CR9069A - Derivados de indol tetraciclicos como agentes antiviricos - Google Patents
Derivados de indol tetraciclicos como agentes antiviricosInfo
- Publication number
- CR9069A CR9069A CR9069A CR9069A CR9069A CR 9069 A CR9069 A CR 9069A CR 9069 A CR9069 A CR 9069A CR 9069 A CR9069 A CR 9069A CR 9069 A CR9069 A CR 9069A
- Authority
- CR
- Costa Rica
- Prior art keywords
- tetraciclic
- antivirical
- agents
- indol derivatives
- indol
- Prior art date
Links
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical class C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 title 1
- 208000006454 hepatitis Diseases 0.000 abstract 1
- 231100000283 hepatitis Toxicity 0.000 abstract 1
- 150000002475 indoles Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000009385 viral infection Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D245/00—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms
- C07D245/04—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- 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
-
- 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
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/22—Eight-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- 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
- C07D491/12—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 three hetero rings
- C07D491/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (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)
Abstract
La presente invencion se refiere a compuestos de indol tetraciclicos de formula ( I ), en la que R1,R2,A,AR,W,X,Y y Z se definen en este documento, y a las sales farmaceuticamente aceptables de los mismos, a composiciones farmaceuticas que los comprenden y a su uso para el tratamiento o prevencion de una infeccion por el virus de la hepatitis.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0423767A GB0423767D0 (en) | 2004-10-26 | 2004-10-26 | Therapeutic compounds |
| GB0512519A GB0512519D0 (en) | 2005-06-21 | 2005-06-21 | Therapeutic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CR9069A true CR9069A (es) | 2007-10-01 |
Family
ID=36101507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CR9069A CR9069A (es) | 2004-10-26 | 2007-04-19 | Derivados de indol tetraciclicos como agentes antiviricos |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US7662809B2 (es) |
| EP (2) | EP1807397A2 (es) |
| JP (2) | JP2008517987A (es) |
| KR (1) | KR20070068427A (es) |
| AR (1) | AR051469A1 (es) |
| AU (2) | AU2005298412B2 (es) |
| BR (1) | BRPI0516972A (es) |
| CA (2) | CA2585084A1 (es) |
| CR (1) | CR9069A (es) |
| EC (1) | ECSP077412A (es) |
| IL (1) | IL182610A0 (es) |
| MA (1) | MA29037B1 (es) |
| MX (1) | MX2007004979A (es) |
| NI (1) | NI200700102A (es) |
| NO (1) | NO20072689L (es) |
| PE (1) | PE20060607A1 (es) |
| RU (1) | RU2007119562A (es) |
| TW (1) | TW200630344A (es) |
| WO (2) | WO2006046039A2 (es) |
Families Citing this family (95)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7270175B2 (en) | 2004-01-09 | 2007-09-18 | United Technologies Corporation | Extended impingement cooling device and method |
| US20070049593A1 (en) | 2004-02-24 | 2007-03-01 | Japan Tobacco Inc. | Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor |
| US7348425B2 (en) | 2004-08-09 | 2008-03-25 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| US7795247B2 (en) | 2004-10-26 | 2010-09-14 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa | Tetracyclic indole derivatives as antiviral agents |
| CA2585084A1 (en) | 2004-10-26 | 2006-05-04 | Immacolata Conte | Tetracyclic indole derivatives as antiviral agents |
