AR122096A2 - Compuestos profármacos de creatina y composiciones que los comprenden - Google Patents
Compuestos profármacos de creatina y composiciones que los comprendenInfo
- Publication number
- AR122096A2 AR122096A2 ARP210101331A ARP210101331A AR122096A2 AR 122096 A2 AR122096 A2 AR 122096A2 AR P210101331 A ARP210101331 A AR P210101331A AR P210101331 A ARP210101331 A AR P210101331A AR 122096 A2 AR122096 A2 AR 122096A2
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- alkyl
- replacement
- cycloalkyl
- arilalquilo
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title abstract 6
- CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical compound NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 title abstract 4
- 229960003624 creatine Drugs 0.000 title abstract 2
- 239000006046 creatine Substances 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title 1
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 21
- 229910052739 hydrogen Inorganic materials 0.000 abstract 14
- 239000001257 hydrogen Substances 0.000 abstract 14
- 150000002431 hydrogen Chemical group 0.000 abstract 11
- 125000003118 aryl group Chemical group 0.000 abstract 10
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 abstract 8
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 8
- 125000004404 heteroalkyl group Chemical group 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- -1 substituted Chemical class 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 230000019439 energy homeostasis Effects 0.000 abstract 1
- 208000028867 ischemia Diseases 0.000 abstract 1
- 230000004770 neurodegeneration Effects 0.000 abstract 1
- 208000015122 neurodegenerative disease Diseases 0.000 abstract 1
- 210000000056 organ Anatomy 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/02—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
- C07D273/06—Seven-membered rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/06—Free radical scavengers or antioxidants
-
- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/04—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton
- C07C279/14—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton being further substituted by carboxyl groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/20—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylguanidines
- C07C279/24—Y being a hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
- C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/02—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
- C07D273/04—Six-membered rings
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Toxicology (AREA)
- Biochemistry (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
Abstract
Compuestos profármacos de creatina, composiciones farmacéuticas que los comprenden y el empleo de los mismos para el tratamiento de enfermedades neurodegenerativas, de la isquemia y para la homeostasis energética en un tejido u órgano entre otros usos. Reivindicación 1: Un compuesto caracterizado porque es de la fórmula (1), fórmula (3), fórmula (5), o una sal, solvato, tautómero o estereoisómero farmacéuticamente aceptable de este: donde el compuesto de la fórmula (1) es: como se muestra a continuación, donde: R es -CH₃ o -CD₃; R¹ es hidrógeno, -OR², -C(O)OR², -C(O)R², o un resto del grupo de fórmulas (2); n es un entero de 1 a 2; cada R² es independientemente hidrógeno, alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, heteroalquilo C₁₋₁₂, heteroalquilo C₁₋₁₂ sustituido, cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂ sustituido, cicloalquilalquilo C₄₋₂₀, cicloalquilalquilo C₄₋₂₀ sustituido, heterocicloalquilalquilo C₄₋₂₀, heterocicloalquilalquilo C₄₋₂₀ sustituido, arilo C₅₋₁₂, arilo C₅₋₁₂ sustituido, heteroarilo C₅₋₁₂, heteroarilo C₅₋₁₂ sustituido, arilalquilo C₆₋₂₀, arilalquilo C₆₋₂₀ sustituido, heteroarilalquilo C₆₋₂₀ o heteroarilalquilo C₆₋₂₀ sustituido; cada R³ y R⁴ es independientemente hidrógeno, alquilo C₁₋₁₂ o alquilo C₁₋₁₂ sustituido; R²³ es hidrógeno, alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, cicloalquilo C₅₋₁₂, cicloalquilo C₅₋₁₂ sustituido, arilo C₅₋₁₂, y arilo C₅₋₁₂ sustituido, -C(O)-OR²² o -C(O)-R²²; R²² es alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, heteroalquilo C₁₋₁₂, heteroalquilo C₁₋₁₂ sustituido, cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂ sustituido, cicloalquilalquilo C₄₋₂₀, cicloalquilalquilo C₄₋₂₀ sustituido, heterocicloalquilalquilo C₄₋₂₀, heterocicloalquilalquilo C₄₋₂₀ sustituido, arilo C₅₋₁₂, arilo C₅₋₁₂ sustituido, heteroarilo C₅₋₁₂, heteroarilo C₅₋₁₂ sustituido, arilalquilo C₆₋₂₀, arilalquilo C₆₋₂₀ sustituido, heteroarilalquilo C₆₋₂₀ o heteroarilalquilo C₆₋₂₀ sustituido; y R⁴⁸ es alquilo C₁₋₁₂ o alquilo C₁₋₁₂ sustituido; donde el compuesto de la fórmula (3) es: como se muestra a continuación, donde: R es -CH₃ o -CD₃; R¹⁰ es hidrógeno, alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, heteroalquilo C₁₋₁₂, heteroalquilo C₁₋₁₂ sustituido, cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂ sustituido, cicloalquilalquilo C₄₋₂₀, cicloalquilalquilo C₄₋₂₀ sustituido, heterocicloalquilalquilo C₄₋₂₀, heterocicloalquilalquilo C₄₋₂₀ sustituido, arilo C₅₋₁₂, arilo C₅₋₁₂ sustituido, heteroarilo C₅₋₁₂, heteroarilo C₅₋₁₂ sustituido, arilalquilo C₆₋₂₀, arilalquilo C₆₋₂₀ sustituido, heteroarilalquilo C₆₋₂₀, heteroarilalquilo C₆₋₂₀ sustituido, -C(O)R⁵, -C(O)OR⁵, -C(O)(NR³R⁴), -C(R³R⁴)-C(O)OR²², -C(R³R⁴)-(O)C(O)R²², -C(R³R⁴)-(O)C(O)-OR²²; o un resto del grupo de fórmulas (4); cada uno de R¹¹ y R¹² es independientemente hidrógeno o -OR¹³; o cada uno de R¹¹ y R¹² es -C(O)R⁵, con la condición de que ambos R¹¹ y R¹² no puedan ser hidrógeno; R¹³ es independientemente hidrógeno, alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, heteroalquilo C₁₋₁₂, heteroalquilo C₁₋₁₂ sustituido, cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂ sustituido, cicloalquilalquilo C₄₋₂₀, cicloalquilalquilo C₄₋₂₀ sustituido, heterocicloalquilalquilo C₄₋₂₀, heterocicloalquilalquilo C₄₋₂₀ sustituido, arilo C₅₋₁₂, arilo C₅₋₁₂ sustituido, heteroarilo C₅₋₁₂, heteroarilo C₅₋₁₂ sustituido, arilalquilo C₆₋₂₀, arilalquilo C₆₋₂₀ sustituido, heteroarilalquilo C₆₋₂₀, heteroarilalquilo C₆₋₂₀ sustituido, -CH(OR⁵), -C(O)R⁵, -C(O)OR⁵ o -C(O)(NR³R⁴); cada R³ y R⁴ es independientemente hidrógeno, alquilo C₁₋₁₂ o alquilo C₁₋₁₂ sustituido; R⁵ es hidrógeno, alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, heteroalquilo C₁₋₁₂, heteroalquilo C₁₋₁₂ sustituido, cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂ sustituido, cicloalquilalquilo C₄₋₂₀, cicloalquilalquilo C₄₋₂₀ sustituido, heterocicloalquilalquilo C₄₋₂₀, heterocicloalquilalquilo C₄₋₂₀ sustituido, arilo C₅₋₁₂, arilo C₅₋₁₂ sustituido, heteroarilo C₅₋₁₂, heteroarilo C₅₋₁₂ sustituido, arilalquilo C₆₋₂₀, arilalquilo C₆₋₂₀ sustituido, heteroarilalquilo C₆₋₂₀ o heteroarilalquilo C₆₋₂₀ sustituido; R²³ es hidrógeno, alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, cicloalquilo C₅₋₁₂, cicloalquilo C₅₋₁₂ sustituido, arilo C₅₋₁₂, y arilo C₅₋₁₂ sustituido, -C(O)-OR²² o -C(O)-R²²; R²² es alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, heteroalquilo C₁₋₁₂, heteroalquilo C₁₋₁₂ sustituido, cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂ sustituido, cicloalquilalquilo C₄₋₂₀, cicloalquilalquilo C₄₋₂₀ sustituido, heterocicloalquilalquilo C₄₋₂₀, heterocicloalquilalquilo C₄₋₂₀ sustituido, arilo C₅₋₁₂, arilo C₅₋₁₂ sustituido, heteroarilo C₅₋₁₂, heteroarilo C₅₋₁₂ sustituido, arilalquilo C₆₋₂₀, arilalquilo C₆₋₂₀ sustituido, heteroarilalquilo C₆₋₂₀ o heteroarilalquilo C₆₋₂₀ sustituido; y n es un entero de 1 a 2; donde el compuesto de la fórmula (5) es: como se muestra