AR121167A1 - DERIVADOS DE PIRROLO[1,2-c]IMIDAZOL COMO INHIBIDORES DE EGFR - Google Patents
DERIVADOS DE PIRROLO[1,2-c]IMIDAZOL COMO INHIBIDORES DE EGFRInfo
- Publication number
- AR121167A1 AR121167A1 ARP200101744A ARP200101744A AR121167A1 AR 121167 A1 AR121167 A1 AR 121167A1 AR P200101744 A ARP200101744 A AR P200101744A AR P200101744 A ARP200101744 A AR P200101744A AR 121167 A1 AR121167 A1 AR 121167A1
- Authority
- AR
- Argentina
- Prior art keywords
- pyrrolo
- isoindolin
- thiazol
- imidazol
- acetamide
- Prior art date
Links
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical class C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 title 1
- 229940121647 egfr inhibitor Drugs 0.000 title 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 abstract 2
- PPUARJAODGRSLP-UHFFFAOYSA-N 2-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-1-yl)-2-[5-[2-[4-[[4-(hydroxymethyl)piperidin-1-yl]methyl]phenyl]ethynyl]-3-oxo-7-(trifluoromethyl)-1H-isoindol-2-yl]-N-(1,3-thiazol-2-yl)acetamide Chemical compound OCC1CCN(CC(C=C2)=CC=C2C#CC2=CC(C(F)(F)F)=C(CN(C(C(NC3=NC=CS3)=O)C3=C(CCC4)N4C=N3)C3=O)C3=C2)CC1 PPUARJAODGRSLP-UHFFFAOYSA-N 0.000 abstract 1
- ACAARKVFRVCUMK-UHFFFAOYSA-N 2-[7-(difluoromethyl)-5-[2-[4-[[4-(hydroxymethyl)piperidin-1-yl]methyl]phenyl]ethynyl]-3-oxo-1H-isoindol-2-yl]-2-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-1-yl)-N-(1,3-thiazol-2-yl)acetamide Chemical compound OCC1CCN(CC(C=C2)=CC=C2C#CC2=CC(C(F)F)=C(CN(C(C(NC3=NC=CS3)=O)C3=C(CCC4)N4C=N3)C3=O)C3=C2)CC1 ACAARKVFRVCUMK-UHFFFAOYSA-N 0.000 abstract 1
- -1 6-hydroxy-2-azaspiro[3.3]heptan-2-yl Chemical group 0.000 abstract 1
- XQWDNSZYUQXOOE-UHFFFAOYSA-N C1(=C2N(C=N1)CCC2)C(C(=O)NC=1SC=CN=1)N1C(C2=CC(=CC(=C2C1)C(F)(F)F)C1=CC=C(C=C1)C1CCN(CC1)CC)=O Chemical compound C1(=C2N(C=N1)CCC2)C(C(=O)NC=1SC=CN=1)N1C(C2=CC(=CC(=C2C1)C(F)(F)F)C1=CC=C(C=C1)C1CCN(CC1)CC)=O XQWDNSZYUQXOOE-UHFFFAOYSA-N 0.000 abstract 1
- UKJOELJLIRFDOW-UHFFFAOYSA-N C1CN(CCC1CO)CC2=CC=C(C=C2)C#CC3=CC4=C(CN(C4=O)C(C5=C6CC(CN6C=N5)F)C(=O)NC7=NC=CS7)C(=C3)C(F)F Chemical compound C1CN(CCC1CO)CC2=CC=C(C=C2)C#CC3=CC4=C(CN(C4=O)C(C5=C6CC(CN6C=N5)F)C(=O)NC7=NC=CS7)C(=C3)C(F)F UKJOELJLIRFDOW-UHFFFAOYSA-N 0.000 abstract 1
- CCXDOHWBGKKXOM-UHFFFAOYSA-N CCN(CC1)CCC1C(C=C1)=CC=C1C1=CC(C(F)F)=C(CN(C(C(NC2=NC=CS2)=O)C2=C(CC(C3)F)N3C=N2)C2=O)C2=C1 Chemical compound CCN(CC1)CCC1C(C=C1)=CC=C1C1=CC(C(F)F)=C(CN(C(C(NC2=NC=CS2)=O)C2=C(CC(C3)F)N3C=N2)C2=O)C2=C1 CCXDOHWBGKKXOM-UHFFFAOYSA-N 0.000 abstract 1
- ICXJDIZDMPRBNH-UHFFFAOYSA-N CCN(CCC1C(C=C2)=CC=C2C2=CC(C(F)F)=C(CN(C(C(NC3=NC=CS3)=O)C3=C(CCC4)N4C=N3)C3=O)C3=C2)CC1F Chemical compound CCN(CCC1C(C=C2)=CC=C2C2=CC(C(F)F)=C(CN(C(C(NC3=NC=CS3)=O)C3=C(CCC4)N4C=N3)C3=O)C3=C2)CC1F ICXJDIZDMPRBNH-UHFFFAOYSA-N 0.000 abstract 1
- NUOXGQPLZTZKPZ-UHFFFAOYSA-N FC(C1=C2CN(C(C2=CC(=C1)C1=CC=C(C=C1)C1CCN(CC1)CC)=O)C(C(=O)NC=1SC=CN=1)C1=C2N(C=N1)CCC2)F Chemical compound FC(C1=C2CN(C(C2=CC(=C1)C1=CC=C(C=C1)C1CCN(CC1)CC)=O)C(C(=O)NC=1SC=CN=1)C1=C2N(C=N1)CCC2)F NUOXGQPLZTZKPZ-UHFFFAOYSA-N 0.000 abstract 1
