AR045367A1 - Compuesto de anillo condensado que contiene nitrogeno y uso del mismo como inhibidor de la integrasa del vih - Google Patents
Compuesto de anillo condensado que contiene nitrogeno y uso del mismo como inhibidor de la integrasa del vihInfo
- Publication number
- AR045367A1 AR045367A1 ARP040102913A ARP040102913A AR045367A1 AR 045367 A1 AR045367 A1 AR 045367A1 AR P040102913 A ARP040102913 A AR P040102913A AR P040102913 A ARP040102913 A AR P040102913A AR 045367 A1 AR045367 A1 AR 045367A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- atom
- optionally substituted
- alkyl
- aryl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title 2
- 239000003112 inhibitor Substances 0.000 title 1
- 229910052757 nitrogen Inorganic materials 0.000 title 1
- 125000001424 substituent group Chemical group 0.000 abstract 12
- 125000000623 heterocyclic group Chemical group 0.000 abstract 11
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 10
- 125000005915 C6-C14 aryl group Chemical group 0.000 abstract 6
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000006701 (C1-C7) alkyl group Chemical group 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 239000002259 anti human immunodeficiency virus agent Substances 0.000 abstract 3
- 229940124411 anti-hiv antiviral agent Drugs 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000005914 C6-C14 aryloxy group Chemical group 0.000 abstract 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000006621 (C3-C8) cycloalkyl-(C1-C6) alkyl group Chemical group 0.000 abstract 1
- 208000030507 AIDS Diseases 0.000 abstract 1
- 125000005974 C6-C14 arylcarbonyl group Chemical group 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- 102100034343 Integrase Human genes 0.000 abstract 1
- 108010061833 Integrases Proteins 0.000 abstract 1
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000010354 integration Effects 0.000 abstract 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 239000003419 rna directed dna polymerase inhibitor Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed 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
-
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- 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)
- Communicable Diseases (AREA)
- Virology (AREA)
- Oncology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La presente se refiere a un compuesto que tiene una actividad inhibidora de la integrase del VIH y es útil como agente para la profilaxis o el tratamiento del SIDA, o como un agente anti-VIH. Además, con el uso combinado con otros agentes anti-VIH tal como un inhibidor de la proteasa, un inhibidor de la transcriptasa inversa y similares, puede ser un agente anti-VIH más efectivo. Como presenta una alta actividad inhibidora específica de la integrasa, el compuesto puede ser un agente farmacéuticamente seguro en el cuerpo humano, el cual provoca sólo una menor cantidad de efectos colaterales. Reivindicación 1: Un compuesto de anillo condensado que contiene N representado por la siguiente fórmula (1) o una de sus sales farmacéuticamente aceptables: en donde R1 es (1) un grupo alquilo C1-6 opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del siguiente grupo A, (2) un grupo alquenilo C2-6 opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del siguiente grupo A o (3) un grupo representado por la fórmula (2) en donde Z es (1´)un enlace; (2´) un alquileno (C1-6); (3´) un alquileno C2-6 o (4´)*-(CH2)m-Q-(CH2)n- en donde Q es (1") -O-; (2") -NR5- en