AR114237A1 - Compuesto de amida heterocíclica que contiene nitrógeno y su uso farmacéutico - Google Patents
Compuesto de amida heterocíclica que contiene nitrógeno y su uso farmacéuticoInfo
- 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
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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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- 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
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- 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
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- 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
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- 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
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- 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
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- 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
Landscapes
- 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)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cardiology (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Hospice & Palliative Care (AREA)
- Biomedical Technology (AREA)
- Vascular Medicine (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Microbiology (AREA)
- General Engineering & Computer Science (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Molecular Biology (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.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2018016328 | 2018-02-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR114237A1 true AR114237A1 (es) | 2020-08-05 |
Family
ID=67479787
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP190100202A AR114237A1 (es) | 2018-02-01 | 2019-01-30 | Compuesto de amida heterocíclica que contiene nitrógeno y su uso farmacéutico |
Country Status (20)
Country | Link |
---|---|
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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112638377A (zh) | 2018-09-11 | 2021-04-09 | 日本烟草产业株式会社 | 含有吡唑酰胺化合物的慢性肾脏病的治疗或预防剂 |
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 |
IL295281A (en) | 2020-02-07 | 2022-10-01 | Gasherbrum Bio Inc | Heterocyclic glp-1 agonists |
CA3166747A1 (en) * | 2020-03-04 | 2021-09-10 | Japan Tobacco Inc. | Fused tricyclic compound and medicinal use thereof |
JP2023540609A (ja) * | 2020-09-10 | 2023-09-25 | 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 |
WO2023032940A1 (ja) | 2021-09-01 | 2023-03-09 | 日本たばこ産業株式会社 | 含窒素三環性化合物及びその医薬用途 |
Family Cites Families (23)
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 |
PE20090319A1 (es) * | 2007-06-01 | 2009-03-27 | Schering Corp | Moduladores de gamma secretasa |
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 |
BR112013033098B8 (pt) | 2011-06-27 | 2021-03-23 | Alectos Therapeutics Inc | inibidores de glicosidade seletivos e usos dos mesmos |
WO2013074388A1 (en) * | 2011-11-15 | 2013-05-23 | Merck Sharp & Dohme Corp. | Substituted cyclopropyl compounds useful as gpr119 agonists |
NZ630488A (en) | 2012-06-12 | 2016-07-29 | Chong Kun Dang Pharm Corp | Piperidine derivatives for gpr119 agonist |
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 | ||
WO2015002119A1 (ja) | 2013-07-01 | 2015-01-08 | 日本たばこ産業株式会社 | ピラゾール-アルコール化合物およびその医薬用途 |
TW201536748A (zh) * | 2013-07-01 | 2015-10-01 | Japan Tobacco Inc | 茀-醯胺化合物及其醫藥用途 |
GB201316823D0 (en) | 2013-09-23 | 2013-11-06 | R & D Vernalis Ltd | New Chemical Entities |
JP6527520B2 (ja) | 2013-12-17 | 2019-06-05 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | ピルビン酸脱水素酵素キナーゼの阻害剤としてのn1−(3,3,3−トリフルオロ−2−ヒドロキソ−2−メチルプロピオニル)−ピペリジン誘導体 |
