JP5179585B2 - 四環系インドール誘導体およびその使用法 - Google Patents
四環系インドール誘導体およびその使用法 Download PDFInfo
- Publication number
- JP5179585B2 JP5179585B2 JP2010522933A JP2010522933A JP5179585B2 JP 5179585 B2 JP5179585 B2 JP 5179585B2 JP 2010522933 A JP2010522933 A JP 2010522933A JP 2010522933 A JP2010522933 A JP 2010522933A JP 5179585 B2 JP5179585 B2 JP 5179585B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- heteroaryl
- haloalkyl
- aryl
- 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.)
- Expired - Fee Related
Links
- 0 C*CCC(C)(C)OC(c1cc2cc(C(F)(F)F)ccc2[n]1)=O Chemical compound C*CCC(C)(C)OC(c1cc2cc(C(F)(F)F)ccc2[n]1)=O 0.000 description 34
- PBNPQVFHAZIWAW-UHFFFAOYSA-N CC(C)(C)OC(N(C(OC(C)(C)C)=O)c1n[n](C(OC(C)(C)C)=O)c2cc(F)c(CBr)cc12)=O Chemical compound CC(C)(C)OC(N(C(OC(C)(C)C)=O)c1n[n](C(OC(C)(C)C)=O)c2cc(F)c(CBr)cc12)=O PBNPQVFHAZIWAW-UHFFFAOYSA-N 0.000 description 2
- BIWOSRSKDCZIFM-UHFFFAOYSA-N OC1CNCCC1 Chemical compound OC1CNCCC1 BIWOSRSKDCZIFM-UHFFFAOYSA-N 0.000 description 2
- LYMGNRHDFKUCDQ-ZETCQYMHSA-N C=C[C@@H]1CNCCC1 Chemical compound C=C[C@@H]1CNCCC1 LYMGNRHDFKUCDQ-ZETCQYMHSA-N 0.000 description 1
- ZVZZUQQFIRPPBU-UHFFFAOYSA-N CC(C)(C)OC([n]1c(ccc(C)c2)c2nc1)=O Chemical compound CC(C)(C)OC([n]1c(ccc(C)c2)c2nc1)=O ZVZZUQQFIRPPBU-UHFFFAOYSA-N 0.000 description 1
- XDHMIYRDRLMAGL-UHFFFAOYSA-N CC(C)(C)OC(c([nH]c1ccc(C(F)(F)F)cc11)c1I)=O Chemical compound CC(C)(C)OC(c([nH]c1ccc(C(F)(F)F)cc11)c1I)=O XDHMIYRDRLMAGL-UHFFFAOYSA-N 0.000 description 1
- KPXVPDCQJPJVNY-UHFFFAOYSA-N CC(C1)C(CBr)=Cc2c1nc[n]2C(OC(C)(C)C)=O Chemical compound CC(C1)C(CBr)=Cc2c1nc[n]2C(OC(C)(C)C)=O KPXVPDCQJPJVNY-UHFFFAOYSA-N 0.000 description 1
- UFKSKQHPOWZJLP-GKAPJAKFSA-N CC(C1)[C@H]1c1nc(cc(C)cc2)c2[nH]1 Chemical compound CC(C1)[C@H]1c1nc(cc(C)cc2)c2[nH]1 UFKSKQHPOWZJLP-GKAPJAKFSA-N 0.000 description 1
- OWVXVOTURDXAMK-UHFFFAOYSA-N CC(CC1C(c2cccnc2O)=C(C=O)N(Cc(cc(cc2)C#N)c2F)C1=C1)=C1F Chemical compound CC(CC1C(c2cccnc2O)=C(C=O)N(Cc(cc(cc2)C#N)c2F)C1=C1)=C1F OWVXVOTURDXAMK-UHFFFAOYSA-N 0.000 description 1
- ZEXSOUBSDGDTRT-UHFFFAOYSA-N CCCC(C(CC1)=Cc2c1ccc(OCc1ccccc1)c2)=O Chemical compound CCCC(C(CC1)=Cc2c1ccc(OCc1ccccc1)c2)=O ZEXSOUBSDGDTRT-UHFFFAOYSA-N 0.000 description 1
- VACSCRRUXJWOCF-UHFFFAOYSA-N CCOC(C(CC1)=C(C)c2c1ccc(C)c2)=O Chemical compound CCOC(C(CC1)=C(C)c2c1ccc(C)c2)=O VACSCRRUXJWOCF-UHFFFAOYSA-N 0.000 description 1
- ULSLPPOVDLNXSG-UHFFFAOYSA-N CCOC(COc(cc(cc1)F)c1Br)OCC Chemical compound CCOC(COc(cc(cc1)F)c1Br)OCC ULSLPPOVDLNXSG-UHFFFAOYSA-N 0.000 description 1
- LAKAVDAOYLZWMI-UHFFFAOYSA-N CCc(c(F)c1)cc2c1[nH]c(C(O)=O)c2 Chemical compound CCc(c(F)c1)cc2c1[nH]c(C(O)=O)c2 LAKAVDAOYLZWMI-UHFFFAOYSA-N 0.000 description 1
