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
- Authority
- AU
- Australia
- Prior art keywords
- compound
- iii
- mmol
- hydrogen
- concentrated
- 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 *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)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (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)
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA3131094A1 (en) | 2012-12-21 | 2014-06-26 | Gilead Sciences, Inc. | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
HUE037347T2 (hu) * | 2013-07-12 | 2018-08-28 | Gilead Sciences Inc | Policiklusos karmaboilpiridon vegyületek és alkalmazásuk HIV fertõzések kezelésére |
NO2865735T3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 2013-07-12 | 2018-07-21 | ||
US10011613B2 (en) | 2014-08-22 | 2018-07-03 | Shionogi & Co., Ltd. | Polycyclic pyridone derivative having integrase inhibitory activity |
MD3097102T2 (ro) | 2015-03-04 | 2018-02-28 | Gilead Sciences Inc | Compuşi de 4,6-diamino-pirido[3,2-D]pirimidină modulatori ai receptorilor de tip Toll |
SI3277691T1 (sl) * | 2015-04-02 | 2019-04-30 | Gilead Sciences, Inc. | Policiklične spojine karbamoilpiridona in njihova farmacevtska uporaba |
AU2016312508A1 (en) | 2015-08-26 | 2018-02-15 | 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 |
EA201890654A1 (ru) * | 2015-11-09 | 2018-10-31 | Джилид Сайэнс, Инк. | Терапевтические композиции для лечения вируса иммунодефицита человека |
CN109923106B (zh) | 2016-09-02 | 2022-09-13 | 吉利德科学公司 | toll样受体调节剂化合物 |
WO2018045150A1 (en) | 2016-09-02 | 2018-03-08 | Gilead Sciences, Inc. | 4,6-diamino-pyrido[3,2-d]pyrimidine derivaties as toll like receptor modulators |
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 |
KR20250002769A (ko) | 2018-05-31 | 2025-01-07 | 시오노기 앤드 컴파니, 리미티드 | 다환성 카바모일피리돈 유도체 |
AU2019277547B2 (en) | 2018-05-31 | 2024-10-10 | Shionogi & Co., Ltd. | Polycyclic pyridone derivative |
MX2021011394A (es) | 2019-03-22 | 2021-10-13 | Gilead Sciences Inc | Compuestos de carbamoilpiridona triciclica puenteada y su uso farmaceutico. |
CA3140708A1 (en) | 2019-06-18 | 2020-12-24 | Helen Horton | 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 |
TW202133858A (zh) | 2019-11-28 | 2021-09-16 | 日商鹽野義製藥股份有限公司 | 以組合整合酶阻礙劑及抗hiv藥為特徵之hiv感染症的預防及治療用醫藥 |
EP4110783A1 (en) | 2020-02-24 | 2023-01-04 | Gilead Sciences, Inc. | Tetracyclic compounds for treating hiv infection |
US20220135565A1 (en) * | 2020-09-30 | 2022-05-05 | Gilead Sciences, Inc. | Bridged tricyclic carbamoylpyridone compounds and uses thereof |
HRP20231654T2 (hr) | 2021-01-19 | 2025-01-03 | Gilead Sciences, Inc. | Supstituirani spojevi piridotriazina i njihove uporabe |
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 |
US6703396B1 (en) | 1990-02-01 | 2004-03-09 | Emory University | Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers |
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 |
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 |
WO1999025345A1 (en) | 1997-11-14 | 1999-05-27 | Merck & Co., Inc. | Alpha-1a adrenergic receptor antagonists |
