AR114237A1 - Compuesto de amida heterocíclica que contiene nitrógeno y su uso farmacéutico - Google Patents

Compuesto de amida heterocíclica que contiene nitrógeno y su uso farmacéutico

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Publication number
AR114237A1
AR114237A1 ARP190100202A ARP190100202A AR114237A1 AR 114237 A1 AR114237 A1 AR 114237A1 AR P190100202 A ARP190100202 A AR P190100202A AR P190100202 A ARP190100202 A AR P190100202A AR 114237 A1 AR114237 A1 AR 114237A1
Authority
AR
Argentina
Prior art keywords
alkyl
independently selected
nitrogen atom
group
atom
Prior art date
Application number
ARP190100202A
Other languages
English (en)
Inventor
Nobutaka Yamaoka
Dai Motoda
Ritsuki Masuo
Masayuki Kotoku
Koichi Suzawa
Takaki Maeba
Original Assignee
Japan Tobacco Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Japan Tobacco Inc filed Critical Japan Tobacco Inc
Publication of AR114237A1 publication Critical patent/AR114237A1/es

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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
    • 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
    • A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/472—Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725—Non-condensed isoquinolines, e.g. papaverine 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
    • A61K31/495—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
    • A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring 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
    • A61K31/495—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
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • 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
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • 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
    • 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
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • 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
    • 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
    • A61P9/12—Antihypertensives
    • 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
    • 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
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/99—Enzyme inactivation by chemical treatment

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Cardiology (AREA)
  • Epidemiology (AREA)
  • Diabetes (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Genetics & Genomics (AREA)
  • Hospice & Palliative Care (AREA)
  • Biomedical Technology (AREA)
  • Pulmonology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Neurology (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Biotechnology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Neurosurgery (AREA)

Abstract

La presente proporciona un compuesto que tiene actividad inhibitoria de PDHK y útil para el tratamiento o profilaxis de diabetes (diabetes tipo 1, diabetes tipo 2, etc.), síndrome de resistencia a la insulina, síndrome metabólico, hiperglucemia, hiperlactacidemia, complicación diabéticas (neuropatía diabética, retinopatía diabética, nefropatía diabética, catarata etc.), insuficiencia cardíaca (insuficiencia cardíaca aguda, insuficiencia cardíaca crónica), cardiomiopatía, isquemia miocárdica, infarto de miocardio, angina de pecho, dislipidemia, aterosclerosis, enfermedad arterial periférica, claudicación intermitente, enfermedad pulmonar obstructiva crónica, isquemia cerebral, apoplejía cerebral, enfermedad mitocondrial, encefalomiopatía mitocondrial, cáncer, hipertensión pulmonar o enfermedad de Alzheimer. La presente se refiere a un compuesto de la fórmula [1] o la fórmula [2], o una de sus sales farmacéuticamente aceptables, donde cada símbolo significa lo mismo como se describe en la memoria descriptiva. Reivindicación 1: Un compuesto de la fórmula [1] o la fórmula [2], o una de sus sales farmacéuticamente aceptables, caracterizado porque un enlace en una línea de puntos es un enlace simple o un enlace doble; X¹ es un átomo de carbono, un átomo de nitrógeno o un átomo de oxígeno; X² es un átomo de carbono o un átomo de nitrógeno; R¹ᵃ es alquilo C₁₋₄ o alquilo C₁₋₄carbonilo; R² es halógeno, ciano o alquilo C₁₋₄; m es 0 ó 1; n es 0, 1 ó 2, cuando n es 2, cada R² es el mismo o diferente; A¹, A², A³, A⁴, A⁵, A⁶ y A⁷ se seleccionan de modo independiente de un átomo de carbono, un átomo de nitrógeno y un átomo de oxígeno; A⁸ se selecciona de un átomo de carbono y un átomo de nitrógeno, y un número total del átomo de nitrógeno y el átomo de oxígeno contenido en una fórmula estructural parcial [3] es 0, 1, 2 ó 3; t es 0 ó 1; r es 0, 1 ó 2, y un total de t y r es 1 ó 2; w es 0 ó 1; R³ y R⁴ son cada uno de modo independiente hidrógeno o alquilo C₁₋₄; Cy¹ es (1) (i) cicloalquilo C₄₋₆; o (ii) heterociclilo saturado o parcialmente saturado de 4 a 6 miembros que tiene un átomo de nitrógeno, el cicloalquilo C₄₋₆ y el heterociclilo saturado o parcialmente saturado está opcionalmente sustituido con un sustituyente seleccionado de modo independiente del grupo que consiste en alquilo C₁₋₄ y oxo, o (2) (i) fenilo o (ii) heteroarilo de 5 ó 6 miembros que tiene 1, 2 ó 3 heteroátomos seleccionados de modo independiente del grupo que consiste en un átomo de nitrógeno y un átomo de oxígeno, el fenilo y el heteroarilo están opcionalmente sustituidos con 1 ó 2 sustituyentes seleccionados de modo independiente del grupo que consiste en halógeno, ciano, carboxi, alquilo C₁₋₄, haloalquilo C₁₋₄ y cicloalquilo C₃₋₆; Cy² es (1) (i) cicloalquilo C₃₋₆ o (ii) heterociclilo saturado de 4 a 6 miembros que tiene 1 ó 2 heteroátomos seleccionados de modo independiente del grupo que consiste en un átomo de nitrógeno y un átomo de oxígeno, y el cicloalquilo C₃₋₆ y el heterociclilo saturado están opcionalmente sustituidos con 1 ó 2 sustituyentes seleccionados de modo independiente del grupo que consiste en halógeno, hidroxi y alquilo C₁₋₄, o (2) (i) fenilo o (ii) heteroarilo de 5 ó 6 miembros que tiene 1, 2, 3 ó 4 átomos de nitrógeno, y el fenilo y el heteroarilo están opcionalmente sustituidos con 1 ó 2 sustituyentes seleccionados de modo independiente del grupo que consiste en halógeno, ciano, alquilo C₁₋₄, alcoxi C₁₋₄; y alquilo C₁₋₄sulfonilo; y v es 0 ó 1.
ARP190100202A 2018-02-01 2019-01-30 Compuesto de amida heterocíclica que contiene nitrógeno y su uso farmacéutico AR114237A1 (es)

