JP4874959B2 - Hivインテグラーゼインヒビターとしての二環式ヘテロ環 - Google Patents
Hivインテグラーゼインヒビターとしての二環式ヘテロ環 Download PDFInfo
- Publication number
- JP4874959B2 JP4874959B2 JP2007515142A JP2007515142A JP4874959B2 JP 4874959 B2 JP4874959 B2 JP 4874959B2 JP 2007515142 A JP2007515142 A JP 2007515142A JP 2007515142 A JP2007515142 A JP 2007515142A JP 4874959 B2 JP4874959 B2 JP 4874959B2
- Authority
- JP
- Japan
- Prior art keywords
- oxo
- methyl
- oxazine
- dimethyl
- hydroxy
- 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.)
- Expired - Fee Related
Links
- 0 CCOC(C(N=C(C(C)(C)OCC1)N1C1=*)=C1OCc1ccccc1)=O Chemical compound CCOC(C(N=C(C(C)(C)OCC1)N1C1=*)=C1OCc1ccccc1)=O 0.000 description 18
- QKHJKSUMZUVHFP-NTUHNPAUSA-N C/N=C/c(ccc(F)c1)c1N(CC1)C1=O Chemical compound C/N=C/c(ccc(F)c1)c1N(CC1)C1=O QKHJKSUMZUVHFP-NTUHNPAUSA-N 0.000 description 1
- SJRNZQAHKUWAKD-UHFFFAOYSA-N CC(C)(C1=NC(/C(/NCc2cccc3c2OCCCO3)=[O]\C)=C2O)NCCN1C2=O Chemical compound CC(C)(C1=NC(/C(/NCc2cccc3c2OCCCO3)=[O]\C)=C2O)NCCN1C2=O SJRNZQAHKUWAKD-UHFFFAOYSA-N 0.000 description 1
- RGTHBLYQXFCOIK-SRZZPIQSSA-N CC(C)(C1=NC(C(/N=C/c(ccc(C)c2)c2P(OC)(OC)=O)=O)=C2O)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(/N=C/c(ccc(C)c2)c2P(OC)(OC)=O)=O)=C2O)OCCN1C2=O RGTHBLYQXFCOIK-SRZZPIQSSA-N 0.000 description 1
- OZDXYSCDXFMZKP-UHFFFAOYSA-N CC(C)(C1=NC(C(NCC(C=C2)=CCC2Cl)=O)=C2O)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(NCC(C=C2)=CCC2Cl)=O)=C2O)OCCN1C2=O OZDXYSCDXFMZKP-UHFFFAOYSA-N 0.000 description 1
- GKOJFMVPNVVZSS-UHFFFAOYSA-N CC(C)(C1=NC(C(NCc(c(C#CCOS(C)(=O)=O)c2)ccc2[I]=C)=O)=C2OCc3ccccc3)OCCN1C2=C Chemical compound CC(C)(C1=NC(C(NCc(c(C#CCOS(C)(=O)=O)c2)ccc2[I]=C)=O)=C2OCc3ccccc3)OCCN1C2=C GKOJFMVPNVVZSS-UHFFFAOYSA-N 0.000 description 1
- PYYHHGCMPCSNFK-UHFFFAOYSA-N CC(C)(C1=NC(C(NCc(cc2)ccc2F)=O)=C2O)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(NCc(cc2)ccc2F)=O)=C2O)OCCN1C2=O PYYHHGCMPCSNFK-UHFFFAOYSA-N 0.000 description 1
- WGWGPCMEWYYSHP-UHFFFAOYSA-N CC(C)(C1=NC(C(NCc(ccc(F)c2)c2-[n]2nc(C(NC)=O)nc2)=O)=C2O)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(NCc(ccc(F)c2)c2-[n]2nc(C(NC)=O)nc2)=O)=C2O)OCCN1C2=O WGWGPCMEWYYSHP-UHFFFAOYSA-N 0.000 description 1
- FONCPLRXMYTFAG-UHFFFAOYSA-N CC(C)(C1=NC(C(NCc(ccc(F)c2)c2-c2nnn[n]2C)=O)=C2O)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(NCc(ccc(F)c2)c2-c2nnn[n]2C)=O)=C2O)OCCN1C2=O FONCPLRXMYTFAG-UHFFFAOYSA-N 0.000 description 1
- SVJAULHTBQDBKW-UHFFFAOYSA-N CC(C)(C1=NC(C(NCc(ccc(F)c2)c2C#CCN(C)C)=O)=C2OCc3c(C)cccc3)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(NCc(ccc(F)c2)c2C#CCN(C)C)=O)=C2OCc3c(C)cccc3)OCCN1C2=O SVJAULHTBQDBKW-UHFFFAOYSA-N 0.000 description 1