WO2000027823A1 (en) | 1998-11-09 | 2000-05-18 | 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 |
CN1178913C (zh) | 1998-12-25 | 2004-12-08 | 盐野义制药株式会社 | 具有hiv整合酶抑制活性的芳族杂环化合物 |
AU2001262732A1 (en) | 2000-06-14 | 2001-12-24 | Shionogi And Co., Ltd. | Inhibitor for enzyme having two divalent metal ions as active centers |
ATE530520T1 (de) | 2001-08-10 | 2011-11-15 | Shionogi & Co | Antivirales mittel |
HUP0402503A2 (hu) | 2001-10-03 | 2005-03-29 | Ucb, S.A. | Pirrolidinonszármazékok és a vegyületeket tartalmazó gyógyászati készítmények |
IL161337A0 (en) | 2001-10-26 | 2004-09-27 | Angeletti P Ist Richerche Bio | N-substituted hydroxypyrimidinone carboxamide inhibitors of hiv integrase |
US7176217B2 (en) | 2001-11-13 | 2007-02-13 | 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 |
EP1549315A4 (en) | 2002-09-11 | 2007-05-23 | Merck & Co Inc | DIHYDROXYPYRIDOPYRAZINE-1,6-DION COMPOUNDS 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 |
CA2512319A1 (en) | 2003-01-14 | 2004-08-05 | Gilead Sciences, Inc. | Compositions and methods for combination antiviral therapy |
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 |
AU2005211349A1 (en) | 2004-01-30 | 2005-08-18 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | N-benzyl-3,4-dihyroxypyridine-2-carboxamide and N-benzyl-2,3-dihydroxypyridine-4-carboxamide compounds useful as HIV integrase inhibitors |
AU2005220767A1 (en) | 2004-03-09 | 2005-09-22 | Merck & Co., Inc. | HIV integrase inhibitors |
WO2005110399A2 (en) | 2004-04-29 | 2005-11-24 | The Regents Of The University Of California | Zinc-binding groups for metalloprotein inhibitors |
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 |
WO2005110414A2 (en) | 2004-05-07 | 2005-11-24 | Merck & Co., Inc. | 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 |
WO2005113509A1 (en) | 2004-05-20 | 2005-12-01 | Japan Tobacco Inc. | Novel 4-oxoquinoline compound and use thereof as hiv integrase inhibitor |
EP2332538A1 (en) | 2004-05-21 | 2011-06-15 | Japan Tobacco, Inc. | Combinations comprising a 4-isoquinolone derivative and anti-HIV agents |
CN101014572B (zh) | 2004-09-15 | 2011-07-06 | 盐野义制药株式会社 | 具有hiv整合酶抑制活性的氨基甲酰基吡啶酮衍生物 |
WO2006066414A1 (en) | 2004-12-23 | 2006-06-29 | Virochem Pharma Inc. | Hydroxydihydropyridopy razine-1,8-diones and methods for inhibiting hiv integrase |
JP5317257B2 (ja) | 2005-02-21 | 2013-10-16 | 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2環性カルバモイルピリドン誘導体 |
AR057023A1 (es) | 2005-05-16 | 2007-11-14 | Gilead Sciences Inc | Compuestos heterociclicos con propiedades inhibidoras de hiv-integrasa |
US20080076740A1 (en) | 2005-07-27 | 2008-03-27 | Gilead Sciences, Inc. | Antiviral compounds |
CA2626956A1 (en) | 2005-10-27 | 2007-05-03 | Shionogi & Co., Ltd. | Polycyclic carbamoylpyridone derivative having hiv integrase inhibitory activity |
JP4676536B2 (ja) | 2005-12-30 | 2011-04-27 | ギリアド サイエンシズ, インコーポレイテッド | Hivインテグラーゼ阻害剤の薬物動態の改善方法 |
US7601844B2 (en) | 2006-01-27 | 2009-10-13 | Bristol-Myers Squibb Company | Piperidinyl derivatives as modulators of chemokine receptor activity |
