[go: up one dir, main page]

AR110753A1 - Inhibidores selectivos de jak1 - Google Patents

Inhibidores selectivos de jak1

Info

Publication number
AR110753A1
AR110753A1 ARP180100104A ARP180100104A AR110753A1 AR 110753 A1 AR110753 A1 AR 110753A1 AR P180100104 A ARP180100104 A AR P180100104A AR P180100104 A ARP180100104 A AR P180100104A AR 110753 A1 AR110753 A1 AR 110753A1
Authority
AR
Argentina
Prior art keywords
methyl
chosen
ethyl
selective inhibitors
jak1 selective
Prior art date
Application number
ARP180100104A
Other languages
English (en)
Inventor
Qibin Su
Matti Juhani Lepist
Jason Grant Kettle
Sameer Pralhad Kawatkar
Johan R Johansson
Anna Ingrid Kristina Berggren
Annika Birgitta Margareta Strand
Karl Magnus Nilsson
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR110753A1 publication Critical patent/AR110753A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/007Pulmonary tract; Aromatherapy
    • A61K9/0073Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
    • A61K9/0075Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/14Drugs for dermatological disorders for baldness or alopecia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Dermatology (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Diabetes (AREA)
  • Pulmonology (AREA)
  • Otolaryngology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Se desvelan en el presente documento compuestos y sales farmacéuticamente aceptables de los mismos. Además, se desvelan composiciones farmacéuticas que comprenden compuestos y métodos de uso de los mismos. Reivindicación 1: Un compuesto de fórmula (1), en la que: cada uno de R¹, R³, y R⁴ se escoge individualmente de hidrógeno y metilo; R² se escoge de hidrógeno, metilo, y -CH₂CH₂OH; n es 1 ó 2; R⁵ se escoge de metilo, etilo, y -CH₂OR⁸; R⁶ se escoge de metilo, cloro, y flúor; R⁷ se selecciona de metilo, etilo, y ciclopropilo; y R⁸ se selecciona de metilo, etilo, y bencilo; o una sal farmacéuticamente aceptable del mismo.
ARP180100104A 2017-01-17 2018-01-17 Inhibidores selectivos de jak1 AR110753A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201762447057P 2017-01-17 2017-01-17

Publications (1)

Publication Number Publication Date
AR110753A1 true AR110753A1 (es) 2019-05-02

Family

ID=61024756

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP180100104A AR110753A1 (es) 2017-01-17 2018-01-17 Inhibidores selectivos de jak1

Country Status (38)

