CA3059107A1 - Isoindolin-1-one derivatives and pharmaceutical compositions thereof useful as aski inhibitor - Google Patents

Isoindolin-1-one derivatives and pharmaceutical compositions thereof useful as aski inhibitor Download PDF

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Publication number
CA3059107A1
CA3059107A1 CA3059107A CA3059107A CA3059107A1 CA 3059107 A1 CA3059107 A1 CA 3059107A1 CA 3059107 A CA3059107 A CA 3059107A CA 3059107 A CA3059107 A CA 3059107A CA 3059107 A1 CA3059107 A1 CA 3059107A1
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CA
Canada
Prior art keywords
group
compound
6alkyl
c6alkyl
pharmaceutically acceptable
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Legal status (The legal status 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 status listed.)
Pending
Application number
CA3059107A
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English (en)
French (fr)
Inventor
Samuel David BROWN
Original Assignee
Seal Rock Therapeutics Inc
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
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Application filed by Seal Rock Therapeutics Inc filed Critical Seal Rock Therapeutics Inc
Publication of CA3059107A1 publication Critical patent/CA3059107A1/en
Pending legal-status Critical Current

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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
    • A61K31/435Heterocyclic 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
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/08Bridged systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Cosmetics (AREA)
CA3059107A 2017-04-05 2018-04-04 Isoindolin-1-one derivatives and pharmaceutical compositions thereof useful as aski inhibitor Pending CA3059107A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201762482085P 2017-04-05 2017-04-05
US62/482,085 2017-04-05
PCT/US2018/026134 WO2018187506A1 (en) 2017-04-05 2018-04-04 Ask1 inhibitor compounds and uses thereof

Publications (1)

Publication Number Publication Date
CA3059107A1 true CA3059107A1 (en) 2018-10-11

Family

ID=63712299

Family Applications (1)

Application Number Title Priority Date Filing Date
CA3059107A Pending CA3059107A1 (en) 2017-04-05 2018-04-04 Isoindolin-1-one derivatives and pharmaceutical compositions thereof useful as aski inhibitor

Country Status (34)

Country Link
US (3) US20210087167A1 (https=)
EP (1) EP3606519B1 (https=)
JP (1) JP7196093B2 (https=)
KR (1) KR102665145B1 (https=)
CN (1) CN110730661B (https=)
AR (1) AR111407A1 (https=)
AU (1) AU2018250217B2 (https=)
CA (1) CA3059107A1 (https=)
CL (1) CL2019002810A1 (https=)
CO (1) CO2019011708A2 (https=)
CR (1) CR20190503A (https=)
CU (1) CU20190080A7 (https=)
DK (1) DK3606519T3 (https=)
DO (1) DOP2019000255A (https=)
EA (1) EA201992299A1 (https=)
EC (1) ECSP19078393A (https=)
ES (1) ES2992084T3 (https=)
FI (1) FI3606519T3 (https=)
HU (1) HUE068103T2 (https=)
IL (1) IL269711B (https=)
JO (1) JOP20190221A1 (https=)
MA (1) MA49047A (https=)
MX (1) MX394098B (https=)
NI (1) NI201900102A (https=)
NZ (1) NZ758345A (https=)
PE (1) PE20200009A1 (https=)
PH (1) PH12019502288A1 (https=)
PL (1) PL3606519T3 (https=)
PT (1) PT3606519T (https=)
RU (1) RU2019134679A (https=)
SG (1) SG11201909155VA (https=)
SI (1) SI3606519T1 (https=)
TW (1) TWI779022B (https=)
WO (1) WO2018187506A1 (https=)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6754505B2 (ja) * 2017-01-22 2020-09-09 福建広生堂薬業股▲ふん▼有限公司 Ask1阻害剤、その調製方法および使用
AU2018266911C1 (en) 2017-05-12 2022-10-20 Enanta Pharmaceuticals, Inc. Apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof
EP3735404B1 (en) 2018-01-02 2023-11-29 Seal Rock Therapeutics, Inc. Ask1 inhibitor compounds and uses thereof
CN110407806B (zh) * 2018-04-28 2021-08-17 深圳微芯生物科技股份有限公司 甲酰胺类化合物、其制备方法及其应用
ES3004523T3 (en) 2018-05-02 2025-03-12 Enanta Pharm Inc Tetrazole containing apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof
WO2020006429A1 (en) * 2018-06-28 2020-01-02 Hepatikos Therapeutics, Llc Ask1 isoindolin-1-one inhibitors and methods of use thereof
WO2020041417A1 (en) 2018-08-22 2020-02-27 Enanta Pharmaceuticals, Inc. Cycloalkyl-containing apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof
WO2020106707A1 (en) 2018-11-19 2020-05-28 Enanta Pharmaceuticals, Inc. Apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof
US11466033B2 (en) 2019-03-25 2022-10-11 Enanta Pharmaceuticals, Inc. Substituted pyridines as apoptosis signal-regulating kinase 1 inhibitors
CN112409332B (zh) * 2019-08-23 2023-12-08 广东东阳光药业股份有限公司 三氮唑衍生物及其在药物中的应用
PE20221283A1 (es) 2019-12-27 2022-09-05 Lupin Ltd Compuestos triciclicos sustituidos
PE20230323A1 (es) 2020-05-01 2023-02-22 Pfizer Compuestos de azalactama como inhibidores de hpk1
WO2021224818A1 (en) * 2020-05-08 2021-11-11 Pfizer Inc. Isoindolone compounds as hpk1 inhibitors
JP7819176B2 (ja) * 2020-08-03 2026-02-24 ノバルティス アーゲー ヘテロアリール置換3-(1-オキソイソインドリン-2-イル)ピペリジン-2,6-ジオン誘導体及びその使用
WO2024020458A1 (en) * 2022-07-20 2024-01-25 Seal Rock Therapeutics, Inc. Method of treating organ diseases or disorders with ask1 inhibitors
TW202547513A (zh) 2024-05-06 2025-12-16 法商Genfit公司 敗血症的治療
WO2026057806A1 (en) 2024-09-13 2026-03-19 Genfit Injectable dosage form of 2-[6-(4-cyclopropyl-4h-1,2,4-triazol-3-yl)-2-pyridyl]-5-morpholinocarbonyl-1-isoindolinone

