AR070361A1 - Compuestos heterociclicos antiviricos - Google Patents
Compuestos heterociclicos antiviricosInfo
- Publication number
- AR070361A1 AR070361A1 ARP090100481A ARP090100481A AR070361A1 AR 070361 A1 AR070361 A1 AR 070361A1 AR P090100481 A ARP090100481 A AR P090100481A AR P090100481 A ARP090100481 A AR P090100481A AR 070361 A1 AR070361 A1 AR 070361A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- hydrogen
- acyl
- optionally substituted
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
- C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D407/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Virology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Furan Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Son inhibidores de la polimerasa NS5b del virus de la hepatitis C. Se describen también composiciones y métodos para tratar una infeccion del HCV y para inhibir la replicacion del HCV. Reivindicacion1: Un compuesto de la formula (1) en la que A1 es fenileno o piridinileno; A2 es fenilo o piridinilo opcionalmente sustituidos por 1-3 grupos elegidos con independencia entre el grupo formado por halogeno, alquilo C1-6, haloalquilo C1-6, ciano y alcoxi C1-6; R1 es hidrogeno, alquilo C1-10, cicloalquilo C3-7, alcoxi C1-10 o halogeno; Y es NR2R3, hidroxialquilo C1-6, acilo C1-6 o heteroarilo elegido entre el grupo formado por pirrolilo, pirazolilo o isoxazolilo, dicho heteroarilo está opcionalmente sustituido por uno o dos grupos elegidos entre alquilo C1-3, haloalquilo C1-3, alcoxi C1-3, halogeno o pirrolidinilo, en el que el átomo de nitrogeno está opcionalmente sustituido por acilo C1-6 o alquilsulfonilo C1-6; en la que (i) R2 es (a) hidrogeno, (b) alquilo C1-10, (c) alquilo C1-10 sustituido de una a cuatro veces por restos elegidos con independencia entre hidroxi, NR7bR8b, alcoxi C1-3, halogeno y ciano; (d) R11S(=O)m[C(R5)2]1-6 en el que R11 es alquilo C1-6 o NR7cR8c;8; (e) alquilo C1-3-S(=O)2NH-[C(R5)2]1-6; (f) R7bR8bNC(=O)-[C(R5)2]1-6; (g) cicloalquilo C3-6 opcionalmente sustituido por -OH, alcoxi C1-3 o -NR7bR8b; (h) heterociclilo; (i) heterociclil-alquilo C1-6, (j) heteroaril-alquilo C1-6, (k) acilo C1-6 opcionalmente sustituido por alquilsulfonilo C1-6; (l) (CH2)pCOX3 en el que p es un numero de uno a seis y X3 es hidroxi, alcoxi C1-6 o NR7cR8c; en el que dicho resto heterociclilo es oxetanilo, tetrahidrofuranilo, tetrahidropiranilo, azetidinilo, pirrolidinilo o piperidinilo, oxazolidin-2-on-4-ilo y dicho resto heteroarilo es piridinilo o pirimidinilo y dichos grupos heterociclilo o heteroarilo están opcionalmente sustituidos por -OH, alcoxi C1-3, alquilo C1-3 o -NR7bR8b; R3 es hidrogeno, alquilo C1-10, S(O)2R6, S(=O)2NR7aR8a, acilo C1-6 o C(=O)NR7aR8a; o bien (ii) R2 y R3 juntos son (CH2)2X1(CH2)2, (CH2)3-4S(=O)2, (CH2)2-3NR10S(=O)2; R4 y R5 son con independencia hidrogeno, alquilo C1-6 o cicloalquilo C3-7; R6 es alquilo C1-6 o cicloalquilo C3-7; R7a y R8a son (i) con independencia hidrogeno, alquilo C1-6, hidroxialquilo C1-6, haloalquilo C1-6 o bien (ii) R7a y R8a juntos son (CH2)2X1(CH2)2; R7b, R8b y R10 son con independencia hidrogeno, alquilo C1-6, acilo C1-6 o alquilsulfonilo C1-6, R7c y R8c son con independencia hidrogeno o alquilo C1-3; R9 es hidrogeno, acilo C1-3, alquilsulfonilo C1-3 o alquilo C1-3; R10 es hidrogeno o alquilo C1-6; X1 es -O-, -NR9-, -S(O)m, (CH2)n; X2 es NHR5 u O; m y n son con independencia un numero entero de 0 a 2; o, una sal farmacéuticamente aceptables del mismo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US2862908P | 2008-02-14 | 2008-02-14 | |
US13860308P | 2008-12-18 | 2008-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR070361A1 true AR070361A1 (es) | 2010-03-31 |
Family
ID=40521706
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP090100481A AR070361A1 (es) | 2008-02-14 | 2009-02-12 | Compuestos heterociclicos antiviricos |
Country Status (18)
Country | Link |
---|---|
US (1) | US8071797B2 (es) |
EP (1) | EP2245023B1 (es) |
JP (1) | JP2011512341A (es) |
KR (1) | KR20100117073A (es) |