- SRSCDTUZRYWMKU-UHFFFAOYSA-N CCc(c(F)c1)cc2c1[nH]c1c2-c2cccnc2OC1=O Chemical compound CCc(c(F)c1)cc2c1[nH]c1c2-c2cccnc2OC1=O SRSCDTUZRYWMKU-UHFFFAOYSA-N 0.000 description 1
- VPEWBEKPUWAFCD-UHFFFAOYSA-N CCc(c(F)c1)cc2c1[n](Cc(cc(cccc1)c1n1)c1Cl)c1c2-c(cccn2)c2OC1=O Chemical compound CCc(c(F)c1)cc2c1[n](Cc(cc(cccc1)c1n1)c1Cl)c1c2-c(cccn2)c2OC1=O VPEWBEKPUWAFCD-UHFFFAOYSA-N 0.000 description 1
- JOSXZUNVEPWEGD-UHFFFAOYSA-N CCc(cc(c(N)c1)I)c1F Chemical compound CCc(cc(c(N)c1)I)c1F JOSXZUNVEPWEGD-UHFFFAOYSA-N 0.000 description 1
- QOGITCLGSMTFOP-YWQZSECXSA-N CCc1ccc2[nH]c(C(OCC)=O)c(/C(/C(/OC)=C\C)=C/C(/Cl)=C\C)c2c1 Chemical compound CCc1ccc2[nH]c(C(OCC)=O)c(/C(/C(/OC)=C\C)=C/C(/Cl)=C\C)c2c1 QOGITCLGSMTFOP-YWQZSECXSA-N 0.000 description 1
- ZHSUEJWJGKIOGI-UHFFFAOYSA-N Cc(c(F)c1)cc(Br)c1N Chemical compound Cc(c(F)c1)cc(Br)c1N ZHSUEJWJGKIOGI-UHFFFAOYSA-N 0.000 description 1
- YAEPXRRKVAJHHQ-UHFFFAOYSA-N Cc(c(F)c1)cc(C#N)c1N Chemical compound Cc(c(F)c1)cc(C#N)c1N YAEPXRRKVAJHHQ-UHFFFAOYSA-N 0.000 description 1
- PYSIAMCBAFHDHQ-UHFFFAOYSA-N Cc(cc(C(C(C=O)N1CC(C(F)=CC2)=CC2C#N)c(cc[nH]2)c2O)c1c1)c1F Chemical compound Cc(cc(C(C(C=O)N1CC(C(F)=CC2)=CC2C#N)c(cc[nH]2)c2O)c1c1)c1F PYSIAMCBAFHDHQ-UHFFFAOYSA-N 0.000 description 1
- DGRGLKZMKWPMOH-UHFFFAOYSA-N Cc(cc1)cc(N)c1N Chemical compound Cc(cc1)cc(N)c1N DGRGLKZMKWPMOH-UHFFFAOYSA-N 0.000 description 1
- XLAFKBXUNAYWQC-UHFFFAOYSA-N Cc(cc1c(N)n[nH]c1c1)c1F Chemical compound Cc(cc1c(N)n[nH]c1c1)c1F XLAFKBXUNAYWQC-UHFFFAOYSA-N 0.000 description 1
- AIHMJRLRPWJDIE-UHFFFAOYSA-N Cc1cc(cccc2)c2nc1[ClH]C Chemical compound Cc1cc(cccc2)c2nc1[ClH]C AIHMJRLRPWJDIE-UHFFFAOYSA-N 0.000 description 1
- RJBROQQUGNXIIP-UHFFFAOYSA-N O=C1Oc2ncccc2-c2c1[nH]c1cc(F)c(CCO3)c3c21 Chemical compound O=C1Oc2ncccc2-c2c1[nH]c1cc(F)c(CCO3)c3c21 RJBROQQUGNXIIP-UHFFFAOYSA-N 0.000 description 1
- HUVAOAVBKOVPBZ-UHFFFAOYSA-N Oc(cc(cc1)F)c1Br Chemical compound Oc(cc(cc1)F)c1Br HUVAOAVBKOVPBZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- 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
-
- 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
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Gastroenterology & Hepatology (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 (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US96868407P | 2007-08-29 | 2007-08-29 | |
US60/968,684 | 2007-08-29 | ||
PCT/US2008/010147 WO2009032123A2 (en) | 2007-08-29 | 2008-08-27 | Tetracyclic indole derivatives and their use for treating or preventing viral infections |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2010537980A JP2010537980A (ja) | 2010-12-09 |
JP5179585B2 true JP5179585B2 (ja) | 2013-04-10 |