JP2009525261A (ja) | 2006-02-01 | 2009-07-09 | 日本たばこ産業株式会社 | レトロウイルス感染症の治療のための、6−(3−クロロ−2−フルオロベンジル)−1−[(2s)−1−ヒドロキシ−3−メチルブタン−2−イル]−7−メトキシ−4−オキソ−1,4−ジヒドロキノリン−3−カルボン酸またはその塩の使用 |
EA017861B9 (ru) | 2006-03-06 | 2014-05-30 | Джапан Тобакко Инк. | Способ получения 4-оксохинолинового соединения |
US8420821B2 (en) | 2006-03-06 | 2013-04-16 | Japan Tobacco Inc. | Process for production of 4-oxoquinoline compound |
US7893055B2 (en) | 2006-06-28 | 2011-02-22 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
US20100092427A1 (en) | 2006-07-19 | 2010-04-15 | The University Of Georgia Research Foundation | Pyridinone Diketo Acids: Inhibitors of HIV Replication in Combination Therapy |
US8853224B2 (en) | 2006-09-07 | 2014-10-07 | Industrial Research Limited | Acyclic amine inhibitors of nucleoside phosphorylases and hydrolases |
SG174787A1 (en) | 2006-09-12 | 2011-10-28 | Gilead Sciences Inc | Process and intermediates for preparing integrase inhibitors |
CA2665538A1 (en) | 2006-10-18 | 2008-04-24 | Merck & Co., Inc. | Hiv integrase inhibitors |
EP3689353A1 (en) | 2007-02-23 | 2020-08-05 | Gilead Sciences, Inc. | Modulators of pharmacokinetic properties of therapeutics |
US20080280945A1 (en) | 2007-05-09 | 2008-11-13 | Sachin Lohani | Crystalline forms of an HIV integrase inhibitor |
AP2965A (en) | 2007-06-29 | 2014-09-30 | Gilead Sciences Inc | Therapeutic compositions and the use thereof |
EP2167089A1 (en) | 2007-06-29 | 2010-03-31 | Gilead Sciences, Inc. | Therapeutic compositions and the use thereof |
WO2009018350A1 (en) | 2007-07-31 | 2009-02-05 | Limerick Biopharma, Inc. | 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 |
EA019259B1 (ru) | 2007-11-16 | 2014-02-28 | Джилид Сайенсиз, Инк. | Ингибиторы репликации вируса иммунодефицита человека |
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 |
CN102149385B (zh) | 2008-07-25 | 2015-04-01 | 盐野义制药株式会社 | 化合物 |
WO2010011819A1 (en) | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
WO2010011818A1 (en) | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
PT2320908E (pt) | 2008-07-25 | 2014-03-06 | Shionogi & Co | Pró-fármacos de dolutegravir |
EP2465858B1 (en) | 2008-07-25 | 2013-12-25 | VIIV Healthcare Company | Process for preparing a pyrido[1,2-a]pyrrolo[1',2':3,4]imidazo[1,2-d]pyrazine-8-carboxamide derivative |
WO2010011815A1 (en) | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
EP3617194B1 (en) | 2008-12-11 | 2023-11-08 | VIIV Healthcare Company | Processes and intermediates for carbamoylpyridone hiv integrase inhibitors |
US8624023B2 (en) | 2008-12-11 | 2014-01-07 | 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 |
PT2444400T (pt) | 2009-06-15 | 2018-06-06 | Shionogi & Co | Derivado de carbamoilpiridona policíclico substituído |
KR101280198B1 (ko) | 2009-09-02 | 2013-06-28 | 이화여자대학교 산학협력단 | 피라졸 유도체, 이의 제조방법 및 이를 포함하는 골다공증 예방 및 치료용 조성물 |
EA032868B1 (ru) | 2010-01-27 | 2019-07-31 | Вайв Хелткер Компани | Комбинация для лечения вич-инфекции |
MX2012009869A (es) | 2010-02-26 | 2012-09-12 | Japan Tobacco Inc | Derivado de 1, 3,4, 8-tetrahidro-2h-pirido[1, 2-a]pirazina y sus uso como inhibidor de la integrasa del vih. |