a continuación, donde: R es -CH₃ o -CD₃; cada R¹⁴ es independientemente hidrógeno, alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, heteroalquilo C₁₋₁₂, heteroalquilo C₁₋₁₂ sustituido, cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂ sustituido, cicloalquilalquilo C₄₋₂₀, cicloalquilalquilo C₄₋₂₀ sustituido, heterocicloalquilalquilo C₄₋₂₀, heterocicloalquilalquilo C₄₋₂₀ sustituido, arilo C₅₋₁₂, arilo C₅₋₁₂ sustituido, heteroarilo C₅₋₁₂, heteroarilo C₅₋₁₂ sustituido, arilalquilo C₆₋₂₀, arilalquilo C₆₋₂₀ sustituido, heteroarilalquilo C₆₋₂₀, heteroarilalquilo C₆₋₂₀ sustituido, -CH(OR⁵), -C(O)R⁵, -C(O)OR⁵ o -C(O)(NR³R⁴); cada R³ y R⁴ es independientemente hidrógeno, alquilo C₁₋₁₂ o alquilo C₁₋₁₂ sustituido; y R⁵ es hidrógeno, alquilo C₁₋₁₂, alquilo C₁₋₁₂ sustituido, heteroalquilo C₁₋₁₂, heteroalquilo C₁₋₁₂ sustituido, cicloalquilo C₃₋₁₂, cicloalquilo C₃₋₁₂ sustituido, cicloalquilalquilo C₄₋₂₀, cicloalquilalquilo C₄₋₂₀ sustituido, heterocicloalquilalquilo C₄₋₂₀, heterocicloalquilalquilo C₄₋₂₀ sustituido, arilo C₅₋₁₂, arilo C₅₋₁₂ sustituido, heteroarilo C₅₋₁₂, heteroarilo C₅₋₁₂ sustituido, arilalquilo C₆₋₂₀, arilalquilo C₆₋₂₀ sustituido, heteroarilalquilo C₆₋₂₀ o heteroarilalquilo C₆₋₂₀ sustituido.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462095295P | 2014-12-22 | 2014-12-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR122096A2 true AR122096A2 (es) | 2022-08-10 |
Family
ID=56128653
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150104265A AR103254A1 (es) | 2014-12-22 | 2015-12-22 | Profármacos de creatina, composiciones y métodos de uso de estos |
| ARP210101331A AR122096A2 (es) | 2014-12-22 | 2021-05-14 | Compuestos profármacos de creatina y composiciones que los comprenden |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150104265A AR103254A1 (es) | 2014-12-22 | 2015-12-22 | Profármacos de creatina, composiciones y métodos de uso de estos |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US9617230B2 (es) |
| EP (2) | EP3771709B1 (es) |
| JP (4) | JP6692372B2 (es) |
| AR (2) | AR103254A1 (es) |
| CA (1) | CA2971729C (es) |
| ES (1) | ES2832333T3 (es) |
| TW (3) | TWI700270B (es) |
| WO (1) | WO2016106284A2 (es) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9617230B2 (en) | 2014-12-22 | 2017-04-11 | Farmington Pharma Development | Creatine prodrugs, compositions and methods of use thereof |
| WO2016160885A1 (en) | 2015-03-30 | 2016-10-06 | Farmington Pharma Development | Creatine phosphate analog prodrugs, compositions and uses thereof |
| US11332438B2 (en) | 2017-12-01 | 2022-05-17 | Ultragenyx Pharmaceutical Inc. | Creatine prodrugs, compositions and methods of use thereof |
| CN110746325A (zh) * | 2018-07-24 | 2020-02-04 | 上海和辉光电有限公司 | 一种基于胍骨架的n型掺杂化合物及其应用 |
| CN114419050B (zh) * | 2022-03-31 | 2022-06-21 | 武汉大学 | 胃黏膜可视化程度量化方法、装置、终端及可读存储介质 |
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| AU4151996A (en) | 1994-11-08 | 1996-05-31 | Avicena Group, Inc. | Use of creatine or creatine analogs for the treatment of diseases of the nervous system |
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| AR103254A1 (es) | 2017-04-26 |
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| JP2020128379A (ja) | 2020-08-27 |
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| EP3771709B1 (en) | 2024-03-20 |
| JP2025118733A (ja) | 2025-08-13 |
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| EP3771709C0 (en) | 2024-03-20 |
| TW202041504A (zh) | 2020-11-16 |
| EP3237391A2 (en) | 2017-11-01 |
| JP6692372B2 (ja) | 2020-05-13 |
| WO2016106284A2 (en) | 2016-06-30 |
| JP7037597B2 (ja) | 2022-03-16 |
| CA2971729A1 (en) | 2016-06-30 |
| US20170342039A1 (en) | 2017-11-30 |
| US20190337909A1 (en) | 2019-11-07 |
| CA2971729C (en) | 2024-02-20 |
| TWI779312B (zh) | 2022-10-01 |
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