AR040411A1 - Inhibidores de la arn polimerasa dependiente de arn del virus de la hepatitis c y composiciones y tratamientos que los usan - Google Patents
Inhibidores de la arn polimerasa dependiente de arn del virus de la hepatitis c y composiciones y tratamientos que los usanInfo
- Publication number
- AR040411A1 AR040411A1 AR20030101630A ARP030101630A AR040411A1 AR 040411 A1 AR040411 A1 AR 040411A1 AR 20030101630 A AR20030101630 A AR 20030101630A AR P030101630 A ARP030101630 A AR P030101630A AR 040411 A1 AR040411 A1 AR 040411A1
- Authority
- AR
- Argentina
- Prior art keywords
- nhc
- integer
- aryl
- group
- cycloalkyl
- Prior art date
Links
- 241000711549 Hepacivirus C Species 0.000 title 1
- 108060004795 Methyltransferase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 238000011282 treatment Methods 0.000 title 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 11
- 229910052736 halogen Inorganic materials 0.000 abstract 11
- 150000002367 halogens Chemical class 0.000 abstract 11
- 125000003118 aryl group Chemical group 0.000 abstract 10
- 125000001072 heteroaryl group Chemical group 0.000 abstract 9
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 9
- 125000001424 substituent group Chemical group 0.000 abstract 9
- 125000003342 alkenyl group Chemical group 0.000 abstract 7
- 125000000304 alkynyl group Chemical group 0.000 abstract 7
- 125000003545 alkoxy group Chemical group 0.000 abstract 6
- 125000004404 heteroalkyl group Chemical group 0.000 abstract 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 4
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 3
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 abstract 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001924 cycloalkanes Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000002207 metabolite Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/32—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
- C07D417/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Reivindicación 1: Un método para inhibir la actividad de la polimerasa de VHC caracterizado porque comprende poner en contacto una polimerasa VHC con una cantidad eficaz de un compuesto representado por la fórmula (1) o una sal, solvato, profármaco, o metabolito del mismo; en la que r es 0, 1, 2, 3, 4 o 5; R1 es hidrógeno, o un grupo arilo, heteroarilo, cicloalquilo, o heterocicloalquilo, sin substituir o substituido con uno o más substituyentes seleccionados entre el grupo substituir o substituido con uno o más substituyentes seleccionados entre el grupo compuesto por grupos halógenos; =O; =S; -CN; -NO2; alcano ramificado o no ramificado; alquilo; heteroalquilo; alquenilo; alquinilo; arilo; cicloalquilo; heterocicloalquilo; heteroarilo; compuesto por halógeno; =O; =S; -CN; -NO2; alquilo; heteroalquilo; alquenilo; alquinilo; arilo; cicloalquilo; heterocicloalquilo; heteroarilo; alcoxi; isopropilo; t-butilo; -(CH2)zCN donde z es un entero de 1 a 