JP6738352B2 - ウイルス感染の治療及び予防のための新規なスルホンイミドイルプリノン化合物及び誘導体 - Google Patents
ウイルス感染の治療及び予防のための新規なスルホンイミドイルプリノン化合物及び誘導体 Download PDFInfo
- Publication number
- JP6738352B2 JP6738352B2 JP2017558397A JP2017558397A JP6738352B2 JP 6738352 B2 JP6738352 B2 JP 6738352B2 JP 2017558397 A JP2017558397 A JP 2017558397A JP 2017558397 A JP2017558397 A JP 2017558397A JP 6738352 B2 JP6738352 B2 JP 6738352B2
- Authority
- JP
- Japan
- Prior art keywords
- purin
- methyl
- amino
- compound
- propylsulfonimidoyl
- 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 *Nc(nc(nc1N2*)S(*)(=N*)=O)c1N(*)C2=O Chemical compound *Nc(nc(nc1N2*)S(*)(=N*)=O)c1N(*)C2=O 0.000 description 3
- XJEVQCHAETXVIB-UHFFFAOYSA-N CCCCC(Nc(nc(nc1N2Cc3ccccc3)S(CCC)=O)c1NC2=O)=O Chemical compound CCCCC(Nc(nc(nc1N2Cc3ccccc3)S(CCC)=O)c1NC2=O)=O XJEVQCHAETXVIB-UHFFFAOYSA-N 0.000 description 2
- KFDGFNQIYSAVAY-UHFFFAOYSA-N CCCS(c(nc1N2Cc3ccccc3)nc(N)c1NC2=O)(=N)=O Chemical compound CCCS(c(nc1N2Cc3ccccc3)nc(N)c1NC2=O)(=N)=O KFDGFNQIYSAVAY-UHFFFAOYSA-N 0.000 description 2
- WXCATEWRWJKDJL-UHFFFAOYSA-N CCCCC(Nc(nc(nc1N2Cc3ccccc3)SCCC)c1NC2=O)=O Chemical compound CCCCC(Nc(nc(nc1N2Cc3ccccc3)SCCC)c1NC2=O)=O WXCATEWRWJKDJL-UHFFFAOYSA-N 0.000 description 1
- APBICSQRGKTYKB-UHFFFAOYSA-N CCCS(c(nc1N)nc(N2Cc3ccc(C(F)(F)F)cc3)c1NC2=O)(=N)=O Chemical compound CCCS(c(nc1N)nc(N2Cc3ccc(C(F)(F)F)cc3)c1NC2=O)(=N)=O APBICSQRGKTYKB-UHFFFAOYSA-N 0.000 description 1
- XMBWXMCTNHNBEU-UHFFFAOYSA-N CCCS(c(nc1N)nc(N2Cc3ccccc3)c1NC2=O)=O Chemical compound CCCS(c(nc1N)nc(N2Cc3ccccc3)c1NC2=O)=O XMBWXMCTNHNBEU-UHFFFAOYSA-N 0.000 description 1
- MBQBYGUMANOLRF-UHFFFAOYSA-N CCCS(c(nc1N2Cc(cc3)cc(Cl)c3Cl)nc(N)c1NC2=O)(=N)=O Chemical compound CCCS(c(nc1N2Cc(cc3)cc(Cl)c3Cl)nc(N)c1NC2=O)(=N)=O MBQBYGUMANOLRF-UHFFFAOYSA-N 0.000 description 1
- WLAWDJREXFPHPH-UHFFFAOYSA-N CCCS(c(nc1N2Cc(cc3)ccc3Cl)nc(N)c1NC2=O)(=N)=O Chemical compound CCCS(c(nc1N2Cc(cc3)ccc3Cl)nc(N)c1NC2=O)(=N)=O WLAWDJREXFPHPH-UHFFFAOYSA-N 0.000 description 1
- MSSXPOADQWRGGF-UHFFFAOYSA-N CCCS(c(nc1N2Cc(cc3)ccc3Cl)nc(NC(C(C)(C)C)=O)c1NC2=O)(=N)=O Chemical compound CCCS(c(nc1N2Cc(cc3)ccc3Cl)nc(NC(C(C)(C)C)=O)c1NC2=O)(=N)=O MSSXPOADQWRGGF-UHFFFAOYSA-N 0.000 description 1
- OMOVBYAITFNLQV-UHFFFAOYSA-N CCCS(c(nc1N2Cc(cn3)ccc3Cl)nc(N)c1NC2=O)(=N)=O Chemical compound CCCS(c(nc1N2Cc(cn3)ccc3Cl)nc(N)c1NC2=O)(=N)=O OMOVBYAITFNLQV-UHFFFAOYSA-N 0.000 description 1