Country Link
US (4) US10961228B2 (es)
EP (2) EP3571192B1 (es)
JP (3) JP6986086B2 (es)
KR (2) KR102585048B1 (es)
CN (2) CN115925693B (es)
AR (1) AR110753A1 (es)
AU (1) AU2018209667B2 (es)
CA (1) CA3049175A1 (es)
CL (1) CL2019001993A1 (es)
CO (1) CO2019007888A2 (es)
CR (1) CR20190332A (es)
DK (1) DK3571192T3 (es)
DO (1) DOP2019000184A (es)
EA (1) EA037067B1 (es)
EC (1) ECSP19051352A (es)
ES (1) ES2938648T3 (es)
FI (1) FI3571192T3 (es)
HR (1) HRP20230069T1 (es)
HU (1) HUE061064T2 (es)
IL (1) IL267851B (es)
JO (1) JOP20190174B1 (es)
LT (1) LT3571192T (es)
MA (1) MA47301B1 (es)
MX (2) MX390625B (es)
MY (1) MY199735A (es)
NI (1) NI201900077A (es)
PE (1) PE20191108A1 (es)
PH (1) PH12019501639B1 (es)
PL (1) PL3571192T3 (es)
PT (1) PT3571192T (es)
RS (1) RS63981B1 (es)
SG (1) SG11201906222WA (es)
SI (1) SI3571192T1 (es)
SM (1) SMT202300051T1 (es)
TW (1) TWI753089B (es)
UA (1) UA124246C2 (es)
WO (1) WO2018134213A1 (es)
ZA (1) ZA201906875B (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI3571192T3 (fi) 2017-01-17 2023-03-06 Astrazeneca Ab Jak1-selektiivisiä inhibiittoreita
PL3514153T3 (pl) 2017-01-26 2022-01-17 Hanmi Pharm. Co., Ltd. Związek pirymidynowy i jego zastosowanie farmaceutyczne
CN112424187B (zh) * 2018-07-18 2024-06-21 阿斯利康(瑞典)有限公司 抑制jak的化合物的昔萘酸盐
KR101954370B1 (ko) 2018-07-25 2019-03-05 한미약품 주식회사 피리미딘 화합물 및 이를 포함하는 암의 예방 또는 치료용 약학 조성물
KR102669660B1 (ko) * 2018-09-21 2024-05-27 상하이 엔노바바이오 파마슈티컬스 씨오 엘티디. 키나아제 억제 활성을 가진 방향족 헤테로고리 화합물
PH12021551985A1 (en) 2019-02-22 2022-08-22 Hanmi Pharmaceutical Co Ltd Pharmaceutical composition comprising flt3 inhibitor and hypomethylating agent for treating acute myeloid leukemia
CA3134174A1 (en) * 2019-04-19 2020-10-22 Dizal (Jiangsu) Pharmaceutical Co., Ltd. Jak1 selective kinase inhibitor
US12350265B2 (en) 2019-06-27 2025-07-08 Hanmi Pharm. Co., Ltd. Pharmaceutical composition for treating acute myeloid leukemia, containing FLT3 inhibitor and chemotherapeutic agents
EP4132920B1 (en) * 2020-04-09 2025-08-13 Disarm Therapeutics, Inc. Indazole derivatives as inhibitors of sarm1
WO2022111499A1 (zh) * 2020-11-26 2022-06-02 深圳铂立健医药有限公司 一种酰胺化合物、药物组合物及其应用
CA3211124A1 (en) * 2021-02-26 2022-09-01 Tyra Biosciences, Inc. Aminopyrimidine compounds and methods of their use
US12240836B2 (en) * 2022-07-05 2025-03-04 Dong-A St Co., Ltd. Compounds as GCN2 inhibitors, pharmaceutical compositions and uses thereof
CN115260128B (zh) * 2022-09-21 2022-12-09 苏州凯瑞医药科技有限公司 一种新型jak抑制剂关键中间体的制备方法
EP4648776A1 (en) * 2023-01-11 2025-11-19 Pfizer Inc. Compositions and methods for the treatment and/or prevention of type 1 diabetes
CN115974845B (zh) * 2023-01-19 2024-09-20 奥锐特药业股份有限公司 奥希替尼中间体的制备方法
AU2024236890A1 (en) * 2023-03-16 2025-09-25 Incyte Corporation Jak1 pathway inhibitors for the treatment of asthma
GB202316063D0 (en) 2023-10-20 2023-12-06 Astrazeneca Ab Dosing regime
GB202403369D0 (en) 2024-03-08 2024-04-24 Astrazeneca Ab Process and intermediates for the production of a jak1 inhibitor

