JP7038063B2 - ピラゾロ[1,5-a]ピリミジニルカルボキサミド化合物および医学的障害の処置におけるその使用 - Google Patents
ピラゾロ[1,5-a]ピリミジニルカルボキサミド化合物および医学的障害の処置におけるその使用 Download PDFInfo
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- JP7038063B2 JP7038063B2 JP2018552683A JP2018552683A JP7038063B2 JP 7038063 B2 JP7038063 B2 JP 7038063B2 JP 2018552683 A JP2018552683 A JP 2018552683A JP 2018552683 A JP2018552683 A JP 2018552683A JP 7038063 B2 JP7038063 B2 JP 7038063B2
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- HSWRDPVAQBDGSC-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3cc(-c4ncncn4)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3cc(-c4ncncn4)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O HSWRDPVAQBDGSC-UHFFFAOYSA-N 0.000 description 1
- UZWQSBRXVLLTNV-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3cc(C(N(C)C)=O)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3cc(C(N(C)C)=O)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O UZWQSBRXVLLTNV-UHFFFAOYSA-N 0.000 description 1
- FHKJYWJCRLTTDT-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3cc(C(NC)=O)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3cc(C(NC)=O)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O FHKJYWJCRLTTDT-UHFFFAOYSA-N 0.000 description 1
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- GDQXXUPADGSRIR-HNNXBMFYSA-N Cc([n]1nc2)cc(-c3cnccc3C(F)(F)F)nc1c2C(N[C@@H](C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3cnccc3C(F)(F)F)nc1c2C(N[C@@H](C1CC1)C(F)(F)F)=O GDQXXUPADGSRIR-HNNXBMFYSA-N 0.000 description 1
- BDIOTSJMSUDGPZ-ZDUSSCGKSA-N Cc([n]1nc2)cc(-c3n[o]cc3)nc1c2C(N[C@@H](C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3n[o]cc3)nc1c2C(N[C@@H](C1CC1)C(F)(F)F)=O BDIOTSJMSUDGPZ-ZDUSSCGKSA-N 0.000 description 1
- BACWZIINSOXLMD-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3nc(-c4ncccn4)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3nc(-c4ncccn4)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O BACWZIINSOXLMD-UHFFFAOYSA-N 0.000 description 1
- JWPZJHZWQLAEDB-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3nc(Cl)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3nc(Cl)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O JWPZJHZWQLAEDB-UHFFFAOYSA-N 0.000 description 1
- YUVGSEDLSFKSSE-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3ncccc3)nc1c2C(Nc(nc1)ccc1-c1ccc[o]1)=O Chemical compound Cc([n]1nc2)cc(-c3ncccc3)nc1c2C(Nc(nc1)ccc1-c1ccc[o]1)=O YUVGSEDLSFKSSE-UHFFFAOYSA-N 0.000 description 1
- MYBMXMBXWQFZDR-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3ncccc3)nc1c2C(Nc1ccc(CCC2)c2c1)=O Chemical compound Cc([n]1nc2)cc(-c3ncccc3)nc1c2C(Nc1ccc(CCC2)c2c1)=O MYBMXMBXWQFZDR-UHFFFAOYSA-N 0.000 description 1
- KYJILWPHEKJSGM-UHFFFAOYSA-N Cc([n]1nc2)cc(N(CCN3CC(F)(F)F)C3=O)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(N(CCN3CC(F)(F)F)C3=O)nc1c2C(NC(C1CC1)C(F)(F)F)=O KYJILWPHEKJSGM-UHFFFAOYSA-N 0.000 description 1
- RUTPHOUZHZTUGE-UHFFFAOYSA-N Cc([o]c(C#N)c1)c1-c(cc(C)[n]1nc2)nc1c2C(N=C)=O Chemical compound Cc([o]c(C#N)c1)c1-c(cc(C)[n]1nc2)nc1c2C(N=C)=O RUTPHOUZHZTUGE-UHFFFAOYSA-N 0.000 description 1
- GSRKHRSALPOTBP-UHFFFAOYSA-N Cc([o]c(C#N)c1)c1-c(cc(C)[n]1nc2)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([o]c(C#N)c1)c1-c(cc(C)[n]1nc2)nc1c2C(NC(C1CC1)C(F)(F)F)=O GSRKHRSALPOTBP-UHFFFAOYSA-N 0.000 description 1
- PHGXUFPYCAWEHK-UHFFFAOYSA-N Cc(cccn1)c1F Chemical compound Cc(cccn1)c1F PHGXUFPYCAWEHK-UHFFFAOYSA-N 0.000 description 1