- CDXQJAFRKMMVJF-UHFFFAOYSA-N CC(C)(C1=NC(C(NCc2cc(Cl)c(C)cc2)=O)=C2O)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(NCc2cc(Cl)c(C)cc2)=O)=C2O)OCCN1C2=O CDXQJAFRKMMVJF-UHFFFAOYSA-N 0.000 description 1
- NOUAILBRPCRINR-UHFFFAOYSA-N CC(C)(C1=NC(C(NCc2ccc(C)c(F)c2F)=O)=C2O)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(NCc2ccc(C)c(F)c2F)=O)=C2O)OCCN1C2=O NOUAILBRPCRINR-UHFFFAOYSA-N 0.000 description 1
- DYEQMHOJJGTSJI-UHFFFAOYSA-N CC(C)(C1=NC(C(NCc2ccccc2Br)=O)=C2O)OCCN1C2=O Chemical compound CC(C)(C1=NC(C(NCc2ccccc2Br)=O)=C2O)OCCN1C2=O DYEQMHOJJGTSJI-UHFFFAOYSA-N 0.000 description 1
- UWBVUZVBBWDSER-UHFFFAOYSA-N CC(C)Oc1cccc(CNC(C(N=C(C(C)(C)OCC2)N2C2=O)=C2O)=O)c1 Chemical compound CC(C)Oc1cccc(CNC(C(N=C(C(C)(C)OCC2)N2C2=O)=C2O)=O)c1 UWBVUZVBBWDSER-UHFFFAOYSA-N 0.000 description 1
- UZCPLTKYCRGACT-UHFFFAOYSA-N CC(CC1=CN1C)(C1=C=CC(C(OC)=O)=C2OCc3ccccc3)OCCN1C2=O Chemical compound CC(CC1=CN1C)(C1=C=CC(C(OC)=O)=C2OCc3ccccc3)OCCN1C2=O UZCPLTKYCRGACT-UHFFFAOYSA-N 0.000 description 1
- KWJKQDDFKPXJLY-UHFFFAOYSA-N CC(N(C)c(cc(cc1)F)c1C#N)=O Chemical compound CC(N(C)c(cc(cc1)F)c1C#N)=O KWJKQDDFKPXJLY-UHFFFAOYSA-N 0.000 description 1
- PJBZNNWANNDADE-UHFFFAOYSA-N CC1(C)OCCN(C2O)C1=NC(C(NCc(ccc(F)c1)c1C#CCSC)=O)=C2OCc1ccccc1 Chemical compound CC1(C)OCCN(C2O)C1=NC(C(NCc(ccc(F)c1)c1C#CCSC)=O)=C2OCc1ccccc1 PJBZNNWANNDADE-UHFFFAOYSA-N 0.000 description 1
- LZBANDBXHOPFFJ-CABQHZTJSA-N CCC(C1)C=CC(CC(CC(C(N=C(C(C)(C)CCC2)N2C2=O)=C2OCc2ccccc2)=O)S)=C1N([C@@](C1)(CC2)[C@@H]1O)C2=O Chemical compound CCC(C1)C=CC(CC(CC(C(N=C(C(C)(C)CCC2)N2C2=O)=C2OCc2ccccc2)=O)S)=C1N([C@@](C1)(CC2)[C@@H]1O)C2=O LZBANDBXHOPFFJ-CABQHZTJSA-N 0.000 description 1
- NZAZNLMUPRADSN-UHFFFAOYSA-N CCC(CC)(C1=NC(C(NCc(cccc2)c2N(CCCC2)S2(=O)=O)=O)=C2O)OCCN1C2=O Chemical compound CCC(CC)(C1=NC(C(NCc(cccc2)c2N(CCCC2)S2(=O)=O)=O)=C2O)OCCN1C2=O NZAZNLMUPRADSN-UHFFFAOYSA-N 0.000 description 1
- RGBVTAWIRQICPI-UHFFFAOYSA-N CCC(N(CCOC)C1=O)=NC(C(NCc(ccc(F)c2)c2C(NC2CC2)=O)=O)=C1O Chemical compound CCC(N(CCOC)C1=O)=NC(C(NCc(ccc(F)c2)c2C(NC2CC2)=O)=O)=C1O RGBVTAWIRQICPI-UHFFFAOYSA-N 0.000 description 1
- DGZOEBPXELBQQU-SLEOGJTISA-N CCCOC(C)(C)/C(/C)=N/C(/C(NCc(ccc(F)c1)c1-c1ccn[nH]1)=O)=C(\C(C)=O)/OC Chemical compound CCCOC(C)(C)/C(/C)=N/C(/C(NCc(ccc(F)c1)c1-c1ccn[nH]1)=O)=C(\C(C)=O)/OC DGZOEBPXELBQQU-SLEOGJTISA-N 0.000 description 1
