AU2015231215B2 - Benzimidazole derivatives as ERBB tyrosine kinase inhibitors for the treatment of cancer - Google Patents
Benzimidazole derivatives as ERBB tyrosine kinase inhibitors for the treatment of cancer Download PDFInfo
- Publication number
- AU2015231215B2 AU2015231215B2 AU2015231215A AU2015231215A AU2015231215B2 AU 2015231215 B2 AU2015231215 B2 AU 2015231215B2 AU 2015231215 A AU2015231215 A AU 2015231215A AU 2015231215 A AU2015231215 A AU 2015231215A AU 2015231215 B2 AU2015231215 B2 AU 2015231215B2
- Authority
- AU
- Australia
- Prior art keywords
- certain embodiments
- substituents
- cancer
- heterocyclyl
- optionally substituted
- 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.)
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- 0 CC1C(*C(C2)C3C(C)[C@@]2C(C2)[C@](C)(C4)C24C2C(C4)C3C4/C=C/CC2)C1 Chemical compound CC1C(*C(C2)C3C(C)[C@@]2C(C2)[C@](C)(C4)C24C2C(C4)C3C4/C=C/CC2)C1 0.000 description 8
- IKNGMZMQIXIFJP-OQHSHRKDSA-N C=CC(N(CCCC1)C[C@@H]1[n]1c(NC(c2cc(O)ccc2)=O)nc2ccc3OCCOc3c12)O Chemical compound C=CC(N(CCCC1)C[C@@H]1[n]1c(NC(c2cc(O)ccc2)=O)nc2ccc3OCCOc3c12)O IKNGMZMQIXIFJP-OQHSHRKDSA-N 0.000 description 1
- HYKAJFUPPJGVRJ-UHFFFAOYSA-N CC1=C(C)OC(N)(N)O1 Chemical compound CC1=C(C)OC(N)(N)O1 HYKAJFUPPJGVRJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461968243P | 2014-03-20 | 2014-03-20 | |
| US61/968,243 | 2014-03-20 | ||
| PCT/US2015/021475 WO2015143161A1 (en) | 2014-03-20 | 2015-03-19 | Benzimidazole derivatives as erbb tyrosine kinase inhibitors for the treatment of cancer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2015231215A1 AU2015231215A1 (en) | 2016-10-06 |
| AU2015231215B2 true AU2015231215B2 (en) | 2019-07-18 |
Family
ID=52808184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2015231215A Active AU2015231215B2 (en) | 2014-03-20 | 2015-03-19 | Benzimidazole derivatives as ERBB tyrosine kinase inhibitors for the treatment of cancer |
Country Status (9)
| Country | Link |
|---|---|
| US (4) | US10202398B2 (OSRAM) |
| EP (1) | EP3119784B1 (OSRAM) |
| JP (1) | JP6568926B2 (OSRAM) |
| KR (1) | KR102409739B1 (OSRAM) |
| CN (1) | CN106661027B (OSRAM) |
| AU (1) | AU2015231215B2 (OSRAM) |
| CA (1) | CA2943231C (OSRAM) |
| TW (1) | TWI705967B (OSRAM) |
| WO (1) | WO2015143161A1 (OSRAM) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102409739B1 (ko) | 2014-03-20 | 2022-06-17 | 카펠라 테라퓨틱스, 인크. | 암 치료용의 erbb 티로신 키나제 억제제로서의 벤즈이미다졸 유도체 |
| EP3922630A1 (en) | 2014-03-20 | 2021-12-15 | Capella Therapeutics, Inc. | Benzimidazole derivatives as erbb tyrosine kinase inhibitors for the treatment of cancer |
| US10590108B2 (en) * | 2015-09-23 | 2020-03-17 | Capella Therapeutics, Inc. | Benzimidazoles for use in the treatment of cancer and inflammatory diseases |
| CN111741954B (zh) | 2018-02-21 | 2024-04-02 | 勃林格殷格翰国际有限公司 | 用作egfr抑制剂的新型苯并咪唑化合物及衍生物 |
| MA52754A (fr) | 2018-05-25 | 2021-04-14 | Incyte Corp | Composés hétérocycliques tricycliques en tant qu'activateurs de sting |
| US10875872B2 (en) | 2018-07-31 | 2020-12-29 | Incyte Corporation | Heteroaryl amide compounds as sting activators |