- WATJDHQAPWIPNM-CQSZACIVSA-N Cc1c(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)[o]nc1 Chemical compound Cc1c(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)[o]nc1 WATJDHQAPWIPNM-CQSZACIVSA-N 0.000 description 1
- OKHCIUYTCGNFHB-UHFFFAOYSA-N Cc1c[o]nc1-c(cc(C)[n]1nc2)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc1c[o]nc1-c(cc(C)[n]1nc2)nc1c2C(NC(C1CC1)C(F)(F)F)=O OKHCIUYTCGNFHB-UHFFFAOYSA-N 0.000 description 1
- TXOHMSSZMJQZAX-CQSZACIVSA-N Cc1cc(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)n[o]1 Chemical compound Cc1cc(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)n[o]1 TXOHMSSZMJQZAX-CQSZACIVSA-N 0.000 description 1
- QLHCLNAQULRANK-UHFFFAOYSA-N Cc1cc(C#N)c(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)[o]1 Chemical compound Cc1cc(C#N)c(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)[o]1 QLHCLNAQULRANK-UHFFFAOYSA-N 0.000 description 1
- UDMNVTJFUISBFD-UHFFFAOYSA-N Cc1cccc(F)n1 Chemical compound Cc1cccc(F)n1 UDMNVTJFUISBFD-UHFFFAOYSA-N 0.000 description 1
- AZFSUHYOECXKOT-CQSZACIVSA-N Cc1n[o]c(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)c1 Chemical compound Cc1n[o]c(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)c1 AZFSUHYOECXKOT-CQSZACIVSA-N 0.000 description 1
- OZQVZLAMNDAUCF-UHFFFAOYSA-N Cc1nc(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)c[o]1 Chemical compound Cc1nc(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)c[o]1 OZQVZLAMNDAUCF-UHFFFAOYSA-N 0.000 description 1
- KAHDUHPHARNQFY-UHFFFAOYSA-N Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(N=C)=O)[o]1 Chemical compound Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(N=C)=O)[o]1 KAHDUHPHARNQFY-UHFFFAOYSA-N 0.000 description 1
- VWIIAOGWLUPWRF-UHFFFAOYSA-N Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)[o]1 Chemical compound Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)[o]1 VWIIAOGWLUPWRF-UHFFFAOYSA-N 0.000 description 1
- VWIIAOGWLUPWRF-CQSZACIVSA-N Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)[o]1 Chemical compound Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)[o]1 VWIIAOGWLUPWRF-CQSZACIVSA-N 0.000 description 1
- HDBGZXSGXLMEOO-UHFFFAOYSA-N FC(CC1[IH]CC1)(F)F Chemical compound FC(CC1[IH]CC1)(F)F HDBGZXSGXLMEOO-UHFFFAOYSA-N 0.000 description 1
- JJQADENPZJYDDI-UHFFFAOYSA-N FC1C=CCCCCC1 Chemical compound FC1C=CCCCCC1 JJQADENPZJYDDI-UHFFFAOYSA-N 0.000 description 1
- JPTMBILBPYBOFL-UHFFFAOYSA-N NC1=CC=CC=[I]1 Chemical compound NC1=CC=CC=[I]1 JPTMBILBPYBOFL-UHFFFAOYSA-N 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N O=C1NCCN1 Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
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- A61P25/16—Anti-Parkinson drugs
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- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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- A—HUMAN NECESSITIES
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- A61P25/22—Anxiolytics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- 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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- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
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- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Neurology (AREA)
- Neurosurgery (AREA)
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- Hospice & Palliative Care (AREA)
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- Hematology (AREA)
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- Pain & Pain Management (AREA)
