SG11202108283QA - Imidazo [2, 1-f] [1, 2, 4] triazin-4-amine derivatives as tlr7 agonist - Google Patents
Imidazo [2, 1-f] [1, 2, 4] triazin-4-amine derivatives as tlr7 agonistInfo
- Publication number
- SG11202108283QA SG11202108283QA SG11202108283QA SG11202108283QA SG11202108283QA SG 11202108283Q A SG11202108283Q A SG 11202108283QA SG 11202108283Q A SG11202108283Q A SG 11202108283QA SG 11202108283Q A SG11202108283Q A SG 11202108283QA SG 11202108283Q A SG11202108283Q A SG 11202108283QA
- Authority
- SG
- Singapore
- Prior art keywords
- triazin
- imidazo
- amine derivatives
- tlr7 agonist
- tlr7
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2019074732 | 2019-02-07 | ||
| CN2019098757 | 2019-07-31 | ||
| CN2020073673 | 2020-01-22 | ||
| PCT/CN2020/074437 WO2020160711A1 (en) | 2019-02-07 | 2020-02-06 | Imidazo [2, 1-f] [1, 2, 4] triazin-4-amine derivatives as tlr7 agonist |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG11202108283QA true SG11202108283QA (en) | 2021-08-30 |
Family
ID=71947004
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11202108283QA SG11202108283QA (en) | 2019-02-07 | 2020-02-06 | Imidazo [2, 1-f] [1, 2, 4] triazin-4-amine derivatives as tlr7 agonist |
| SG11202108284TA SG11202108284TA (en) | 2019-02-07 | 2020-02-06 | Imidazo [2, 1-f] [1, 2, 4] triazin-4-amine derivatives as tlr7 agonist |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11202108284TA SG11202108284TA (en) | 2019-02-07 | 2020-02-06 | Imidazo [2, 1-f] [1, 2, 4] triazin-4-amine derivatives as tlr7 agonist |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US12281119B2 (en) |
| EP (2) | EP3921320B1 (en) |
| JP (2) | JP7637328B2 (en) |
| KR (2) | KR20210125026A (en) |
| CN (2) | CN113423708B (en) |
| AU (2) | AU2020218383B2 (en) |
| BR (2) | BR112021015012A2 (en) |
| CA (2) | CA3129178A1 (en) |
| IL (2) | IL285315B2 (en) |
| MX (2) | MX2021009439A (en) |
| SG (2) | SG11202108283QA (en) |
| TW (2) | TWI841679B (en) |
| WO (2) | WO2020160710A1 (en) |
| ZA (2) | ZA202105338B (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2019262978B2 (en) | 2018-05-01 | 2023-07-13 | Revolution Medicines, Inc. | C40-, C28-, and C-32-linked rapamycin analogs as mTOR inhibitors |
| WO2019212991A1 (en) | 2018-05-01 | 2019-11-07 | Revolution Medicines, Inc. | C26-linked rapamycin analogs as mtor inhibitors |
| BR112021015012A2 (en) | 2019-02-07 | 2021-10-05 | Beigene, Ltd. | COMPOUNDS, PHARMACEUTICAL COMPOSITION, METHOD OF MODULATION OF TLR7, AND METHOD OF TREATMENT OF A DISEASE OR DISORDER IN A PATIENT |
| CN114206872A (en) * | 2019-08-02 | 2022-03-18 | 百济神州有限公司 | Imidazo [2,1-F ] [1,2,4] triazin-4-amine derivatives as TLR8 agonists |
| TW202200589A (en) * | 2020-05-28 | 2022-01-01 | 瑞士商諾華公司 | Mll1 inhibitors and anti-cancer agents |
| CN114057746B (en) * | 2020-08-04 | 2025-01-28 | 百济神州(北京)生物科技有限公司 | Preparation of imidazo[2,1-F][1,2,4]triazine-4-amine derivatives as TLR7 agonists |
