CN102574854B - 大环整合酶抑制剂 - Google Patents
大环整合酶抑制剂 Download PDFInfo
- Publication number
- CN102574854B CN102574854B CN201080046163.3A CN201080046163A CN102574854B CN 102574854 B CN102574854 B CN 102574854B CN 201080046163 A CN201080046163 A CN 201080046163A CN 102574854 B CN102574854 B CN 102574854B
- Authority
- CN
- China
- Prior art keywords
- methyl
- compound
- amino
- naphthyridine
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 0 CC(O*SC(N)=N)=O Chemical compound CC(O*SC(N)=N)=O 0.000 description 3
- RHMUDIXGIYUAMW-UHFFFAOYSA-N CC(C)(C)OC(NCCCCCCNc(nc1C(O)=O)c(cccn2)c2c1OCc1ccccc1)=O Chemical compound CC(C)(C)OC(NCCCCCCNc(nc1C(O)=O)c(cccn2)c2c1OCc1ccccc1)=O RHMUDIXGIYUAMW-UHFFFAOYSA-N 0.000 description 1
- BECNIMHEHYREGE-UHFFFAOYSA-N CC(C)(C)OC(NCCCCCS(N(C)c(c1cccnc11)nc(C(OC)=O)c1O)(=O)=O)=O Chemical compound CC(C)(C)OC(NCCCCCS(N(C)c(c1cccnc11)nc(C(OC)=O)c1O)(=O)=O)=O BECNIMHEHYREGE-UHFFFAOYSA-N 0.000 description 1
- NNIUUBUNPYASGC-UHFFFAOYSA-N CC(C)(C)OC(NCCCCCS(N(C)c(nc1C(O)=O)c(cccn2)c2c1OCc1ccccc1)(=O)=O)=O Chemical compound CC(C)(C)OC(NCCCCCS(N(C)c(nc1C(O)=O)c(cccn2)c2c1OCc1ccccc1)(=O)=O)=O NNIUUBUNPYASGC-UHFFFAOYSA-N 0.000 description 1
- DMRJMORGJFLEAM-UHFFFAOYSA-N CC(C)(C)OC(NCCCCS(N(C)c(nc1C(OC)=O)c(cccn2)c2c1OS(c1ccc(C)cc1)(=O)=O)(=O)=O)=O Chemical compound CC(C)(C)OC(NCCCCS(N(C)c(nc1C(OC)=O)c(cccn2)c2c1OS(c1ccc(C)cc1)(=O)=O)(=O)=O)=O DMRJMORGJFLEAM-UHFFFAOYSA-N 0.000 description 1
- UUEGXEMADNBIAK-UHFFFAOYSA-N CC(C)(C)OC(NCc(c(C(NCCCCS(N(C)c(nc1C(O)=O)c(cccn2)c2c1OS(c1ccc(C)cc1)(=O)=O)(=O)=O)=O)c1)ccc1F)=O Chemical compound CC(C)(C)OC(NCc(c(C(NCCCCS(N(C)c(nc1C(O)=O)c(cccn2)c2c1OS(c1ccc(C)cc1)(=O)=O)(=O)=O)=O)c1)ccc1F)=O UUEGXEMADNBIAK-UHFFFAOYSA-N 0.000 description 1
- JHOAWXLTTNQAHU-UHFFFAOYSA-N CCOC(CCCCOc1c(CNC(OC(C)(C)C)=O)ccc(F)c1)=O Chemical compound CCOC(CCCCOc1c(CNC(OC(C)(C)C)=O)ccc(F)c1)=O JHOAWXLTTNQAHU-UHFFFAOYSA-N 0.000 description 1
- HKJMICNUGXQFIT-UHFFFAOYSA-N CNS(CCCCI)(=O)=O Chemical compound CNS(CCCCI)(=O)=O HKJMICNUGXQFIT-UHFFFAOYSA-N 0.000 description 1
- IJNIEANLYFXCFR-UHFFFAOYSA-N Cc(cc1)ccc1S(Oc1c2ncccc2c(N(C)S(CCCCNC(c2cc(F)ccc2CN)=O)(=O)=O)nc1C(O)=O)(=O)=O Chemical compound Cc(cc1)ccc1S(Oc1c2ncccc2c(N(C)S(CCCCNC(c2cc(F)ccc2CN)=O)(=O)=O)nc1C(O)=O)(=O)=O IJNIEANLYFXCFR-UHFFFAOYSA-N 0.000 description 1
- ORUPRLBUOQIKEC-UHFFFAOYSA-N Oc(c1c2cccn1)c(C(NCc(cc1)c3cc1F)=O)nc2NCCCCCNC3=O Chemical compound Oc(c1c2cccn1)c(C(NCc(cc1)c3cc1F)=O)nc2NCCCCCNC3=O ORUPRLBUOQIKEC-UHFFFAOYSA-N 0.000 description 1
- DKHHQXQSYABQJL-UHFFFAOYSA-N Oc1c2ncccc2c(N(CC2)CCN2C(CCCCOc2c(CN3)ccc(F)c2)=O)nc1C3=O Chemical compound Oc1c2ncccc2c(N(CC2)CCN2C(CCCCOc2c(CN3)ccc(F)c2)=O)nc1C3=O DKHHQXQSYABQJL-UHFFFAOYSA-N 0.000 description 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D513/18—Bridged 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- 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
- C07D471/12—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 three hetero rings
- C07D471/18—Bridged 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
- C07D498/18—Bridged 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
- C07D498/22—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 four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D515/18—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09172853 | 2009-10-13 | ||