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2007114080A (ru) 2004-10-13 2008-11-27 Вайет (Us) N-бензилсульфонил-замещенные аналоги анилинопиримидина
GB2431927B (en) * 2005-11-04 2010-03-17 Amira Pharmaceuticals Inc 5-Lipoxygenase-activating protein (FLAP) inhibitors
CN101421250A (zh) * 2006-01-30 2009-04-29 埃克塞里艾克西斯公司 作为jak-2调节剂的4-芳基-2-氨基-嘧啶或4-芳基-2-氨基烷基-嘧啶及包含它们的药物组合物
JP2010518025A (ja) * 2007-02-05 2010-05-27 アミラ ファーマシューティカルス,インコーポレーテッド 5−リポキシゲナーゼ活性化タンパク質(flap)インヒビターとしての逆インドール
JP2010540641A (ja) * 2007-10-05 2010-12-24 アミラ ファーマシューティカルス,インコーポレーテッド 5−リポキシゲナーゼ活性化タンパク質(flap)阻害剤
WO2009046416A1 (en) * 2007-10-05 2009-04-09 Targegen Inc. Anilinopyrimidines as jak kinase inhibitors
GB0805477D0 (en) * 2008-03-26 2008-04-30 Univ Nottingham Pyrimidines triazines and their use as pharmaceutical agents
UA110324C2 (en) * 2009-07-02 2015-12-25 Genentech Inc Jak inhibitory compounds based on pyrazolo pyrimidine
SI3354652T1 (sl) 2010-03-10 2020-08-31 Incyte Holdings Corporation Derivati piperidin-4-il azetidina kot inhibitorji JAK1
CA2812087A1 (en) * 2010-09-15 2012-03-22 F. Hoffmann-La Roche Ag Azabenzothiazole compounds, compositions and methods of use
JP2016539927A (ja) 2013-10-24 2016-12-22 アッヴィ・インコーポレイテッド Jak1選択的阻害剤とその使用
RU2760359C2 (ru) 2015-09-25 2021-11-24 Дизал (Цзянсу) Фармасьютикалз Ко., Лимитед Соединения и способы для ингибирования JAK
FI3571192T3 (fi) * 2017-01-17 2023-03-06 Astrazeneca Ab Jak1-selektiivisiä inhibiittoreita

Also Published As

Publication number Publication date
HRP20230069T1 (hr) 2023-03-17
FI3571192T3 (fi) 2023-03-06
UA124246C2 (uk) 2021-08-11
WO2018134213A1 (en) 2018-07-26
US20260028329A1 (en) 2026-01-29
MA47301A (fr) 2019-11-27
AU2018209667A1 (en) 2019-08-22
SI3571192T1 (sl) 2023-03-31
HUE061064T2 (hu) 2023-05-28
ECSP19051352A (es) 2019-07-31
MX2022002976A (es) 2022-04-06
SG11201906222WA (en) 2019-08-27
PT3571192T (pt) 2023-02-21
CR20190332A (es) 2019-09-13
SMT202300051T1 (it) 2023-03-17
US20210188821A1 (en) 2021-06-24
CN115925693A (zh) 2023-04-07
EP3571192A1 (en) 2019-11-27
IL267851B (en) 2021-08-31
KR102659213B1 (ko) 2024-04-18
US11897869B2 (en) 2024-02-13
US10961228B2 (en) 2021-03-30
EP3571192B1 (en) 2022-11-30
AU2018209667B2 (en) 2020-05-07
LT3571192T (lt) 2023-02-27
MX390625B (es) 2025-03-19
MY199735A (en) 2023-11-21
KR20190104215A (ko) 2019-09-06
PL3571192T3 (pl) 2023-03-20
JP2022043059A (ja) 2022-03-15
PH12019501639A1 (en) 2020-07-06
RS63981B1 (sr) 2023-03-31
CN115925693B (zh) 2024-11-12
US20240208947A1 (en) 2024-06-27
DK3571192T3 (da) 2023-02-06
EP4219470A1 (en) 2023-08-02
JP7394820B2 (ja) 2023-12-08
IL267851A (en) 2019-09-26
CN110461830B (zh) 2022-11-01
EA201991700A1 (ru) 2020-01-28
JOP20190174A1 (ar) 2019-07-14
ES2938648T3 (es) 2023-04-13
ZA201906875B (en) 2021-05-26
JOP20190174B1 (ar) 2023-09-17
CO2019007888A2 (es) 2019-07-31
CN110461830A (zh) 2019-11-15
JP6986086B2 (ja) 2021-12-22
CA3049175A1 (en) 2018-07-26
MA47301B1 (fr) 2023-02-28
PE20191108A1 (es) 2019-08-26
NZ756069A (en) 2025-08-29
KR102585048B1 (ko) 2023-10-05
TW201838984A (zh) 2018-11-01
PH12019501639B1 (en) 2023-09-08
US12473272B2 (en) 2025-11-18
JP2024010041A (ja) 2024-01-23
KR20230141938A (ko) 2023-10-10
US20190367490A1 (en) 2019-12-05
EA037067B1 (ru) 2021-02-02
CL2019001993A1 (es) 2019-12-27
NI201900077A (es) 2020-03-18
JP2020506171A (ja) 2020-02-27
MX418519B (es) 2024-12-09
MX2019008435A (es) 2019-09-09
JP7626819B2 (ja) 2025-02-04
TWI753089B (zh) 2022-01-21
BR112019014526A2 (pt) 2020-02-27
DOP2019000184A (es) 2019-08-15