- HJPNICYHBIWMIN-UHFFFAOYSA-N CCCS(c(nc1N2Cc3cc(Cl)c(C)cc3)nc(N)c1NC2=O)=O Chemical compound CCCS(c(nc1N2Cc3cc(Cl)c(C)cc3)nc(N)c1NC2=O)=O HJPNICYHBIWMIN-UHFFFAOYSA-N 0.000 description 1
- YXFJJQUVGAPZKB-UHFFFAOYSA-N CCCS(c(nc1N2Cc3ccc(C)cc3)nc(N)c1NC2=O)(=N)=O Chemical compound CCCS(c(nc1N2Cc3ccc(C)cc3)nc(N)c1NC2=O)(=N)=O YXFJJQUVGAPZKB-UHFFFAOYSA-N 0.000 description 1
- AOIPJFRADPKAFS-UHFFFAOYSA-N CCCS(c(nc1N2Cc3ccc(C)nc3)nc(NCC)c1NC2=O)=O Chemical compound CCCS(c(nc1N2Cc3ccc(C)nc3)nc(NCC)c1NC2=O)=O AOIPJFRADPKAFS-UHFFFAOYSA-N 0.000 description 1
- LHRAYRPXCNIOOH-UHFFFAOYSA-N CCCS(c(nc1N2Cc3ccccc3)nc(N)c1N(C(C)OC(C)=O)C2=O)(=N)=O Chemical compound CCCS(c(nc1N2Cc3ccccc3)nc(N)c1N(C(C)OC(C)=O)C2=O)(=N)=O LHRAYRPXCNIOOH-UHFFFAOYSA-N 0.000 description 1
- TWWIKYSVNRCTOK-UHFFFAOYSA-N CCCS(c(nc1N2Cc3ccccc3)nc(NCC)c1NC2=O)=O Chemical compound CCCS(c(nc1N2Cc3ccccc3)nc(NCC)c1NC2=O)=O TWWIKYSVNRCTOK-UHFFFAOYSA-N 0.000 description 1
- POOOKUXMUVRWEZ-UHFFFAOYSA-N CCCSc(nc1Cl)nc(NCc(cc2)cc(C)c2Cl)c1N Chemical compound CCCSc(nc1Cl)nc(NCc(cc2)cc(C)c2Cl)c1N POOOKUXMUVRWEZ-UHFFFAOYSA-N 0.000 description 1
- YEOAWWOBFYFPBW-UHFFFAOYSA-N CCCSc(nc1N)nc(N2Cc(cc3)ccc3Br)c1NC2=O Chemical compound CCCSc(nc1N)nc(N2Cc(cc3)ccc3Br)c1NC2=O YEOAWWOBFYFPBW-UHFFFAOYSA-N 0.000 description 1
- FBFBHKHVBSHQDY-UHFFFAOYSA-N CCCSc(nc1N2Cc(cc3)ccc3Cl)nc(N)c1NC2=O Chemical compound CCCSc(nc1N2Cc(cc3)ccc3Cl)nc(N)c1NC2=O FBFBHKHVBSHQDY-UHFFFAOYSA-N 0.000 description 1
- WSLPWOKZOATGMZ-UHFFFAOYSA-N CCCSc(nc1N2Cc(cc3)ccc3Cl)nc(NC(C)=O)c1NC2=O Chemical compound CCCSc(nc1N2Cc(cc3)ccc3Cl)nc(NC(C)=O)c1NC2=O WSLPWOKZOATGMZ-UHFFFAOYSA-N 0.000 description 1
- HMWSWNCISULJJJ-UHFFFAOYSA-N CCCSc(nc1N2Cc3cc(Cl)c(C)cc3)nc(N)c1NC2=O Chemical compound CCCSc(nc1N2Cc3cc(Cl)c(C)cc3)nc(N)c1NC2=O HMWSWNCISULJJJ-UHFFFAOYSA-N 0.000 description 1
- SRNUMMPVJTYPCV-UHFFFAOYSA-N CCCSc(nc1N2Cc3cc(N)ccc3)nc(N)c1NC2=O Chemical compound CCCSc(nc1N2Cc3cc(N)ccc3)nc(N)c1NC2=O SRNUMMPVJTYPCV-UHFFFAOYSA-N 0.000 description 1
- SAZWABVFGVSDDB-UHFFFAOYSA-N CCCSc(nc1N2Cc3cccc(N)c3)nc(Cl)c1NC2=O Chemical compound CCCSc(nc1N2Cc3cccc(N)c3)nc(Cl)c1NC2=O SAZWABVFGVSDDB-UHFFFAOYSA-N 0.000 description 1
- MCBGAVARLDFVPY-UHFFFAOYSA-N CCCSc(nc1N2Cc3ccccc3)nc(N)c1NC2=O Chemical compound CCCSc(nc1N2Cc3ccccc3)nc(N)c1NC2=O MCBGAVARLDFVPY-UHFFFAOYSA-N 0.000 description 1
- FDLQLLZNIHGIRR-UHFFFAOYSA-N CCCSc(nc1NCc(cc2)cc(Cl)c2Cl)nc(Cl)c1[N+]([O-])=O Chemical compound CCCSc(nc1NCc(cc2)cc(Cl)c2Cl)nc(Cl)c1[N+]([O-])=O FDLQLLZNIHGIRR-UHFFFAOYSA-N 0.000 description 1