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- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662318929P | 2016-04-06 | 2016-04-06 | |
| US62/318,929 | 2016-04-06 | ||
| PCT/US2017/026280 WO2017176960A1 (en) | 2016-04-06 | 2017-04-06 | Pyrazolo[1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019510790A JP2019510790A (ja) | 2019-04-18 |
| JP2019510790A5 JP2019510790A5 (https=) | 2021-11-04 |
| JP7038063B2 true JP7038063B2 (ja) | 2022-03-17 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| JP2018552683A Expired - Fee Related JP7038063B2 (ja) | 2016-04-06 | 2017-04-06 | ピラゾロ[1,5-a]ピリミジニルカルボキサミド化合物および医学的障害の処置におけるその使用 |
Country Status (12)
| Country | Link |
|---|---|
| US (4) | US11192892B2 (https=) |
| EP (1) | EP3440080A4 (https=) |
| JP (1) | JP7038063B2 (https=) |
| KR (2) | KR20180133461A (https=) |
| CN (1) | CN109311887B (https=) |
| AU (1) | AU2017246455B2 (https=) |
| BR (1) | BR112018070586A8 (https=) |
| CA (1) | CA3020287A1 (https=) |
| IL (1) | IL262177B (https=) |
| MX (1) | MX2018012211A (https=) |
| SG (1) | SG11201808830YA (https=) |
| WO (1) | WO2017176960A1 (https=) |
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| HRP20240644T1 (hr) | 2014-11-06 | 2024-08-02 | Bial-R&D Investments, S.A. | Supstituirani pirazolo(1,5-a)pirimidini i njihova uporaba u liječenju medicinskih poremećaja |
| WO2016073889A1 (en) | 2014-11-06 | 2016-05-12 | Lysosomal Therapeutics Inc. | Substituted imidazo[1,5-a]pyrimidines and their use in the treatment of medical disorders |
| AU2015342883B2 (en) | 2014-11-06 | 2020-07-02 | Bial - R&D Investments, S.A. | Substituted pyrrolo(1,2-a)pyrimidines and their use in the treatment of medical disorders |
| CA3020305A1 (en) * | 2016-04-06 | 2017-10-12 | Lysosomal Therapeutics Inc. | Imidazo [1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
| US11192892B2 (en) | 2016-04-06 | 2021-12-07 | Bial—R&D Investments, S.A. | Substituted pyrazolo[1,5-a]pyrimidines for the treatment of medical disorders |
| EP3440081A4 (en) | 2016-04-06 | 2019-09-18 | Lysosomal Therapeutics Inc. | PYRROLO [1,2-A] PYRIMIDINYL-CARBOXAMIDE COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDER |
| SG11201809693SA (en) | 2016-05-05 | 2018-11-29 | Lysosomal Therapeutics Inc | SUBSTITUTED IMIDAZO[1,2-b]PYRIDAZINES, SUBSTITUTED IMIDAZO[1,5-b]PYRIDAZINES, RELATED COMPOUNDS, AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS |
| EP3452455A4 (en) | 2016-05-05 | 2019-11-13 | Lysosomal Therapeutics Inc. | SUBSTITUTED IMDAZO [1,2-] PYRIDINES, SUBSTITUTED IMIDAZO [1,2-] PYRAZINES, RELATED COMPOUNDS AND THEIR USE IN THE TREATMENT OF ILLNESSES |
| CN110698484B (zh) * | 2019-06-05 | 2021-11-05 | 陕西理工大学 | 含吡唑并[1,5-a]嘧啶的衍生物、药用组合物及应用 |
| CN115108972A (zh) * | 2022-08-29 | 2022-09-27 | 北京迪泰医药科技有限公司 | 一种2-甲基-3-氟-5-溴吡啶的合成方法 |
| WO2025014639A2 (en) * | 2023-07-07 | 2025-01-16 | The Johns Hopkins University | Neutral sphingomyelinase inhibitors |
| WO2025146216A1 (zh) * | 2024-01-05 | 2025-07-10 | 成都赜灵生物医药科技有限公司 | 六并五氮杂环酰胺类化合物及其用途 |
| CN118184599A (zh) * | 2024-02-29 | 2024-06-14 | 重庆药友制药有限责任公司 | 一种阿莫奈韦中间体的制备方法 |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004277337A (ja) | 2003-03-14 | 2004-10-07 | Sumitomo Pharmaceut Co Ltd | ピラゾロ[1,5−a]ピリミジン誘導体 |
| WO2005113004A2 (en) | 2004-05-14 | 2005-12-01 | The Cleveland Clinic Founfation | Small molecule inhibitors for mrp1 and other multidrug transporters |
| WO2007048066A2 (en) | 2005-10-21 | 2007-04-26 | Exelixis, Inc. | Pyrazolo-pyrimidines as casein kinase ii (ck2) modulators |
