSC-UHFFFAOYSA-N CN(C)c(c(F)c-12)c-1c1c2[nH]cc1N Chemical compound CN(C)c(c(F)c-12)c-1c1c2[nH]cc1N PMSMTNPHJSWSSC-UHFFFAOYSA-N 0.000 description 1
- YAODSTOIAVANEI-UHFFFAOYSA-N COC(c([nH]c1ccc2)cc1c2O)=O Chemical compound COC(c([nH]c1ccc2)cc1c2O)=O YAODSTOIAVANEI-UHFFFAOYSA-N 0.000 description 1
- JRGNNZOCANCPLM-UHFFFAOYSA-N Cc(c(Cl)c1)cc(I)c1F Chemical compound Cc(c(Cl)c1)cc(I)c1F JRGNNZOCANCPLM-UHFFFAOYSA-N 0.000 description 1
- CWXYAAPFPRHTQR-UHFFFAOYSA-N Cc(c(F)c1)cc(C=O)c1NN Chemical compound Cc(c(F)c1)cc(C=O)c1NN CWXYAAPFPRHTQR-UHFFFAOYSA-N 0.000 description 1
- PBWOJASKNNGEQT-UHFFFAOYSA-N Cc(cc(C)c(Cl)c1)c1F Chemical compound Cc(cc(C)c(Cl)c1)c1F PBWOJASKNNGEQT-UHFFFAOYSA-N 0.000 description 1
- PFEIMKNQOIFKSW-UHFFFAOYSA-N Cc1cc(Cl)nc2c1cccc2 Chemical compound Cc1cc(Cl)nc2c1cccc2 PFEIMKNQOIFKSW-UHFFFAOYSA-N 0.000 description 1
- UZFRMQVCYQOAPI-UHFFFAOYSA-N Clc1nc(nccc2)c2cc1CBr Chemical compound Clc1nc(nccc2)c2cc1CBr UZFRMQVCYQOAPI-UHFFFAOYSA-N 0.000 description 1
- MXDGVDQYVPICSI-UHFFFAOYSA-N Nc1cc(CCl)c(cccc2)c2n1 Chemical compound Nc1cc(CCl)c(cccc2)c2n1 MXDGVDQYVPICSI-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Nc1ccccc1 Chemical compound Nc1ccccc1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- QKAKHHXCHOVWOU-UHFFFAOYSA-N O=C1Oc2ncccc2-c2c1[nH]c1cc(F)c(cc[o]3)c3c21 Chemical compound O=C1Oc2ncccc2-c2c1[nH]c1cc(F)c(cc[o]3)c3c21 QKAKHHXCHOVWOU-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61P31/12—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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Molecular Biology (AREA)
- Gastroenterology & Hepatology (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 (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6134408P | 2008-06-13 | 2008-06-13 | |
| US61/061,344 | 2008-06-13 | ||
| US61/061344 | 2008-06-13 | ||
| PCT/US2009/046822 WO2009152200A1 (en) | 2008-06-13 | 2009-06-10 | Tricyclic indole derivatives and methods of use thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102159579A CN102159579A (zh) | 2011-08-17 |
| CN102159579B true CN102159579B (zh) | 2015-03-25 |
Family
ID=40943627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980131569.9A Active CN102159579B (zh) | 2008-06-13 | 2009-06-10 | 三环吲哚衍生物及其使用方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8901139B2 (https=) |
| EP (1) | EP2303893B1 (https=) |
| JP (1) | JP5580814B2 (https=) |
| CN (1) | CN102159579B (https=) |
| AR (1) | AR072088A1 (https=) |
| CA (1) | CA2727620A1 (https=) |
| MX (1) | MX2010013630A (https=) |
| TW (1) | TW201011030A (https=) |
| WO (1) | WO2009152200A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8557848B2 (en) | 2006-12-22 | 2013-10-15 | Merck Sharp & Dohme Corp. | 4,5-ring annulated indole derivatives for treating or preventing of HCV and related viral infections |
| WO2014044722A1 (en) | 2012-09-20 | 2014-03-27 | Basf Se | Azadibenzofurans for electronic applications |
| WO2015143257A1 (en) * | 2014-03-21 | 2015-09-24 | Bristol-Myers Squibb Company | 6h-furo[2,3-e]indole compounds for the treatment of hepatitis c |