Family
ID=40319417
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2010522933A Expired - Fee Related JP5179585B2 (ja) | 2007-08-29 | 2008-08-27 | 四環系インドール誘導体およびその使用法 |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP2197884A2 (ko) |
JP (1) | JP5179585B2 (ko) |
KR (1) | KR20100061819A (ko) |
CN (1) | CN101842376A (ko) |
AR (1) | AR068109A1 (ko) |
AU (1) | AU2008295483B2 (ko) |
CA (1) | CA2697451A1 (ko) |
MX (1) | MX2010002316A (ko) |
TW (1) | TW200918536A (ko) |
WO (1) | WO2009032123A2 (ko) |
ZA (1) | ZA201001391B (ko) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101945872B (zh) | 2008-01-11 | 2014-07-23 | 阿尔巴尼分子研究公司 | 作为mch拮抗剂的(1-吖嗪酮)-取代的吡啶并吲哚 |
AR072088A1 (es) * | 2008-06-13 | 2010-08-04 | Schering Corp | Derivados de indol triciclicos y sus metodos de uso |
AU2009273327A1 (en) | 2008-07-23 | 2010-01-28 | F. Hoffmann-La Roche Ag | Heterocyclic antiviral compounds |
CN102164909A (zh) | 2008-09-26 | 2011-08-24 | 弗·哈夫曼-拉罗切有限公司 | 用于治疗hcv的吡啶或吡嗪衍生物 |
EP2421831A1 (en) | 2009-04-25 | 2012-02-29 | F. Hoffmann-La Roche AG | Heterocyclic antiviral compounds |
WO2010138791A1 (en) | 2009-05-29 | 2010-12-02 | Schering Corporation | Antiviral compounds composed of three linked aryl moieties to treat diseases such as hepatitis c |
AR077004A1 (es) | 2009-06-09 | 2011-07-27 | Hoffmann La Roche | Compuestos heterociclicos antivirales |
BRPI1011744A2 (pt) | 2009-06-24 | 2016-03-22 | Hoffmann La Roche | composto antiviral heterocíclico. |
WO2011003021A1 (en) | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof |
US8629158B2 (en) | 2009-07-01 | 2014-01-14 | Albany Molecular Research, Inc. | Azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof |
US8618299B2 (en) | 2009-07-01 | 2013-12-31 | Albany Molecular Research, Inc. | Azinone-substituted azapolycycle MCH-1 antagonists, methods of making, and use thereof |
EP2448585B1 (en) | 2009-07-01 | 2014-01-01 | Albany Molecular Research, Inc. | Azinone-substituted azepino[b]indole and pyrido-pyrrolo-azepine mch-1 antagonists, methods of making, and use thereof |
CN102498100A (zh) | 2009-09-21 | 2012-06-13 | 弗·哈夫曼-拉罗切有限公司 | 抗病毒杂环化合物 |
WO2011066241A1 (en) | 2009-11-25 | 2011-06-03 | Schering Corporation | Fused tricyclic compounds and derivatives thereof useful for the treatment of viral diseases |
US20130156731A1 (en) | 2009-12-22 | 2013-06-20 | Kevin X. Chen | Fused tricyclic compounds and methods of use thereof for the treatment of viral diseas |
ES2558554T3 (es) | 2010-03-09 | 2016-02-05 | Merck Sharp & Dohme Corp. | Compuestos de sililo tricíclicos condensados y métodos de uso de los mismos para el tratamiento de enfermedades víricas |