| JP2008530155A (ja) | 2005-02-17 | 2008-08-07 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | ピラゾロピリミジン類 |
| WO2010086040A1 (en) | 2009-01-29 | 2010-08-05 | Biomarin Iga, Ltd. | Pyrazolo-pyrimidines for treatment of duchenne muscular dystrophy |
| WO2012075393A2 (en) | 2010-12-02 | 2012-06-07 | President And Fellows Of Harvard College | Activators of proteasomal degradation and uses thereof |
| WO2012078855A1 (en) | 2010-12-08 | 2012-06-14 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Substituted pyrazolopyrimidines as glucocerebrosidase activators |
| WO2014141129A2 (en) | 2013-03-14 | 2014-09-18 | Grueneberg Dorre A | Novel methods, compounds, and compositions for inhibition of ros |
| WO2015012328A1 (ja) | 2013-07-24 | 2015-01-29 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2015073267A1 (en) | 2013-11-15 | 2015-05-21 | Calitor Sciences, Llc | Substituted heteroaryl compounds and methods of use |
Family Cites Families (94)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4838925A (en) | 1986-04-25 | 1989-06-13 | E. I. Du Pont De Nemours And Company | Heterocyclic acyl sulfonamides |
| JP3763997B2 (ja) | 1999-05-13 | 2006-04-05 | 富士写真フイルム株式会社 | 感熱記録材料 |
| JP4331823B2 (ja) | 1999-05-21 | 2009-09-16 | 富士フイルム株式会社 | ピロロ[1,2−a]−1,3,5−トリアジン−4−オン系化合物 |
| WO2001051919A2 (en) | 2000-01-07 | 2001-07-19 | Transform Pharmaceuticals, Inc. | High-throughput formation, identification, and analysis of diverse solid-forms |
| TWI243164B (en) | 2001-02-13 | 2005-11-11 | Aventis Pharma Gmbh | Acylated indanyl amines and their use as pharmaceuticals |
| JP4070966B2 (ja) | 2001-06-28 | 2008-04-02 | 株式会社カネボウ化粧品 | 新規ガラクトシルセラミド類縁体及び用途 |
| ATE307812T1 (de) | 2001-10-22 | 2005-11-15 | Pfizer | Imidazopyridinverbindungen als 5-ht4- rezeptormodulatoren |
| US20050096322A1 (en) | 2002-03-01 | 2005-05-05 | Susumu Igarashi | Nitrogen-containing heterocyclic compound |
| DOP2003000703A (es) | 2002-09-20 | 2004-03-31 | Pfizer | Compuestos de imidazopiradina como agonistas del receptor 5-ht4 |
| MXPA05003065A (es) | 2002-09-20 | 2005-05-27 | Pfizer | Compuestos de piperidinil-imidazopiridina n-sustituidos como moduladores del receptor 5-ht4. |
| US7550470B2 (en) | 2002-12-11 | 2009-06-23 | Merck & Co. Inc. | Substituted pyrazolo[1,5-A]pyrimidines as tyrosine kinase inhibitors |
| MXPA05011270A (es) | 2003-04-21 | 2006-01-24 | Pfizer | Compuestos de imidazopiridina que tienen actividad agonista del receptor 5-ht4 y actividad antagonista del receptor 5-ht3. |
| EP1682504B1 (en) | 2003-11-12 | 2012-12-26 | Amicus Therapeutics Inc. | Hydroxy piperidine derivatives to treat gaucher disease |
| GB0329214D0 (en) | 2003-12-17 | 2004-01-21 | Glaxo Group Ltd | Novel compounds |
| GB0400812D0 (en) | 2004-01-14 | 2004-02-18 | Celltech R&D Ltd | Novel compounds |
| AU2005212096B2 (en) | 2004-02-18 | 2010-12-16 | Msd K.K. | Nitrogenous fused heteroaromatic ring derivative |
| HRP20080070T3 (en) * | 2004-06-21 | 2008-05-31 | F. Hoffmann - La Roche Ag | Pyrrazolo-pyrimidine derivatives |
| JP2008508337A (ja) | 2004-08-02 | 2008-03-21 | シュバルツ ファルマ アクチェンゲゼルシャフト | インドリジンカルボキサミド並びにそのアザ及びジアザ誘導体 |
| DE102004049363A1 (de) | 2004-10-08 | 2006-04-13 | Henkel Kgaa | Mittel zum Färben von keratinhaltigen Fasern |
| WO2006078676A2 (en) | 2005-01-19 | 2006-07-27 | Merck & Co., Inc. | Bicyclic pyrimidines as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes |
| CN101115755B (zh) * | 2005-02-11 | 2013-01-16 | 弗·哈夫曼-拉罗切有限公司 | 作为mglur2拮抗剂的吡唑并-嘧啶衍生物 |
| JPWO2006115168A1 (ja) | 2005-04-21 | 2008-12-18 | 大日本住友製薬株式会社 | N−置換フェニルアセトアミド誘導体およびそれを含有する医薬組成物 |