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 |
EA201291300A1 (ru) | 2010-07-02 | 2013-06-28 | Джилид Сайэнс, Инк. | Производные нафт-2-илуксусной кислоты для лечения спида |
KR20130124291A (ko) | 2010-07-02 | 2013-11-13 | 길리애드 사이언시즈, 인코포레이티드 | Hiv 항바이러스 화합물로서의 2-퀴놀리닐-아세트산 유도체 |
EP2595986A2 (en) | 2010-07-14 | 2013-05-29 | Addex Pharma SA | Novel 2-amino-4-pyrazolyl-thiazole derivatives and their use as allosteric modulators of metabotropic glutamate receptors |
RS61796B1 (sr) | 2010-08-05 | 2021-06-30 | Shionogi & Co | Postupak za proizvodnju jedinjenja koja imaju inhibitornu aktivnost u odnosu na hiv integrazu |
ES2683153T3 (es) | 2010-09-24 | 2018-09-25 | Shionogi & Co., Ltd. | Profármaco derivado de carbamoil piridona policíclica sustituida |
WO2012106534A2 (en) | 2011-02-02 | 2012-08-09 | The Regents Of The University Of California | Hiv integrase inhibitors |
UA111841C2 (uk) | 2011-04-21 | 2016-06-24 | Гіліад Сайєнсіз, Інк. | Сполуки бензотіазолу та їх фармацевтичне застосування |
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 |
PT2729448E (pt) | 2011-07-06 | 2015-12-02 | Gilead Sciences Inc | Compostos para o tratamento de vih |
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 |
WO2013038407A1 (en) | 2011-09-14 | 2013-03-21 | Mapi Pharma Ltd. | Amorphous form of dolutegravir |
JP6163428B2 (ja) | 2011-10-12 | 2017-07-12 | 塩野義製薬株式会社 | インテグラーゼ阻害活性を有する多環性ピリドン誘導体 |
CA2858685A1 (en) | 2011-12-12 | 2013-06-20 | Bayer Intellectual Property Gmbh | Amino-substituted imidazopyridazines |
AU2013249041B2 (en) | 2012-04-20 | 2016-11-03 | 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 |
US20150166520A1 (en) | 2012-07-20 | 2015-06-18 | Merck Sharp & Dohme Corp. | Amido-substituted pyrimidinone derivatives useful for the treatment of hiv infection |
EP2877469A4 (en) | 2012-07-25 | 2016-04-06 | Merck Sharp & Dohme | SUBSTITUTED NAPHTHYRIDEINDION DERIVATIVES AS HIV INTEGRASE INHIBITORS |
PT2880017T (pt) | 2012-08-03 | 2016-12-14 | Gilead Sciences Inc | Processo e intermediários para preparar inibidores da integrase |
JP6204484B2 (ja) | 2012-11-08 | 2017-09-27 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | キナーゼモジュレーターとして有用なヘテロアリール置換ピリジル化合物 |
CN104902905A (zh) | 2012-12-14 | 2015-09-09 | 葛兰素史克有限责任公司 | 药物组合物 |
EP2931730B1 (en) | 2012-12-17 | 2019-08-07 | Merck Sharp & Dohme Corp. | 4-pyridinonetriazine derivatives as hiv integrase inhibitors |
EP2934482A4 (en) | 2012-12-21 | 2016-07-20 | Merck Sharp & Dohme | ADMINISTRATIVE FORMULATIONS |
CA3131094A1 (en) | 2012-12-21 | 2014-06-26 | Gilead Sciences, Inc. | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
US20140221355A1 (en) | 2012-12-21 | 2014-08-07 | Gilead Sciences, Inc. | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
KR20150102069A (ko) | 2012-12-27 | 2015-09-04 | 니뽄 다바코 산교 가부시키가이샤 | 치환된 스피로피리도[1,2-a]피라진 유도체 및 그의 HIV 인테그라제 저해제로서의 의약 용도 |
EP3008044B1 (en) | 2013-06-13 | 2018-11-21 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds as hiv integrase inhibitors |
HUE037347T2 (hu) * | 2013-07-12 | 2018-08-28 | Gilead Sciences Inc | Policiklusos karmaboilpiridon vegyületek és alkalmazásuk HIV fertõzések kezelésére |
