MX2009008541A - Fenilcarbamatos macrociclicos que inhiben el virus de hepatitis c. - Google Patents
Fenilcarbamatos macrociclicos que inhiben el virus de hepatitis c.Info
- Publication number
- MX2009008541A MX2009008541A MX2009008541A MX2009008541A MX2009008541A MX 2009008541 A MX2009008541 A MX 2009008541A MX 2009008541 A MX2009008541 A MX 2009008541A MX 2009008541 A MX2009008541 A MX 2009008541A MX 2009008541 A MX2009008541 A MX 2009008541A
- Authority
- MX
- Mexico
- Prior art keywords
- phenylcarbamates
- compounds
- hcv inhibiting
- macrocyclic
- pharmaceutically acceptable
- Prior art date
Links
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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/538—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring 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
-
- 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
- C07D255/00—Heterocyclic compounds containing rings having three nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D249/00 - C07D253/00
- C07D255/04—Heterocyclic compounds containing rings having three nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D249/00 - C07D253/00 condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- 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
- C07D498/12—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 three hetero rings
- C07D498/14—Ortho-condensed systems
Abstract
Compuestos de la fórmula I: (ver fórmula (I)) incluyendo un estereoisómero del mismo, o un N-óxido; una sal de adición farmacéuticamente aceptable o un solvato de adición farmacéuticamente aceptable de los mismos; útiles como inhibidores de HCV; procedimientos para preparar estos compuestos así como composiciones farmacéuticas que comprenden estos compuestos como ingrediente activo.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07102006 | 2007-02-08 | ||
EP07102008 | 2007-02-08 | ||
EP07102007 | 2007-02-08 | ||
PCT/EP2008/051556 WO2008096001A1 (en) | 2007-02-08 | 2008-02-08 | Hcv inhibiting macrocyclic phenylcarbamates |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009008541A true MX2009008541A (es) | 2009-08-18 |
Family
ID=39110518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009008541A MX2009008541A (es) | 2007-02-08 | 2008-02-08 | Fenilcarbamatos macrociclicos que inhiben el virus de hepatitis c. |
Country Status (14)
Country | Link |
---|---|
US (1) | US8383584B2 (es) |
EP (1) | EP2111396B1 (es) |
JP (1) | JP5554570B2 (es) |
KR (1) | KR20090111326A (es) |
CN (1) | CN101627020B (es) |
AU (1) | AU2008212760B2 (es) |
BR (1) | BRPI0807482A2 (es) |
CA (1) | CA2677015C (es) |
DK (1) | DK2111396T3 (es) |
ES (1) | ES2432590T3 (es) |
IL (1) | IL199640A0 (es) |
MX (1) | MX2009008541A (es) |
RU (1) | RU2490261C2 (es) |
WO (1) | WO2008096001A1 (es) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
US8207341B2 (en) | 2008-09-04 | 2012-06-26 | Bristol-Myers Squibb Company | Process or synthesizing substituted isoquinolines |
UY32099A (es) * | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
WO2010033466A1 (en) * | 2008-09-16 | 2010-03-25 | Phenomix Corporation | Macrocyclic inhibitors of hepatitis c protease |
PT2382198E (pt) * | 2008-12-23 | 2013-10-01 | Janssen Pharmaceuticals Inc | Processos e intermediários para a preparação de um inibidor macrocíclico de protease do vhc |
TW201040181A (en) | 2009-04-08 | 2010-11-16 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitors |
WO2011017389A1 (en) | 2009-08-05 | 2011-02-10 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors useful against viral infections, particularly hcv |
CN103534256B (zh) | 2010-12-30 | 2016-08-10 | 益安药业 | 大环丙型肝炎丝氨酸蛋白酶抑制剂 |
JP2014506255A (ja) | 2010-12-30 | 2014-03-13 | エナンタ ファーマシューティカルズ インコーポレイテッド | フェナントリジン大環状c型肝炎セリンプロテアーゼ阻害剤 |
US9353100B2 (en) | 2011-02-10 | 2016-05-31 | Idenix Pharmaceuticals Llc | Macrocyclic serine protease inhibitors, pharmaceutical compositions thereof, and their use for treating HCV infections |
US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
US8691757B2 (en) | 2011-06-15 | 2014-04-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
ES2613766T3 (es) | 2012-10-19 | 2017-05-25 | Bristol-Myers Squibb Company | Derivados de carbamato de hexadecahidrociclopropa(e)pirrolo(1,2-a)(1,4)diazaciclopentadecinilo sustituidos con 9-metilo como inhibidores de la proteasa no estructural 3 (NS3) para el tratamiento de infecciones del virus de la hepatitis C |
US9598433B2 (en) | 2012-11-02 | 2017-03-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US9643999B2 (en) | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
EP2914598B1 (en) | 2012-11-02 | 2017-10-18 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
US9409943B2 (en) | 2012-11-05 | 2016-08-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
