CR20190200A - Deribados de 5-[2-(pirldin-2-ilamino)-1,3-tiazol-5-il]-2,3-dihidro-1h-isoindol-1-ona y su uso como inhibidores dobles de fosfatidilinositol-3-cinasa delta y gamma campo técnico - Google Patents

Deribados de 5-[2-(pirldin-2-ilamino)-1,3-tiazol-5-il]-2,3-dihidro-1h-isoindol-1-ona y su uso como inhibidores dobles de fosfatidilinositol-3-cinasa delta y gamma campo técnico

Info

Publication number
CR20190200A
CR20190200A CR20190200A CR20190200A CR20190200A CR 20190200 A CR20190200 A CR 20190200A CR 20190200 A CR20190200 A CR 20190200A CR 20190200 A CR20190200 A CR 20190200A CR 20190200 A CR20190200 A CR 20190200A
Authority
CR
Costa Rica
Prior art keywords
phosphatidylinositol
gamma
kinase
compounds
isoindol
Prior art date
Application number
CR20190200A
Other languages
English (en)
Inventor
Jeans Petersen
Peter Bold
Christian Tyrchan
Ulf Börjesson
Matthew Perry
Kostantinos Karabelas
Antonios Nikitidis
Mickael Mogemark
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 CR20190200A publication Critical patent/CR20190200A/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/427Thiazoles not condensed and containing further heterocyclic rings
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pulmonology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Se dan a conocer ciertos compuestos nuevos (que incluyen sales farmacéuticamente aceptables de estos), que inhiben la actividad de fosfatidilinositol¿¿3-cinasa gamma (PI3Kd) y fosfatidilinositol¿¿3-cinasa gamma (PI3Ky), a su utilidad en el tratamiento y/o la prevención de afecciones clínicas que incluyen enfermedades respiratorias, tales como el asma y la enfermedad pulmonar obstructiva crónica (EPOC), a su uso en terapia, a composiciones farmacéuticas que los contienen y a procesos para preparar tales compuestos.There are disclosed certain novel compounds (including pharmaceutically acceptable salts thereof) (I) that inhibit phosphatidylinositol 3-kinase gamma (PI3Kd) and phosphatidylinositol 3-kinase gamma (¿¿3¿¿) activity, to their utility in treating and/or preventing clinical conditions including respiratory diseases, such as asthma and chronic obstructive pulmonary disease (COPD), to their use in therapy, to pharmaceutical compositions containing them and to processes for preparing such compounds.
CR20190200A 2016-09-22 2017-09-21 Deribados de 5-[2-(pirldin-2-ilamino)-1,3-tiazol-5-il]-2,3-dihidro-1h-isoindol-1-ona y su uso como inhibidores dobles de fosfatidilinositol-3-cinasa delta y gamma campo técnico CR20190200A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662398006P 2016-09-22 2016-09-22
PCT/EP2017/073916 WO2018055040A1 (en) 2016-09-22 2017-09-21 5-[2-(pyridin-2-ylamino)-1,3-thiazol-5-yl]-2,3-dihydro-1 h-isoindol-1 -one derivatives and their use as dual inhibitors of phosphatidylinositol 3-kinase delta & gamma

Publications (1)

Publication Number Publication Date
CR20190200A true CR20190200A (es) 2019-06-07

Family

ID=59966739

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20190200A CR20190200A (es) 2016-09-22 2017-09-21 Deribados de 5-[2-(pirldin-2-ilamino)-1,3-tiazol-5-il]-2,3-dihidro-1h-isoindol-1-ona y su uso como inhibidores dobles de fosfatidilinositol-3-cinasa delta y gamma campo técnico

Country Status (36)

Country Link
US (2) US10961236B2 (es)
EP (1) EP3515910B1 (es)
JP (1) JP6765516B2 (es)
KR (1) KR102226098B1 (es)
CN (1) CN109715623A (es)
AR (1) AR109706A1 (es)
AU (1) AU2017331940B2 (es)
BR (1) BR112019004719A2 (es)
CA (1) CA3036304A1 (es)
CL (1) CL2019000707A1 (es)
CO (1) CO2019003440A2 (es)
CR (1) CR20190200A (es)
CY (1) CY1123346T1 (es)
DK (1) DK3515910T3 (es)
DO (1) DOP2019000073A (es)
EA (1) EA036176B1 (es)
EC (1) ECSP19027780A (es)
ES (1) ES2818583T3 (es)
HR (1) HRP20201175T1 (es)
HU (1) HUE051634T2 (es)
IL (1) IL265298B (es)
JO (1) JOP20190052A1 (es)
LT (1) LT3515910T (es)
MA (1) MA46268B1 (es)
MX (2) MX381898B (es)
PE (1) PE20190909A1 (es)
PH (1) PH12019500615A1 (es)
PL (1) PL3515910T3 (es)
PT (1) PT3515910T (es)
RS (1) RS60764B1 (es)
SI (1) SI3515910T1 (es)
SM (1) SMT202000481T1 (es)
SV (1) SV2019005857A (es)
TW (1) TW201813967A (es)
UA (1) UA123558C2 (es)
WO (1) WO2018055040A1 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020102216A1 (en) 2018-11-13 2020-05-22 Incyte Corporation Substituted heterocyclic derivatives as pi3k inhibitors
US11161838B2 (en) 2018-11-13 2021-11-02 Incyte Corporation Heterocyclic derivatives as PI3K inhibitors
US11078204B2 (en) 2018-11-13 2021-08-03 Incyte Corporation Heterocyclic derivatives as PI3K inhibitors
JP7644023B2 (ja) * 2019-04-10 2025-03-11 ナンジン ゼンシャイン ファーマシューティカルズ カンパニー リミテッド ホスファチジルイノシトール3-キナーゼ阻害剤
CN114206332B (zh) 2019-06-04 2024-08-23 艾库斯生物科学有限公司 2,3,5-三取代吡唑并[1,5-a]嘧啶化合物
WO2022017371A1 (zh) * 2020-07-21 2022-01-27 中国医药研究开发中心有限公司 具有磷脂酰肌醇3-激酶δ和γ的双重抑制剂活性的杂环化合物及其医药用途
WO2022023456A1 (en) 2020-07-29 2022-02-03 Astrazeneca Ab Pharmaceutical compositions comprising nano embedded microparticles and methods of use
CN116813608B (zh) * 2023-06-08 2024-03-22 英矽智能科技(上海)有限公司 噻唑类化合物及其应用