- NDLYEMYNTIAPIE-UHFFFAOYSA-N CCN(C(C(C)(C)O)=NC(C(NCc(ccc(F)c1)c1S(N1CCC1)(=O)=O)=O)=C1O)C1=O Chemical compound CCN(C(C(C)(C)O)=NC(C(NCc(ccc(F)c1)c1S(N1CCC1)(=O)=O)=O)=C1O)C1=O NDLYEMYNTIAPIE-UHFFFAOYSA-N 0.000 description 1
- JDSHYTVCADTHTI-UHFFFAOYSA-N CCOC(C(N=C(C(C)(C)CCC1)N1C1=C)=C1OCc1ccccc1)=O Chemical compound CCOC(C(N=C(C(C)(C)CCC1)N1C1=C)=C1OCc1ccccc1)=O JDSHYTVCADTHTI-UHFFFAOYSA-N 0.000 description 1
- VZZZXJBDFSPRBI-UHFFFAOYSA-O CCOC(C(N=C(COCC[S+](C)I)NC1=O)=C1OCc1ccccc1)=O Chemical compound CCOC(C(N=C(COCC[S+](C)I)NC1=O)=C1OCc1ccccc1)=O VZZZXJBDFSPRBI-UHFFFAOYSA-O 0.000 description 1
- CFTRKGCBMZSAED-UHFFFAOYSA-N CCOC(CSc1c(C)cccc1)OCC Chemical compound CCOC(CSc1c(C)cccc1)OCC CFTRKGCBMZSAED-UHFFFAOYSA-N 0.000 description 1
- VGFNLLKQWAOFLA-UHFFFAOYSA-N CCOP(c1c(CNC(C(N=C(C(C)(C)OCC2)N2C2=O)=C2O)=O)ccc(F)c1)(OCC)=O Chemical compound CCOP(c1c(CNC(C(N=C(C(C)(C)OCC2)N2C2=O)=C2O)=O)ccc(F)c1)(OCC)=O VGFNLLKQWAOFLA-UHFFFAOYSA-N 0.000 description 1
- KGYXKRGMSUHYCY-UHFFFAOYSA-N COc1cc(F)ccc1Br Chemical compound COc1cc(F)ccc1Br KGYXKRGMSUHYCY-UHFFFAOYSA-N 0.000 description 1
- APCOZTPKAPXGEX-UHFFFAOYSA-N N#Cc(c(-[n]1nccn1)c1)ccc1F Chemical compound N#Cc(c(-[n]1nccn1)c1)ccc1F APCOZTPKAPXGEX-UHFFFAOYSA-N 0.000 description 1
- QSIXUEFTANPJDE-UHFFFAOYSA-N N#Cc1cccc(F)c1N(CCCC1)S1(=O)=O Chemical compound N#Cc1cccc(F)c1N(CCCC1)S1(=O)=O QSIXUEFTANPJDE-UHFFFAOYSA-N 0.000 description 1
- DYJYKTJWPYSHKW-UHFFFAOYSA-N N=Cc(cccc1)c1-[n]1ncnc1 Chemical compound N=Cc(cccc1)c1-[n]1ncnc1 DYJYKTJWPYSHKW-UHFFFAOYSA-N 0.000 description 1
- QLMHMZMBMHLRCV-UHFFFAOYSA-N NCc(c(OCC(N1CCOCC1)=O)c1)ccc1F Chemical compound NCc(c(OCC(N1CCOCC1)=O)c1)ccc1F QLMHMZMBMHLRCV-UHFFFAOYSA-N 0.000 description 1
- CAYVWMSNEPGBCX-UHFFFAOYSA-N NCc(ccc(F)c1)c1N(CCO1)C1=O Chemical compound NCc(ccc(F)c1)c1N(CCO1)C1=O CAYVWMSNEPGBCX-UHFFFAOYSA-N 0.000 description 1
- PVBIYRKDWMPTLU-UHFFFAOYSA-N Nc(cccc1)c1N(CC1)C1=O Chemical compound Nc(cccc1)c1N(CC1)C1=O PVBIYRKDWMPTLU-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
-
- 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)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- AIDS & HIV (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US57551304P | 2004-05-28 | 2004-05-28 | |
| US60/575,513 | 2004-05-28 | ||
| US60337104P | 2004-08-20 | 2004-08-20 | |
| US60/603,371 | 2004-08-20 | ||
| US11/126,891 | 2005-05-11 | ||
| US11/126,891 US7176196B2 (en) | 2004-05-28 | 2005-05-11 | Bicyclic heterocycles as HIV integrase inhibitors |
| PCT/US2005/016473 WO2005118593A1 (en) | 2004-05-28 | 2005-05-12 | Bicyclic heterocycles as hiv integrase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008501018A JP2008501018A (ja) | 2008-01-17 |