| WO2015160636A1 (en) | 2014-04-16 | 2015-10-22 | Merck Sharp & Dohme Corp. | Factor ixa inhibitors |
| WO2018151239A1 (ja) * | 2017-02-17 | 2018-08-23 | 第一三共株式会社 | 3,6-ジヒドロ-2H-フロ[2,3-e]インドール化合物 |
| CN116063310A (zh) * | 2022-12-23 | 2023-05-05 | 齐鲁工业大学 | 一种呋喃并[3,4-b]吲哚衍生物及其合成方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1863528A (zh) * | 2003-10-10 | 2006-11-15 | P.安杰莱蒂分子生物学研究所 | 作为抗病毒剂的吲哚和吖吲哚 |
| CN101098695A (zh) * | 2004-03-01 | 2008-01-02 | 维洛药品公司 | 吡喃并吲哚衍生物及其用于治疗丙型肝炎病毒感染或者疾病的用途 |
| WO2008082484A1 (en) * | 2006-12-22 | 2008-07-10 | Schering Corporation | 4,5-ring annulated indole derivatives for treating or preventing of hcv and related viral infections |
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| DE648639C (de) | 1935-05-19 | 1937-08-05 | I G Farbenindustrie Akt Ges | Verfahren zur Darstellung von Dipyrrolen |
| US3632805A (en) | 1967-12-08 | 1972-01-04 | Sumitomo Chemical Co | Process for producing 1-aminoalkyl-benzodiazepine derivatives |
| AU575854B2 (en) | 1983-10-04 | 1988-08-11 | Shionogi & Co., Ltd. | 7beta-(carboxyalkenamido) cephalosporins |
| US5017380A (en) | 1986-07-02 | 1991-05-21 | Shionogi & Co., Ltd. | Gelatin hard capsule containing crystalline hydrate of oral cephalosporin |
| NZ220764A (en) | 1986-07-02 | 1989-09-27 | Shionogi & Co | Crystalline form of 7beta((z)-2-(2-aminothiazol-4-yl)-4- carboxybut-2-enoylamino)-3-cephem-4-carboxylic acid and pharmaceutical compositions |
| CA2038925A1 (en) | 1990-03-26 | 1991-09-27 | Takashi Sohda | Indole derivatives, their production and use |
| JPH04149429A (ja) | 1990-10-12 | 1992-05-22 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー反転写真感光材料およびそれを用いた画像形成方法 |
| IT1278077B1 (it) | 1995-05-25 | 1997-11-17 | Angeletti P Ist Richerche Bio | Metodologia per riprodurre in vitro le attivita' di rna polimerasi rna-dipendente e di nucleotidiltransferasi terminale codificate dal |
| US5922757A (en) | 1996-09-30 | 1999-07-13 | The Regents Of The University Of California | Treatment and prevention of hepatic disorders |
| KR100509388B1 (ko) | 1996-10-18 | 2005-08-23 | 버텍스 파마슈티칼스 인코포레이티드 | 세린 프로테아제, 특히 간염 c 바이러스 ns3 프로테아제의 저해제 |
| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| ES2234144T3 (es) | 1997-08-11 | 2005-06-16 | Boehringer Ingelheim (Canada) Ltd. | Analogos de peptidos inhibidores de la hepatitis c. |
| FR2768146B1 (fr) | 1997-09-05 | 2000-05-05 | Oreal | Nouveaux composes de la famille des indole-carboxyliques et leur utilisation |
| AR029903A1 (es) | 2000-04-05 | 2003-07-23 | Schering Corp | Inhibidores macrociclicos de la ns3-serina proteasa, del virus de la hepatitis c, que comprenden partes p2 n-ciclicas, composiciones farmaceuticas y utilizacion de los mismos para la manufactura de un medicamento |
| CN101580536A (zh) | 2000-04-19 | 2009-11-18 | 先灵公司 | 含有烷基和芳基丙氨酸p2部分的丙型肝炎病毒的大环ns3-丝氨酸蛋白酶抑制剂 |
| KR20030081297A (ko) | 2000-07-21 | 2003-10-17 | 쉐링 코포레이션 | C형 간염 바이러스의 ns3-세린 프로테아제억제제로서의 신규한 펩티드 |
| DK1385870T3 (da) | 2000-07-21 | 2010-07-05 | Schering Corp | Peptider som inhibitorer af NS3-serinprotease fra hepatitis C-virus |