CN (1) | CN101910145A (es) |
AR (1) | AR070361A1 (es) |
AT (1) | ATE539070T1 (es) |
AU (1) | AU2009214194B2 (es) |
BR (1) | BRPI0907885A2 (es) |
CA (1) | CA2714254A1 (es) |
CL (1) | CL2009000305A1 (es) |
ES (1) | ES2377280T3 (es) |
IL (1) | IL204736A0 (es) |
MX (1) | MX2010004623A (es) |
PE (1) | PE20091458A1 (es) |
RU (1) | RU2010137635A (es) |
TW (1) | TW200936573A (es) |
WO (1) | WO2009101022A1 (es) |
Families Citing this family (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8293909B2 (en) | 2008-09-11 | 2012-10-23 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
US8048887B2 (en) * | 2008-09-11 | 2011-11-01 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
US8198449B2 (en) | 2008-09-11 | 2012-06-12 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
US7994171B2 (en) | 2008-09-11 | 2011-08-09 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
JP2013505912A (ja) * | 2009-09-24 | 2013-02-21 | エフ.ホフマン−ラ ロシュ アーゲー | 複素環式抗ウイルス化合物 |
US8324212B2 (en) | 2010-02-25 | 2012-12-04 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
US8354410B2 (en) | 2010-03-11 | 2013-01-15 | Bristol-Meyers Squibb Company | Compounds for the treatment of hepatitis C |
JP2013522192A (ja) * | 2010-03-11 | 2013-06-13 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎の処置のための化合物 |
US8324239B2 (en) | 2010-04-21 | 2012-12-04 | Novartis Ag | Furopyridine compounds and uses thereof |
US8445497B2 (en) | 2010-06-30 | 2013-05-21 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
MX2013004655A (es) | 2010-10-26 | 2013-08-27 | Presidio Pharmaceuticals Inc | Inhibidores del virus de la hepatitis c. |
US8507683B2 (en) | 2010-12-09 | 2013-08-13 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
WO2012087833A1 (en) | 2010-12-22 | 2012-06-28 | Abbott Laboratories | Hepatitis c inhibitors and uses thereof |
EP2744342B1 (en) | 2011-08-17 | 2019-04-24 | GlaxoSmithKline LLC | Therapeutic methods |
WO2013028371A1 (en) * | 2011-08-19 | 2013-02-28 | Glaxo Group Limited | Benzofuran compounds for the treatment of hepatitis c virus infections |
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 |
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 |
US9303020B2 (en) | 2012-02-08 | 2016-04-05 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
WO2013148620A1 (en) | 2012-03-27 | 2013-10-03 | Bristol-Myers Squibb Company | Benzofuran derivatives for the treatment of hepatitis c |
JP2016505011A (ja) * | 2013-01-10 | 2016-02-18 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎の治療用の大環状ベンゾフランおよびアザベンゾフラン化合物 |
US8962651B2 (en) | 2013-03-13 | 2015-02-24 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
WO2014159559A1 (en) | 2013-03-14 | 2014-10-02 | Bristol-Myers Squibb Company | Fused furans for the treatment of hepatitis c |
EP3119769A1 (en) * | 2014-03-21 | 2017-01-25 | Bristol-Myers Squibb Pharma Company | Cyanoamino (aza)benzofuran compounds for the treatment of hepatitis c |
ES2688147T3 (es) | 2014-03-21 | 2018-10-31 | Bristol-Myers Squibb Company | Compuestos de 6H-furo[2,3-e]indol para el tratamiento de la hepatitis C |
AR099820A1 (es) | 2014-03-21 | 2016-08-17 | Bristol Myers Squibb Co | Ciano que contiene compuestos de azabenzofuran para el tratamiento de la hepatitis c |
US9840511B2 (en) | 2014-05-21 | 2017-12-12 | Bristol-Meyers Squibb Company | 2-(aryl or heteroaryl-)phenyl (AZA)benzofuran compounds for the treatment of hepatitis C |
US10214534B2 (en) | 2014-06-11 | 2019-02-26 | Bristol-Myers Squibb Company | Substituted 2-phenyl (AZA)benzofuran compounds for the treatment of hepatitis C |
WO2016022513A1 (en) | 2014-08-05 | 2016-02-11 | Bristol-Myers Squibb Company | Furopyridine compounds for the treatment of hepatitis c |
BR112017006117A2 (pt) | 2014-09-26 | 2017-12-19 | Changzhou Yinsheng Pharmaceutical Co Ltd | análogo de benzofurano como inibidor de ns4b |
EP3201202A1 (en) | 2014-10-02 | 2017-08-09 | Bristol-Myers Squibb Company | Macrocyclic benzofuran compounds for the treatment of hepatitis c |
US10131645B2 (en) | 2015-02-19 | 2018-11-20 | Bristol-Myers Squibb Company | Benzofurans substituted with primary benzamide as HCV inhibitors |