| JP2008501018A5 JP2008501018A5 (enExample) | 2008-06-19 |
| JP4874959B2 true JP4874959B2 (ja) | 2012-02-15 |
Family
ID=35456854
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007515142A Expired - Fee Related JP4874959B2 (ja) | 2004-05-28 | 2005-05-12 | Hivインテグラーゼインヒビターとしての二環式ヘテロ環 |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US7176196B2 (enExample) |
| EP (1) | EP1749011B1 (enExample) |
| JP (1) | JP4874959B2 (enExample) |
| KR (1) | KR101097623B1 (enExample) |
| AR (1) | AR049124A1 (enExample) |
| AT (1) | ATE412656T1 (enExample) |
| AU (1) | AU2005250356C1 (enExample) |
| BR (1) | BRPI0511623A (enExample) |
| CA (1) | CA2568356C (enExample) |
| CY (1) | CY1110266T1 (enExample) |
| DE (1) | DE602005010690D1 (enExample) |
| DK (1) | DK1749011T3 (enExample) |
| ES (1) | ES2315875T3 (enExample) |
| HR (1) | HRP20090005T3 (enExample) |
| IL (1) | IL179455A (enExample) |
| MX (1) | MXPA06013835A (enExample) |
| NO (1) | NO20065879L (enExample) |
| NZ (1) | NZ551282A (enExample) |
| PE (1) | PE20060242A1 (enExample) |
| PL (1) | PL1749011T3 (enExample) |
| PT (1) | PT1749011E (enExample) |
| RS (1) | RS50700B (enExample) |
| RU (1) | RU2381228C2 (enExample) |
| SI (1) | SI1749011T1 (enExample) |
| TW (1) | TWI366567B (enExample) |
| WO (1) | WO2005118593A1 (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7115601B2 (en) | 2004-05-18 | 2006-10-03 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| EP1866313A1 (en) * | 2005-03-31 | 2007-12-19 | Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. | Hiv integrase inhibitors |
| US7494984B2 (en) * | 2005-08-31 | 2009-02-24 | Bristol-Myers Squibb Company | Substituted imidazo[1,2-a]pyrimidines as HIV viral DNA integrase inhibitors |
| JP5094725B2 (ja) | 2005-10-04 | 2012-12-12 | イステイチユート・デイ・リチエルケ・デイ・ビオロジア・モレコラーレ・ピ・アンジエレツテイ・エツセ・エルレ・エルレ | Hivインテグラーゼ阻害剤 |
| US7902182B2 (en) * | 2005-11-16 | 2011-03-08 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| WO2007064316A1 (en) * | 2005-11-30 | 2007-06-07 | Bristol-Myers Squibb Company | Bicyclic heterocycles as hiv integrase inhibitors |
| WO2007064502A1 (en) * | 2005-12-01 | 2007-06-07 | Bristol-Myers Squibb Company | Forms of n-[(4-fluorophenyl)methyl]-4,6,7,9-tetrahydro-3-hydroxy-9,9-dimethyl-4-oxo-pyrimido[2,1-c][1,4]oxazine-2-carboxamide |
| US20070129379A1 (en) * | 2005-12-01 | 2007-06-07 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