| JP5079500B2 (ja) | 2005-04-28 | 2012-11-21 | 協和発酵キリン株式会社 | 2−アミノキナゾリン誘導体 |
| US7632837B2 (en) | 2005-06-17 | 2009-12-15 | Bristol-Myers Squibb Company | Bicyclic heterocycles as cannabinoid-1 receptor modulators |
| US7723336B2 (en) | 2005-09-22 | 2010-05-25 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful as kinase modulators |
| CN101316847A (zh) | 2005-10-06 | 2008-12-03 | 先灵公司 | 用作蛋白激酶抑制剂的吡唑并(1,5a)嘧啶化合物 |
| CN101296699B (zh) * | 2005-10-21 | 2013-01-02 | 田边三菱制药株式会社 | 吡唑并[1,5-a]嘧啶化合物 |
| AU2006322187A1 (en) | 2005-12-08 | 2007-06-14 | Novartis Ag | Pyrazolo[1,5-a]pyridine-3-carboxylic acids as EphB and VEGFR2 kinase inhibitors |
| TW200800997A (en) | 2006-03-22 | 2008-01-01 | Astrazeneca Ab | Chemical compounds |
| JP5303458B2 (ja) | 2006-06-23 | 2013-10-02 | アミークス セラピューティックス インコーポレイテッド | β−グルコセレブロシダーゼの活性増強による神経学的疾患の治療方法 |
| AR061793A1 (es) | 2006-07-05 | 2008-09-24 | Mitsubishi Tanabe Pharma Corp | Compuesto de pirazolo[1,5-a] pirimidina y composicion farmaceutica |
| US7553846B2 (en) | 2006-08-07 | 2009-06-30 | Albany Molecular Research, Inc. | 2-alkylbenzoxazole carboxamides as 5-HT3 modulators |
| AU2007321923A1 (en) | 2006-11-20 | 2008-05-29 | Alantos Pharmaceuticals Holding, Inc. | Heterobicyclic matrix metalloprotease inhibitors |
| WO2008063671A2 (en) | 2006-11-20 | 2008-05-29 | Alantos Pharmaceuticals Holding, Inc. | Heterobicyclic metalloprotease inhibitors |
| US20080255153A1 (en) | 2007-03-28 | 2008-10-16 | Biovitrum Ab (Publ) | New compounds |
| AR067326A1 (es) | 2007-05-11 | 2009-10-07 | Novartis Ag | Imidazopiridinas y pirrolo -pirimidinas sustituidas como inhibidores de cinasa de lipido |
| WO2008157575A1 (en) | 2007-06-21 | 2008-12-24 | Irm Llc | Protein kinase inhibitors and methods for using thereof |
| WO2009060835A1 (ja) | 2007-11-05 | 2009-05-14 | Kyoto University | 新規ユビキリン結合性小分子 |
| EP2217601A1 (en) | 2007-11-08 | 2010-08-18 | Centro Nacional de Investigaciones Oncológicas (CNIO) | Imidazopyridazines for use as protein kinase inhibitors |
| MX2010005950A (es) | 2007-11-28 | 2010-06-17 | Schering Corp | 2-fluoropirazolo[1,5-a]pirimidinas como inhibidores de proteina quinasa. |
| WO2009100375A1 (en) | 2008-02-06 | 2009-08-13 | Bristol-Myers Squibb Company | Substituted imidazopyridazines useful as kinase inhibitors |
| WO2009119088A1 (ja) | 2008-03-25 | 2009-10-01 | 武田薬品工業株式会社 | 複素環化合物 |
| EA021938B1 (ru) | 2008-05-01 | 2015-10-30 | Сертрис Фармасьютикалз, Инк. | Хинолины и их аналоги в качестве модуляторов сиртуина |
| CN102245605B (zh) | 2008-10-14 | 2016-01-27 | 阿斯利康(瑞典)有限公司 | 用于治疗细菌感染的稠合、螺环杂芳族化合物 |
| CN102271515B (zh) | 2008-10-31 | 2014-07-02 | 健泰科生物技术公司 | 吡唑并嘧啶jak抑制剂化合物和方法 |
| AR077468A1 (es) * | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
| PE20121148A1 (es) | 2009-08-17 | 2012-09-07 | Intellikine Llc | Compuestos heterociclicos y usos de los mismos |
| JP5985473B2 (ja) | 2010-07-13 | 2016-09-06 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | IRAK4モジュレーターとしてのピラゾロ[1,5a]ピリミジン及びチエノ[3,2b]ピリミジン誘導体 |
| WO2012034095A1 (en) | 2010-09-09 | 2012-03-15 | Irm Llc | Compounds and compositions as trk inhibitors |
| TW201217312A (en) | 2010-09-22 | 2012-05-01 | Gruenenthal Gmbh | Substituted benzamide compounds |
| WO2012116237A2 (en) | 2011-02-23 | 2012-08-30 | Intellikine, Llc | Heterocyclic compounds and uses thereof |
| WO2012129258A1 (en) | 2011-03-22 | 2012-09-27 | Merck Sharp & Dohme Corp. | Amidopyrazole inhibitors of interleukin receptor-associated kinases |