Applications Claiming Priority (1)

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JP2018016328 2018-02-01

Publications (1)

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AR114237A1 true AR114237A1 (es) 2020-08-05

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US (2) US10800784B2 (es)
EP (1) EP3747888A4 (es)
JP (2) JP7241556B2 (es)
KR (1) KR20200115566A (es)
CN (1) CN111655692B (es)
AR (1) AR114237A1 (es)
AU (1) AU2019214048B2 (es)
BR (1) BR112020014177A2 (es)
CA (1) CA3090219A1 (es)
CL (1) CL2020002003A1 (es)
CO (1) CO2020009420A2 (es)
IL (1) IL276386B2 (es)
MX (1) MX2020008126A (es)
PE (1) PE20211273A1 (es)
PH (1) PH12020500613A1 (es)
SA (1) SA520412473B1 (es)
SG (1) SG11202006916SA (es)
TW (1) TWI803570B (es)
WO (1) WO2019151274A1 (es)
ZA (1) ZA202004548B (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020054734A1 (ja) 2018-09-11 2020-03-19 日本たばこ産業株式会社 ピラゾール－アミド化合物を含有する慢性腎臓病の治療又は予防剤
CN110407744A (zh) * 2019-08-13 2019-11-05 上海毕得医药科技有限公司 一种1-(4-氨基吡啶-2-基)乙酮的合成方法
JP2023513272A (ja) 2020-02-07 2023-03-30 ガシャーブラム・バイオ・インコーポレイテッド ヘテロ環ｇｌｐ－１アゴニスト
US20230025880A1 (en) * 2020-03-04 2023-01-26 Japan Tobacco Inc. Fused tricyclic compound and medicinal use thereof
CN116368140A (zh) * 2020-09-10 2023-06-30 加舒布鲁姆生物公司 杂环glp-1激动剂
TW202319051A (zh) 2021-09-01 2023-05-16 日商日本煙草產業股份有限公司 含氮三環性化合物及其醫藥用途

