MA47301B1 - Inhibiteurs sélectifs de jak1 - Google Patents

Inhibiteurs sélectifs de jak1

Info

Publication number
MA47301B1
MA47301B1 MA47301A MA47301A MA47301B1 MA 47301 B1 MA47301 B1 MA 47301B1 MA 47301 A MA47301 A MA 47301A MA 47301 A MA47301 A MA 47301A MA 47301 B1 MA47301 B1 MA 47301B1
Authority
MA
Morocco
Prior art keywords
selective jak1
jak1 inhibitors
formula
compounds
inhibitors
Prior art date
Application number
MA47301A
Other languages
English (en)
Other versions
MA47301A (fr
Inventor
Karl Nilsson
Annika Åstrand
Anna Berggren
Johan Johansson
Matti Lepistö
Sameer Kawatkar
Qibin Su
Jason Kettle
Original Assignee
Astrazeneca Ab 151 85 Soedertaelje
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 151 85 Soedertaelje filed Critical Astrazeneca Ab 151 85 Soedertaelje
Publication of MA47301A publication Critical patent/MA47301A/fr
Publication of MA47301B1 publication Critical patent/MA47301B1/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • 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
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/007—Pulmonary tract; Aromatherapy
    • A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
    • A61K9/0075—Sprays 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/14—Drugs for dermatological disorders for baldness or alopecia
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/04—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic 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)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (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

L'invention concerne d'une manière générale des composés de formule (i) et des sels pharmaceutiquement acceptables de ceux-ci. Dans la formule (i), r1-r8 peuvent prendre une quelconque des significations définies dans la description. L'invention concerne également des compositions pharmaceutiques comprenant des composés de formule (i) et leurs procédés d'utilisation.
MA47301A 2017-01-17 2018-01-16 Inhibiteurs sélectifs de jak1 MA47301B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762447057P 2017-01-17 2017-01-17
PCT/EP2018/051038 WO2018134213A1 (fr) 2017-01-17 2018-01-16 Inhibiteurs sélectifs de jak1

Publications (2)

Publication Number Publication Date
MA47301A MA47301A (fr) 2019-11-27
MA47301B1 true MA47301B1 (fr) 2023-02-28

Family

ID=61024756

Family Applications (1)

Application Number Title Priority Date Filing Date
MA47301A MA47301B1 (fr) 2017-01-17 2018-01-16 Inhibiteurs sélectifs de jak1

Country Status (38)

Country Link
US (4) US10961228B2 (fr)
EP (2) EP3571192B1 (fr)
JP (3) JP6986086B2 (fr)
KR (2) KR102659213B1 (fr)
CN (2) CN115925693B (fr)
AR (1) AR110753A1 (fr)
AU (1) AU2018209667B2 (fr)
CA (2) CA3306538A1 (fr)
CL (1) CL2019001993A1 (fr)
CO (1) CO2019007888A2 (fr)
CR (1) CR20190332A (fr)
DK (1) DK3571192T3 (fr)
DO (1) DOP2019000184A (fr)
EA (1) EA037067B1 (fr)
EC (1) ECSP19051352A (fr)
ES (1) ES2938648T3 (fr)
FI (1) FI3571192T3 (fr)
HR (1) HRP20230069T1 (fr)
HU (1) HUE061064T2 (fr)
IL (1) IL267851B (fr)
JO (1) JOP20190174B1 (fr)
LT (1) LT3571192T (fr)
MA (1) MA47301B1 (fr)
MX (2) MX390625B (fr)
MY (1) MY199735A (fr)
NI (1) NI201900077A (fr)
PE (1) PE20191108A1 (fr)
PH (1) PH12019501639B1 (fr)
PL (1) PL3571192T3 (fr)
PT (1) PT3571192T (fr)
RS (1) RS63981B1 (fr)
SG (1) SG11201906222WA (fr)
SI (1) SI3571192T1 (fr)
SM (1) SMT202300051T1 (fr)
TW (1) TWI753089B (fr)
UA (1) UA124246C2 (fr)
WO (1) WO2018134213A1 (fr)
ZA (1) ZA201906875B (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20191108A1 (es) * 2017-01-17 2019-08-26 Astrazeneca Ab Inhibidores selectivos de jak1
TWI810172B (zh) 2017-01-26 2023-08-01 南韓商韓美藥品股份有限公司 嘧啶化合物及包括其的藥學組成物
US11149029B2 (en) * 2018-07-18 2021-10-19 Astrazeneca Ab Salts of IJAK inhibitors and methods of using the same
KR101954370B1 (ko) 2018-07-25 2019-03-05 한미약품 주식회사 피리미딘 화합물 및 이를 포함하는 암의 예방 또는 치료용 약학 조성물
EP3854793A4 (fr) * 2018-09-21 2022-06-01 Shanghai Ennovabio Pharmaceuticals Co., Ltd. Composé hétérocyclique aromatique ayant une activité inhibitrice de kinase
BR112021016522A2 (pt) 2019-02-22 2021-10-26 Hanmi Pharm. Co., Ltd. Composição farmacêutica para o tratamento da leucemia mieloide aguda
AU2020258619C1 (en) * 2019-04-19 2026-01-29 Dizal (Jiangsu) Pharmaceutical Co., Ltd. JAK1 selective kinase inhibitor
EP3991733A4 (fr) 2019-06-27 2023-07-05 Hanmi Pharm. Co., Ltd. Composition pharmaceutique pour le traitement de la leucémie myéloïde aiguë contenant un inhibiteur de flt3 et des agents de chimiothérapie
CA3174321A1 (fr) 2020-04-09 2021-10-14 Disarm Therapeutics, Inc. Derives d'indazole utiles en tant qu'inhibiteurs de sarm1
WO2022111499A1 (fr) 2020-11-26 2022-06-02 深圳铂立健医药有限公司 Composé amide, composition pharmaceutique et leur utilisation
EP4297873A1 (fr) * 2021-02-26 2024-01-03 Tyra Biosciences, Inc. Composés d'aminopyrimidine et leurs procédés d'utilisation
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
WO2024150110A1 (fr) * 2023-01-11 2024-07-18 Pfizer Inc. Compositions et méthodes pour le traitement et/ou la prévention du diabète de type 1
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
KR20250174908A (ko) * 2023-03-16 2025-12-15 인사이트 코포레이션 천식의 치료를 위한 jak1 경로 저해제
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
WO2026132265A1 (fr) 2024-12-19 2026-06-25 Astrazeneca Ab Inhalateur à poudre sèche

