AU2014286995B2 - Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections - Google Patents
Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections Download PDFInfo
- Publication number
- AU2014286995B2 AU2014286995B2 AU2014286995A AU2014286995A AU2014286995B2 AU 2014286995 B2 AU2014286995 B2 AU 2014286995B2 AU 2014286995 A AU2014286995 A AU 2014286995A AU 2014286995 A AU2014286995 A AU 2014286995A AU 2014286995 B2 AU2014286995 B2 AU 2014286995B2
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- compound
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- hydrogen
- concentrated
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- 0 *C(*)(*)NC(C(C1=O)=CN(CC2(*C3)IC3CN2C2=O)C2=C1O)=O Chemical compound *C(*)(*)NC(C(C1=O)=CN(CC2(*C3)IC3CN2C2=O)C2=C1O)=O 0.000 description 8
- HFMMTTCKCHKWAS-OSPHWJPCSA-N CCOC(C(C1=O)=CN(C[C@@](C2)(CCC[C@H]2C2)N2C2=O)C2=C1OCc1ccccc1)=O Chemical compound CCOC(C(C1=O)=CN(C[C@@](C2)(CCC[C@H]2C2)N2C2=O)C2=C1OCc1ccccc1)=O HFMMTTCKCHKWAS-OSPHWJPCSA-N 0.000 description 2
- QGCVRZHDWDRLPI-CMVXHFHISA-N C=C/C(/CNC(C(C1=O)=CN(C[C@@](C2)(CCC[C@H]2C2)N2C2=O)C2=C1O)=O)=C/F Chemical compound C=C/C(/CNC(C(C1=O)=CN(C[C@@](C2)(CCC[C@H]2C2)N2C2=O)C2=C1O)=O)=C/F QGCVRZHDWDRLPI-CMVXHFHISA-N 0.000 description 1
- MMDXARSCRJYPDY-UHFFFAOYSA-N CC1=C(C(NC(C2)=C)=C)N2C=C(C(N)=C)C1=O Chemical compound CC1=C(C(NC(C2)=C)=C)N2C=C(C(N)=C)C1=O MMDXARSCRJYPDY-UHFFFAOYSA-N 0.000 description 1
- HXPAFCPLUPJFQF-XYNXFOTISA-N CC1C(CC(CC[C@]2(C3)CN(C=C4C(NCc(c(F)cc(F)c5)c5F)=O)C5=C(C)C4=O)[C@H]3CN2C5=C)C1 Chemical compound CC1C(CC(CC[C@]2(C3)CN(C=C4C(NCc(c(F)cc(F)c5)c5F)=O)C5=C(C)C4=O)[C@H]3CN2C5=C)C1 HXPAFCPLUPJFQF-XYNXFOTISA-N 0.000 description 1
- LRXBHPOPQODAGZ-PTVXEPTESA-N Cc1cc(F)cc(F)c1CNC(C(C1O)=CN(C[C@](C2)(CCC[C@@H]2C2)N2C2=O)C2=C1O)=C Chemical compound Cc1cc(F)cc(F)c1CNC(C(C1O)=CN(C[C@](C2)(CCC[C@@H]2C2)N2C2=O)C2=C1O)=C LRXBHPOPQODAGZ-PTVXEPTESA-N 0.000 description 1
- OBYYGQMAUDYBAV-UHFFFAOYSA-N Cc1ccc(CNC(C(C2=O)=CN(CC(C(C3)CC3C3)N3C3=O)C3=C2O)=O)c(F)c1 Chemical compound Cc1ccc(CNC(C(C2=O)=CN(CC(C(C3)CC3C3)N3C3=O)C3=C2O)=O)c(F)c1 OBYYGQMAUDYBAV-UHFFFAOYSA-N 0.000 description 1
- VLMDAUAZUOVFKU-QRQCRPRQSA-N NC(C(C1=O)=CN(C[C@@](C2)(CCC[C@H]2C2)N2C2=O)C2=C1OCc1ccccc1)=O Chemical compound NC(C(C1=O)=CN(C[C@@](C2)(CCC[C@H]2C2)N2C2=O)C2=C1OCc1ccccc1)=O VLMDAUAZUOVFKU-QRQCRPRQSA-N 0.000 description 1
- VBTQFGJFGWVPLY-RBSBEOHCSA-N O=C(C(C1=O)=CN(C[C@](C2)(CCC[C@@H]2C2)N2C2=O)C2=C1OCc1ccccc1)NCc(c(F)cc(F)c1)c1F Chemical compound O=C(C(C1=O)=CN(C[C@](C2)(CCC[C@@H]2C2)N2C2=O)C2=C1OCc1ccccc1)NCc(c(F)cc(F)c1)c1F VBTQFGJFGWVPLY-RBSBEOHCSA-N 0.000 description 1
- UGKYRBKXBKAWIZ-UULLZXFKSA-N O=C(C(C1=O)=CN(C[C@](CC2)(C[C@@H]2C2)N2C2=O)C2=C1OCc1ccccc1)NCc(c(F)cc(F)c1)c1F Chemical compound O=C(C(C1=O)=CN(C[C@](CC2)(C[C@@H]2C2)N2C2=O)C2=C1OCc1ccccc1)NCc(c(F)cc(F)c1)c1F UGKYRBKXBKAWIZ-UULLZXFKSA-N 0.000 description 1
- ZNYMMMAYIVJGJI-OYHNWAKOSA-N OC(C(C1=O)=CN(C[C@](C2)(CCC[C@@H]2C2)N2C2=O)C2=C1OCc1ccccc1)=O Chemical compound OC(C(C1=O)=CN(C[C@](C2)(CCC[C@@H]2C2)N2C2=O)C2=C1OCc1ccccc1)=O ZNYMMMAYIVJGJI-OYHNWAKOSA-N 0.000 description 1