4; =NH; -NHOH; -OH; -OCH3; -OCH2-; -OCH2CH3; -C(O)H; -OC(O)H; -C(O)OH; -CH2CH(O)OCH3; -OC(O)OH; -OC(O)OC(O)H; -OOH; -C(NH)NH2; -NHC(NH)NH2; -C(S)NH2; -NHC(S)NH2; -NHC(O)NH2; -S(O2)H; -S(O)H; -NH2; -C(O)NH2; -OC(O)NH2; -NHC(O)H; -NHC(O)OH; -C(O)NHC(O)H; -OS(O2)H; -OS(O)H; -OSH; -SC(O)H; -S(O)C(O)OH; -SO2C(O)OH; -SO2CH3; -NHSH; -NHS(O)H; -NHSO2H; -C(O)SH; -C(O)S(O)H; -C(O)S(O2)H; -C(S)OH; -C(SO)OH; -C(SO2)OH; -NHC(S) H; -OC(S)H; -OC(S)OH; -OC(SO2)H; -S(O2)NH2; -S(O)NH2; -SNH2; -NHCS(O2)H; -NHC(SO)H; -NHC(S)H; y -SH, sin alcoxi; -(CH2)zCN donde z es un entero de 1 a 4; =NH; -NHOH; -OH; -C(O)H; -OC(O)H; -C(O)OH; -C(O)OC(CH3)n, donde n es un entero de 1 a 3; -OC(O)OH; -OC(O)OC(O)H; -OOH; -C(NH)NH2; -NHC(NH)NH2; -C(S)NH2; -NHC(S)NH2; -NHC(O)NH2; -S(O2)H; -S(O)H; -NH2; -C(O)NH2; -OC(O)NH2; -NHC(O)H; -NHC(O)OH; -C(O)NHC(O)H; -OS(O2)H; -OS(O)H; -OSH; -SC(O)H; -SCH2CH3; -S(O)C(O)OH; -SO2C(O)OH; -NHSH; -NHS(O)H; -NHSO2H; -C(O)SH; -C(O)S(O)H; -C(O)S (O2)H; -C(S)H; -C(SO)OH; -C(SO2)OH; -NHC(S)H; -OC(S)H; -OC(S)OH; -OC(SO2)H; -S(O2)NH2; -S(O)NH2; -SNH2; -NHCS(O2)H; -NHC(SO)H; -NHC(S)H; y -SH sin substituir o substituidos con uno o más substituyentes seleccionados entre el grupo compuesto por halógenos; fenilo; cicloalcano; -O-; -OH; y CH3; R2 es un grupo isopropilo, ciclopentilo, o ciclohexilo, sin substituir o substituido con uno o más substituyentes seleccionados entre el grupo compuesto por halógenos; =O; =S; -CN; -NO2; alquilo; alquenilo; alquinilo; arilo; cicloalquilo; heterocicloalquilo; heteroarilo; -(CH2)zCN donde z es un entero de 1 a 4; =NH; -NHOH; -OH; -C(O)H; -OC(O)H; -C(O)OH; -OC(O)OH; -OC(O)OC(O)H; -OOH; -C(NH)NH2; -NHC(NH)NH2; -C(S)NH2; -NHC(S)NH2; -NHC(O)NH2; -S(O2)H; -S(O)H; -NH2; -C(O)NH2; -OC(O)NH2; -NHC(O)H; -NHC(O)OH; -C(O)NHC(O)H; OS(O2)H; -OS(O)H; -OSH; -SC(O)H; -S(O)C(O)OH; -SO2C(O)OH; -NHSH; -NHS(O)H; -NHSO2H; -C(O)SH; -C(O)S(O)H; -C(O)S(O2)H; -C(S)OH; -C(SO)OH; -C(SO2)OH; -NHC(S)H; -OC(S)H; -OC(S)OH; -OC(SO2)H; -S(O2)NH2; -S(O)NH2; -SNH2; -NHCS (O2) H; -NHC(SO)H; -NHC(S)H; y -SH; R3 es hidrógeno; halógeno; =S; -SH; -S-(CH2)z-heteroarilo donde z es un entero de 0 a 4; -S-(CH2)z-heterocicloalquilo donde z es un entero de 0 a 4; -S-(CH2)z-arilo donde z es un entero de 0 a 4; -(CH2)z-arilo donde z es un entero de 0 a 4; -O-arilo; -C(O)H; -C(O)-alquilo; amino; o un halógeno, sin substituir o substituido con un grupo arilo, halógenos; =O; =S; -CN; -NO2; alquilo; heteroalquilo; alquenilo; alquinilo; arilo; cicloalquilo; heterocicloalquilo; heteroarilo; alcoxi; isopropilo; t-butilo; - (CH2)zCN donde z es un entero de 1 a 4; =NH; -NHOH; -OH; -OCH3, -OCH2-; -OCH2CH3; -C(O)H; -OC(O)H; -C(O)OH; -OS(O2)H; -OS(O)H; -OSH; -SC(O)H; -S(O)C(O)OH; -SO2C(O)OH; -SO2CH3; -NHSH; -NHS(O)H; -NHSO2H; -C(O)SH; -C(O)S(O)H; -C(O)S(O2)H; -C(S)OH; -C(SO)OH; -C(SO2)OH; -NHC(S)H; -OC(S)H; -OC(S)OH; -OC(SO2)H; -S(O2)NH2; -S(O)NH2; -SNH2; -NHCS(O2)H; -NHC(SO)H; -NHC(S)H; y -SH, sin substituir o substituido con uno o más substituyentes seleccionados entre el grupo compuesto por halógenos; =O; =S; -CN; -NO2; alcano, ramificado o no ramificado; alquilo; heteroalquilo; alquenilo; alquinilo; arilo; cicloalquilo; heterocicloalquilo; heteroarilo; alcoxi; -(CH2)zCN donde z es un entero de 1 a 4; =NH; -NHOH; -OH; -C(O)H; -OC(O)H; -C(O)OH; -C(O)OC(CH3)n, donde n es un entero de 1 a 