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7799915B2 (en) 2004-10-13 2010-09-21 Wyeth Llc Anilino-pyrimidine analogs
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
WO2008097930A1 (fr) 2007-02-05 2008-08-14 Amira Pharmaceuticals, Inc. Indoles inverses en tant qu'inhibiteurs de la protéine d'activation de la 5-lipoxygénase (flap)
EP2207547A4 (fr) 2007-10-05 2010-11-17 Amira Pharmaceuticals Inc Inhibiteurs de protéine activant la 5-lipoxygénase
WO2009046416A1 (fr) * 2007-10-05 2009-04-09 Targegen Inc. Anilinopyrimidines en tant qu'inhibiteurs de kinases jak
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
CA2792508C (fr) 2010-03-10 2018-01-16 Incyte Corporation Derives de piperidin-4-yl azetidine en tant qu'inhibiteurs de jak1
RU2013114352A (ru) * 2010-09-15 2014-10-20 Ф. Хоффманн-Ля Рош Аг Азабензотиазолы, композиции и способы применения
EP3060234A1 (fr) 2013-10-24 2016-08-31 AbbVie Inc. Inhibiteur sélectif de jak1 et ses utilisations
KR102774784B1 (ko) * 2015-09-25 2025-02-27 디잘 (지앙수) 파마슈티칼 씨오., 리미티드 Jak를 억제하기 위한 화합물 및 방법
PE20191108A1 (es) * 2017-01-17 2019-08-26 Astrazeneca Ab Inhibidores selectivos de jak1

Also Published As

Publication number Publication date
CN115925693B (zh) 2024-11-12
US20240208947A1 (en) 2024-06-27
JP6986086B2 (ja) 2021-12-22
MX2019008435A (es) 2019-09-09
US11897869B2 (en) 2024-02-13
BR112019014526A2 (pt) 2020-02-27
EA037067B1 (ru) 2021-02-02
EP3571192A1 (fr) 2019-11-27
TWI753089B (zh) 2022-01-21
ES2938648T3 (es) 2023-04-13
EP3571192B1 (fr) 2022-11-30
JOP20190174A1 (ar) 2019-07-14
JP2020506171A (ja) 2020-02-27
US10961228B2 (en) 2021-03-30
WO2018134213A1 (fr) 2018-07-26
KR102585048B1 (ko) 2023-10-05
US20210188821A1 (en) 2021-06-24
DK3571192T3 (da) 2023-02-06
CN110461830B (zh) 2022-11-01
TW201838984A (zh) 2018-11-01
JP7394820B2 (ja) 2023-12-08
JP7626819B2 (ja) 2025-02-04
JP2024010041A (ja) 2024-01-23
KR20190104215A (ko) 2019-09-06
AU2018209667A1 (en) 2019-08-22
ECSP19051352A (es) 2019-07-31
JOP20190174B1 (ar) 2023-09-17
SG11201906222WA (en) 2019-08-27
CL2019001993A1 (es) 2019-12-27
CA3049175A1 (fr) 2018-07-26
KR20230141938A (ko) 2023-10-10
SMT202300051T1 (it) 2023-03-17
CN115925693A (zh) 2023-04-07
MY199735A (en) 2023-11-21
US20190367490A1 (en) 2019-12-05
HUE061064T2 (hu) 2023-05-28
PH12019501639B1 (en) 2023-09-08
US12473272B2 (en) 2025-11-18
JP2022043059A (ja) 2022-03-15
PH12019501639A1 (en) 2020-07-06
DOP2019000184A (es) 2019-08-15
CN110461830A (zh) 2019-11-15
PT3571192T (pt) 2023-02-21
CR20190332A (es) 2019-09-13
LT3571192T (lt) 2023-02-27
SI3571192T1 (sl) 2023-03-31
EA201991700A1 (ru) 2020-01-28
PL3571192T3 (pl) 2023-03-20
MX390625B (es) 2025-03-19
MA47301A (fr) 2019-11-27
EP4219470A1 (fr) 2023-08-02
IL267851B (en) 2021-08-31
UA124246C2 (uk) 2021-08-11
AR110753A1 (es) 2019-05-02
US20260028329A1 (en) 2026-01-29
KR102659213B1 (ko) 2024-04-18
AU2018209667B2 (en) 2020-05-07
IL267851A (en) 2019-09-26
FI3571192T3 (fi) 2023-03-06
NI201900077A (es) 2020-03-18
CA3306538A1 (en) 2026-05-13
HRP20230069T1 (hr) 2023-03-17
MX2022002976A (es) 2022-04-06
NZ756069A (en) 2025-08-29
MX418519B (es) 2024-12-09
CO2019007888A2 (es) 2019-07-31
PE20191108A1 (es) 2019-08-26
RS63981B1 (sr) 2023-03-31
ZA201906875B (en) 2021-05-26

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