MA46268A - Dérivés de 5-[2-(pyridin-2-ylamino)-1,3-thiazol-5-yl]-2,3-dihydro-1h-isoindol-1-one et leur utilisation en tant qu'inhibiteurs doubles de phosphatidylinositol 3-kinase delta & gamma - Google Patents

Dérivés de 5-[2-(pyridin-2-ylamino)-1,3-thiazol-5-yl]-2,3-dihydro-1h-isoindol-1-one et leur utilisation en tant qu'inhibiteurs doubles de phosphatidylinositol 3-kinase delta & gamma

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Publication number
MA46268A
MA46268A MA046268A MA46268A MA46268A MA 46268 A MA46268 A MA 46268A MA 046268 A MA046268 A MA 046268A MA 46268 A MA46268 A MA 46268A MA 46268 A MA46268 A MA 46268A
Authority
MA
Morocco
Prior art keywords
phosphatidylinositol
gamma
isoindol
ylamino
thiazol
Prior art date
Application number
MA046268A
Other languages
English (en)
Other versions
MA46268B1 (fr
Inventor
Peter Bold
Ulf Börjesson
Konstantinos Karabelas
Mickael Mogemark
Antonios Nikitidis
Matthew Perry
Jens Petersen
Christian Tyrchan
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 MA46268A publication Critical patent/MA46268A/fr
Publication of MA46268B1 publication Critical patent/MA46268B1/fr

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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)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Pulmonology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (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

La présente invention concerne certains nouveaux composés (y compris des sels pharmaceutiquement acceptables de ceux-ci) qui inhibent l'activité de la phosphatidylinositol 3-kinase gamma (pi3kδ), et l'activité de la phosphatidylinositol 3-kinase gamma (ρι3κγ), leur utilité dans le traitement et/ou la prévention d'affections cliniques comprenant les maladies respiratoires, telles que l'asthme et la broncho-pneumopathie chronique obstructive (bpco), leur utilisation en thérapie, des compositions pharmaceutiques les contenant et des procédés pour préparer ces composés.
MA46268A 2016-09-22 2017-09-21 Dérivés de 5-[2-(pyridin-2-ylamino)-1 ,3-thiazol-5-yl]-2,3-dihydro-1h-isoindol-1-one et leur utilisation en tant qu'inhibiteurs doubles de phosphatidylinositol 3-kinase delta & gamma MA46268B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662398006P 2016-09-22 2016-09-22
PCT/EP2017/073916 WO2018055040A1 (fr) 2016-09-22 2017-09-21 Dérivés de 5-[2-(pyridin-2-ylamino)-1,3-thiazol-5-yl]-2,3-dihydro-1 h-isoindol-1 -one et leur utilisation en tant qu'inhibiteurs doubles de phosphatidylinositol 3-kinase delta & gamma

Publications (2)

Publication Number Publication Date
MA46268A true MA46268A (fr) 2019-07-31
MA46268B1 MA46268B1 (fr) 2020-08-31

Family

ID=59966739

Family Applications (1)

Application Number Title Priority Date Filing Date
MA46268A MA46268B1 (fr) 2016-09-22 2017-09-21 Dérivés de 5-[2-(pyridin-2-ylamino)-1 ,3-thiazol-5-yl]-2,3-dihydro-1h-isoindol-1-one et leur utilisation en tant qu'inhibiteurs doubles de phosphatidylinositol 3-kinase delta & gamma

Country Status (36)