WO2016133961A1 (en) | 2015-02-19 | 2016-08-25 | Bristol-Myers Squibb Company | Benzofurans substituted with bicyclic secondary benzamide as hcv inhibitors |
US10125111B2 (en) | 2015-02-19 | 2018-11-13 | Bristol-Myers Squibb Company | Benzofuran compounds for the treatment of hepatitis C |
WO2016133963A1 (en) | 2015-02-19 | 2016-08-25 | Bristol-Myers Squibb Company | Benzofurans substituted with secondary benzamide as hcv inhibitors |
WO2016133972A1 (en) | 2015-02-19 | 2016-08-25 | Bristol-Myers Squibb Company | Substituted benzofuran compounds for the treatment of hepatitis c |
TWI731854B (zh) | 2015-03-23 | 2021-07-01 | 美商共結晶製藥公司 | C型肝炎病毒聚合酶之抑制劑 |
CN105732602B (zh) * | 2015-09-23 | 2017-04-19 | 常州寅盛药业有限公司 | 作为ns4b抑制剂的苯并呋喃类似物 |
BR112018007876B1 (pt) * | 2015-11-19 | 2023-10-17 | Shanghai Hengrui Pharmaceutical Co., Ltd. | Derivado de benzofurano, seus usos e seu processo de preparação, e composição farmacêutica |
EP3380199A4 (en) | 2015-11-24 | 2019-05-22 | L'oreal | DEVICE FOR TREATING HAIR |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HN2003000348A (es) * | 2002-11-01 | 2008-10-14 | Viropharma Inc | Compuestos de benzofurano, composiciones y metodos para tratamiento y profilaxis de infeccion virales de hepatitis c y enfermedades asociadas. |
CL2007000361A1 (es) * | 2006-02-09 | 2008-01-25 | Wyeth Corp | Combinacion que comprende un inhibidor de la arn polimerasa del virus de la hepatitis c (vhc) y un inhibidor de la proteasa del vhc; composicion farmaceutica que la comprende; y uso de la combinacion para tratar trastornos asociados con vhc. |
MX2009008439A (es) * | 2007-02-12 | 2009-08-13 | Intermune Inc | Nuevos inhibidores de la replicacion del virus de hepatitis c. |
-
2009
- 2009-02-05 EP EP09710988A patent/EP2245023B1/en not_active Not-in-force
- 2009-02-05 ES ES09710988T patent/ES2377280T3/es active Active
- 2009-02-05 KR KR1020107017891A patent/KR20100117073A/ko not_active Application Discontinuation
- 2009-02-05 AT AT09710988T patent/ATE539070T1/de active
- 2009-02-05 AU AU2009214194A patent/AU2009214194B2/en not_active Ceased
- 2009-02-05 CN CN2009801015270A patent/CN101910145A/zh active Pending
- 2009-02-05 CA CA2714254A patent/CA2714254A1/en not_active Abandoned
- 2009-02-05 JP JP2010546292A patent/JP2011512341A/ja active Pending
- 2009-02-05 WO PCT/EP2009/051306 patent/WO2009101022A1/en active Application Filing
- 2009-02-05 BR BRPI0907885-1A patent/BRPI0907885A2/pt not_active IP Right Cessation
- 2009-02-05 RU RU2010137635/04A patent/RU2010137635A/ru not_active Application Discontinuation
- 2009-02-05 MX MX2010004623A patent/MX2010004623A/es active IP Right Grant
- 2009-02-11 TW TW098104353A patent/TW200936573A/zh unknown
- 2009-02-11 CL CL2009000305A patent/CL2009000305A1/es unknown
- 2009-02-12 AR ARP090100481A patent/AR070361A1/es not_active Application Discontinuation
- 2009-02-12 US US12/378,346 patent/US8071797B2/en not_active Expired - Fee Related
- 2009-02-13 PE PE2009000213A patent/PE20091458A1/es not_active Application Discontinuation
-
2010
- 2010-03-25 IL IL204736A patent/IL204736A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
MX2010004623A (es) | 2010-06-07 |
CN101910145A (zh) | 2010-12-08 |
IL204736A0 (en) | 2010-11-30 |
WO2009101022A1 (en) | 2009-08-20 |
EP2245023A1 (en) | 2010-11-03 |
TW200936573A (en) | 2009-09-01 |
PE20091458A1 (es) | 2009-09-24 |
CL2009000305A1 (es) | 2010-02-19 |
AU2009214194A1 (en) | 2009-08-20 |
US8071797B2 (en) | 2011-12-06 |
RU2010137635A (ru) | 2012-03-20 |
CA2714254A1 (en) | 2009-08-20 |
US20090208449A1 (en) | 2009-08-20 |
AU2009214194B2 (en) | 2012-05-17 |
KR20100117073A (ko) | 2010-11-02 |
ATE539070T1 (de) | 2012-01-15 |
EP2245023B1 (en) | 2011-12-28 |
BRPI0907885A2 (pt) | 2015-07-21 |
JP2011512341A (ja) | 2011-04-21 |
ES2377280T3 (es) | 2012-03-26 |
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Legal Events
Date | Code | Title | Description |
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FA | Abandonment or withdrawal |