| US7659263B2 (en) | 2004-11-12 | 2010-02-09 | Japan Tobacco Inc. | Thienopyrrole compound and use thereof as HCV polymerase inhibitor |
| WO2006119061A2 (en) | 2005-05-02 | 2006-11-09 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
| KR20080036598A (ko) | 2005-08-01 | 2008-04-28 | 머크 앤드 캄파니 인코포레이티드 | Hcv ns3 프로테아제 억제제로서의 마크로사이클릭펩티드 |
| US7399758B2 (en) | 2005-09-12 | 2008-07-15 | Meanwell Nicholas A | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| US7473688B2 (en) | 2005-09-13 | 2009-01-06 | Bristol-Myers Squibb Company | Indolobenzazepine HCV NS5B inhibitors |
| GB0522881D0 (en) * | 2005-11-10 | 2005-12-21 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| WO2007092000A1 (en) * | 2006-02-06 | 2007-08-16 | Bristol-Myers Squibb Company | Inhibitors of hcv replication |
| US7456165B2 (en) | 2006-02-08 | 2008-11-25 | Bristol-Myers Squibb Company | HCV NS5B inhibitors |
| GB0608928D0 (en) * | 2006-05-08 | 2006-06-14 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| CN101443336B (zh) * | 2006-05-17 | 2012-07-04 | 百时美施贵宝公司 | 环丙基稠合的[吲哚]并[苯并氮杂*]hcv ns5b抑制剂 |
| US7456166B2 (en) * | 2006-05-17 | 2008-11-25 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| US7521443B2 (en) | 2006-05-17 | 2009-04-21 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| US7521441B2 (en) * | 2006-05-22 | 2009-04-21 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| WO2007140200A2 (en) | 2006-05-25 | 2007-12-06 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine hcv ns5b inhibitors |
| ES2343914T3 (es) * | 2006-05-25 | 2010-08-12 | Bristol-Myers Squibb Company | Inhibidores de ns5b de hcv de indolobenzazepina condensada con ciclopropilo. |
| US7452876B2 (en) | 2006-06-08 | 2008-11-18 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| GB0612423D0 (en) | 2006-06-23 | 2006-08-02 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| US20080045498A1 (en) * | 2006-07-20 | 2008-02-21 | Genelabs Technologies, Inc. | Polycyclic viral inhibitors |
| AU2007309488B2 (en) | 2006-10-24 | 2012-10-11 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| AU2007309546A1 (en) | 2006-10-24 | 2008-05-02 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | HCV NS3 protease inhibitors |
| EP2079479B1 (en) | 2006-10-24 | 2014-11-26 | Merck Sharp & Dohme Corp. | Hcv ns3 protease inhibitors |
| CN101568346B (zh) | 2006-10-27 | 2015-11-25 | 默沙东公司 | Hcv ns3蛋白酶抑制剂 |
| CA2667031C (en) | 2006-10-27 | 2013-01-22 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
| GB0625349D0 (en) | 2006-12-20 | 2007-01-31 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| GB0625345D0 (en) | 2006-12-20 | 2007-01-31 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| CA2672250C (en) * | 2006-12-20 | 2013-04-30 | Ian Stansfield | Antiviral indoles |
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| US7541351B2 (en) | 2007-01-11 | 2009-06-02 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US7541352B2 (en) * | 2007-02-02 | 2009-06-02 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
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| EP3728266A1 (en) | 2017-12-20 | 2020-10-28 | Novartis AG | Fused tricyclic pyrazolo-dihydropyrazinyl-pyridone compounds as antivirals |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5206382A (en) * | 1991-06-27 | 1993-04-27 | Fidia Georgetown Institute For The Neurosciences | Indole derivatives, pharmaceutical compositions and methods of treating neurological and psychiatric disorders |
| 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 |
| EP2050822B1 (en) | 2001-01-23 | 2013-07-31 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Hepatitis C virus replicons and replicon enhanced cells |