| WO2012177997A1 (en) | 2011-06-22 | 2012-12-27 | The General Hospital Corporation | Treatment of proteinopathies |
| CN103857657B (zh) | 2011-08-18 | 2016-04-20 | 日本新药株式会社 | 杂环衍生物及医药 |
| CN104039784B (zh) | 2011-09-02 | 2017-08-22 | 拜耳知识产权有限责任公司 | 取代的增环嘧啶及其用途 |
| WO2013059119A1 (en) | 2011-10-17 | 2013-04-25 | The Regents Of The University Of Michigan | Glucosylceramide synthase inhibitors and therapeutic methods using the same |
| RU2014120166A (ru) * | 2011-10-20 | 2015-11-27 | ГЛЭКСОСМИТКЛАЙН ЭлЭлСи | Замещенные бициклические аза-гетероциклы и их аналоги в качестве модуляторов сиртуина |
| EP2794592A1 (en) | 2011-12-23 | 2014-10-29 | Novartis AG | Compounds for inhibiting the interaction of bcl2 with binding partners |
| US9340549B2 (en) | 2012-03-05 | 2016-05-17 | Amgen Inc. | Oxazolidinone compounds and derivatives thereof |
| RU2014140739A (ru) | 2012-03-09 | 2016-04-27 | Лексикон Фармасьютикалз, Инк. | Соединения на основе имидазо[1, 2-b]пиридазина, композиции таких соединений и способы их применения |
| DK2822555T3 (en) | 2012-03-09 | 2018-02-05 | Lexicon Pharmaceuticals Inc | Inhibition of adapter-associated kinase 1 for the treatment of pain |
| WO2013148333A1 (en) | 2012-03-28 | 2013-10-03 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Salicylic acid derivatives useful as glucocerebrosidase activators |
| KR20150020228A (ko) | 2012-05-31 | 2015-02-25 | 에프. 호프만-라 로슈 아게 | 아미노퀴나졸린 및 피리도피리미딘 유도체 |
| EP2865671B1 (en) | 2012-06-22 | 2017-11-01 | Sumitomo Chemical Company, Ltd | Fused heterocyclic compound |
| WO2014025651A1 (en) | 2012-08-06 | 2014-02-13 | Amgen Inc. | Chroman derivatives as trpm8 inhibitors |
| EA201590482A1 (ru) | 2012-09-05 | 2015-07-30 | Байер Кропсайенс Аг | Применение замещенных 2-амидобензимидазолов, 2-амидобензоксазолов и 2-амидобензотиазолов или их солей в качестве биологически активных веществ против абиотического стресса растений |
| US9573954B2 (en) | 2012-11-16 | 2017-02-21 | University Health Network | Pyrazolopyrimidine compounds |
| WO2014085607A1 (en) | 2012-11-29 | 2014-06-05 | Karyopharm Therapeutics Inc. | Substituted 2,3-dihydrobenzofuranyl compounds and uses thereof |
| SI2941432T1 (en) | 2012-12-07 | 2018-07-31 | Vertex Pharmaceuticals Incorporated | 2-AMINO-6-FLUORO-N- (5-FLUORO-4- (4- (4- (OXETHAN-3-YL) PIPERAZIN-1-CARBONYL) PIPERIDIN-1-YLIPRIDIN-3-YL) 1,5 ALFA) PYRIMIDINE-3-CARBOXAMIDE AS ATR KINAZE INHIBITOR |
| KR20140086002A (ko) | 2012-12-28 | 2014-07-08 | 한미약품 주식회사 | Fms 키나아제 저해 활성을 갖는 피리다진 접합고리 유도체 |
| EP2970266B1 (en) | 2013-03-15 | 2018-01-31 | Epizyme, Inc. | 1-phenoxy-3-(alkylamino)-propan-2-ol derivatives as carm1 inhibitors and uses thereof |
| EP3035921A1 (en) | 2013-08-20 | 2016-06-29 | Bristol-Myers Squibb Company | Imidazopyridazine kinase inhibitors useful to treating a disease or disorder mediated by aak1, such as alzheimer's disease, bipolar disorder, pain, schizophrenia |
| CN105658653A (zh) | 2013-08-23 | 2016-06-08 | 因赛特公司 | 可用作pim激酶抑制剂的呋喃并-和噻吩并-吡啶甲酰胺化合物 |
| TW201542550A (zh) | 2013-09-06 | 2015-11-16 | Lexicon Pharmaceuticals Inc | 吡唑并[1,5-a]嘧啶基化合物、包含彼之組合物以及使用彼之方法 |
| AR097543A1 (es) | 2013-09-06 | 2016-03-23 | Lexicon Pharmaceuticals Inc | COMPUESTOS BASADOS EN IMIDAZO[1,2-b]PIRIDAZINA, COMPOSICIONES QUE LOS COMPRENDEN Y SUS MÉTODOS DE USO |
| ES2895490T3 (es) | 2014-03-27 | 2022-02-21 | Acad Medisch Ct | Iminoazúcares N-(5-(bifen-4-ilmetiloxi)pentil)-sustituidos como inhibidores de glucosilceramida sintasa |
| TW201613925A (en) | 2014-07-10 | 2016-04-16 | Incyte Corp | Imidazopyrazines as LSD1 inhibitors |