- QERPVLPCCZNVKX-SZNDQCEHSA-N OC(C(C1=O)=CN(C[C@](CC2)(C[C@@H]2C2)N2C2=O)C2=C1OCc1ccccc1)=O Chemical compound OC(C(C1=O)=CN(C[C@](CC2)(C[C@@H]2C2)N2C2=O)C2=C1OCc1ccccc1)=O QERPVLPCCZNVKX-SZNDQCEHSA-N 0.000 description 1
- SBWPHTTXWNSHCB-UZJPJQLHSA-N OC1=C(C(N(C[C@H](CC2)C3)[C@@]23C2)=O)N2C=C(C(NCc(c(F)cc(F)c2)c2F)=O)C1=O Chemical compound OC1=C(C(N(C[C@H](CC2)C3)[C@@]23C2)=O)N2C=C(C(NCc(c(F)cc(F)c2)c2F)=O)C1=O SBWPHTTXWNSHCB-UZJPJQLHSA-N 0.000 description 1
- KHPMSEOFOMMZME-LMRGUYSOSA-N OC1=C(C(N(C[C@H](CC2)CC3)[C@@]23C2)=O)N2C=C(C(NCc(c(F)c2)ccc2F)=O)C1=O Chemical compound OC1=C(C(N(C[C@H](CC2)CC3)[C@@]23C2)=O)N2C=C(C(NCc(c(F)c2)ccc2F)=O)C1=O KHPMSEOFOMMZME-LMRGUYSOSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic 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
-
- 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
- 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
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)
- Epidemiology (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2018236701A AU2018236701B2 (en) | 2013-07-12 | 2018-09-24 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections |
AU2020202368A AU2020202368A1 (en) | 2013-07-12 | 2020-04-03 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361845807P | 2013-07-12 | 2013-07-12 | |
US61/845,807 | 2013-07-12 | ||
PCT/US2014/046415 WO2015006733A1 (en) | 2013-07-12 | 2014-07-11 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of hiv infections |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2018236701A Division AU2018236701B2 (en) | 2013-07-12 | 2018-09-24 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2014286995A1 AU2014286995A1 (en) | 2016-03-03 |
AU2014286995B2 true AU2014286995B2 (en) | 2018-10-18 |
Family
ID=51257630
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2014286995A Active AU2014286995B2 (en) | 2013-07-12 | 2014-07-11 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections |
AU2018236701A Active AU2018236701B2 (en) | 2013-07-12 | 2018-09-24 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections |
AU2020202368A Abandoned AU2020202368A1 (en) | 2013-07-12 | 2020-04-03 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2018236701A Active AU2018236701B2 (en) | 2013-07-12 | 2018-09-24 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections |
AU2020202368A Abandoned AU2020202368A1 (en) | 2013-07-12 | 2020-04-03 | Polycyclic-carbamoylpyridone compounds and their use for the treatment of HIV infections |
Country Status (18)
Country | Link |
---|---|
US (6) | US9458159B2 (en:Method) |
EP (2) | EP3252053B1 (en:Method) |
JP (1) | JP6411492B2 (en:Method) |
AU (3) | AU2014286995B2 (en:Method) |
CA (1) | CA2918055C (en:Method) |
CY (1) | CY1119545T1 (en:Method) |
DK (1) | DK3019499T3 (en:Method) |
ES (2) | ES2856867T3 (en:Method) |
HR (1) | HRP20171807T1 (en:Method) |
HU (1) | HUE037343T2 (en:Method) |
LT (1) | LT3019499T (en:Method) |