- XORLOGUGADHHPK-UHFFFAOYSA-N OC1CCN(CC(C=C2)=CC=C2C#CC2=CC(C(F)(F)F)=C(CN(C(C(NC3=NC=CS3)=O)C3=C(CC(C4)F)N4C=N3)C3=O)C3=C2)CCC1 Chemical compound OC1CCN(CC(C=C2)=CC=C2C#CC2=CC(C(F)(F)F)=C(CN(C(C(NC3=NC=CS3)=O)C3=C(CC(C4)F)N4C=N3)C3=O)C3=C2)CCC1 XORLOGUGADHHPK-UHFFFAOYSA-N 0.000 abstract 1
- OAMMGHIKSQTVCM-UHFFFAOYSA-N OCC1CCN(CC(C=C2)=CC=C2C#CC2=CC(C(F)(F)F)=C(CN(C(C(NC3=NC=CS3)=O)C3=C(CC(C4)F)N4C=N3)C3=O)C3=C2)CC1 Chemical compound OCC1CCN(CC(C=C2)=CC=C2C#CC2=CC(C(F)(F)F)=C(CN(C(C(NC3=NC=CS3)=O)C3=C(CC(C4)F)N4C=N3)C3=O)C3=C2)CC1 OAMMGHIKSQTVCM-UHFFFAOYSA-N 0.000 abstract 1
- 206010041067 Small cell lung cancer Diseases 0.000 abstract 1
- 230000003281 allosteric effect Effects 0.000 abstract 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- 102000052116 epidermal growth factor receptor activity proteins Human genes 0.000 abstract 1
- 108700015053 epidermal growth factor receptor activity proteins Proteins 0.000 abstract 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 1
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 abstract 1
- 150000002460 imidazoles Chemical class 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- YOHYSYJDKVYCJI-UHFFFAOYSA-N n-[3-[[6-[3-(trifluoromethyl)anilino]pyrimidin-4-yl]amino]phenyl]cyclopropanecarboxamide Chemical compound FC(F)(F)C1=CC=CC(NC=2N=CN=C(NC=3C=C(NC(=O)C4CC4)C=CC=3)C=2)=C1 YOHYSYJDKVYCJI-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 208000000587 small cell lung carcinoma Diseases 0.000 abstract 1
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
- A61K31/41—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
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Steroid Compounds (AREA)
Abstract
Compuestos derivados de pirrolo[1,2-c]imidazol con actividad inhibitoria alostérica de EGFR, composición farmacéutica que los comprende y su uso en el tratamiento del cáncer de pulmón de células pequeñas. Reivindicación 1: Un compuesto seleccionado de 2-(6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il)-2-[6-[4-(1-etil-4-piperidil)fenil]-1-oxo-4-(trifluorometil)isoindolin-2-il]-N-tiazol-2-il-acetamida; 2-(6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il)-2-[6-[2-[4-[[4-(hidroximetil)-1-piperidil]metil]fenil]etinil]-1-oxo-4-(trifluorometil)isoindolin-2-il]-N-tiazol-2-il-acetamida; 2-[4-(difluorometil)-6-[4-(1-etil-4-piperidil)fenil]-1-oxo-isoindolin-2-il]-2-(6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il)-N-tiazol-2-il-acetamida; 2-[4-(difluorometil)-6-[2-[4-[[4-(hidroximetil)-1-piperidil]metil]fenil]etinil]-1-oxo-isoindolin-2-il]-2-(6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il)-N-tiazol-2-il-acetamida; 2-[6-[2-[4-[[4-(hidroximetil)-1-piperidil]metil]fenil]etinil]-1-oxo-4-(trifluorometil)isoindolin-2-il]-2-[rac-(6R)-6-fluoro-6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il]-N-tiazol-2-il-acetamida; 2-[4-(difluorometil)-6-[4-(1-etil-4-piperidil)fenil]-1-oxo-isoindolin-2-il]-2-[rac-(6R)-6-fluoro-6,7-dihidro-5Hpirrolo[1,2-c]imidazol-1-il]-N-tiazol-2-il-acetamida; 2-[4-(difluorometil)-1-oxo-6-[4-[rac-(3R,4R)-1-etil-3-fluoro-4-piperidil]fenil]isoindolin-2-il]-2-(6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il)-N-tiazol-2-il-acetamida; 