donde R5 es un átomo de H o un grupo alquilo C1-6, (3") -CO-, (4") -SO-; (5") -SO2- o (6") **-CO-NR6- en donde R6 es un átomo de H o un grupo alquilo C1-6 y ** indica el lado a ser unido con (CH2)m; m es 0 o un número entero de 1 a 4; n es 0 o un número entero de 1 a 4 y * indica el lado a ser unido con un átomo de N del anillo A, y anillo D es (1´) un grupo del anillo de C C3-10 opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del siguiente grupo B o (2´) un grupo heterocíclico opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del siguiente grupo B en donde el grupo heterocíclico contiene al menos un heteroátomo seleccionado de átomo de N, átomo de O y átomo de S; X es: (1) -C(Rx1)(Rx2)- , (2) -C(Rx1)(Rx2)-C(Rx3)(Rx4)- , (3) -C(Rx1)(Rx2)-C(Rx3)(Rx4)-C(Rx5)(Rx6)- , (4) -C(Rx7)=C(Rx8)- , (5) -C(Rx1)(Rx2)-C(Rx7)=C(Rx8)- , (6) -C(Rx7)=C(Rx8)-C(Rx1)(Rx2)- , (7) -N=C(Rx9)- o (8) -C(Rx10)=N- en donde indica el lado a ser unido con Y1 del anillo B, Rx1 a Rx10 se seleccionan cada uno, de modo independiente, del siguiente grupo C, Rx1 y Rx2, Rx3 y Rx4, y Rx5 y Rx6 forman cada uno opcionalmente, de modo independiente, un cicloalquilo C3-8 junto con el átomo de C adyacente; el resto de fórmula (3) del anillo B es (1) C=C(Ry1)-N(Ry2), (2) N-C(Ry1)=N, (3) N-C(Ry1)=C(Ry2), (4) C=N-N(Ry2) o (5) N-N=C(Ry3) en donde Ry1 a Ry3 se seleccionan cada uno, de modo independiente, del siguiente grupo C, cuando el resto de fórmula (3) es N-C(Ry1)=C(Ry2), el anillo B está opcionalmente condensado con un anillo benceno para formar un anillo condensado representado por la fórmula (4) en donde R4 se selecciona del siguiente grupo C; y R2 es (1) un átomo de h, (2) un grupo alquilo C1-6; (3) un grupo aril C6-14-alquilo C1-6 o (4) -SO2Rd1 en donde Rd1 es un átomo de H, un grupo alquilo C1-7 opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del siguiente grupo A o un grupo arilo C6-14; grupo A: (1) un átomo de halógeno; (2) un grupo ciano; (3) -ORa1; (4) -SRa1; (5) -CO2Ra1; (6) -CONRa2Ra3; (7) -CORa4; (8) -SO2NRa2Ra3, (9) -SO2Ra4; (10) un grupo ariloxi C6-14, (11) un grupo aril C6-14-alquiloxicarbonilo C1-6, (12) un grupo alquilcarboniloxi C1-6 opcionalmente sustituido con átomos de halógeno, (13) un grupo arilo C6-14 opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del grupo integrado por un átomo de halógeno, un grupo alquilo C1-6, un grupo alquilsulfonilo C1-6, un grupo di(alquil C1-6)amino y un grupo alquilcarbonilamino C1-6 y (14) un grupo heterocíclico opcionalmente sustituido con un grupo alquiloxi C1-6, en donde Ra1, Ra2, Ra3, y Ra4 son cada uno, de modo independiente, un átomo de H o un grupo alquilo c1-6; grupo B: (1) un átomo de halógeno; (2) un grupo ciano, 3) un grupo alquilo C1-6; (4) un grupo haloalquilo C1-6; (5) -ORb1; (6) -SRb1, (7) -CO2Rb1, (8) -CONRb3Rb3; (9) -CORb4; (10) -SO2NRb2Rb3; (11) -SO2Rb4; (12) un grupo ariloxi C6-14; (13) un grupo aril C6-14-alquiloxicarbonilo C1-6; (14) un grupo aril C6-14-alquiloxi C1-6 y (15) -NRb5CORb6, en donde Rb1, Rb2, Rb3, Rb4, Rb5 y Rb6 son cada uno, de modo independiente, un átomo de H o un grupo alquilo C1-6; grupo C: (1) un átomo de h, (2) un grupo cicloalquil C3-8-alquilo C1-6; (3) un grupo ciano; (4) un átomo de halógeno; (5) un grupo alquilo C1-7; (6) un grupo alquenilo C2-6; (7) un grupo alquinilo C2-6; (8) un grupo arilo C6-14; (9) un grupo heterocíclico, en donde dicho grupo heterocíclico es un heteromonociclo saturado o insaturado de 5 miembros o de 6 miembros que contiene al menos un heteroátomo