NO (1) | NO2865735T3 (en:Method) |
PL (1) | PL3019499T3 (en:Method) |
PT (1) | PT3019499T (en:Method) |
RS (1) | RS56539B1 (en:Method) |
SI (2) | SI3019499T1 (en:Method) |
SM (1) | SMT201700525T1 (en:Method) |
WO (1) | WO2015006733A1 (en:Method) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI3067358T1 (sl) | 2012-12-21 | 2019-12-31 | Gilead Sciences, Inc. | Policiklične spojine karbamoilpiridona in njihova farmacevtska uporaba |
WO2015006731A1 (en) * | 2013-07-12 | 2015-01-15 | Gilead Sciences, Inc. | Polycyclic-carbamoylpyridone compounds and their use for the treatment of hiv infections |
NO2865735T3 (en:Method) * | 2013-07-12 | 2018-07-21 | ||
US10011613B2 (en) | 2014-08-22 | 2018-07-03 | Shionogi & Co., Ltd. | Polycyclic pyridone derivative having integrase inhibitory activity |
SI3321265T1 (sl) | 2015-03-04 | 2020-07-31 | Gilead Sciences, Inc. | Spojine 4,6-diamino-pirido(3,2-d)pirimidina in njihova uporaba kot modulatorji toličnih receptorjev |
NZ735575A (en) * | 2015-04-02 | 2018-11-30 | Gilead Sciences Inc | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
WO2017035230A1 (en) | 2015-08-26 | 2017-03-02 | Gilead Sciences, Inc. | Deuterated toll-like receptor modulators |
JP2018527366A (ja) | 2015-09-15 | 2018-09-20 | ギリアード サイエンシーズ, インコーポレイテッド | HIVを処置するためのtoll様レセプターのモジュレーター |
WO2017083304A1 (en) | 2015-11-09 | 2017-05-18 | Gilead Sciences, Inc. | Therapeutic compositions for treatment of human immunodeficiency virus |
US10640499B2 (en) | 2016-09-02 | 2020-05-05 | Gilead Sciences, Inc. | Toll like receptor modulator compounds |
US10370342B2 (en) | 2016-09-02 | 2019-08-06 | Gilead Sciences, Inc. | Toll like receptor modulator compounds |
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) |
CN110526930B (zh) * | 2018-05-23 | 2022-06-03 | 莫云芬 | 抗hiv病毒的含硫多环-羟基吡啶酮甲酰胺类似物及其应用 |
CN112513042B (zh) | 2018-05-31 | 2023-09-29 | 盐野义制药株式会社 | 多环氨基甲酰基吡啶酮衍生物 |
MY203593A (en) | 2018-05-31 | 2024-07-05 | Shionogi & Co | Polycyclic pyridone derivative |
KR102714084B1 (ko) | 2019-03-22 | 2024-10-08 | 길리애드 사이언시즈, 인코포레이티드 | 가교된 트리시클릭 카르바모일피리돈 화합물 및 그의 제약 용도 |
WO2020255038A1 (en) | 2019-06-18 | 2020-12-24 | Janssen Sciences Ireland Unlimited Company | Combination of hepatitis b virus (hbv) vaccines and pyridopyrimidine derivatives |
US20200398978A1 (en) | 2019-06-20 | 2020-12-24 | Bell Helicopter Textron Inc. | Low-drag rotor blade extension |
EP4066839A4 (en) | 2019-11-28 | 2023-12-27 | Shionogi & Co., Ltd | PROPHYLACTIC AND THERAPEUTIC PHARMACEUTICAL AGENT FOR HIV INFECTIOUS DISEASES, CHARACTERIZED IN THAT IT COMPRISES A COMBINATION OF AN INTEGRASE INHIBITOR AND AN ANTI-HIV AGENT |
PE20221569A1 (es) | 2020-02-24 | 2022-10-06 | Gilead Sciences Inc | Compuestos tetraciclicos para el tratamiento de infecciones por vih |
AU2021351491C1 (en) * | 2020-09-30 | 2025-06-12 | Gilead Sciences, Inc. | Bridged tricyclic carbamoylpyridone compounds and uses thereof |
DK4196479T5 (da) | 2021-01-19 | 2025-01-02 | Gilead Sciences Inc | Substituerede pyridotriazinforbindelser og anvendelser deraf |