| AU2015342883B2 (en) | 2014-11-06 | 2020-07-02 | Bial - R&D Investments, S.A. | Substituted pyrrolo(1,2-a)pyrimidines and their use in the treatment of medical disorders |
| WO2016073889A1 (en) | 2014-11-06 | 2016-05-12 | Lysosomal Therapeutics Inc. | Substituted imidazo[1,5-a]pyrimidines and their use in the treatment of medical disorders |
| HRP20240644T1 (hr) | 2014-11-06 | 2024-08-02 | Bial-R&D Investments, S.A. | Supstituirani pirazolo(1,5-a)pirimidini i njihova uporaba u liječenju medicinskih poremećaja |
| CN108290894A (zh) | 2015-07-01 | 2018-07-17 | 西北大学 | 被取代的4-甲基-吡咯并[1,2-a]嘧啶-8-甲酰胺类化合物及其调节葡糖脑苷脂酶活性的用途 |
| JP2018525345A (ja) | 2015-07-01 | 2018-09-06 | ノースウェスタン ユニバーシティ | 置換キナゾリン化合物及びグルコセレブロシダーゼ活性の調節のためのその使用 |
| WO2017040877A1 (en) | 2015-09-04 | 2017-03-09 | Lysosomal Therapeutics Inc. | Heterobicyclic pyrimidinone compounds and their use in the treatment of medical disorders |
| RS63359B1 (sr) | 2015-11-06 | 2022-07-29 | Incyte Corp | Heterociklična jedinjenja kao inhibitori pi3k-gama |
| US10479793B2 (en) | 2015-11-18 | 2019-11-19 | Bristol-Myers Squibb Company | Imidazopyridazine compounds useful as modulators of IL-12, IL-23 and/or IFN alpha responses |
| EP3416967B1 (en) | 2016-02-18 | 2022-02-09 | F. Hoffmann-La Roche AG | Therapeutic compounds, compositions and methods of use thereof |
| US11192892B2 (en) | 2016-04-06 | 2021-12-07 | Bial—R&D Investments, S.A. | Substituted pyrazolo[1,5-a]pyrimidines for the treatment of medical disorders |
| CA3020305A1 (en) | 2016-04-06 | 2017-10-12 | Lysosomal Therapeutics Inc. | Imidazo [1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
| EP3440081A4 (en) | 2016-04-06 | 2019-09-18 | Lysosomal Therapeutics Inc. | PYRROLO [1,2-A] PYRIMIDINYL-CARBOXAMIDE COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDER |
| EP3452045A1 (en) | 2016-05-04 | 2019-03-13 | Lysosomal Therapeutics Inc. | Methods of treatment and combination therapies using gcase activator heterobicyclic and related compounds |
| SG11201809693SA (en) | 2016-05-05 | 2018-11-29 | Lysosomal Therapeutics Inc | SUBSTITUTED IMIDAZO[1,2-b]PYRIDAZINES, SUBSTITUTED IMIDAZO[1,5-b]PYRIDAZINES, RELATED COMPOUNDS, AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS |
| WO2017192929A1 (en) | 2016-05-05 | 2017-11-09 | Lysosomal Therapeutics Inc. | SUBSTITUTED PYRROLO[1,2-α]TRIAZINES AND RELATED COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS |
| EP3452455A4 (en) | 2016-05-05 | 2019-11-13 | Lysosomal Therapeutics Inc. | SUBSTITUTED IMDAZO [1,2-] PYRIDINES, SUBSTITUTED IMIDAZO [1,2-] PYRAZINES, RELATED COMPOUNDS AND THEIR USE IN THE TREATMENT OF ILLNESSES |
| JP2021506920A (ja) | 2017-12-21 | 2021-02-22 | リソソーマル・セラピューティクス・インコーポレイテッドLysosomal Therapeutics Inc. | 結晶性の置換シクロヘキシルピラゾロ[1,5−a]ピリミジニルカルボキサミド化合物およびその治療的使用 |
-
2017
- 2017-04-06 US US16/091,311 patent/US11192892B2/en active Active
- 2017-04-06 WO PCT/US2017/026280 patent/WO2017176960A1/en not_active Ceased
- 2017-04-06 JP JP2018552683A patent/JP7038063B2/ja not_active Expired - Fee Related
- 2017-04-06 KR KR1020187032153A patent/KR20180133461A/ko not_active Ceased
- 2017-04-06 AU AU2017246455A patent/AU2017246455B2/en not_active Ceased
- 2017-04-06 MX MX2018012211A patent/MX2018012211A/es unknown
- 2017-04-06 BR BR112018070586A patent/BR112018070586A8/pt not_active Application Discontinuation
- 2017-04-06 CN CN201780034861.3A patent/CN109311887B/zh not_active Expired - Fee Related
- 2017-04-06 KR KR1020237021557A patent/KR20230104752A9/ko not_active Withdrawn
- 2017-04-06 SG SG11201808830YA patent/SG11201808830YA/en unknown