JP6132352B2 (ja) | 2010-05-02 | 2017-05-24 | エックスジェット エルティーディー. | セルフパージ、沈澱防止、および、ガス除去の構造を備えた印刷システム |
WO2012018534A2 (en) | 2010-07-26 | 2012-02-09 | Schering Corporation | Substituted biphenylene compounds and methods of use thereof for the treatment of viral diseases |
WO2012041227A1 (en) * | 2010-09-29 | 2012-04-05 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds for treating hepatitis c viral infection |
EP2621279B1 (en) | 2010-09-29 | 2018-04-04 | Merck Sharp & Dohme Corp. | Fused tetracycle derivatives and methods of use thereof for the treatment of viral diseases |
US8697700B2 (en) | 2010-12-21 | 2014-04-15 | Albany Molecular Research, Inc. | Piperazinone-substituted tetrahydro-carboline MCH-1 antagonists, methods of making, and uses thereof |
WO2012088124A2 (en) | 2010-12-21 | 2012-06-28 | Albany Molecular Research, Inc. | Tetrahydro-azacarboline mch-1 antagonists, methods of making, and uses thereof |
WO2012142075A1 (en) | 2011-04-13 | 2012-10-18 | Merck Sharp & Dohme Corp. | 2'-azido substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
EA201391519A1 (ru) | 2011-04-13 | 2014-03-31 | Мерк Шарп И Доум Корп. | 2'-замещенные нуклеозидные производные и способы их применения для лечения вирусных заболеваний |
WO2013033901A1 (en) | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Heterocyclic-substituted benzofuran derivatives and methods of use thereof for the treatment of viral diseases |
WO2013033899A1 (en) | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Substituted benzofuran compounds and methods of use thereof for the treatment of viral diseases |
WO2013033900A1 (en) | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of viral diseases |
WO2013039876A1 (en) | 2011-09-14 | 2013-03-21 | Merck Sharp & Dohme Corp. | Silyl-containing heterocyclic compounds and methods of use thereof for the treatment of viral diseases |
US9242988B2 (en) | 2012-10-17 | 2016-01-26 | Merck Sharp & Dohme Corp. | 2′-cyano substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
AR092959A1 (es) | 2012-10-17 | 2015-05-06 | Merck Sharp & Dohme | Derivados de nucleosidos 2-metil sustituidos y metodos de uso de los mismos para el tratamiento de enfermedades virales |
WO2014059902A1 (en) | 2012-10-17 | 2014-04-24 | Merck Sharp & Dohme Corp. | 2'-disubstituted substituted nucleoside derivatives and methods of use thereof for treatment of viral diseases |
WO2014078463A1 (en) | 2012-11-19 | 2014-05-22 | Merck Sharp & Dohme Corp. | 2 -alkynyl substituted nucleoside derivatives for treating viral diseases |
WO2014204831A1 (en) | 2013-06-18 | 2014-12-24 | Merck Sharp & Dohme Corp. | Cyclic phosphonate substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