TWI843506B (zh) | 2022-04-06 | 2024-05-21 | 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 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006116764A1 (en) * | 2005-04-28 | 2006-11-02 | Smithkline Beecham Corporation | Polycyclic carbamoylpyridone derivative having hiv integrase inhibitory activity |
Family Cites Families (114)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE788516A (fr) | 1971-09-10 | 1973-03-07 | Lonza Ag | Procede de fabrication d'esters alcoxyacetylacetiques |
GB1528382A (en) | 1974-12-26 | 1978-10-11 | Teijin Ltd | Cyclopentene diols and acyl esters thereof and processes for their preparation |
DE2658401A1 (de) | 1976-12-23 | 1978-07-06 | Merck Patent Gmbh | Cyclopentan-1-amine, verfahren zu ihrer herstellung und diese verbindungen enthaltende mittel |
US4575694A (en) | 1984-03-05 | 1986-03-11 | Allied Corporation | Coaxial connector |
DE3900735A1 (de) | 1989-01-12 | 1990-07-26 | Hoechst Ag | Neue mehrfunktionelle (alpha)-diazo-(beta)-ketoester, verfahren zu ihrer herstellung und deren verwendung |
US5204466A (en) | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
US5914331A (en) | 1990-02-01 | 1999-06-22 | Emory University | Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane |
US6703396B1 (en) | 1990-02-01 | 2004-03-09 | Emory University | Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers |
DE4014649A1 (de) | 1990-05-08 | 1991-11-14 | Hoechst Ag | Neue mehrfunktionelle verbindungen mit (alpha)-diazo-ss-ketoester- und sulfonsaeureester-einheiten, verfahren zu ihrer herstellung und deren verwendung |
GB9301000D0 (en) | 1993-01-20 | 1993-03-10 | Glaxo Group Ltd | Chemical compounds |
US5922695A (en) | 1996-07-26 | 1999-07-13 | Gilead Sciences, Inc. | Antiviral phosphonomethyoxy nucleotide analogs having increased oral bioavarilability |
SE9702772D0 (sv) | 1997-07-22 | 1997-07-22 | Astra Pharma Prod | Novel compounds |
US5935946A (en) | 1997-07-25 | 1999-08-10 | Gilead Sciences, Inc. | Nucleotide analog composition and synthesis method |
AU1403099A (en) | 1997-11-14 | 1999-06-07 | Merck & Co., Inc. | Alpha-1a adrenergic receptor antagonists |
AU1061500A (en) | 1998-11-09 | 2000-05-29 | James Black Foundation Limited | Gastrin and cholecystokinin receptor ligands |
GB2345058A (en) | 1998-12-01 | 2000-06-28 | Cerebrus Pharm Ltd | Hydroxypyridone compounds useful in the treatment of oxidative damage to the central nervous system |
US6620841B1 (en) | 1998-12-25 | 2003-09-16 | Shionogi & Co., Ltd. | Aromatic heterocycle compounds having HIV integrase inhibiting activities |
WO2001095905A1 (en) | 2000-06-14 | 2001-12-20 | Shionogi & Co., Ltd. | Inhibitor for enzyme having two divalent metal ions as active centers |
KR100977701B1 (ko) | 2001-08-10 | 2010-08-24 | 시오노기세이야쿠가부시키가이샤 | 항바이러스제 |
JP2005523238A (ja) | 2001-10-03 | 2005-08-04 | ユ セ ベ ソシエテ アノニム | ピロリジノン誘導体 |
ES2258668T3 (es) | 2001-10-26 | 2006-09-01 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Hidroxipirimidina carboxamidas n-sustituidas inhibidoras de hiv integrasa. |