| AR029851A1 (es) | 2000-07-21 | 2003-07-16 | Dendreon Corp | Nuevos peptidos como inhibidores de ns3-serina proteasa del virus de hepatitis c |
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| KR20030091946A (ko) | 2000-12-12 | 2003-12-03 | 쉐링 코포레이션 | C형 간염 바이러스의 ns3-세린 프로테아제억제제로서의 디아릴 펩티드 |
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| CN101611025A (zh) | 2006-12-22 | 2009-12-23 | 先灵公司 | 5,6-环化的吲哚衍生物及其使用方法 |
| WO2008082488A1 (en) | 2006-12-22 | 2008-07-10 | Schering Corporation | 4, 5-ring annulated indole derivatives for treating or preventing of hcv and related viral infections |
| WO2009032116A1 (en) | 2007-08-29 | 2009-03-12 | Schering Corporation | 2, 3-substituted indole derivatives for treating viral infections |
| AU2008295483B2 (en) * | 2007-08-29 | 2013-11-21 | Merck Sharp & Dohme Corp. | Tetracyclic indole derivatives and their use for treating or preventing viral infections |
| EP2408761B1 (en) | 2007-08-29 | 2014-01-01 | Merck Sharp & Dohme Corp. | Substituted indole derivatives and methods of use thereof |
| ATE541845T1 (de) | 2007-08-29 | 2012-02-15 | Schering Corp | 2,3-substituierte azaindolderivate zur behandlung von virusinfektionen |
| MX2010005356A (es) | 2007-11-16 | 2010-05-27 | Schering Corp | Derivados de indol 3-heterociclico sustituidos y metodos de uso de los mismos. |
| US8377928B2 (en) | 2007-11-16 | 2013-02-19 | Merck Sharp & Dohme Corp. | 3-aminosulfonyl substituted indole derivatives and methods of use thereof |
-
2009
- 2009-06-10 MX MX2010013630A patent/MX2010013630A/es active IP Right Grant
- 2009-06-10 AR ARP090102091A patent/AR072088A1/es not_active Application Discontinuation
- 2009-06-10 EP EP09763490.1A patent/EP2303893B1/en not_active Not-in-force
- 2009-06-10 JP JP2011513649A patent/JP5580814B2/ja active Active
- 2009-06-10 CN CN200980131569.9A patent/CN102159579B/zh active Active
- 2009-06-10 CA CA2727620A patent/CA2727620A1/en not_active Abandoned
- 2009-06-10 WO PCT/US2009/046822 patent/WO2009152200A1/en not_active Ceased
- 2009-06-10 US US12/997,654 patent/US8901139B2/en active Active
- 2009-06-11 TW TW098119583A patent/TW201011030A/zh unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1863528A (zh) * | 2003-10-10 | 2006-11-15 | P.安杰莱蒂分子生物学研究所 | 作为抗病毒剂的吲哚和吖吲哚 |
| CN101098695A (zh) * | 2004-03-01 | 2008-01-02 | 维洛药品公司 | 吡喃并吲哚衍生物及其用于治疗丙型肝炎病毒感染或者疾病的用途 |
| WO2008082484A1 (en) * | 2006-12-22 | 2008-07-10 | Schering Corporation | 4,5-ring annulated indole derivatives for treating or preventing of hcv and related viral infections |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5580814B2 (ja) | 2014-08-27 |
| AR072088A1 (es) | 2010-08-04 |
| EP2303893A1 (en) | 2011-04-06 |
| WO2009152200A1 (en) | 2009-12-17 |
| US8901139B2 (en) | 2014-12-02 |
| TW201011030A (en) | 2010-03-16 |
| MX2010013630A (es) | 2010-12-21 |
| CA2727620A1 (en) | 2009-12-17 |
| JP2011524359A (ja) | 2011-09-01 |
| EP2303893B1 (en) | 2016-12-07 |
| US20110189127A1 (en) | 2011-08-04 |
| CN102159579A (zh) | 2011-08-17 |
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