| US7897593B2 (en) * | 2006-05-30 | 2011-03-01 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US7893055B2 (en) * | 2006-06-28 | 2011-02-22 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| AU2007275805A1 (en) * | 2006-07-19 | 2008-01-24 | University Of Georgia Research Foundation, Inc. | Pyridinone diketo acids: Inhibitors of HIV replication in combination therapy |
| US7763630B2 (en) * | 2007-06-06 | 2010-07-27 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US8129398B2 (en) * | 2008-03-19 | 2012-03-06 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| WO2009120841A1 (en) * | 2008-03-27 | 2009-10-01 | Bristol-Myers Squibb Company | Crystalline form of n-[[4-fluoro-2-(5-methyl-1h-1,2,4-triazol-1-yl)phenyl]methyl]-4,6,7,9-tetrahydro-3-hydroxy-9,9-dimethyl-4-oxo-pyrimido[2,1-c][1,4]oxazine-2-carboxamide, sodium salt monohydrate |
| EP2349276B1 (en) * | 2008-10-06 | 2019-11-27 | Merck Sharp & Dohme Corp. | Hiv integrase inhibitors |
| US8143244B2 (en) * | 2009-02-26 | 2012-03-27 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| ES2446720T3 (es) | 2009-10-13 | 2014-03-10 | Elanco Animal Health Ireland Limited | Inhibidores de la integrasa macrocíclica |
| US8383639B2 (en) * | 2009-10-15 | 2013-02-26 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| KR20120094098A (ko) | 2009-12-07 | 2012-08-23 | 유니버시티 오브 조지아 리서치 파운데이션, 인코포레이티드 | 피리디논 하이드록시사이클로펜틸 카복사미드: 치료 용도의 hiv 인테그라제 억제제 |
| EA032868B1 (ru) | 2010-01-27 | 2019-07-31 | Вайв Хелткер Компани | Комбинация для лечения вич-инфекции |
| RU2567385C2 (ru) | 2010-04-02 | 2015-11-10 | ЯНССЕН Ар ЭНД Ди АЙРЛЭНД | Макроциклические ингибиторы интегразы |
| JP5996532B2 (ja) | 2010-07-15 | 2016-09-21 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 有害生物防除剤としての新規複素環式化合物 |
| US8791108B2 (en) | 2011-08-18 | 2014-07-29 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| US9089574B2 (en) | 2011-11-30 | 2015-07-28 | Emory University | Antiviral JAK inhibitors useful in treating or preventing retroviral and other viral infections |
| EP2807149A2 (en) * | 2012-01-26 | 2014-12-03 | CRO Consulting Limited | Agents for treating neurodegenerative disorders |
| WO2014099586A1 (en) | 2012-12-17 | 2014-06-26 | Merck Sharp & Dohme Corp. | 4-pyridinonetriazine derivatives as hiv integrase inhibitors |
| EP2986291B1 (en) | 2013-04-16 | 2020-05-27 | Merck Sharp & Dohme Corp. | 4-pyridone derivative compounds and uses thereof as hiv integrase inhibitors |
| ES2656696T3 (es) | 2013-05-17 | 2018-02-28 | Merck Sharp & Dohme Corp. | Compuestos heterocíclicos tricíclicos condensados como inhibidores de la integrasa del VIH |