- 2017-04-06 CA CA3020287A patent/CA3020287A1/en active Pending
- 2017-04-06 EP EP17779797.4A patent/EP3440080A4/en not_active Withdrawn
- 2017-08-16 US US15/678,474 patent/US9840510B1/en active Active
-
2018
- 2018-10-07 IL IL262177A patent/IL262177B/en unknown
-
2019
- 2019-03-18 US US16/356,564 patent/US10934298B2/en active Active
-
2021
- 2021-10-25 US US17/509,353 patent/US12116369B2/en active Active
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004277337A (ja) | 2003-03-14 | 2004-10-07 | Sumitomo Pharmaceut Co Ltd | ピラゾロ[1,5−a]ピリミジン誘導体 |
| WO2005113004A2 (en) | 2004-05-14 | 2005-12-01 | The Cleveland Clinic Founfation | Small molecule inhibitors for mrp1 and other multidrug transporters |
| JP2008530155A (ja) | 2005-02-17 | 2008-08-07 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | ピラゾロピリミジン類 |
| WO2007048066A2 (en) | 2005-10-21 | 2007-04-26 | Exelixis, Inc. | Pyrazolo-pyrimidines as casein kinase ii (ck2) modulators |
| WO2010086040A1 (en) | 2009-01-29 | 2010-08-05 | Biomarin Iga, Ltd. | Pyrazolo-pyrimidines for treatment of duchenne muscular dystrophy |
| WO2012075393A2 (en) | 2010-12-02 | 2012-06-07 | President And Fellows Of Harvard College | Activators of proteasomal degradation and uses thereof |
| WO2012078855A1 (en) | 2010-12-08 | 2012-06-14 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Substituted pyrazolopyrimidines as glucocerebrosidase activators |
| WO2014141129A2 (en) | 2013-03-14 | 2014-09-18 | Grueneberg Dorre A | Novel methods, compounds, and compositions for inhibition of ros |
| WO2015012328A1 (ja) | 2013-07-24 | 2015-01-29 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2015073267A1 (en) | 2013-11-15 | 2015-05-21 | Calitor Sciences, Llc | Substituted heteroaryl compounds and methods of use |
Non-Patent Citations (4)
| Title |
|---|
| AHMETAJ,Sizana,Parallel synthesis of 7-heteroaryl-pyrazolo[1,5-a]pyrimidine-3-carboxamides,Mol.Divers,2013年,17,731-743 |
| DALINGER, IGOR L.,Liquid-phase synthesis of combinatorial libraries based on 7-trifluoromethyl-substituted pyrazolo[1,5-a]pyrimidine scaffold,Journal of Conbinatorial Chemistry [ONLINE],2005年,7(2),236-245 |
| PATNAIK, S.,Discovery, Structure-Activity Relationship, and Biological Evaluation of Noninhibitory Small Molecul,Journal of Medicinal Chemistry,2012年,55(12),5734-5748 |
| WANG, X.,Discovery of novel pyrazolo[1,5-a]pyrimidines as potent pan-Pim inhibitors by structure- and propert,Bioorganic & Medicinal Chemistry Letters,2013年,23(11),3149-3153 |
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| EP3440080A1 (en) | 2019-02-13 |
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| BR112018070586A2 (pt) | 2019-02-05 |
| CN109311887A (zh) | 2019-02-05 |
| AU2017246455B2 (en) | 2021-09-30 |
| WO2017176960A1 (en) | 2017-10-12 |
| US20200017507A1 (en) | 2020-01-16 |
| IL262177B (en) | 2022-06-01 |
| AU2017246455A1 (en) | 2018-10-25 |
| EP3440080A4 (en) | 2020-01-22 |
| RU2018138688A3 (https=) | 2020-08-31 |
| US20170349598A1 (en) | 2017-12-07 |
| US11192892B2 (en) | 2021-12-07 |
| BR112018070586A8 (pt) | 2023-03-14 |
| US20190330213A1 (en) | 2019-10-31 |
| KR20230104752A (ko) | 2023-07-10 |
| SG11201808830YA (en) | 2018-11-29 |
| IL262177A (en) | 2018-11-29 |
| JP2019510790A (ja) | 2019-04-18 |
| MX2018012211A (es) | 2019-03-28 |
| KR20230104752A9 (ko) | 2024-11-15 |
| CA3020287A1 (en) | 2017-10-12 |
| RU2018138688A (ru) | 2020-05-19 |
| US12116369B2 (en) | 2024-10-15 |
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