| CN115119508B (en) * | 2021-01-20 | 2024-05-24 | 上海维申医药有限公司 | Macrocyclic TLR7 agonist, preparation method, pharmaceutical composition and use thereof |
| WO2022216900A2 (en) * | 2021-04-09 | 2022-10-13 | Revolution Medicines, Inc. | Synthesis of rapamycin analog compounds |
| US20240327354A1 (en) * | 2021-07-23 | 2024-10-03 | Institut National de la Santé et de la Recherche Médicale | Gram-negative bacteria efflux pump inhibitors |
| JP2025509240A (en) * | 2022-03-10 | 2025-04-11 | ナミ セラピューティクス, インコーポレイテッド | Formulated and/or co-formulated lipid nanocarrier compositions containing toll-like receptor ("TLR") agonist prodrugs useful in the treatment of cancer and methods thereof |
| WO2023230577A1 (en) | 2022-05-25 | 2023-11-30 | Revolution Medicines, Inc. | Methods of treating cancer with an mtor inhibitor |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2210891A1 (en) * | 2009-01-26 | 2010-07-28 | Domain Therapeutics | New adenosine receptor ligands and uses thereof |
| EP2396328A2 (en) | 2009-02-11 | 2011-12-21 | The Regents of The University of California | Toll-like receptor modulators and treatment of diseases |
| BR112012006261B1 (en) | 2009-09-21 | 2021-12-21 | Gilead Sciences, Inc | ANALOG COMPOUNDS OF 2'-FLUORINE SUBSTITUTED CARBANUCLEOSIDE, USEFUL COMPOUND FOR THE PREPARATION OF THE SAME, PHARMACEUTICAL COMPOSITION AND USE OF ANALOG COMPOUNDS OF 2'-FLUORIDE SUBSTITUTED CARBANUCLEOSIDE |
| JO3407B1 (en) | 2012-05-31 | 2019-10-20 | Eisai R&D Man Co Ltd | Tetrahydropyrazolopyrimidines |
| TW201414737A (en) * | 2012-07-13 | 2014-04-16 | 必治妥美雅史谷比公司 | Imidazotriazinecarbonitriles useful as kinase inhibitors |
| JP5900234B2 (en) | 2012-08-09 | 2016-04-06 | ダイキン工業株式会社 | Humidifier |
| WO2014035140A2 (en) * | 2012-08-30 | 2014-03-06 | Kainos Medicine, Inc. | Compounds and compositions for modulating histone methyltransferase activity |
| EP2906563B1 (en) | 2012-10-10 | 2018-02-28 | Janssen Sciences Ireland UC | Pyrrolo[3,2-d]pyrimidine derivatives for the treatment of viral infections and other diseases |
| CN105367576A (en) | 2014-08-15 | 2016-03-02 | 正大天晴药业集团股份有限公司 | Pyrrolopyrimidine compounds as TLR7 agonists |
| SG11201701169XA (en) | 2014-08-15 | 2017-03-30 | Chia Tai Tianqing Pharmaceutical Group Co Ltd | Pyrrolopyrimidine compounds used as tlr7 agonist |
| EA029789B1 (en) * | 2014-12-19 | 2018-05-31 | Янссен Фармацевтика Нв | IMIDAZOPYRIDAZINE DERIVATIVES AS PI3Kβ INHIBITORS |
| BR112017024163A2 (en) * | 2015-05-12 | 2018-07-17 | Kalyra Pharmaceuticals Inc | bicyclic compounds |
| PL3889145T3 (en) | 2015-12-17 | 2024-07-01 | Merck Patent Gmbh | 8-cyano-5-piperidine-quinolines as TLR7/8 antagonists and their use in the treatment of immunological disorders |
| US10138248B2 (en) * | 2016-06-24 | 2018-11-27 | Incyte Corporation | Substituted imidazo[2,1-f][1,2,4]triazines, substituted imidazo[1,2-a]pyridines, substituted imidazo[1,2-b]pyridazines and substituted imidazo[1,2-a]pyrazines as PI3K-γ inhibitors |