- TWTXTWSFXYSAGO-UHFFFAOYSA-N CCCSc(nc1NCc(cc2)ccc2Br)nc(Cl)c1[N+]([O-])=O Chemical compound CCCSc(nc1NCc(cc2)ccc2Br)nc(Cl)c1[N+]([O-])=O TWTXTWSFXYSAGO-UHFFFAOYSA-N 0.000 description 1
- KUISQZDVMKSVNP-UHFFFAOYSA-N CCCSc(nc1NCc(cc2)ccc2S(C)(=O)=O)nc(Cl)c1[N+]([O-])=O Chemical compound CCCSc(nc1NCc(cc2)ccc2S(C)(=O)=O)nc(Cl)c1[N+]([O-])=O KUISQZDVMKSVNP-UHFFFAOYSA-N 0.000 description 1
- BRSQFEYCEJEYCJ-UHFFFAOYSA-N CCS(c(nc1N2Cc3ccc(C)cc3)nc(N)c1NC2=O)(=N)=O Chemical compound CCS(c(nc1N2Cc3ccc(C)cc3)nc(N)c1NC2=O)(=N)=O BRSQFEYCEJEYCJ-UHFFFAOYSA-N 0.000 description 1
- LHRSFBRLPAJSMK-UHFFFAOYSA-N CCSc(nc1N2Cc3ccc(C)cc3)nc(N)c1NC2=O Chemical compound CCSc(nc1N2Cc3ccc(C)cc3)nc(N)c1NC2=O LHRSFBRLPAJSMK-UHFFFAOYSA-N 0.000 description 1
- RKOAQZHSBQHMDM-UHFFFAOYSA-N COCCS(c(nc1N2Cc3ccccc3)nc(N)c1NC2=O)=O Chemical compound COCCS(c(nc1N2Cc3ccccc3)nc(N)c1NC2=O)=O RKOAQZHSBQHMDM-UHFFFAOYSA-N 0.000 description 1
- GJZZDPHTUXZRDP-UHFFFAOYSA-N CS(c(nc1N2Cc3ccccc3)nc(N)c1NC2=O)(=N)=O Chemical compound CS(c(nc1N2Cc3ccccc3)nc(N)c1NC2=O)(=N)=O GJZZDPHTUXZRDP-UHFFFAOYSA-N 0.000 description 1
- OWHOVQKHZCNMAL-UHFFFAOYSA-N CSc(nc1N2Cc3cccnc3)nc(N)c1NC2=O Chemical compound CSc(nc1N2Cc3cccnc3)nc(N)c1NC2=O OWHOVQKHZCNMAL-UHFFFAOYSA-N 0.000 description 1
- FAVREULOXHXCQX-UHFFFAOYSA-N Cc(cc(CN)cc1)c1Cl Chemical compound Cc(cc(CN)cc1)c1Cl FAVREULOXHXCQX-UHFFFAOYSA-N 0.000 description 1
- NZPFQOXRHLUPRT-UHFFFAOYSA-N Cc1ncc(CN)cc1 Chemical compound Cc1ncc(CN)cc1 NZPFQOXRHLUPRT-UHFFFAOYSA-N 0.000 description 1
- JJNLGGQLCGZEIB-UHFFFAOYSA-N NC(N1Cc2ccccc2)=C(C#N)NC1=O Chemical compound NC(N1Cc2ccccc2)=C(C#N)NC1=O JJNLGGQLCGZEIB-UHFFFAOYSA-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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
-
- 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
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/24—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one nitrogen and one sulfur atom
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2015078507 | 2015-05-08 | ||
| CNPCT/CN2015/078507 | 2015-05-08 | ||
| CN2016078785 | 2016-04-08 | ||
| CNPCT/CN2016/078785 | 2016-04-08 | ||
| PCT/EP2016/059961 WO2016180695A1 (en) | 2015-05-08 | 2016-05-04 | Novel sulfonimidoylpurinone compounds and derivatives for the treatment and prophylaxis of virus infection |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018515509A JP2018515509A (ja) | 2018-06-14 |