EP1452527B1 (en) | 2001-11-13 | 2009-03-04 | Shiseido Co., Ltd. | Azabicyclo compound, matrix metalloprotease inhibitor, and skin preparation |
US7109186B2 (en) | 2002-07-09 | 2006-09-19 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
WO2004024078A2 (en) | 2002-09-11 | 2004-03-25 | Merck & Co., Inc. | Dihydroxypyridopyrazine-1,6-dione compounds useful as hiv integrase inhibitors |
AU2003302029B8 (en) | 2002-11-20 | 2006-08-17 | Japan Tobacco Inc. | 4-oxoquinoline compound and utilization thereof as HIV integrase inhibitor |
MXPA05007016A (es) | 2003-01-14 | 2005-09-12 | Gilead Sciences Inc | Composiciones y metodos para terapia antiviral de combinacion. |
TW200510425A (en) | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
TW200528440A (en) | 2003-10-31 | 2005-09-01 | Fujisawa Pharmaceutical Co | 2-cyanopyrrolidinecarboxamide compound |
WO2005074513A2 (en) | 2004-01-30 | 2005-08-18 | Merck & Co., Inc. | N-benzyl-3,4-dihyroxypyridine-2-carboxamide and n-benzyl-2,3-dihydroxypyridine-4-carboxamide compounds useful as hiv integrase inhibitors |
CN101014574A (zh) | 2004-03-09 | 2007-08-08 | 默克公司 | Hiv整合酶抑制剂 |
WO2006028523A2 (en) | 2004-04-29 | 2006-03-16 | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, SAN DIEGO USDC Technology Transfer Office | Hydroxypyridinone, hydroxypyridinethione, pyrone, and thiopyrone metalloprotein inhibitors |
WO2005110399A2 (en) | 2004-04-29 | 2005-11-24 | The Regents Of The University Of California | Zinc-binding groups for metalloprotein inhibitors |
AU2005244157B2 (en) | 2004-05-07 | 2010-11-11 | Merck Sharp & Dohme Corp. | HIV integrase inhibitors |
US7273859B2 (en) | 2004-05-12 | 2007-09-25 | Bristol-Myers Squibb Company | HIV integrase inhibitors: cyclic pyrimidinone compounds |
MY134672A (en) | 2004-05-20 | 2007-12-31 | Japan Tobacco Inc | Stable crystal of 4-oxoquinoline compound |
US7531554B2 (en) | 2004-05-20 | 2009-05-12 | Japan Tobacco Inc. | 4-oxoquinoline compound and use thereof as HIV integrase inhibitor |
JP4629104B2 (ja) | 2004-05-21 | 2011-02-09 | 日本たばこ産業株式会社 | 4−オキソキノリン誘導体および抗hiv剤を含む併用剤 |
WO2006030807A1 (ja) | 2004-09-15 | 2006-03-23 | Shionogi & Co., Ltd. | 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 |
CA2634499A1 (en) | 2004-12-23 | 2006-06-29 | Virochem Pharma Inc. | Hydroxydihydropyridopy razine-1,8-diones and methods for inhibiting hiv integrase |
ATE516026T1 (de) | 2005-02-21 | 2011-07-15 | Shionogi & Co | Bicyclisches carbamoylpyridonderivat mit hiv- integrase-hemmender wirkung |
AR057023A1 (es) | 2005-05-16 | 2007-11-14 | Gilead Sciences Inc | Compuestos heterociclicos con propiedades inhibidoras de hiv-integrasa |
EP1906971A2 (en) | 2005-07-27 | 2008-04-09 | Gilead Sciences, Inc. | Antiviral compounds |
JP5131689B2 (ja) | 2005-10-27 | 2013-01-30 | 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多環性カルバモイルピリドン誘導体 |