| EP09172853.5 | 2009-10-13 | ||
| PCT/EP2010/065300 WO2011045330A1 (en) | 2009-10-13 | 2010-10-13 | Macrocyclic integrase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102574854A CN102574854A (zh) | 2012-07-11 |
| CN102574854B true CN102574854B (zh) | 2014-04-16 |
Family
ID=41720665
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201080046163.3A Active CN102574854B (zh) | 2009-10-13 | 2010-10-13 | 大环整合酶抑制剂 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US8497270B2 (https=) |
| EP (1) | EP2488521B1 (https=) |
| JP (1) | JP5624148B2 (https=) |
| KR (1) | KR20120087916A (https=) |
| CN (1) | CN102574854B (https=) |
| AU (1) | AU2010305805B2 (https=) |
| BR (1) | BR112012008586A2 (https=) |
| CA (1) | CA2777664C (https=) |
| EA (1) | EA019558B1 (https=) |
| ES (1) | ES2446720T3 (https=) |
| IL (1) | IL218845A0 (https=) |
| MX (1) | MX2012004426A (https=) |
| NZ (1) | NZ598766A (https=) |
| WO (1) | WO2011045330A1 (https=) |
| ZA (1) | ZA201202516B (https=) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2487176A1 (en) * | 2011-02-14 | 2012-08-15 | Elanco Animal Health Ireland Limited | Macrocyclic integrase inhibitors for use in the treatment of feline immunodeficiency virus |
| WO2014008636A1 (en) * | 2012-07-11 | 2014-01-16 | Merck Sharp & Dohme Corp. | Macrocyclic compounds as hiv integrase inhibitors |
| EP2931730B1 (en) | 2012-12-17 | 2019-08-07 | Merck Sharp & Dohme Corp. | 4-pyridinonetriazine derivatives as hiv integrase inhibitors |
| US9493479B2 (en) | 2013-04-16 | 2016-11-15 | Merck Sharp & Dohme Corp. | Substituted pyrido[1,2-a]pyrazines as HIV integrase inhibitors |
| RS56701B1 (sr) | 2013-05-17 | 2018-03-30 | Merck Sharp & Dohme | Fuzionisana triciklična heterociklična jedinjenja kao inhibitori hiv integraze |
| EP3008044B1 (en) | 2013-06-13 | 2018-11-21 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds as hiv integrase inhibitors |
| UA117499C2 (uk) | 2013-09-27 | 2018-08-10 | Мерк Шарп Енд Доум Корп. | Заміщені похідні хінолізину, які можна використовувати як інгібітори інтегрази віл |
| ES2933350T3 (es) | 2014-01-24 | 2023-02-06 | Turning Point Therapeutics Inc | Macrociclos de diarilo como moduladores de proteína quinasas |
| WO2016187788A1 (en) | 2015-05-25 | 2016-12-01 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds useful for treating hiv infection |
| AU2016287568B2 (en) | 2015-07-02 | 2020-08-20 | Turning Point Therapeutics, Inc. | Chiral diaryl macrocycles as modulators of protein kinases |
| RU2765181C2 (ru) | 2015-07-06 | 2022-01-26 | Тёрнинг Поинт Терапьютикс, Инк. | Полиморфная форма диарильного макроцикла |
| PT3733187T (pt) | 2015-07-21 | 2024-11-08 | Turning Point Therapeutics Inc | Macrociclo de diarilo quiral e utilização do mesmo no tratamento do cancro |
| US10548910B2 (en) | 2015-11-17 | 2020-02-04 | Merck Sharp & Dohme Corp. | Amido-substituted pyridotriazine derivatives useful as HIV integrase inhibitors |
| US10544155B2 (en) | 2015-12-15 | 2020-01-28 | Merck Sharp & Dohme Corp. | Spirocyclic quinolizine derivatives useful as HIV integrase inhibitors |
| WO2017113288A1 (en) | 2015-12-31 | 2017-07-06 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds as hiv integrase inhibitors |