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7943617B2 (en) * 2006-11-27 2011-05-17 Bristol-Myers Squibb Company Heterobicyclic compounds useful as kinase inhibitors
WO2008132162A1 (en) * 2007-04-26 2008-11-06 Boehringer Ingelheim International Gmbh 3- (sulphonylamino) -phenyl-2 -hydroxy-ethylamino derivatives useful as beta-agonists, processes for preparing them and their use as medicaments
CA2689930A1 (en) * 2007-06-01 2008-12-18 Schering Corporation Gamma secretase modulators
EP2090576A1 (en) 2008-02-01 2009-08-19 Merz Pharma GmbH & Co.KGaA 6-halo-pyrazolo[1,5-a]pyridines, a process for their preparation and their use as metabotropic glutamate receptor (mGluR) modulators
AR074797A1 (es) * 2008-10-10 2011-02-16 Japan Tobacco Inc Compuesto de fluoreno , composiciones farmaceuticas , inhibidores de pdhk y pdhk2 , metodos de tratamiento , usos de los mismos y kit comercial
KR102054744B1 (ko) * 2011-06-27 2019-12-11 알렉토스 테라퓨틱스 인크. 선택적인 글리코시다아제 저해제 및 이의 용도
EP2780337B1 (en) 2011-11-15 2017-12-20 Merck Sharp & Dohme Corp. Substituted cyclopropyl compounds useful as gpr119 agonists
ES2759010T3 (es) * 2012-06-12 2020-05-07 Chong Kun Dang Pharmaceutical Corp Derivados de piperidina como agonistas del GPR119
CN103570725B (zh) 2012-08-01 2017-03-22 中国科学院上海药物研究所 哌嗪并三唑类化合物及其制备方法和用途
NO2975028T3 (es) * 2013-03-15 2018-07-21
TW201536749A (zh) * 2013-07-01 2015-10-01 Japan Tobacco Inc 吡唑－醇化合物及其醫藥用途
JP2015028010A (ja) * 2013-07-01 2015-02-12 日本たばこ産業株式会社 フルオレン−アミド化合物およびその医薬用途
GB201316823D0 (en) 2013-09-23 2013-11-06 R & D Vernalis Ltd New Chemical Entities
CA2933927C (en) * 2013-12-17 2021-11-16 Merck Patent Gmbh N1-(3,3,3-trifluoro-2-hydroxo-2-methylpropionyl)-piperidine derivatives as inhibitors of pyruvate dehydrogenase kinase
US10526325B2 (en) 2015-07-31 2020-01-07 Merck Patent Gmbh Bicyclic heterocyclic derivatives
CA3019240A1 (en) 2016-03-29 2017-10-05 Merck Patent Gmbh N1-(3,3,3-trifluoro-2-hydroxy-2-methylpropionyl)-piperidine derivatives as inhibitors of pyruvate dehydrogenase kinase
CA3022231A1 (en) * 2016-04-28 2017-11-02 Merck Patent Gmbh Piperidinyl derivatives
US10981877B2 (en) * 2016-07-29 2021-04-20 Japan Tobacco Inc. Production method for pyrazole-amide compound
US10414774B2 (en) 2016-08-15 2019-09-17 Merck Sharp & Dohme Corp. Compound useful for altering the levels of bile acids for the treatment of diabetes and cardiometabolc disease
KR20190075068A (ko) 2016-10-28 2019-06-28 하. 룬드벡 아크티에셀스카브 정신 및/또는 인지 장애의 치료를 위한 이미다조피라지논을 포함하는 병용 치료
WO2018078042A1 (en) 2016-10-28 2018-05-03 H. Lundbeck A/S Combination treatments comprising administration of imidazopyrazinones
US20230025880A1 (en) * 2020-03-04 2023-01-26 Japan Tobacco Inc. Fused tricyclic compound and medicinal use thereof
TW202319051A (zh) * 2021-09-01 2023-05-16 日商日本煙草產業股份有限公司 含氮三環性化合物及其醫藥用途

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BR112020014177A2 (pt) 2020-12-08
PE20211273A1 (es) 2021-07-19
US10800784B2 (en) 2020-10-13
JP7241556B2 (ja) 2023-03-17
IL276386A (en) 2020-09-30
CN111655692B (zh) 2023-10-10
CL2020002003A1 (es) 2020-10-23
US20210284644A1 (en) 2021-09-16
US20200017505A1 (en) 2020-01-16
CN111655692A (zh) 2020-09-11
WO2019151274A1 (ja) 2019-08-08
IL276386B2 (en) 2023-06-01
PH12020500613A1 (en) 2021-05-31
JP2019131544A (ja) 2019-08-08
AU2019214048B2 (en) 2023-03-16
SA520412473B1 (ar) 2023-02-12
KR20200115566A (ko) 2020-10-07
EP3747888A4 (en) 2021-12-15
CA3090219A1 (en) 2019-08-08
MX2020008126A (es) 2020-09-18
CO2020009420A2 (es) 2020-08-10
TWI803570B (zh) 2023-06-01
TW201934553A (zh) 2019-09-01
ZA202004548B (en) 2021-10-27
AU2019214048A1 (en) 2020-06-25
JP2023071925A (ja) 2023-05-23
RU2020128593A (ru) 2022-03-03
SG11202006916SA (en) 2020-08-28
EP3747888A1 (en) 2020-12-09

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