EA201201496A1 (ru) | 2005-12-30 | 2013-07-30 | Джилид Сайэнс, Инк. | Способ ингибирования интегразы вич, способ улучшения фармакокинетики 6-(3-хлор-2-фторбензил)-1-[(2s)-1-гидрокси-3-метилбутан-2-ил]-7-метокси-4-оксо-1,4-дигидрохинолин-3-карбоновой кислоты (варианты), набор, фармацевтическая композиция (варианты) и антиретровирусный агент (варианты) |
US7601844B2 (en) | 2006-01-27 | 2009-10-13 | Bristol-Myers Squibb Company | Piperidinyl derivatives as modulators of chemokine receptor activity |
US20090018162A1 (en) | 2006-02-01 | 2009-01-15 | Yuji Matsuzaki | 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 |
IN2014CN00532A (en:Method) | 2006-03-06 | 2015-04-03 | Japan Tobacco Inc | |
EA017861B9 (ru) | 2006-03-06 | 2014-05-30 | Джапан Тобакко Инк. | Способ получения 4-оксохинолинового соединения |
US7893055B2 (en) | 2006-06-28 | 2011-02-22 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
JP2009543865A (ja) | 2006-07-19 | 2009-12-10 | ユニバーシティ オブ ジョージア リサーチ ファウンデーション, インコーポレーテッド | ピリジノンジケト酸:併用療法におけるhiv複製の阻害剤 |
EP2395005A1 (en) | 2006-09-07 | 2011-12-14 | Industrial Research Limited | Acyclic amine inhibitors of nucleoside phosphorylases and hydrolases |
EP2644587A3 (en) | 2006-09-12 | 2013-10-23 | Gilead Sciences, Inc. | Process and intermediates for preparing integrase inhibitors |
JP2010506913A (ja) | 2006-10-18 | 2010-03-04 | メルク エンド カムパニー インコーポレーテッド | Hivインテグラーゼ阻害剤 |
LT2487162T (lt) | 2007-02-23 | 2016-11-10 | Gilead Sciences, Inc. | Terapinių agentų farmakokinetinių savybių moduliatoriai |
US20080280945A1 (en) | 2007-05-09 | 2008-11-13 | Sachin Lohani | Crystalline forms of an HIV integrase inhibitor |
CA2692101A1 (en) | 2007-06-29 | 2009-01-08 | Gilead Sciences, Inc. | Combination of 6-(3-chloro-2-fluorobenzyl)-1-[(2s)-1-hydroxy-3-methylbutan-2-yl]-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid and a compound that inhibits a ugt pathway or ugt metabolism |
MX2009013828A (es) | 2007-06-29 | 2010-03-10 | Gilead Sciences Inc | Composiciones terapeuticas y su uso. |
US20090258939A1 (en) | 2007-07-31 | 2009-10-15 | Wendye Robbins | Pyrone analog compositions and methods |
AR068403A1 (es) | 2007-09-11 | 2009-11-18 | Gilead Sciences Inc | Proceso e intermediarios para la preparacion de inhibidores de integrasa |
EP2220046B1 (en) | 2007-11-16 | 2014-06-18 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
GB0803019D0 (en) | 2008-02-19 | 2008-03-26 | Btg Int Ltd | Fluorinated compounds |
US8129398B2 (en) | 2008-03-19 | 2012-03-06 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
US20100272811A1 (en) | 2008-07-23 | 2010-10-28 | Alkermes,Inc. | Complex of trospium and pharmaceutical compositions thereof |
ES2448766T3 (es) | 2008-07-25 | 2014-03-17 | Viiv Healthcare Company | Profármacos de dolutegravir |
EP2330902B1 (en) | 2008-07-25 | 2012-11-14 | GlaxoSmithKline LLC | Chemical compounds |
WO2010011818A1 (en) | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
WO2010011814A1 (en) | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
WO2010011815A1 (en) | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