| JP2018515509A5 JP2018515509A5 (OSRAM) | 2020-06-18 |
| JP6738352B2 true JP6738352B2 (ja) | 2020-08-12 |
Family
ID=55910966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017558397A Active JP6738352B2 (ja) | 2015-05-08 | 2016-05-04 | ウイルス感染の治療及び予防のための新規なスルホンイミドイルプリノン化合物及び誘導体 |
Country Status (32)
| Country | Link |
|---|---|
| US (3) | US9708325B2 (OSRAM) |
| EP (1) | EP3294740B1 (OSRAM) |
| JP (1) | JP6738352B2 (OSRAM) |
| KR (1) | KR102690131B1 (OSRAM) |
| CN (1) | CN107580596B (OSRAM) |
| AR (1) | AR104528A1 (OSRAM) |
| AU (3) | AU2016260683B2 (OSRAM) |
| BR (1) | BR112017023959B1 (OSRAM) |
| CA (1) | CA2982704C (OSRAM) |
| CL (1) | CL2017002745A1 (OSRAM) |
| CO (1) | CO2017009994A2 (OSRAM) |
| CR (1) | CR20170496A (OSRAM) |
| DK (1) | DK3294740T3 (OSRAM) |
| ES (1) | ES2753777T3 (OSRAM) |
| HR (1) | HRP20191942T1 (OSRAM) |
| HU (1) | HUE045906T2 (OSRAM) |
| IL (2) | IL254947B (OSRAM) |
| LT (1) | LT3294740T (OSRAM) |
| MX (2) | MX393198B (OSRAM) |
| MY (1) | MY182353A (OSRAM) |
| NZ (2) | NZ775222A (OSRAM) |
| PE (1) | PE20171620A1 (OSRAM) |
| PH (1) | PH12017502009A1 (OSRAM) |
| PL (1) | PL3294740T3 (OSRAM) |
| PT (1) | PT3294740T (OSRAM) |
| RS (1) | RS59435B1 (OSRAM) |
| RU (1) | RU2745269C2 (OSRAM) |
| SG (1) | SG10202108841YA (OSRAM) |
| SI (1) | SI3294740T1 (OSRAM) |
| TW (2) | TWI706954B (OSRAM) |
| UA (1) | UA120450C2 (OSRAM) |
| WO (1) | WO2016180695A1 (OSRAM) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ775222A (en) * | 2015-05-08 | 2024-09-27 | Hoffmann La Roche | Novel sulfonimidoylpurinone compounds and derivatives for the treatment and prophylaxis of virus infection |
| IL284255B (en) | 2016-08-29 | 2022-07-01 | Hoffmann La Roche | 7-substituted sulfonimidoylpurinone compounds for the treatment and prophylaxis of virus infection |
| TWI720250B (zh) * | 2016-09-13 | 2021-03-01 | 瑞士商赫孚孟拉羅股份公司 | 利用tlr7促效劑及hbv蛋白殼組裝抑制劑之組合治療 |
| CN111699187A (zh) | 2018-02-12 | 2020-09-22 | 豪夫迈·罗氏有限公司 | 用于治疗和预防病毒感染的新的砜化合物和衍生物 |
| JP7089596B2 (ja) * | 2018-02-28 | 2022-06-22 | エフ・ホフマン－ラ・ロシュ・アクチェンゲゼルシャフト | 肝がんの治療及び予防のための７位置換スルホンイミドイルプリノン化合物及び誘導体 |
| CN111072667A (zh) * | 2018-10-22 | 2020-04-28 | 罗欣药业(上海)有限公司 | 五元或六元杂环并嘧啶类化合物及其用途 |
| WO2020168017A1 (en) * | 2019-02-12 | 2020-08-20 | Ambrx, Inc. | Compositions containing, methods and uses of antibody-tlr agonist conjugates |