Similar Documents

Publication Publication Date Title
AR110753A1 (es) Inhibidores selectivos de jak1
AR119424A1 (es) Derivados de 3-oxo-4h-quinoxalina y oxo-1h-naftiridina como inhibidores de parp
AR111820A1 (es) Derivados de indolina sustituidos como inhibidores de la replicación de virus del dengue
AR111233A1 (es) Inhibidores de tyk2, usos y métodos para la producción de los mismos
ECSP17007208A (es) Derivados de indano e indolina y el uso de los mismos como activadores de la guanilato ciclasa soluble
NI201700020A (es) Compuestos de aminopirimidinilo como inhibidores de jak
AR087711A1 (es) Inhibidores de quinurenina-3-monooxigenasa, composiciones farmaceuticas y uso de los mismos para el tratamiento de trastornos neurodegenerativos
UY37133A (es) Derivados de pirazolo[1,5-a]pirazin-4-ilo
AR090590A1 (es) COMPUESTOS 1,3,4-OXADIAZOL Y 1,3,4-TIADIAZOL COMO INHIBIDORES DE b-LACTAMASA
AR088535A1 (es) Derivados de amidas de aminoacidos sustituidos con n-urea como moduladores de receptor formil peptido del receptor del tipo 1 (fprl-1)
GT200900283A (es) "terapia de combinación con un compuesto actuando como un inhibidor del receptor adp plaquetario".
CR20150371A (es) Inhibidores de prmt5 y sus usos
AR101189A1 (es) Heterociclos nitrogenados antiproliferativos y sus métodos de uso
UY33501A (es) Derivados de acil sulfonamida y sus sales farmacéuticamente aceptables para uso en medicina
AR107927A1 (es) Compuestos de pirrolidina, sal farmacéuticamente aceptable del mismo, composición farmacéutica que lo comprende y su uso para la fabricación de un medicamento
AR089143A1 (es) Triazolopiridinas sustituidas con actividad inhibidora de ttk
AR111315A1 (es) Derivados de indolina sustituidos como inhibidores de la replicación vírica de dengue
AR100806A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
CO2019006220A2 (es) Compuestos de pirazolopirimidina y métodos de uso de los mismos
CU24434B1 (es) Compuestos derivados de n-(1,5-dimetil-3-oxo-2,3-dihidro-1h-pirazol-4-il)-4-metil-5-isoxazol-3-carboxamida activos como inhibidores selectivos de smurf-1
PE20211246A1 (es) Compuestos biciclicos para su uso como inhibidores de rip1 quinasa
AR118729A1 (es) Inhibidor selectivo de la jak1 quinasa
CU20190042A7 (es) Compuestos derivados de naftiridinona
JOP20190050A1 (ar) مثبطات دوبامين-b-هيدروكسيلاز تخترق حاجز المخ الدموي
ECSP20026023A (es) Derivados de piridinona y su uso como inhibidores selectivos de alk–2.