| CN108069969B (en) | 2016-11-11 | 2020-09-18 | 南京海璞医药科技有限公司 | Nitrogen-containing heterocyclic compound, preparation method, intermediate, pharmaceutical composition and application |
| CA3044903A1 (en) | 2016-11-28 | 2018-05-31 | Jiangsu Hengrui Medicine Co., Ltd. | Pyrazolo-heteroaryl derivative, preparation method and medical use thereof |
| WO2018210298A1 (en) * | 2017-05-18 | 2018-11-22 | 江苏恒瑞医药股份有限公司 | Heteroaryl-pyrazole derivative, and preparation method therefor and medical application thereof |
| BR112021015012A2 (en) | 2019-02-07 | 2021-10-05 | Beigene, Ltd. | COMPOUNDS, PHARMACEUTICAL COMPOSITION, METHOD OF MODULATION OF TLR7, AND METHOD OF TREATMENT OF A DISEASE OR DISORDER IN A PATIENT |
| CN114206872A (en) | 2019-08-02 | 2022-03-18 | 百济神州有限公司 | Imidazo [2,1-F ] [1,2,4] triazin-4-amine derivatives as TLR8 agonists |
-
2020
- 2020-02-06 BR BR112021015012-9A patent/BR112021015012A2/en not_active Application Discontinuation
- 2020-02-06 BR BR112021015016-1A patent/BR112021015016A2/en unknown
- 2020-02-06 CN CN202080013393.3A patent/CN113423708B/en active Active
- 2020-02-06 CA CA3129178A patent/CA3129178A1/en active Pending
- 2020-02-06 EP EP20752173.3A patent/EP3921320B1/en active Active
- 2020-02-06 IL IL285315A patent/IL285315B2/en unknown
- 2020-02-06 SG SG11202108283QA patent/SG11202108283QA/en unknown
- 2020-02-06 MX MX2021009439A patent/MX2021009439A/en unknown
- 2020-02-06 SG SG11202108284TA patent/SG11202108284TA/en unknown
- 2020-02-06 WO PCT/CN2020/074436 patent/WO2020160710A1/en not_active Ceased
- 2020-02-06 KR KR1020217027572A patent/KR20210125026A/en not_active Ceased
- 2020-02-06 AU AU2020218383A patent/AU2020218383B2/en active Active
- 2020-02-06 EP EP20752096.6A patent/EP3921319B1/en active Active
- 2020-02-06 KR KR1020217027571A patent/KR102853071B1/en active Active
- 2020-02-06 MX MX2021009444A patent/MX2021009444A/en unknown
- 2020-02-06 JP JP2021546210A patent/JP7637328B2/en active Active
- 2020-02-06 WO PCT/CN2020/074437 patent/WO2020160711A1/en not_active Ceased
- 2020-02-06 US US17/428,856 patent/US12281119B2/en active Active
- 2020-02-06 CA CA3129234A patent/CA3129234A1/en active Pending
- 2020-02-06 JP JP2021546230A patent/JP7564112B2/en active Active
- 2020-02-06 CN CN202080013422.6A patent/CN113454086B/en active Active
- 2020-02-06 AU AU2020218872A patent/AU2020218872A1/en not_active Abandoned
- 2020-02-06 US US17/428,853 patent/US20230167117A1/en active Pending
- 2020-02-07 TW TW109103808A patent/TWI841679B/en active
- 2020-02-07 TW TW109103823A patent/TWI835999B/en not_active IP Right Cessation
-
2021
- 2021-07-28 ZA ZA2021/05338A patent/ZA202105338B/en unknown
- 2021-07-28 ZA ZA2021/05339A patent/ZA202105339B/en unknown
- 2021-08-02 IL IL285311A patent/IL285311A/en unknown
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