| EP4031544B1 (en) | 2019-09-20 | 2024-02-28 | Syngenta Crop Protection AG | Pesticidally active heterocyclic derivatives with sulfur and sulfoximine containing substituents |
| WO2021154662A1 (en) * | 2020-01-27 | 2021-08-05 | Bristol-Myers Squibb Company | 1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS |
| JP7684316B2 (ja) * | 2020-01-27 | 2025-05-27 | ブリストル－マイヤーズ スクイブ カンパニー | トール様受容体７（ＴＬＲ７）アゴニストとしての１Ｈ－ピラゾロ［４，３－ｄ］ピリミジン化合物 |
| EP4554678A1 (en) | 2022-07-14 | 2025-05-21 | F. Hoffmann-La Roche AG | Phosphorylpurinone compounds for the treatment of cancer |
| CN118724963A (zh) * | 2023-03-30 | 2024-10-01 | 浙江养生堂天然药物研究所有限公司 | 含磷或含硫的大环化合物及其用途 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4189048B2 (ja) * | 1997-12-26 | 2008-12-03 | 大日本住友製薬株式会社 | 複素環化合物 |
| EA200702235A1 (ru) * | 2005-05-04 | 2008-04-28 | Пфайзер Лимитед | Производные 2-амидо-6-амино-8-оксопурина в качестве модуляторов toll-подобных рецепторов для лечения рака и вирусных инфекций, таких как гепатит с |
| CN101239980B (zh) | 2008-02-18 | 2011-06-22 | 靳广毅 | 免疫受体调节剂偶联体前体和偶联体及其应用 |
| CA2745295C (en) * | 2008-12-09 | 2017-01-10 | Gilead Sciences, Inc. | Modulators of toll-like receptors |
| US20110150836A1 (en) | 2009-12-22 | 2011-06-23 | Gilead Sciences, Inc. | Methods of treating hbv and hcv infection |
| TWI555737B (zh) | 2011-05-24 | 2016-11-01 | 拜耳知識產權公司 | 含有硫醯亞胺基團之４－芳基－ｎ－苯基－１，３，５－三氮雜苯－２－胺 |
| EP2776439B1 (en) * | 2011-11-09 | 2018-07-04 | Janssen Sciences Ireland UC | Purine derivatives for the treatment of viral infections |
| BR112015024411B1 (pt) | 2013-03-29 | 2022-02-22 | Janssen Sciences Ireland Uc | Desaza-purinonas macrocíclicas para o tratamento de infeções virais e composição farmacêutica que os compreende |
| AU2015303558B2 (en) | 2014-08-15 | 2018-07-12 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Pyrrolopyrimidine compounds used as TLR7 agonist |
| NZ775222A (en) * | 2015-05-08 | 2024-09-27 | Hoffmann La Roche | Novel sulfonimidoylpurinone compounds and derivatives for the treatment and prophylaxis of virus infection |
| IL284255B (en) * | 2016-08-29 | 2022-07-01 | Hoffmann La Roche | 7-substituted sulfonimidoylpurinone compounds for the treatment and prophylaxis of virus infection |
-
2016
- 2016-05-04 NZ NZ775222A patent/NZ775222A/en unknown
- 2016-05-04 PE PE2017002102A patent/PE20171620A1/es unknown
- 2016-05-04 UA UAA201712023A patent/UA120450C2/uk unknown
- 2016-05-04 PT PT167204213T patent/PT3294740T/pt unknown
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