MA46268B1 - 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
MA46268B1
MA46268B1 MA46268A MA46268A MA46268B1 MA 46268 B1 MA46268 B1 MA 46268B1 MA 46268 A MA46268 A MA 46268A MA 46268 A MA46268 A MA 46268A MA 46268 B1 MA46268 B1 MA 46268B1
Authority
MA
Morocco
Prior art keywords
phosphatidylinositol
gamma
isoindol
ylamino
thiazol
Prior art date
Application number
MA46268A
Other languages
English (en)
Other versions
MA46268A (fr
Inventor
Matthew Perry
Konstantinos Karabelas
Mickael Mogemark
Peter Bold
Christian Tyrchan
Antonios Nikitidis
Jens Petersen
Ulf Börjesson
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 (pi3kd), et l'activité de la phosphatidylinositol 3-kinase gamma (??3??), 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 MA46268A (fr) 2019-07-31
MA46268B1 true 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 (35)

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) MX2019003194A (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)
SV (1) SV2019005857A (fr)
TW (1) TW201813967A (fr)
UA (1) UA123558C2 (fr)
WO (1) WO2018055040A1 (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11078204B2 (en) 2018-11-13 2021-08-03 Incyte Corporation Heterocyclic derivatives as PI3K inhibitors
US11396502B2 (en) 2018-11-13 2022-07-26 Incyte Corporation Substituted heterocyclic derivatives as PI3K inhibitors
US11161838B2 (en) 2018-11-13 2021-11-02 Incyte Corporation Heterocyclic derivatives as PI3K inhibitors
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

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4405726B2 (ja) * 2000-12-21 2010-01-27 ブリストル−マイヤーズ スクイブ カンパニー Tecファミリーチロシンキナーゼのチアゾリルインヒビター
GB0305152D0 (en) * 2003-03-06 2003-04-09 Novartis Ag Organic compounds
GB0320197D0 (en) * 2003-08-28 2003-10-01 Novartis Ag Organic compounds
AU2006258101A1 (en) * 2005-06-09 2006-12-21 Merck Sharp & Dohme Corp. Inhibitors of checkpoint kinases
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
AR088218A1 (es) 2011-07-19 2014-05-21 Infinity Pharmaceuticals Inc Compuestos heterociclicos utiles como inhibidores de pi3k
WO2013012915A1 (fr) 2011-07-19 2013-01-24 Infinity Pharmaceuticals Inc. Composés hétérocycliques et leurs utilisations
CA2846431A1 (fr) 2011-08-29 2013-03-07 Infinity Pharmaceuticals Inc. Composes heterocycliques et leurs utilisations
WO2013052699A2 (fr) 2011-10-04 2013-04-11 Gilead Calistoga Llc Nouveaux inhibiteurs de quinoxaline de la voie 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
WO2015001491A1 (fr) 2013-07-02 2015-01-08 Rhizen Pharmaceuticals Sa Inhibiteurs de protéine kinase pi3k, en particulier inhibiteurs delta et/ou gamma
UY35675A (es) 2013-07-24 2015-02-27 Novartis Ag Derivados sustituidos de quinazolin-4-ona
CA2951370A1 (fr) 2014-06-27 2015-12-30 Rhizen Pharmaceuticals Sa Derives substitues de chromene en tant qu'inhibiteurs doubles selectifs des inhibiteurs de la pi3 delta proteine kinase et de la pi3 gamma proteine kinase

Also Published As

Publication number Publication date
BR112019004719A2 (pt) 2019-05-28
JP6765516B2 (ja) 2020-10-07
EP3515910A1 (fr) 2019-07-31
ECSP19027780A (es) 2019-04-30
CR20190200A (es) 2019-06-07
HRP20201175T1 (hr) 2020-11-13
WO2018055040A1 (fr) 2018-03-29
EA201990664A1 (ru) 2019-08-30
LT3515910T (lt) 2020-10-12
KR102226098B1 (ko) 2021-03-09
MX2019003194A (es) 2019-06-17
JP2019529445A (ja) 2019-10-17
IL265298A (en) 2019-05-30
US20200308164A1 (en) 2020-10-01
SI3515910T1 (sl) 2020-09-30
ES2818583T3 (es) 2021-04-13
PH12019500615A1 (en) 2019-06-03
DK3515910T3 (da) 2020-08-31
DOP2019000073A (es) 2019-04-15
PT3515910T (pt) 2020-09-16
CY1123346T1 (el) 2022-03-24
CO2019003440A2 (es) 2019-04-12
IL265298B (en) 2020-09-30
US20210246130A1 (en) 2021-08-12
EA036176B1 (ru) 2020-10-09
TW201813967A (zh) 2018-04-16
SV2019005857A (es) 2019-05-06
US10961236B2 (en) 2021-03-30
CN109715623A (zh) 2019-05-03
MX2021004748A (es) 2021-06-08
AR109706A1 (es) 2019-01-16
AU2017331940B2 (en) 2020-03-12
EP3515910B1 (fr) 2020-07-15
PL3515910T3 (pl) 2021-02-22
AU2017331940A1 (en) 2019-05-02
KR20190049867A (ko) 2019-05-09
UA123558C2 (uk) 2021-04-21
CA3036304A1 (fr) 2018-03-29
JOP20190052A1 (ar) 2019-03-21
RS60764B1 (sr) 2020-10-30
CL2019000707A1 (es) 2019-05-31
HUE051634T2 (hu) 2021-03-01
MA46268A (fr) 2019-07-31
PE20190909A1 (es) 2019-06-26

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