JP6342922B2 (ja) | 2013-03-07 | 2018-06-13 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎ウイルス阻害剤 |
CN104557954A (zh) * | 2013-10-16 | 2015-04-29 | 上海唐润医药科技有限公司 | 抗hcv的大环化合物 |
EP3089757A1 (en) | 2014-01-03 | 2016-11-09 | AbbVie Inc. | Solid antiviral dosage forms |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA74546C2 (en) * | 1999-04-06 | 2006-01-16 | Boehringer Ingelheim Ca Ltd | Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition |
CA2369711A1 (en) * | 2002-01-30 | 2003-07-30 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis c virus |
AU2003299519A1 (en) * | 2002-05-20 | 2004-05-04 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
JP5248783B2 (ja) * | 2004-01-30 | 2013-07-31 | メディヴィル・アクチエボラーグ | Hcvns−3セリンプロテアーゼインヒビター |
ATE516293T1 (de) | 2004-07-16 | 2011-07-15 | Gilead Sciences Inc | Antivirale verbindungen |
MY141245A (en) * | 2005-07-29 | 2010-03-31 | Tibotec Pharm Ltd | Macrocylic inhibitors of hepatitis c virus |
EP1919898B1 (en) * | 2005-07-29 | 2011-01-26 | Tibotec Pharmaceuticals | Macrocyclic inhibitors of hepatitis c virus |
US7772183B2 (en) * | 2005-10-12 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
-
2008
- 2008-02-08 EP EP08708828.2A patent/EP2111396B1/en not_active Not-in-force
- 2008-02-08 CA CA2677015A patent/CA2677015C/en not_active Expired - Fee Related
- 2008-02-08 CN CN200880004388.5A patent/CN101627020B/zh not_active Expired - Fee Related
- 2008-02-08 MX MX2009008541A patent/MX2009008541A/es active IP Right Grant
- 2008-02-08 AU AU2008212760A patent/AU2008212760B2/en not_active Ceased
- 2008-02-08 US US12/526,085 patent/US8383584B2/en not_active Expired - Fee Related
- 2008-02-08 WO PCT/EP2008/051556 patent/WO2008096001A1/en active Application Filing
- 2008-02-08 DK DK08708828.2T patent/DK2111396T3/da active
- 2008-02-08 RU RU2009133470/04A patent/RU2490261C2/ru not_active IP Right Cessation
- 2008-02-08 BR BRPI0807482-8A2A patent/BRPI0807482A2/pt not_active IP Right Cessation
- 2008-02-08 JP JP2009548694A patent/JP5554570B2/ja not_active Expired - Fee Related
- 2008-02-08 KR KR1020097016996A patent/KR20090111326A/ko active IP Right Grant
- 2008-02-08 ES ES08708828T patent/ES2432590T3/es active Active
-
2009
- 2009-07-01 IL IL199640A patent/IL199640A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO2008096001A1 (en) | 2008-08-14 |
KR20090111326A (ko) | 2009-10-26 |
CN101627020A (zh) | 2010-01-13 |
JP5554570B2 (ja) | 2014-07-23 |
AU2008212760B2 (en) | 2014-02-27 |
IL199640A0 (en) | 2010-04-15 |
US8383584B2 (en) | 2013-02-26 |
US20100041728A1 (en) | 2010-02-18 |
JP2010518049A (ja) | 2010-05-27 |
WO2008096001A8 (en) | 2009-07-23 |
CA2677015C (en) | 2015-05-26 |
ES2432590T3 (es) | 2013-12-04 |
RU2490261C2 (ru) | 2013-08-20 |
EP2111396A1 (en) | 2009-10-28 |
CN101627020B (zh) | 2015-06-17 |
AU2008212760A1 (en) | 2008-08-14 |
BRPI0807482A2 (pt) | 2014-05-13 |
EP2111396B1 (en) | 2013-08-07 |
CA2677015A1 (en) | 2008-08-14 |
DK2111396T3 (da) | 2013-11-04 |
RU2009133470A (ru) | 2011-03-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX2009008541A (es) | Fenilcarbamatos macrociclicos que inhiben el virus de hepatitis c. | |
MX2009008540A (es) | Inhibidores de virus de hepatitis c macrociclicos sustituidos con pirimidina. | |
WO2012030685A3 (en) | Indazole derivatives useful as erk inhibitors | |
EP4071149A3 (en) | Heterocyclic compounds and uses thereof | |
MX2011011136A (es) | Eteres diarilicos. | |
MY174452A (en) | Substituted piperidines that increase p53 activity and the uses thereof | |
TW200613243A (en) | Novel compounds | |
WO2009155121A3 (en) | Inhibitors of pi3 kinase | |
SE0400284D0 (sv) | Novel compounds | |
UA94833C2 (en) | Substituted bicyclolactams | |
WO2007087548A3 (en) | Chemical compounds | |
MX2009008275A (es) | Formas polimorficas de un inhibidor macrociclico del virus de la hepatitis c. | |
MX2009000884A (es) | Derivados de piridizinona. | |
EP1714961A4 (en) | INDAZOL COMPOUND AND THEIR PHARMACEUTICAL USE | |
EA200900135A1 (ru) | Производные пиразола в качестве ингибиторов цитохрома р450 | |
MX2010003155A (es) | Derivados de ciclopropil aril amida y uso de los mismos. | |
WO2008154642A3 (en) | Antibacterial agents | |
WO2007002313A3 (en) | Phenylglycinamide and pyridylglycinamide derivatives useful as anticoagulants | |
WO2010026436A3 (en) | 1,3, 4, 6, 7, 11b-hexahydro-benzo[alpha]quinolizines for the treatment of hyperkinetic movement and related disorders | |
MY151986A (en) | Adamantyl diamide derivatives and uses of same | |
TW200806291A (en) | Pharmaceutical formulations | |
UA97348C2 (en) | HETEROCYCLIC NF-kB INHIBITORS | |
TW200639156A (en) | New compounds | |
MX2011011776A (es) | Nuevos profarmacos de triptolite. | |
WO2009140341A3 (en) | Atorvastatin compositions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
HH | Correction or change in general | ||
FG | Grant or registration |