3; -OC(O)OH; -OC(O)OC(O)H; -OOH; -C(NH)NH2; -NHC(NH)NH2; -C(S)NH2; -NHC(S)NH2; -NHC(O)NH2; -S(O2)H; -S(O)H; -NH2; -C(O)NH2; -OC(O)NH2; -NHC(O)H; -NHC(O)OH; -C(O)NHC(O)H; -OS(O2)H; -OS(O)H; -OSH; -SC(O)H; -SCH2CH3; -S(O)C(O)OH; -SO2C(O)OH; -NHSH; -NHS(O)H; -NHSO2H; -C(O)SH; -C(O)S(O)H; -C(O)S(O2)H; -C(S)H; -C(SO)OH; -C(SO2)OH; -NHC(S)H; -OC(S)H; -OC(S)OH; -OC(SO2)H; -S(O2)NH2; -S(O)NH2; -SNH2; -NHCS(O2)H; -NHC(SO)H; -NHC(S)H; y -SH, sin substituir o substituido con uno o más substituyentes seleccionados entre el grupo compuesto por halógenos; fenilo; cicloalcano; -O-; -OH; y CH3; R4 es =O ó -OR5; X-W es C-CH cuando R4 es =O, y X-W es C=C cuando R4 es -OR5; o R3 y R4 junto con X y W forman un grupo cicloalquilo, heteroarilo, cicloalquilo, o heterocicloalquilo sin substituir o substituidos con uno o más substituyentes seleccionados entre el grupo compuesto por halógenos; =O; =S; -CN; -NO2; alquilo; heteroalquilo; alquenilo; alquinilo; arilo; cicloalquilo; heterocicloalquilo; heteroarilo; alcoxi; isopropilo; t-butilo; -(CH2)zCN donde z es un entero de 1 a 4; =NH; -NHOH; -OH; -OCH3, -OCH2-; -OCH2CH3; -C(O)H; -OC(O)H; -C(O)OH; -CH2CH(O)OCH3; -OC(O)OH; -OC(O)OC(O)H; -OOH; -C(NH)NH2; -NHC(NH)NH2; -C(S)NH2; -NHC(S)NH2; -NHC(O)NH2; -S(O2)H; -S(O)H; -NH2; -C(O)NH2; -OC(O)NH2; -NHC(O)H; -NHC(O)OH; -NHC(NH)NH2; -C(S)NH2; -NHC(S)NH2; -NHC(O)NH2; -S(O2)H; -S(O)H; -NH2; -C(O)NH2; -OC(O)NH2; -NHC(O)H; -NHC(O)OH; -C(O)NHC(O)H; -OS(O2)H; -OS(O)H; -OSH; -SC(O)H; -S(O)C(O)OH; -SO2C(O)OH; -SO2CH3; -NHSH; -NHS(O)H; -NHSO2H; -C(O)SH; -C(O)S(O)H; -C(O)S(O2)H; -C(S)OH; -C(SO)OH; -C (SO2)OH; -NHC(S)H; -OC(S)H; -OC(S)OH; -OC(SO2)H; -S(O2)NH2; -S(O)NH2; -SNH2; -NHCS(O2)H; -NHC(SO)H; -NHC(S)H; y -SH, sin substituir o substituidos con uno o más substituyentes seleccionados entre el grupo compuesto por halógenos; =O; =S; -CN; -NO2; alcano, ramificado o no ramificado; alquilo; heteroalquilo; alquenilo; alquinilo; arilo; cicloalquilo; heterocicloalquilo; heteroarilo; alcoxi; -(CH2)zCN donde z es un entero de 1 a 4; =NH; -NHOH; -OH; -C(O)H; -OC(O)H; -C(O)OH; -C(O)OC(CH3)n, donde n es un entero de 1 a 3; -OC(O)OH; -OC(O)OC(O)H; -OOH; -C(NH)NH2; -NHC(NH)NH2; -C(S)NH2; -NHC(S)NH2; -NHC(O)NH2; -S(O2)H; -S(O)H; -NH2; -C(O)NH2; -OC(O)NH2; -NHC(O)H; -NHC(O)OH; -C(O)NHC(O)H; -OS(O2)H; -OS(O)H; -OSH; -SC(O)H; -SCH2CH3; -S(O)C(O)OH; -SO2C(O)OH; -NHSH; -NHS(O)H; -NHSO2H; -C(O)SH; -C (O)S(O)H; -C(O)S(O2)H; -C(S)H; -C(SO)OH; -C(SO2)OH; -NHC(S)H; -OC(S)H; -OC(S)OH; -OC(SO2)H; -S(O2)NH2; -S(O)NH2; -SNH2; -NHCS(O2)H; -NHC(SO)H; -NHC(S)H; y -SH sin substituir o substituido con uno o más substituyentes seleccionados entre el grupo compuesto por halógenos; arilo; cicloalquilo; -OR5; haloalquilo; y alquilo; y R5 es un alquilo o H.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37943302P | 2002-05-10 | 2002-05-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR040411A1 true AR040411A1 (es) | 2005-04-06 |
Family
ID=29420530
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AR20030101630A AR040411A1 (es) | 2002-05-10 | 2003-05-09 | Inhibidores de la arn polimerasa dependiente de arn del virus de la hepatitis c y composiciones y tratamientos que los usan |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7115658B2 (es) |
| AR (1) | AR040411A1 (es) |
| AU (1) | AU2003224371A1 (es) |