2-[6-[2-[4-[(6-hidroxi-2-azaspiro[3.3]heptan-2-il)metil]fenil]etinil]-1-oxo-4-(trifluorometil)isoindolin-2-il]-2-[rac-(6R)-6-fluoro-6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il]-N-tiazol-2-il-acetamida; 2-[4-(difluorometil)-6-[2-[4-[[4-(hidroximetil)-1-piperidil]metil]fenil]etinil]-1-oxo-isoindolin-2-il]-2-[rac-(6R)-6-fluoro-6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il]-N-tiazol-2-il-acetamida; 2-[6-[2-[4-[(4-hidroxiazepan-1-il)metil]fenil]etinil]-1-oxo-4-(trifluorometil)isoindolin-2-il]-2-[rac-(6R)-6-fluoro-6,7-dihidro-5H-pirrolo[1,2-c]imidazol-1-il]-N-tiazol-2-il-acetamida.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP19181772 | 2019-06-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR121167A1 true AR121167A1 (es) | 2022-04-27 |
Family
ID=67001684
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP200101746A AR119207A1 (es) | 2019-06-21 | 2020-06-19 | DERIVADOS DE PIRROLO[1,2-c]IMIDAZOL COMO INHIBIDORES DE EGFR |
| ARP200101744A AR121167A1 (es) | 2019-06-21 | 2020-06-19 | DERIVADOS DE PIRROLO[1,2-c]IMIDAZOL COMO INHIBIDORES DE EGFR |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP200101746A AR119207A1 (es) | 2019-06-21 | 2020-06-19 | DERIVADOS DE PIRROLO[1,2-c]IMIDAZOL COMO INHIBIDORES DE EGFR |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US20220315591A1 (es) |
| EP (2) | EP3986567B1 (es) |
| JP (2) | JP7530390B2 (es) |
| KR (1) | KR20220024096A (es) |
| CN (2) | CN113993590B (es) |
| AR (2) | AR119207A1 (es) |
| AU (1) | AU2020296933A1 (es) |
| BR (1) | BR112021024810A2 (es) |
| CA (1) | CA3139171A1 (es) |
| CL (1) | CL2021003373A1 (es) |
| CO (1) | CO2021016967A2 (es) |
| CR (1) | CR20210614A (es) |
| IL (1) | IL287806A (es) |
| MA (1) | MA56507A (es) |
| MX (1) | MX2021015889A (es) |
| PE (1) | PE20220807A1 (es) |
| PH (1) | PH12021553018A1 (es) |
| TW (2) | TW202115070A (es) |
| WO (2) | WO2020254547A1 (es) |
| ZA (1) | ZA202108775B (es) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113993873B (zh) * | 2019-06-21 | 2024-08-02 | 豪夫迈·罗氏有限公司 | 用于治疗癌症的egfr抑制剂 |
| TW202115070A (zh) * | 2019-06-21 | 2021-04-16 | 瑞士商赫孚孟拉羅股份公司 | 新穎的egfr抑制劑 |
| JOP20220107A1 (ar) | 2019-11-11 | 2023-01-30 | Dana Farber Cancer Inst Inc | مثبطات egfr تفارغية وطرق استخدامها |
| CR20230218A (es) * | 2020-12-01 | 2023-07-07 | Hoffmann La Roche | Nuevos derivados de indazol acetileno |
| CR20250458A (es) | 2023-03-30 | 2025-11-21 | Revolution Medicines Inc | Composiciones para inducir la hidrólisis de ras gtp y sus usos |
| AU2024265078A1 (en) | 2023-05-04 | 2025-12-11 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
| US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| US20250154171A1 (en) | 2023-10-12 | 2025-05-15 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025240847A1 (en) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025255438A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025265060A1 (en) | 2024-06-21 | 2025-12-26 | Revolution Medicines, Inc. | Therapeutic compositions and methods for managing treatment-related effects |
| WO2026006747A1 (en) | 2024-06-28 | 2026-01-02 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026015801A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015790A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015825A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Use of ras inhibitor for treating pancreatic cancer |