| JOP20190130A1 (ar) | 2016-12-02 | 2019-06-02 | Merck Sharp & Dohme | مركبات حلقية غير متجانسة رباعية الحلقات مفيدة كمثبطات إنزيم مدمج لفيروس نقص المناعة البشرية (hiv) |
| CA3042314A1 (en) | 2016-12-02 | 2018-06-07 | Merck Sharp & Dohme Corp. | Tricyclic heterocycle compounds useful as hiv integrase inhibitors |
| TWI808958B (zh) | 2017-01-25 | 2023-07-21 | 美商特普醫葯公司 | 涉及二芳基巨環化合物之組合療法 |
| EP3573984A4 (en) | 2017-01-26 | 2020-07-29 | Merck Sharp & Dohme Corp. | USEFUL SUBSTITUTE QUINOLIZINE DERIVATIVES AS HIV INTEGRASE INHIBITORS |
| CN111182903A (zh) | 2017-07-28 | 2020-05-19 | 特普医药公司 | 巨环化合物及其用途 |
| LT3728271T (lt) | 2017-12-19 | 2022-12-12 | Turning Point Therapeutics, Inc. | Makrocikliniai junginiai, skirti ligų gydymui |
| MY201239A (en) | 2019-03-22 | 2024-02-13 | Gilead Sciences Inc | Bridged tricyclic carbamoylpyridone compounds and their pharmaceutical use |
| PE20221569A1 (es) | 2020-02-24 | 2022-10-06 | Gilead Sciences Inc | Compuestos tetraciclicos para el tratamiento de infecciones por vih |
| ES3064867T3 (en) | 2020-09-30 | 2026-04-29 | Gilead Sciences Inc | Bridged tricyclic carbamoylpyridone compounds for a use in the treatment of hiv |
| CN112358477A (zh) * | 2020-11-10 | 2021-02-12 | 牡丹江医学院 | 一种用于治疗胆囊炎的药物及其制备方法 |
| US11613546B2 (en) | 2021-01-19 | 2023-03-28 | Gilead Sciences, Inc. | Substituted pyridotriazine compounds and uses thereof |
| TW202446773A (zh) | 2022-04-06 | 2024-12-01 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
| CN115974886A (zh) * | 2022-11-22 | 2023-04-18 | 国科大杭州高等研究院 | 一种含有二氢苯并呋喃骨架的大环内酰胺化合物及其制备方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002030931A2 (en) * | 2000-10-12 | 2002-04-18 | Merck & Co., Inc. | Aza- and polyaza-naphthalenyl carboxamides useful as hiv integrase inhibitors |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CS210880B1 (cs) | 1979-10-19 | 1982-01-29 | Jiri Krepelka | Substituované imidy kyselin 4-arylnaftalen-2,3-dikarboxylových |
| CS225002B1 (cs) | 1980-12-12 | 1984-02-13 | Krepelka Jiri | Deriváty 9-fenyl-1H-benzo/f/isoindol-1,3-dionu a způsob jejich výroby |
| JPH04217684A (ja) | 1990-05-30 | 1992-08-07 | Shionogi & Co Ltd | アルド−ス還元酵素阻害物質 |
| EP0729950A4 (en) * | 1994-09-13 | 2001-02-07 | Kyowa Hakko Kogyo Kk | ANTI-HIV MEDICINAL PRODUCTS |
| ATE345129T1 (de) | 2000-10-12 | 2006-12-15 | Merck & Co Inc | Aza- und polyaza-naphthalenylcarbonsäureamide als hiv-integrase-hemmer |
| WO2002036734A2 (en) | 2000-10-12 | 2002-05-10 | Merck & Co., Inc. | Aza-and polyaza-naphthalenyl ketones useful as hiv integrase inhibitors |
| EP1326611B1 (en) | 2000-10-12 | 2007-06-13 | Merck & Co., Inc. | Aza- and polyaza-naphthalenyl-carboxamides useful as hiv integrase inhibitors |
| WO2004035577A2 (en) | 2002-10-16 | 2004-04-29 | Gilead Sciences, Inc. | Pre-organized tricyclic integrase inhibitor compounds |
| SK2662004A3 (sk) | 2002-11-20 | 2005-06-02 | Japan Tobacco, Inc. | Zlúčenina s obsahom 4-oxochinolínu a jej použitie ako inhibítora integráz |
| NZ540729A (en) | 2002-12-27 | 2008-03-28 | Angeletti P Ist Richerche Bio | Tetrahydro-4H-pyrido[1,2-a]pyrimidines and related compounds useful as HIV integrase inhibitors |