| DO (1) | DOP2003000641A (es) |
| GT (1) | GT200300105A (es) |
| PA (1) | PA8573401A1 (es) |
| PE (1) | PE20040472A1 (es) |
| TW (1) | TW200306813A (es) |
| UY (1) | UY27798A1 (es) |
| WO (1) | WO2003095441A1 (es) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7148226B2 (en) * | 2003-02-21 | 2006-12-12 | Agouron Pharmaceuticals, Inc. | Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same |
| BRPI0507861A (pt) | 2004-02-20 | 2007-07-17 | Boehringer Ingelheim Int | inibidores de polimerase viral |
| GEP20094751B (en) * | 2004-08-18 | 2009-08-10 | Pfizer | Inhibitors of hepatitis c virus rna-dependent rna polymerase, and compositions and treatments using the same |
| MX2007005177A (es) | 2004-10-29 | 2007-06-26 | Schering Corp | 5-oxo pirazoles y [1,2,4]triazoles sustituidos como agentes antivirales. |
| CA2619077C (en) | 2005-08-24 | 2011-09-13 | Pfizer Inc. | Methods for the preparation of hcv polymerase inhibitors |
| RU2401268C2 (ru) * | 2005-08-24 | 2010-10-10 | Пфайзер Инк. | КРИСТАЛЛИЧЕСКАЯ ФОРМА (R)-6-ЦИКЛОПЕНТИЛ-6-(2-(2,6-ДИЭТИЛПИРИДИН-4-ИЛ)ЭТИЛ)-3-((5,7-ДИМЕТИЛ-[1,2,4]ТРИАЗОЛО[1,5-a]ПИРИМИДИН-2-ИЛ)МЕТИЛ)-4-ГИДРОКСИ-5,6-ДИГИДРОПИРАН-2-ОНА, ЕЕ ПРИМЕНЕНИЕ И ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, СОДЕРЖАЩАЯ ЕЕ |
| DK2320905T3 (en) | 2008-08-11 | 2017-09-18 | Glaxosmithkline Llc Corp Service Company | New adenine derivatives |
| UA103195C2 (uk) | 2008-08-11 | 2013-09-25 | Глаксосмитклайн Ллк | Похідні пурину для застосування у лікуванні алергій, запальних та інфекційних захворювань |
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| WO2011098451A1 (en) | 2010-02-10 | 2011-08-18 | Glaxosmithkline Llc | Purine derivatives and their pharmaceutical uses |
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| EP3107915B1 (en) | 2014-02-20 | 2017-11-08 | Glaxosmithkline Intellectual Property (No. 2) Limited | Pyrrolo[3,2-d]pyrimidine derivatives as inducers of human interferon |
| CA2967248A1 (en) | 2014-11-13 | 2016-05-19 | Glaxosmithkline Biologicals Sa | Adenine derivatives which are useful in the treatment of allergic diseases or other inflammatory conditions |
| HK1250032A1 (zh) | 2015-12-03 | 2018-11-23 | Glaxosmithkline Intellectual Property Development Limited | 作为sting调节剂的环状嘌呤二核苷酸 |
| MX387354B (es) | 2016-04-07 | 2025-03-18 | Glaxosmithkline Ip Dev Ltd | Amidas heterocíclicas útiles como moduladores de proteínas. |
| CN109563081A (zh) | 2016-04-07 | 2019-04-02 | 葛兰素史克知识产权开发有限公司 | 可用作蛋白调节剂的杂环酰胺类 |
| US11377440B2 (en) | 2017-10-05 | 2022-07-05 | Glaxosmithkline Intellectual Property Development Limited | Modulators of stimulator of interferon genes (STING) |
| EP3692033A1 (en) | 2017-10-05 | 2020-08-12 | GlaxoSmithKline Intellectual Property Development Limited | Modulators of stimulator of interferon genes (sting) useful in treating hiv |
| GB201807924D0 (en) | 2018-05-16 | 2018-06-27 | Ctxt Pty Ltd | Compounds |
| US20220227761A1 (en) | 2019-05-16 | 2022-07-21 | Stingthera, Inc. | Oxoacridinyl acetic acid derivatives and methods of use |
| CN114391015A (zh) | 2019-05-16 | 2022-04-22 | 斯汀塞拉股份有限公司 | 苯并[b][1,8]萘啶乙酸衍生物和使用方法 |
| GB201910305D0 (en) | 2019-07-18 | 2019-09-04 | Ctxt Pty Ltd | Compounds |