NO2865735T3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 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 |
TN2016000090A1 (en) | 2013-09-27 | 2017-07-05 | Merck Sharp & Dohme | Substituted quinolizine derivatives useful as hiv integrase inhibitors. |
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 |
US9856271B2 (en) | 2014-01-21 | 2018-01-02 | Laurus Labs Limited | Process for the preparation of dolutegravir and pharmaceutically acceptable salts thereof |
-
2012
- 2012-03-29 NO NO15151831A patent/NO2865735T3/no unknown
-
2014
- 2014-07-11 PT PT147450530T patent/PT3019499T/pt unknown
- 2014-07-11 LT LTEP14745053.0T patent/LT3019499T/lt unknown
- 2014-07-11 ES ES17177428T patent/ES2856867T3/es active Active
- 2014-07-11 EP EP17177428.4A patent/EP3252053B1/en active Active
- 2014-07-11 US US14/329,697 patent/US9458159B2/en active Active
- 2014-07-11 JP JP2016525820A patent/JP6411492B2/ja active Active
- 2014-07-11 DK DK14745053.0T patent/DK3019499T3/da active
- 2014-07-11 WO PCT/US2014/046415 patent/WO2015006733A1/en active Application Filing
- 2014-07-11 CA CA2918055A patent/CA2918055C/en active Active
- 2014-07-11 ES ES14745053.0T patent/ES2647216T3/es active Active
- 2014-07-11 SM SM20170525T patent/SMT201700525T1/it unknown
- 2014-07-11 HU HUE14745053A patent/HUE037343T2/hu unknown
- 2014-07-11 SI SI201430410T patent/SI3019499T1/sl unknown
- 2014-07-11 EP EP14745053.0A patent/EP3019499B1/en active Active
- 2014-07-11 SI SI201431750T patent/SI3252053T1/sl unknown
- 2014-07-11 AU AU2014286995A patent/AU2014286995B2/en active Active
- 2014-07-11 PL PL14745053T patent/PL3019499T3/pl unknown
- 2014-07-11 RS RS20171143A patent/RS56539B1/sr unknown
- 2014-07-11 HR HRP20171807TT patent/HRP20171807T1/hr unknown
-
2016
- 2016-09-06 US US15/257,528 patent/US20170128444A1/en not_active Abandoned
-
2017
- 2017-11-02 CY CY20171101152T patent/CY1119545T1/el unknown
-
2018
- 2018-05-17 US US15/982,197 patent/US10456395B2/en active Active
- 2018-09-24 AU AU2018236701A patent/AU2018236701B2/en active Active
-
2019
- 2019-09-16 US US16/572,159 patent/US11213523B2/en active Active
-
2020
- 2020-04-03 AU AU2020202368A patent/AU2020202368A1/en not_active Abandoned
-
2021
- 2021-11-22 US US17/532,148 patent/US11883397B2/en active Active
-
2023
- 2023-12-18 US US18/543,923 patent/US20240238285A1/en active Pending
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 |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11883397B2 (en) | Substituted pyrido[1,2-a]pyrrolo[1,2-d]pyrazines for treating viral infections | |
US10668064B2 (en) | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use | |
CA3131094A1 (en) | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use | |
NZ716774B2 (en) | Polycyclic-carbamoylpyridone compounds and their use for the treatment of hiv infections | |
NZ716794B2 (en) | Polycyclic-carbamoylpyridone compounds and their use for the treatment of hiv infections |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FGA | Letters patent sealed or granted (standard patent) |