| TW200400963A (en) | 2002-05-21 | 2004-01-16 | Wyeth Corp | R-enantiomers of pyranoindole derivatives and the use thereof for the treatment of hepatitis C virus infection or disease |
| JPWO2004029725A1 (ja) * | 2002-09-27 | 2006-01-26 | 三菱製紙株式会社 | 電子写真用転写紙 |
| GB0307891D0 (en) | 2003-04-04 | 2003-05-14 | Angeletti P Ist Richerche Bio | Chemical compounds,compositions and uses |
| PT1719773E (pt) | 2004-02-24 | 2009-06-03 | Japan Tobacco Inc | Compostos heterotetracíclicos fundidos e a sua utilização como inibidores da polimerase do hcv |
| US7153848B2 (en) * | 2004-08-09 | 2006-12-26 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| CA2585084A1 (en) | 2004-10-26 | 2006-05-04 | Immacolata Conte | Tetracyclic indole derivatives as antiviral agents |
| US7795247B2 (en) | 2004-10-26 | 2010-09-14 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa | Tetracyclic indole derivatives as antiviral agents |
-
2005
- 2005-10-25 CA CA002585084A patent/CA2585084A1/en not_active Abandoned
- 2005-10-25 CA CA002585113A patent/CA2585113A1/en not_active Abandoned
- 2005-10-25 RU RU2007119562/04A patent/RU2007119562A/ru not_active Application Discontinuation
- 2005-10-25 KR KR1020077009541A patent/KR20070068427A/ko not_active Withdrawn
- 2005-10-25 PE PE2005001247A patent/PE20060607A1/es not_active Application Discontinuation
- 2005-10-25 MX MX2007004979A patent/MX2007004979A/es active IP Right Grant
- 2005-10-25 JP JP2007538504A patent/JP2008517987A/ja active Pending
- 2005-10-25 AU AU2005298412A patent/AU2005298412B2/en not_active Ceased
- 2005-10-25 EP EP05798382A patent/EP1807397A2/en not_active Withdrawn
- 2005-10-25 US US11/666,583 patent/US7662809B2/en not_active Expired - Fee Related
- 2005-10-25 AU AU2005298403A patent/AU2005298403A1/en not_active Abandoned
- 2005-10-25 WO PCT/GB2005/004144 patent/WO2006046039A2/en not_active Ceased
- 2005-10-25 EP EP05798379A patent/EP1807403A2/en not_active Withdrawn
- 2005-10-25 BR BRPI0516972-0A patent/BRPI0516972A/pt not_active IP Right Cessation
- 2005-10-25 JP JP2007538502A patent/JP2008517986A/ja active Pending
- 2005-10-25 WO PCT/GB2005/004127 patent/WO2006046030A2/en not_active Ceased
- 2005-10-26 TW TW094137552A patent/TW200630344A/zh unknown
- 2005-10-26 AR ARP050104493A patent/AR051469A1/es unknown
-
2007
- 2007-04-16 NI NI200700102A patent/NI200700102A/es unknown
- 2007-04-17 IL IL182610A patent/IL182610A0/en unknown
- 2007-04-19 CR CR9069A patent/CR9069A/es not_active Application Discontinuation
- 2007-04-23 EC EC2007007412A patent/ECSP077412A/es unknown
- 2007-05-23 MA MA29932A patent/MA29037B1/fr unknown
- 2007-05-25 NO NO20072689A patent/NO20072689L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006046039A2 (en) | 2006-05-04 |
| AU2005298412B2 (en) | 2011-06-09 |
| CA2585084A1 (en) | 2006-05-04 |
| WO2006046039A3 (en) | 2006-07-06 |
| JP2008517987A (ja) | 2008-05-29 |
| AU2005298412A1 (en) | 2006-05-04 |
| US7662809B2 (en) | 2010-02-16 |
| TW200630344A (en) | 2006-09-01 |
| MA29037B1 (fr) | 2007-11-01 |
| ECSP077412A (es) | 2007-05-30 |
| RU2007119562A (ru) | 2008-12-10 |
| EP1807397A2 (en) | 2007-07-18 |
| US20080261938A1 (en) | 2008-10-23 |
| MX2007004979A (es) | 2007-06-14 |
| AR051469A1 (es) | 2007-01-17 |
| CA2585113A1 (en) | 2006-05-04 |
| WO2006046030A2 (en) | 2006-05-04 |
| NO20072689L (no) | 2007-07-17 |
| BRPI0516972A (pt) | 2008-09-30 |
| AU2005298403A1 (en) | 2006-05-04 |
| WO2006046030A3 (en) | 2006-07-06 |
| IL182610A0 (en) | 2007-07-24 |
| JP2008517986A (ja) | 2008-05-29 |
| NI200700102A (es) | 2007-10-18 |
| PE20060607A1 (es) | 2006-07-14 |
| KR20070068427A (ko) | 2007-06-29 |
| EP1807403A2 (en) | 2007-07-18 |
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| FA | Abandonment or withdrawal (granting procedure) |