WO2010011819A1 (en) | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
US8552187B2 (en) | 2008-12-11 | 2013-10-08 | Shionogi & Co., Ltd. | Processes and intermediates for carbamoylpyridone HIV integrase inhibitors |
CA2744019C (en) | 2008-12-11 | 2017-03-14 | Shionogi & Co., Ltd. | Synthesis of carbamoylpyridone hiv integrase inhibitors and intermediates |
TWI518084B (zh) | 2009-03-26 | 2016-01-21 | 鹽野義製藥股份有限公司 | 哌喃酮與吡啶酮衍生物之製造方法 |
JP5697163B2 (ja) | 2009-03-26 | 2015-04-08 | 塩野義製薬株式会社 | 置換された3−ヒドロキシ−4−ピリドン誘導体 |
US8338441B2 (en) | 2009-05-15 | 2012-12-25 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
EP2444400B1 (en) | 2009-06-15 | 2018-03-28 | Shionogi&Co., Ltd. | Substituted polycyclic carbamoylpyridone derivative |
WO2011028044A2 (ko) | 2009-09-02 | 2011-03-10 | 이화여자대학교 산학협력단 | 피라졸 유도체, 이의 제조방법 및 이를 포함하는 골다공증 예방 및 치료용 조성물 |
CN105311033B (zh) | 2010-01-27 | 2019-05-07 | Viiv保健公司 | 抗病毒治疗 |
KR20120130185A (ko) | 2010-02-26 | 2012-11-29 | 니뽄 다바코 산교 가부시키가이샤 | 1,3,4,8―테트라히드로―2H―피리도[1,2―a]피라진 유도체 및 그의 HIV 인테그라제 저해제로서의 이용 |
TWI582097B (zh) | 2010-03-23 | 2017-05-11 | Viiv醫療保健公司 | 製備胺甲醯吡啶酮衍生物及中間體之方法 |
WO2011139637A1 (en) | 2010-05-03 | 2011-11-10 | Philadelphia Health & Education Corporation | Small-molecule modulators of hiv-1 capsid stability and methods thereof |
AU2011274323B2 (en) | 2010-07-02 | 2015-08-06 | Gilead Sciences, Inc. | 2 -quinolinyl- acetic acid derivatives as HIV antiviral compounds |
CA2802308C (en) | 2010-07-02 | 2018-08-28 | Lianhong Xu | Napht-2-ylacetic acid derivatives to treat aids |
US20130210809A1 (en) | 2010-07-14 | 2013-08-15 | Christelle Boléa | Novel 2-amino-4-pyrazolyl-thiazole derivatives and their use as allosteric modulators of metabotropic glutamate receptors |
SG187683A1 (en) | 2010-08-05 | 2013-03-28 | Shionogi & Co | Process for preparing compound having hiv integrase inhibitory activity |
US8987441B2 (en) | 2010-09-24 | 2015-03-24 | Shionogi & Co., Ltd. | Substituted polycyclic carbamoyl pyridone derivative prodrug |
WO2012106534A2 (en) | 2011-02-02 | 2012-08-09 | The Regents Of The University Of California | Hiv integrase inhibitors |
US9006229B2 (en) | 2011-04-21 | 2015-04-14 | Gilead Sciences, Inc. | Benzothiazole compounds and their pharmaceutical use |
US20140213553A1 (en) | 2011-05-03 | 2014-07-31 | Concert Pharmaceuticals Inc. | Carbamoylpyridone derivatives |
WO2012151567A1 (en) | 2011-05-05 | 2012-11-08 | St. Jude Children's Research Hospital | Pyrimidinone compounds and methods for preventing and treating influenza |
AU2012278976B2 (en) | 2011-07-06 | 2017-05-11 | Gilead Sciences, Inc. | Compounds for the treatment of HIV |
CN102863512B (zh) | 2011-07-07 | 2016-04-20 | 上海泓博智源医药技术有限公司 | 抗病毒化合物 |
EP2742051B1 (en) | 2011-09-14 | 2016-10-12 | Mapi Pharma Limited | Amorpous form of the dolutegravir sodium salt |
EP2774928B1 (en) | 2011-10-12 | 2017-08-30 | Shionogi & Co., Ltd. | Polycyclic pyridone derivative having integrase-inhibiting activity |