| US6890942B2 (en) | 2003-05-16 | 2005-05-10 | Bristol-Myers Squibb Company | Acyl sulfonamides as inhibitors of HIV integrase |
| CA2537325A1 (en) | 2003-09-19 | 2005-03-31 | Gilead Sciences, Inc. | Aza-quinolinol phosphonate integrase inhibitor compounds |
| US20070161639A1 (en) | 2004-03-09 | 2007-07-12 | Philip Jones | Hiv integrase inhibitors |
| US7176196B2 (en) | 2004-05-28 | 2007-02-13 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
| KR101363875B1 (ko) | 2005-04-28 | 2014-02-21 | 시오노기세야쿠 가부시키가이샤 | Ｈｉｖ 통합효소 억제 활성을 가지는 다환식카르바모일피리돈 유도체 |
| US20080214527A1 (en) * | 2005-08-04 | 2008-09-04 | Takashi Kawasuji | Hiv Integrase Inhibitors |
| MX2008005137A (es) * | 2005-10-27 | 2008-09-29 | Shionogi & Co | Derivado de carbamoilpiridona policiclica que tiene actividad inhibidora en vih integrasa. |
| US8039458B2 (en) * | 2005-11-17 | 2011-10-18 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| TW200811153A (en) | 2006-06-23 | 2008-03-01 | Japan Tobacco Inc | 6-(heterocyclyl-substituted benzyl)-4-oxoquinoline compound and use thereof as HIV integrase inhibitor |
| US8318929B2 (en) * | 2008-03-10 | 2012-11-27 | Janssen Pharmaceutica Nv | 4-aryl-2-anilino-pyrimidines |
-
2010
- 2010-10-13 ES ES10772998.0T patent/ES2446720T3/es active Active
- 2010-10-13 CN CN201080046163.3A patent/CN102574854B/zh active Active
- 2010-10-13 AU AU2010305805A patent/AU2010305805B2/en active Active
- 2010-10-13 KR KR1020127009345A patent/KR20120087916A/ko not_active Abandoned
- 2010-10-13 NZ NZ598766A patent/NZ598766A/xx not_active IP Right Cessation
- 2010-10-13 EA EA201270540A patent/EA019558B1/ru not_active IP Right Cessation
- 2010-10-13 CA CA2777664A patent/CA2777664C/en active Active
- 2010-10-13 EP EP10772998.0A patent/EP2488521B1/en active Active
- 2010-10-13 MX MX2012004426A patent/MX2012004426A/es active IP Right Grant
- 2010-10-13 BR BR112012008586A patent/BR112012008586A2/pt not_active IP Right Cessation
- 2010-10-13 WO PCT/EP2010/065300 patent/WO2011045330A1/en not_active Ceased
- 2010-10-13 US US13/395,891 patent/US8497270B2/en active Active
- 2010-10-13 JP JP2012533614A patent/JP5624148B2/ja active Active
-
2012
- 2012-03-26 IL IL218845A patent/IL218845A0/en unknown
- 2012-04-05 ZA ZA2012/02516A patent/ZA201202516B/en unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002030931A2 (en) * | 2000-10-12 | 2002-04-18 | Merck & Co., Inc. | Aza- and polyaza-naphthalenyl carboxamides useful as hiv integrase inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2013507423A (ja) | 2013-03-04 |
| EP2488521B1 (en) | 2013-12-18 |
| EP2488521A1 (en) | 2012-08-22 |
| US20120172367A1 (en) | 2012-07-05 |
| ES2446720T3 (es) | 2014-03-10 |
| AU2010305805B2 (en) | 2014-04-03 |
| MX2012004426A (es) | 2012-07-30 |
| WO2011045330A1 (en) | 2011-04-21 |
| AU2010305805A1 (en) | 2012-04-19 |
| EA019558B1 (ru) | 2014-04-30 |
| NZ598766A (en) | 2013-09-27 |
| IL218845A0 (en) | 2012-06-28 |
| JP5624148B2 (ja) | 2014-11-12 |
| BR112012008586A2 (pt) | 2016-11-29 |
| KR20120087916A (ko) | 2012-08-07 |
| EA201270540A1 (ru) | 2012-09-28 |
| CA2777664A1 (en) | 2011-04-21 |
| US8497270B2 (en) | 2013-07-30 |
| ZA201202516B (en) | 2013-09-25 |
| CA2777664C (en) | 2014-06-10 |
| CN102574854A (zh) | 2012-07-11 |
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