seleccionado de átomo de N, átomo de O y átomo de S, o un anillo condensado de tales heterociclos, o un anillo condensado de un anillo de C seleccionado de benceno, ciclopentano y ciclohexano y el heterociclo antes definido, (10) un grupo ariloxi C1-6; (11) un grupo aril C6-14-alquilo C1-6; (12) un grupo aril C6-14-alquiloxi C1-6; (13) -CO2Rc1; (14) -CONRc2Rc3; (15) -CORc4; (16) -SO2NRc2Rc3; (17) un grupo arilcarboniloC6-14; (18) -NRc4Rc5; (19) -NRc6CORc7; (20) -NRc8SO2Rc9; (21) -SRc10; (22) -SORc11; (23) -SO2Rc12, (24) -NRc13CONRc14Rc15; (25) -NRc16CO2Rc17 y (26) -NRc18COCORc19; en donde Rc1, Rc2, Rc3, Rc4, Rc5, Rc6, Rc7, Rc8, Rc9, Rc10, Rc11, Rc12, Rc13, Rc14, Rc15, Rc16, Rc17, Rc18 y Rc19 son cada uno, de modo independiente, (1´) un átomo de H; (2´) un grupo alquilo C1-7 opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del grupo A antes mencionado, (3´) un grupo arilo C6-14 opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del grupo B antes mencionado, (4´) un grupo heterocíclico opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del grupo B antes mencionado o (5´) un grupo cicloalquilo C3-8, en donde Rc2 y Rc3 forman opcionalmente, junto con el átomo de N adyacente, un heterociclo que contiene N opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del grupo B antes mencionado; el grupo alquilo C1-7, el resto de alquilo C1-6, el grupo alquenilo C2-6 y el grupo alquinilo C2-6 del grupo C antes mencionado están opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados del grupo A antes mencionado, o un grupo heterocíclico; y el grupo arilo C6-14, el resto de arilo C6-14 y el grupo heterocíclico del grupo C antes mencionado están opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados del grupo B antes mencionado.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003293117 | 2003-08-13 | ||
| JP2004134896 | 2004-04-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR045367A1 true AR045367A1 (es) | 2005-10-26 |
Family
ID=34197143
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040102913A AR045367A1 (es) | 2003-08-13 | 2004-08-13 | Compuesto de anillo condensado que contiene nitrogeno y uso del mismo como inhibidor de la integrasa del vih |
Country Status (15)
| Country | Link |
|---|---|
| US (3) | US20050054645A1 (es) |
| EP (2) | EP2042502A1 (es) |
| JP (1) | JP3814631B2 (es) |
| AR (1) | AR045367A1 (es) |
| AT (1) | ATE411315T1 (es) |
| CA (1) | CA2577239A1 (es) |
| CL (1) | CL2004002061A1 (es) |
| DE (1) | DE602004017108D1 (es) |
| DK (1) | DK1544199T3 (es) |
| ES (1) | ES2315700T3 (es) |
| PE (1) | PE20050361A1 (es) |
| PT (1) | PT1544199E (es) |
| SI (1) | SI1544199T1 (es) |
| TW (1) | TW200510425A (es) |
| WO (1) | WO2005016927A1 (es) |
Families Citing this family (123)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006232849A (ja) * | 2003-08-13 | 2006-09-07 | Japan Tobacco Inc | 含窒素縮合環化合物及びそのｈｉｖインテグラーゼ阻害剤としての利用 |
| US7732616B2 (en) * | 2003-11-19 | 2010-06-08 | Array Biopharma Inc. | Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof |
| CN1905873A (zh) * | 2003-11-19 | 2007-01-31 | 阵列生物制药公司 | Mek的杂环抑制剂及其使用方法 |
| US7517994B2 (en) * | 2003-11-19 | 2009-04-14 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
| US20050182252A1 (en) | 2004-02-13 | 2005-08-18 | Reddy K. R. | Novel 2'-C-methyl nucleoside derivatives |
| US20070161639A1 (en) * | 2004-03-09 | 2007-07-12 | Philip Jones | Hiv integrase inhibitors |
| CN101014574A (zh) * | 2004-03-09 | 2007-08-08 | 默克公司 | Hiv整合酶抑制剂 |