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

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020102198A1 (fr) 2018-11-13 2020-05-22 Incyte Corporation Dérivés hétérocycliques utilisés en tant qu'inhibiteurs de pi3k
WO2020102150A1 (fr) 2018-11-13 2020-05-22 Incyte Corporation Dérivés hétérocycliques utilisés comme inhibiteurs de pi3k
WO2020102216A1 (fr) 2018-11-13 2020-05-22 Incyte Corporation Dérivés hétécycliques substitués utiles en tant qu'inhibiteurs de pi3k
CN115677692A (zh) * 2019-04-10 2023-02-03 南京征祥医药有限公司 磷脂酰肌醇3-激酶抑制剂
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 (fr) * 2020-07-21 2022-01-27 中国医药研究开发中心有限公司 Composé hétérocylique présentant une double activité inhibitrice de phosphatidylinositol 3-kinase δ et γ et son utilisation médicale
WO2022023456A1 (fr) 2020-07-29 2022-02-03 Astrazeneca Ab Compositions pharmaceutiques comprenant des microparticules nano-intégrées et procédés d'utilisation
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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* Cited by examiner, † Cited by third party
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WO2002050071A1 (fr) * 2000-12-21 2002-06-27 Bristol-Myers Squibb Company Inhibiteurs thiazolyl des tyrosine kinases de la famille tec
GB0305152D0 (en) 2003-03-06 2003-04-09 Novartis Ag Organic compounds
GB0320197D0 (en) * 2003-08-28 2003-10-01 Novartis Ag Organic compounds
EP1893607A4 (fr) * 2005-06-09 2010-07-21 Merck Sharp & Dohme Inhibiteurs de kinases checkpoint
TW200911798A (en) * 2007-08-02 2009-03-16 Amgen Inc PI3 kinase modulators and methods of use
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
AR088218A1 (es) 2011-07-19 2014-05-21 Infinity Pharmaceuticals Inc Compuestos heterociclicos utiles como inhibidores de pi3k
HK1198443A1 (en) 2011-07-19 2015-04-24 无限药品股份有限公司 Heterocyclic compounds and uses thereof
MX2014002542A (es) 2011-08-29 2014-07-09 Infinity Pharmaceuticals Inc Compuestos heterociclicos y usos de los mismos.
HK1201065A1 (en) * 2011-10-04 2015-08-21 Gilead Calistoga Llc Novel quinoxaline inhibitors of pi3k
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
TW201446767A (zh) 2013-02-15 2014-12-16 Almirall Sa 作為磷脂肌醇3-激酶抑製劑之吡咯並三嗪衍生物
CN105431437B (zh) 2013-07-02 2020-03-10 理森制药股份公司 PI3K蛋白激酶抑制剂,特别是δ抑制剂和/或γ抑制剂
UY35675A (es) 2013-07-24 2015-02-27 Novartis Ag Derivados sustituidos de quinazolin-4-ona
AP2017009670A0 (en) 2014-06-27 2017-01-31 Rhizen Pharmaceuticals Sa Substituted chromene derivatives as selective dual inhibitors of PI3 delta and gamma protein kinases

Also Published As

Publication number Publication date
IL265298A (en) 2019-05-30
HRP20201175T1 (hr) 2020-11-13
US20200308164A1 (en) 2020-10-01
HUE051634T2 (hu) 2021-03-01
CL2019000707A1 (es) 2019-05-31
PE20190909A1 (es) 2019-06-26
CO2019003440A2 (es) 2019-04-12
CA3036304A1 (fr) 2018-03-29
PL3515910T3 (pl) 2021-02-22
SMT202000481T1 (it) 2020-11-10
PT3515910T (pt) 2020-09-16
JP2019529445A (ja) 2019-10-17
DOP2019000073A (es) 2019-04-15
BR112019004719A2 (pt) 2019-05-28
JP6765516B2 (ja) 2020-10-07
KR102226098B1 (ko) 2021-03-09
JOP20190052A1 (ar) 2019-03-21
AR109706A1 (es) 2019-01-16
UA123558C2 (uk) 2021-04-21
EA036176B1 (ru) 2020-10-09
EP3515910B1 (fr) 2020-07-15
MX381898B (es) 2025-03-13
MA46268B1 (fr) 2020-08-31
KR20190049867A (ko) 2019-05-09
LT3515910T (lt) 2020-10-12
MX2021004748A (es) 2021-06-08
EP3515910A1 (fr) 2019-07-31
AU2017331940B2 (en) 2020-03-12
DK3515910T3 (da) 2020-08-31
SI3515910T1 (sl) 2020-09-30
CR20190200A (es) 2019-06-07
TW201813967A (zh) 2018-04-16
IL265298B (en) 2020-09-30
AU2017331940A1 (en) 2019-05-02
RS60764B1 (sr) 2020-10-30
US10961236B2 (en) 2021-03-30
PH12019500615A1 (en) 2019-06-03
US20210246130A1 (en) 2021-08-12
CN109715623A (zh) 2019-05-03
WO2018055040A1 (fr) 2018-03-29
ES2818583T3 (es) 2021-04-13
CY1123346T1 (el) 2022-03-24
EA201990664A1 (ru) 2019-08-30
SV2019005857A (es) 2019-05-06
MX2019003194A (es) 2019-06-17
ECSP19027780A (es) 2019-04-30

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