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AU3113902A (en) * 2000-12-21 2002-07-01 Bristol Myers Squibb Co Thiazolyl inhibitors of tec family tyrosine kinases
GB0305152D0 (en) * 2003-03-06 2003-04-09 Novartis Ag Organic compounds
GB0320197D0 (en) * 2003-08-28 2003-10-01 Novartis Ag Organic compounds
JP2008543754A (ja) * 2005-06-09 2008-12-04 メルク エンド カムパニー インコーポレーテッド チェックポイントキナーゼの阻害剤
US7928140B2 (en) * 2007-08-02 2011-04-19 Amgen Inc. Benzothiazole PI3 kinase modulators for cancer treatment
UY33337A (es) 2010-10-18 2011-10-31 Respivert Ltd DERIVADOS SUSTITUIDOS DE 1H-PIRAZOL[ 3,4-d]PIRIMIDINA COMO INHIBIDORES DE LAS FOSFOINOSITIDA 3-QUINASAS
US9056877B2 (en) 2011-07-19 2015-06-16 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
JP6027610B2 (ja) 2011-07-19 2016-11-16 インフィニティー ファーマシューティカルズ, インコーポレイテッド 複素環式化合物及びその使用
EP2751093A1 (en) 2011-08-29 2014-07-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
AU2012318580A1 (en) 2011-10-04 2014-05-22 Gilead Calistoga Llc Novel quinoxaline inhibitors of PI3K
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
UY35332A (es) 2013-02-15 2014-11-28 Almirall Sa Derivados de pirrolotriazina como inhibidores de pi3k
CA2915418C (en) 2013-07-02 2022-05-03 Rhizen Pharmaceuticals Sa Novel selective pi3k delta and/or gamma protein kinase inhibitors
UY35675A (es) 2013-07-24 2015-02-27 Novartis Ag Derivados sustituidos de quinazolin-4-ona
EP3160968B1 (en) 2014-06-27 2018-10-31 Rhizen Pharmaceuticals S.A. Substituted chromene derivatives as selective dual inhibitors of pi3 delta and gamma protein kinases

Also Published As

Publication number Publication date
JP6765516B2 (ja) 2020-10-07
CA3036304A1 (en) 2018-03-29
SMT202000481T1 (it) 2020-11-10
WO2018055040A1 (en) 2018-03-29
PH12019500615A1 (en) 2019-06-03
EP3515910B1 (en) 2020-07-15
DOP2019000073A (es) 2019-04-15
LT3515910T (lt) 2020-10-12
CN109715623A (zh) 2019-05-03
EP3515910A1 (en) 2019-07-31
IL265298B (en) 2020-09-30
RS60764B1 (sr) 2020-10-30
KR102226098B1 (ko) 2021-03-09
MA46268A (fr) 2019-07-31
JOP20190052A1 (ar) 2019-03-21
MX2019003194A (es) 2019-06-17
MX381898B (es) 2025-03-13
ECSP19027780A (es) 2019-04-30
DK3515910T3 (da) 2020-08-31
IL265298A (en) 2019-05-30
EA201990664A1 (ru) 2019-08-30
CL2019000707A1 (es) 2019-05-31
US20200308164A1 (en) 2020-10-01
PL3515910T3 (pl) 2021-02-22
PT3515910T (pt) 2020-09-16
US20210246130A1 (en) 2021-08-12
HRP20201175T1 (hr) 2020-11-13
AR109706A1 (es) 2019-01-16
SV2019005857A (es) 2019-05-06
SI3515910T1 (sl) 2020-09-30
ES2818583T3 (es) 2021-04-13
PE20190909A1 (es) 2019-06-26
HUE051634T2 (hu) 2021-03-01
MA46268B1 (fr) 2020-08-31
UA123558C2 (uk) 2021-04-21
AU2017331940A1 (en) 2019-05-02
EA036176B1 (ru) 2020-10-09
AU2017331940B2 (en) 2020-03-12
TW201813967A (zh) 2018-04-16
BR112019004719A2 (pt) 2019-05-28
MX2021004748A (es) 2021-06-08
US10961236B2 (en) 2021-03-30
CO2019003440A2 (es) 2019-04-12
JP2019529445A (ja) 2019-10-17
KR20190049867A (ko) 2019-05-09
CY1123346T1 (el) 2022-03-24

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