WO2017020981A1 (en) | 2015-07-31 | 2017-02-09 | Merck Patent Gmbh | Bicyclic heterocyclic derivatives |
JP6923551B2 (ja) | 2016-03-29 | 2021-08-18 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | ピルバートデヒドロゲナーゼキナーゼのインヒビターとしてのn1−(3,3,3−トリフルオロ−2−ヒドロキシ−2−メチルプロピオニル)−ピペリジン誘導体 |
JP7028792B2 (ja) * | 2016-04-28 | 2022-03-02 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | ピペリジニル誘導体 |
RU2736722C2 (ru) * | 2016-07-29 | 2020-11-19 | Джапан Тобакко Инк. | Способ получения соединения пиразоламида |
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 |
BR112018013247A2 (pt) | 2016-10-28 | 2018-12-04 | H Lundbeck As | tratamentos de combinação compreendendo imidazopirazinonas para o tratamento de distúrbios psiquiátricos e/ou cognitivos |
EP3532053A1 (en) | 2016-10-28 | 2019-09-04 | H. Lundbeck A/S | Combination treatments comprising administration of imidazopyrazinones |
CA3166747A1 (en) * | 2020-03-04 | 2021-09-10 | Japan Tobacco Inc. | Fused tricyclic compound and medicinal use thereof |
WO2023032940A1 (ja) * | 2021-09-01 | 2023-03-09 | 日本たばこ産業株式会社 | 含窒素三環性化合物及びその医薬用途 |
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2019
- 2019-01-30 SG SG11202006916SA patent/SG11202006916SA/en unknown
- 2019-01-30 TW TW108103504A patent/TWI803570B/zh active
- 2019-01-30 CN CN201980010396.9A patent/CN111655692B/zh active Active
- 2019-01-30 EP EP19747660.9A patent/EP3747888A4/en active Pending
- 2019-01-30 AU AU2019214048A patent/AU2019214048B2/en active Active
- 2019-01-30 KR KR1020207024426A patent/KR20200115566A/ko not_active Application Discontinuation
- 2019-01-30 WO PCT/JP2019/003052 patent/WO2019151274A1/ja active Application Filing
- 2019-01-30 PE PE2020001125A patent/PE20211273A1/es unknown
- 2019-01-30 CA CA3090219A patent/CA3090219A1/en active Pending
- 2019-01-30 AR ARP190100202A patent/AR114237A1/es unknown
- 2019-01-30 JP JP2019013745A patent/JP7241556B2/ja active Active
- 2019-01-30 MX MX2020008126A patent/MX2020008126A/es unknown
- 2019-01-30 US US16/261,792 patent/US10800784B2/en active Active
- 2019-01-30 BR BR112020014177-1A patent/BR112020014177A2/pt unknown
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2020
- 2020-07-14 PH PH12020500613A patent/PH12020500613A1/en unknown
- 2020-07-21 SA SA520412473A patent/SA520412473B1/ar unknown
- 2020-07-22 ZA ZA2020/04548A patent/ZA202004548B/en unknown
- 2020-07-29 IL IL276386A patent/IL276386B2/en unknown
- 2020-07-29 CO CONC2020/0009420A patent/CO2020009420A2/es unknown
- 2020-07-30 CL CL2020002003A patent/CL2020002003A1/es unknown
- 2020-10-08 US US17/065,679 patent/US20210284644A1/en not_active Abandoned
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2023
- 2023-03-07 JP JP2023034806A patent/JP2023071925A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
MX2020008126A (es) | 2020-09-18 |
EP3747888A1 (en) | 2020-12-09 |
US20200017505A1 (en) | 2020-01-16 |
JP2023071925A (ja) | 2023-05-23 |
CO2020009420A2 (es) | 2020-08-10 |
JP2019131544A (ja) | 2019-08-08 |
SG11202006916SA (en) | 2020-08-28 |
RU2020128593A (ru) | 2022-03-03 |
US10800784B2 (en) | 2020-10-13 |
CN111655692A (zh) | 2020-09-11 |
TW201934553A (zh) | 2019-09-01 |
EP3747888A4 (en) | 2021-12-15 |
AU2019214048A1 (en) | 2020-06-25 |
AU2019214048B2 (en) | 2023-03-16 |
ZA202004548B (en) | 2021-10-27 |
CL2020002003A1 (es) | 2020-10-23 |
PE20211273A1 (es) | 2021-07-19 |
CN111655692B (zh) | 2023-10-10 |
IL276386B2 (en) | 2023-06-01 |
IL276386A (en) | 2020-09-30 |
SA520412473B1 (ar) | 2023-02-12 |
US20210284644A1 (en) | 2021-09-16 |
KR20200115566A (ko) | 2020-10-07 |
JP7241556B2 (ja) | 2023-03-17 |
BR112020014177A2 (pt) | 2020-12-08 |
WO2019151274A1 (ja) | 2019-08-08 |
TWI803570B (zh) | 2023-06-01 |
PH12020500613A1 (en) | 2021-05-31 |
CA3090219A1 (en) | 2019-08-08 |
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