| GB201910304D0 (en) | 2019-07-18 | 2019-09-04 | Ctxt Pty Ltd | Compounds |
| CA3164751A1 (en) | 2019-12-18 | 2021-06-24 | Benjamin Joseph MORROW | Compounds |
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| US4326058A (en) * | 1979-02-05 | 1982-04-20 | Sumitomo Chemical Company, Limited | Organo-phosphoric esters and their production and use |
| US4489077A (en) * | 1983-03-23 | 1984-12-18 | Warner-Lambert Company | 3-Isoxa-zolyl-2H-1,2-benzothiazine-3-carboxamide, 1,1-dioxides |
| US6174868B1 (en) * | 1992-09-10 | 2001-01-16 | Isis Pharmaceuticals, Inc. | Compositions and methods for treatment of hepatitis C virus-associated diseases |
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| CA2167537A1 (en) * | 1993-07-19 | 1995-02-02 | Tsuneo Ozeki | Hepatitis c virus proliferation inhibitor |
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| US5840751A (en) * | 1993-11-19 | 1998-11-24 | Warner-Lambert Company | 5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents |
| EP0729463B1 (en) * | 1993-11-19 | 2002-05-22 | PARKE DAVIS & COMPANY | 5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents |
| US5504104A (en) * | 1993-11-19 | 1996-04-02 | Warner-Lambert Company | Tricyclic pyrone derivatives as protease inhibitors and antiviral agents |
| US5808062A (en) * | 1993-11-19 | 1998-09-15 | Warner-Lambert Company | Pyrone derivatives as protease inhibitors and antiviral agents |
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| WO1999014210A1 (en) * | 1997-09-15 | 1999-03-25 | Warner-Lambert Company | Process for the preparation of substituted 5,6-dihydro-2h-pyran-2-ones |
| EP1112269A2 (en) * | 1998-09-11 | 2001-07-04 | Warner-Lambert Company | Hiv protease inhibitors |
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| CA2480583C (en) * | 2002-04-01 | 2008-07-15 | Pfizer Inc. | Pyranon and pyrandion inhibitors of hepatitis c virus rna-dependent rna polymerase |
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2003
- 2003-05-02 DO DO2003000641A patent/DOP2003000641A/es unknown
- 2003-05-07 AU AU2003224371A patent/AU2003224371A1/en not_active Abandoned
- 2003-05-07 PE PE2003000446A patent/PE20040472A1/es not_active Application Discontinuation
- 2003-05-07 WO PCT/IB2003/001905 patent/WO2003095441A1/en not_active Ceased
- 2003-05-07 GT GT200300105A patent/GT200300105A/es unknown
- 2003-05-08 PA PA20038573401A patent/PA8573401A1/es unknown
- 2003-05-08 UY UY27798A patent/UY27798A1/es not_active Application Discontinuation
- 2003-05-09 TW TW092112696A patent/TW200306813A/zh unknown
- 2003-05-09 US US10/434,702 patent/US7115658B2/en not_active Expired - Fee Related
- 2003-05-09 AR AR20030101630A patent/AR040411A1/es not_active Application Discontinuation
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| AU2003224371A1 (en) | 2003-11-11 |
| US7115658B2 (en) | 2006-10-03 |
| GT200300105A (es) | 2004-03-17 |
| US20040023958A1 (en) | 2004-02-05 |
| UY27798A1 (es) | 2003-12-31 |
| TW200306813A (en) | 2003-12-01 |
| PA8573401A1 (es) | 2003-12-10 |
| DOP2003000641A (es) | 2003-11-15 |
| WO2003095441A1 (en) | 2003-11-20 |
| PE20040472A1 (es) | 2004-08-12 |
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