| WO2026015796A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2307365B1 (en) | 2008-06-25 | 2013-03-27 | Merck Sharp & Dohme Corp. | Synthesis and use of heterocyclic antibacterial agents |
| US8420661B2 (en) | 2010-04-13 | 2013-04-16 | Hoffmann-La Roche Inc. | Arylethynyl derivatives |
| BR112017024481B1 (pt) | 2015-05-14 | 2020-11-17 | The Wistar Institute Of Anatomy And Biology | composto inibidor de ebna1, composição farmacêutica compreendendo dito composto e usos terapêuticos do mesmo |
| EP3317273B1 (en) * | 2015-06-30 | 2021-12-29 | Dana-Farber Cancer Institute, Inc. | Inhibitors of egfr and methods of use thereof |
| AR113299A1 (es) * | 2017-06-02 | 2020-04-08 | Hoffmann La Roche | Compuestos de isoindolina |
| MA53003A (fr) * | 2018-06-29 | 2021-05-05 | Hoffmann La Roche | Composés |
| EP3986565B1 (en) | 2019-06-21 | 2023-08-30 | F. Hoffmann-La Roche AG | New egfr inhibitors |
| CN113993873B (zh) * | 2019-06-21 | 2024-08-02 | 豪夫迈·罗氏有限公司 | 用于治疗癌症的egfr抑制剂 |
| TW202115070A (zh) * | 2019-06-21 | 2021-04-16 | 瑞士商赫孚孟拉羅股份公司 | 新穎的egfr抑制劑 |
-
2020
- 2020-06-19 TW TW109120780A patent/TW202115070A/zh unknown
- 2020-06-19 JP JP2021576027A patent/JP7530390B2/ja active Active
- 2020-06-19 EP EP20734489.6A patent/EP3986567B1/en active Active
- 2020-06-19 KR KR1020217041503A patent/KR20220024096A/ko not_active Ceased
- 2020-06-19 PE PE2021002083A patent/PE20220807A1/es unknown
- 2020-06-19 PH PH1/2021/553018A patent/PH12021553018A1/en unknown
- 2020-06-19 BR BR112021024810A patent/BR112021024810A2/pt not_active IP Right Cessation
- 2020-06-19 AU AU2020296933A patent/AU2020296933A1/en not_active Abandoned
- 2020-06-19 AR ARP200101746A patent/AR119207A1/es not_active Application Discontinuation
- 2020-06-19 AR ARP200101744A patent/AR121167A1/es not_active Application Discontinuation
- 2020-06-19 US US17/620,238 patent/US20220315591A1/en not_active Abandoned
- 2020-06-19 JP JP2021576026A patent/JP7561779B2/ja active Active
- 2020-06-19 CN CN202080044132.8A patent/CN113993590B/zh active Active
- 2020-06-19 TW TW109120820A patent/TW202115073A/zh unknown
- 2020-06-19 MX MX2021015889A patent/MX2021015889A/es unknown
- 2020-06-19 CR CR20210614A patent/CR20210614A/es unknown
- 2020-06-19 EP EP20734487.0A patent/EP3986566B1/en active Active
- 2020-06-19 MA MA056507A patent/MA56507A/fr unknown
- 2020-06-19 WO PCT/EP2020/067057 patent/WO2020254547A1/en not_active Ceased
- 2020-06-19 CA CA3139171A patent/CA3139171A1/en active Pending
- 2020-06-19 CN CN202080045318.5A patent/CN113993591A/zh active Pending
- 2020-06-19 WO PCT/EP2020/067055 patent/WO2020254546A1/en not_active Ceased
-
2021
- 2021-11-02 IL IL287806A patent/IL287806A/en unknown
- 2021-11-08 ZA ZA2021/08775A patent/ZA202108775B/en unknown
- 2021-12-14 CO CONC2021/0016967A patent/CO2021016967A2/es unknown
- 2021-12-16 CL CL2021003373A patent/CL2021003373A1/es unknown
- 2021-12-21 US US17/558,108 patent/US20220112199A1/en not_active Abandoned
Also Published As
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