| US9951079B2 (en) | 2013-06-13 | 2018-04-24 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds as HIV integrase inhibitors |
| MX367057B (es) | 2013-09-27 | 2019-08-02 | Merck Sharp & Dohme | Derivados de quinolizina sustituidos utiles como inhibidores de integrasa del vih. |
| WO2016187788A1 (en) | 2015-05-25 | 2016-12-01 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds useful for treating hiv infection |
| 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) |
| AU2017367714B2 (en) | 2016-12-02 | 2020-11-12 | Merck Sharp & Dohme Corp. | Tricyclic heterocycle compounds useful as HIV integrase inhibitors |
| EP3573984A4 (en) | 2017-01-26 | 2020-07-29 | Merck Sharp & Dohme Corp. | USEFUL SUBSTITUTE QUINOLIZINE DERIVATIVES AS HIV INTEGRASE INHIBITORS |
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| CN113912622B (zh) * | 2020-07-10 | 2023-12-01 | 上海纽思克生物科技有限公司 | 三环嘧啶酮类化合物、其制备方法、其组合物和用途 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US5693641A (en) * | 1996-08-16 | 1997-12-02 | Berlex Laboratories Inc. | Bicyclic pyrimidine derivatives and their use as anti-coagulants |
| EP1441735B1 (en) | 2001-10-26 | 2006-02-22 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | N-substituted hydroxypyrimidinone carboxamide inhibitors of hiv integrase |
| DE60218511T2 (de) | 2001-10-26 | 2007-10-25 | Istituto Di Richerche Di Biologia Molecolare P. Angeletti S.P.A. | Dihydroxypyrimidin-carbonsäueramid-hemmer der hiv-integrase |
| US7094783B2 (en) * | 2002-06-26 | 2006-08-22 | Bristol-Myers Squibb Company | Bicyclic pyrimidinones as coagulation cascade inhibitors |
| AU2003292436B2 (en) | 2002-12-27 | 2009-07-30 | Msd Italia S.R.L. | Tetrahydro-4H-pyrido[1,2-A]pyrimidines and related compounds useful as HIV integrase inhibitors |
| AR046938A1 (es) | 2003-12-12 | 2006-01-04 | Merck & Co Inc | Procedimiento para preparar hexahidropirimido[1,2-a]azepin-2-carboxilatos y compuetos similares |
| TW200526635A (en) | 2003-12-22 | 2005-08-16 | Shionogi & Co | Hydroxypyrimidinone derivative having HIV integrase inhibitory activity |
| MX2007006637A (es) | 2004-12-03 | 2007-06-19 | Merck & Co Inc | Uso de atazanavir para mejorar los parametros farmacocineticos de farmacos metabolizados por isoforma 1a1 de udp-glucuronosil- transferasa. |
| EP1866313A1 (en) | 2005-03-31 | 2007-12-19 | Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. | Hiv integrase inhibitors |
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