| WO2020028565A1 (en) | 2018-07-31 | 2020-02-06 | Incyte Corporation | Tricyclic heteraryl compounds as sting activators |
| US12336995B2 (en) | 2018-09-10 | 2025-06-24 | Mirati Therapeutics, Inc. | Combination therapies |
| US11596692B1 (en) | 2018-11-21 | 2023-03-07 | Incyte Corporation | PD-L1/STING conjugates and methods of use |
| US12129267B2 (en) | 2019-01-07 | 2024-10-29 | Incyte Corporation | Heteroaryl amide compounds as sting activators |
| US20220380382A1 (en) | 2019-06-24 | 2022-12-01 | Boehringer Ingelheim International Gmbh | New macrocyclic compounds and derivatives as egfr inhibitors |
| CN111855192B (zh) * | 2020-07-31 | 2021-04-23 | 北京航空航天大学 | 一种用于编码器信号去噪的奇异值分解方法 |
| WO2022090481A1 (en) | 2020-11-02 | 2022-05-05 | Boehringer Ingelheim International Gmbh | Substituted 1h-pyrazolo[4,3-c]pyridines and derivatives as egfr inhibitors |
| BR112023021111A2 (pt) | 2021-04-13 | 2023-12-19 | Nuvalent Inc | Composto, composição farmacêutica, método de tratamento de câncer, método para inibir seletivamente her2, método de regulação de um nível de her2, método para aumentar um nível de her2, método de diminuição da fosforilação de her2 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US8461328B2 (en) * | 2010-01-12 | 2013-06-11 | Genentech, Inc. | Tricyclic heterocyclic compounds, compositions and methods of use thereof |
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| WO2015134210A1 (en) | 2014-03-03 | 2015-09-11 | Principia Biopharma, Inc. | BENZIMIDAZOLE DERIVATIVES AS RLK and ITK INHIBITORS |
| EP3922630A1 (en) | 2014-03-20 | 2021-12-15 | Capella Therapeutics, Inc. | Benzimidazole derivatives as erbb tyrosine kinase inhibitors for the treatment of cancer |
| KR102409739B1 (ko) | 2014-03-20 | 2022-06-17 | 카펠라 테라퓨틱스, 인크. | 암 치료용의 erbb 티로신 키나제 억제제로서의 벤즈이미다졸 유도체 |
| CN104447765A (zh) | 2014-12-31 | 2015-03-25 | 深圳铂立健医药有限公司 | 三环化合物及其药物组合物和应用 |
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Patent Citations (1)
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| US8461328B2 (en) * | 2010-01-12 | 2013-06-11 | Genentech, Inc. | Tricyclic heterocyclic compounds, compositions and methods of use thereof |
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| KR102409739B1 (ko) | 2022-06-17 |
| JP6568926B2 (ja) | 2019-08-28 |
| US20190169204A1 (en) | 2019-06-06 |
| EP3119784B1 (en) | 2020-07-22 |
| TW201620912A (zh) | 2016-06-16 |
| WO2015143161A1 (en) | 2015-09-24 |
| US11713322B2 (en) | 2023-08-01 |
| US20210061816A1 (en) | 2021-03-04 |
| US20170174697A1 (en) | 2017-06-22 |
| KR20170004969A (ko) | 2017-01-11 |
| CA2943231A1 (en) | 2015-09-24 |
| US20220298167A1 (en) | 2022-09-22 |
| US10202398B2 (en) | 2019-02-12 |
| TWI705967B (zh) | 2020-10-01 |
| CN106661027A (zh) | 2017-05-10 |
| US10683304B2 (en) | 2020-06-16 |
| CN106661027B (zh) | 2019-12-24 |
| EP3119784A1 (en) | 2017-01-25 |
| US11242352B2 (en) | 2022-02-08 |
| AU2015231215A1 (en) | 2016-10-06 |
| JP2017508816A (ja) | 2017-03-30 |
| CA2943231C (en) | 2023-10-24 |
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