WO2014205592A1 (en) | 2013-06-24 | 2014-12-31 | Merck Sharp & Dohme Corp. | Heterocyclic compounds and methods of use thereof for treatment of hepatitis c |
WO2014205593A1 (en) | 2013-06-24 | 2014-12-31 | Merck Sharp & Dohme Corp. | Substituted benzofuran compounds and methods of use thereof for treatment of viral diseases |
US10167298B2 (en) | 2013-10-30 | 2019-01-01 | Merck Sharp & Dohme Corp. | Pseudopolymorphs of an HCV NS5A inhibitor and uses thereof |
US10899788B2 (en) | 2016-06-20 | 2021-01-26 | Merck Sharp & Dohme Corp. | Cyclic phosphate substituted nucleoside compounds and methods of use thereof for the treatment of viral diseases |
CN112898312B (zh) * | 2021-01-29 | 2021-11-12 | 湖南南新制药股份有限公司 | 一种稠合多环吡啶酮衍生物及其用途 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7153848B2 (en) * | 2004-08-09 | 2006-12-26 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
JP2008514611A (ja) * | 2004-09-23 | 2008-05-08 | ワイス | C型肝炎ウイルスによる感染を処置するためのカルバゾールおよびシクロペンタインドールの誘導体 |
GB0518390D0 (en) * | 2005-09-09 | 2005-10-19 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
MX2008004024A (es) * | 2005-09-23 | 2009-02-27 | Schering Corp | Antagonistas de receptor de glutamato metabotropico-1 tetraciclicos fusionados como agentes terapeuticos. |
-
2008
- 2008-08-27 MX MX2010002316A patent/MX2010002316A/es not_active Application Discontinuation
- 2008-08-27 TW TW097132762A patent/TW200918536A/zh unknown
- 2008-08-27 AU AU2008295483A patent/AU2008295483B2/en not_active Ceased
- 2008-08-27 JP JP2010522933A patent/JP5179585B2/ja not_active Expired - Fee Related
- 2008-08-27 EP EP08795628A patent/EP2197884A2/en not_active Withdrawn
- 2008-08-27 WO PCT/US2008/010147 patent/WO2009032123A2/en active Application Filing
- 2008-08-27 AR ARP080103718A patent/AR068109A1/es not_active Application Discontinuation
- 2008-08-27 KR KR1020107006704A patent/KR20100061819A/ko not_active Application Discontinuation
- 2008-08-27 CA CA2697451A patent/CA2697451A1/en not_active Abandoned
- 2008-08-27 CN CN200880113543A patent/CN101842376A/zh active Pending
-
2010
- 2010-02-25 ZA ZA2010/01391A patent/ZA201001391B/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO2009032123A3 (en) | 2009-06-11 |
JP2010537980A (ja) | 2010-12-09 |
AU2008295483B2 (en) | 2013-11-21 |
KR20100061819A (ko) | 2010-06-09 |
TW200918536A (en) | 2009-05-01 |
CA2697451A1 (en) | 2009-03-12 |
MX2010002316A (es) | 2010-03-22 |
CN101842376A (zh) | 2010-09-22 |
AR068109A1 (es) | 2009-11-04 |
EP2197884A2 (en) | 2010-06-23 |
ZA201001391B (en) | 2010-11-24 |
WO2009032123A2 (en) | 2009-03-12 |
AU2008295483A1 (en) | 2009-03-12 |
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