JP6147761B2 (ja) | 2011-12-12 | 2017-06-14 | 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 | アミノ置換イミダゾピリダジン |
EP2788336B1 (en) | 2012-04-20 | 2016-03-02 | Gilead Sciences, Inc. | Benzothiazol-6-yl acetic acid derivatives and their use for treating an hiv infection |
WO2014008636A1 (en) | 2012-07-11 | 2014-01-16 | Merck Sharp & Dohme Corp. | Macrocyclic compounds as hiv integrase inhibitors |
EP2875024A4 (en) | 2012-07-20 | 2015-12-23 | Merck Sharp & Dohme | HIV TREATMENT WITH AMIDOSUBSTITUTED PYRIMIDINONE DERIVATIVES |
US20150218164A1 (en) | 2012-07-25 | 2015-08-06 | Merck Sharp & Dohme Corp. | Substituted naphthyridinedione derivatives as hiv integrase inhibitors |
CN104520275B (zh) | 2012-08-03 | 2016-11-02 | 吉利德科学公司 | 用于制备整合酶抑制剂的方法和中间产物 |
MX2015005562A (es) | 2012-11-08 | 2015-07-23 | Squibb Bristol Myers Co | Compuestos de piridilo sustituidos con heteroarilo utiles como moduladores de cinasa. |
SG11201503807TA (en) | 2012-12-14 | 2015-06-29 | Glaxosmithkline Llc | Pharmaceutical compositions |
WO2014099586A1 (en) * | 2012-12-17 | 2014-06-26 | Merck Sharp & Dohme Corp. | 4-pyridinonetriazine derivatives as hiv integrase inhibitors |
SI3067358T1 (sl) * | 2012-12-21 | 2019-12-31 | Gilead Sciences, Inc. | Policiklične spojine karbamoilpiridona in njihova farmacevtska uporaba |
US20140221355A1 (en) | 2012-12-21 | 2014-08-07 | Gilead Sciences, Inc. | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
EP2934482A4 (en) | 2012-12-21 | 2016-07-20 | Merck Sharp & Dohme | ADMINISTRATIVE FORMULATIONS |
RU2015131006A (ru) | 2012-12-27 | 2017-01-30 | Джапан Тобакко Инк. | ЗАМЕЩЕННОЕ ПРОИЗВОДНОЕ СПИРОПИРИДО[1,2-a]ПИРАЗИНА И ЕГО ПРИМЕНЕНИЕ В МЕДИЦИНЕ В КАЧЕСТВЕ ИНГИБИТОРА ИНТЕГРАЗЫ ВИРУСА ИММУНОДЕФИЦИТА ЧЕЛОВЕКА (ВИЧ) |
WO2014200880A1 (en) | 2013-06-13 | 2014-12-18 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds as hiv integrase inhibitors |
WO2015006731A1 (en) * | 2013-07-12 | 2015-01-15 | Gilead Sciences, Inc. | Polycyclic-carbamoylpyridone compounds and their use for the treatment of hiv infections |
NO2865735T3 (en:Method) * | 2013-07-12 | 2018-07-21 | ||
WO2015039348A1 (en) * | 2013-09-23 | 2015-03-26 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds useful as hiv integrase inhibitors |
CN105744936B (zh) | 2013-09-27 | 2019-07-30 | 默沙东公司 | 可用作hiv整合酶抑制剂的取代喹嗪衍生物 |
US20150146340A1 (en) | 2013-11-26 | 2015-05-28 | Qualcomm Incorporated | Multilayer ceramic capacitor including at least one slot |
WO2015089847A1 (en) | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | Spirocyclic heterocycle compounds useful as hiv integrase inhibitors |
ES2770050T3 (es) | 2014-01-21 | 2020-06-30 | Laurus Labs Ltd | Nuevo procedimiento para la preparación de dolutegravir y sus sales farmacéuticamente aceptables |
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006116764A1 (en) * | 2005-04-28 | 2006-11-02 | Smithkline Beecham Corporation | Polycyclic carbamoylpyridone derivative having hiv integrase inhibitory activity |
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