| US7820680B2 (en) * | 2004-03-09 | 2010-10-26 | Merck & Co., Inc. | HIV integrase inhibitors |
| JP4625838B2 (ja) * | 2004-03-09 | 2011-02-02 | メルク・シャープ・エンド・ドーム・コーポレイション | Ｈｉｖインテグラーゼ阻害薬 |
| US7115601B2 (en) * | 2004-05-18 | 2006-10-03 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| EP1758581A1 (en) * | 2004-05-21 | 2007-03-07 | Japan Tobacco, Inc. | Combinations comprising a 4-isoquinolone derivative and anti-hiv agents |
| JP4953297B2 (ja) * | 2004-09-15 | 2012-06-13 | 塩野義製薬株式会社 | Ｈｉｖインテグラーゼ阻害活性を有するカルバモイルピリドン誘導体 |
| US7745459B2 (en) * | 2004-09-21 | 2010-06-29 | Japan Tobacco Inc. | Quinolizinone compound and use thereof as HIV integrase inhibitor |
| ATE516026T1 (de) * | 2005-02-21 | 2011-07-15 | Shionogi & Co | Bicyclisches carbamoylpyridonderivat mit hiv- integrase-hemmender wirkung |
| CA2600832C (en) * | 2005-03-31 | 2011-12-13 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Hiv integrase inhibitors |
| KR101363875B1 (ko) | 2005-04-28 | 2014-02-21 | 시오노기세야쿠 가부시키가이샤 | Ｈｉｖ 통합효소 억제 활성을 가지는 다환식카르바모일피리돈 유도체 |
| AU2006242475B2 (en) | 2005-05-02 | 2011-07-07 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| WO2006121831A2 (en) * | 2005-05-10 | 2006-11-16 | Merck & Co., Inc. | Hiv integrase inhibitors |
| ES2405785T3 (es) * | 2005-05-18 | 2013-06-03 | Array Biopharma Inc. | Inhibidores heterocíclicos de MEK y métodos de uso de los mismos |
| JP2006342115A (ja) * | 2005-06-10 | 2006-12-21 | Shionogi & Co Ltd | Ｈｉｖインテグラーゼ阻害活性を有する多環性化合物 |
| EP1906971A2 (en) * | 2005-07-27 | 2008-04-09 | Gilead Sciences, Inc. | Antiviral compounds |
| BRPI0614205A2 (pt) | 2005-08-01 | 2016-11-22 | Merck & Co Inc | composto, composição farmacêutica, e, uso de composto |
| US7939537B2 (en) * | 2005-10-04 | 2011-05-10 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | HIV integrase inhibitors |
| MX2008005137A (es) * | 2005-10-27 | 2008-09-29 | Shionogi & Co | Derivado de carbamoilpiridona policiclica que tiene actividad inhibidora en vih integrasa. |
| EP2452682A1 (en) * | 2006-02-01 | 2012-05-16 | Japan Tobacco, Inc. | Use of 6-(3-chloro-2-fluorobenzyl)-1-[(2s)-1-hydroxy-3-methylbutan-2-yl]-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or salt thereof for treating retrovirus infection |
| GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| AU2007254190A1 (en) * | 2006-05-16 | 2007-11-29 | Gilead Sciences, Inc. | Integrase inhibitors |
| GB0612423D0 (en) | 2006-06-23 | 2006-08-02 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| WO2008048538A1 (en) * | 2006-10-18 | 2008-04-24 | Merck & Co., Inc. | Hiv integrase inhibitors |
| US8138164B2 (en) | 2006-10-24 | 2012-03-20 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| CN101583372A (zh) | 2006-10-24 | 2009-11-18 | 默克公司 | Hcv ns3蛋白酶抑制剂 |
| JP2010507656A (ja) | 2006-10-24 | 2010-03-11 | メルク エンド カムパニー インコーポレーテッド | Ｈｃｖｎｓ３プロテアーゼ阻害剤 |
| WO2008057209A1 (en) | 2006-10-27 | 2008-05-15 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
| AU2007318164B2 (en) | 2006-10-27 | 2013-02-07 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| CN103224506A (zh) | 2006-12-20 | 2013-07-31 | P.安杰莱蒂分子生物学研究所 | 抗病毒的吲哚 |
| 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 |
| JP2010515680A (ja) | 2007-01-05 | 2010-05-13 | メルク・シャープ・エンド・ドーム・コーポレイション | Ｒｎａ依存性ｒｎａウイルス感染症の治療用としてのヌクレオシドアリールホスホロアミデート |
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| JP3814631B2 (ja) | 2006-08-30 |
| SI1544199T1 (sl) | 2009-04-30 |
| DK1544199T3 (da) | 2009-01-12 |
| CA2577239A1 (en) | 2005-02-24 |
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