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4229447A (en) 1979-06-04 1980-10-21 American Home Products Corporation Intraoral methods of using benzodiazepines
US4596795A (en) 1984-04-25 1986-06-24 The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives
US4755386A (en) 1986-01-22 1988-07-05 Schering Corporation Buccal formulation
US5739136A (en) 1989-10-17 1998-04-14 Ellinwood, Jr.; Everett H. Intraoral dosing method of administering medicaments
TWI598347B (zh) * 2009-07-13 2017-09-11 基利科學股份有限公司 調節細胞凋亡信號之激酶的抑制劑
PL2531501T3 (pl) * 2010-02-03 2014-05-30 Takeda Pharmaceuticals Co Inhibitory kinazy 1 regulującej sygnał apoptotyczny
WO2012079022A1 (en) * 2010-12-10 2012-06-14 Concert Pharmaceuticals, Inc. Substituted dioxopiperidinyl phthalimide derivatives
ES2617339T3 (es) * 2010-12-16 2017-06-16 Calchan Limited Derivados de pirrolopirimidina inhibidores de ASK1
MX2017003933A (es) * 2014-09-24 2017-06-30 Gilead Sciences Inc Metodos de tratamiento de la enfermedad hepatica.
US10669242B2 (en) 2016-06-10 2020-06-02 Venenum Biodesign, LLC Clostridium difficile toxin inhibitors
WO2018133866A1 (zh) 2017-01-22 2018-07-26 福建广生堂药业股份有限公司 作为ask1抑制剂的吡啶衍生物及其制备方法和应用
JP6754505B2 (ja) * 2017-01-22 2020-09-09 福建広生堂薬業股▲ふん▼有限公司 Ask1阻害剤、その調製方法および使用
EP3580224B1 (en) 2017-02-07 2022-07-13 Biogen MA Inc. Ask1 inhibiting agents
CN109071498B (zh) 2017-02-16 2021-03-30 四川科伦博泰生物医药股份有限公司 激酶抑制剂及其制备方法和用途
WO2018151830A1 (en) 2017-02-17 2018-08-23 Fronthera U.S. Pharmaceuticals Llc Pyridinyl based apoptosis signal-regulation kinase inhibitors
WO2018157277A1 (en) 2017-02-28 2018-09-07 Eli Lilly And Company Isoquinolin and naphthydrin compounds
US11136324B2 (en) 2017-03-03 2021-10-05 Jiangsu Hansoh Pharmaceutical Group Co., Ltd. Substituted imidazoles as apoptosis signal regulating kinase 1 inhibitors
JP2020512976A (ja) 2017-03-27 2020-04-30 ファーマケア,インク. アポトーシスシグナル調節キナーゼ1(ask1)阻害剤化合物
EP3681499A4 (en) * 2017-09-13 2021-04-21 D.E. Shaw Research, LLC CONNECTIONS AS RAS INHIBITORS AND THEIR USE
WO2020006429A1 (en) * 2018-06-28 2020-01-02 Hepatikos Therapeutics, Llc Ask1 isoindolin-1-one inhibitors and methods of use thereof

Also Published As

Publication number Publication date
JOP20190221A1 (ar) 2019-09-23
KR20190141166A (ko) 2019-12-23
TW201838983A (zh) 2018-11-01
MX394098B (es) 2025-03-24
US20180291002A1 (en) 2018-10-11
PT3606519T (pt) 2024-08-06
KR102665145B1 (ko) 2024-05-09
NI201900102A (es) 2020-05-15
JP2020515589A (ja) 2020-05-28
JP7196093B2 (ja) 2022-12-26
EP3606519A4 (en) 2020-12-02
NZ758345A (en) 2022-02-25
DK3606519T3 (da) 2024-08-12
MA49047A (fr) 2020-02-12
IL269711A (en) 2019-11-28
SG11201909155VA (en) 2019-10-30
US20250304552A1 (en) 2025-10-02
CU20190080A7 (es) 2020-10-20
PE20200009A1 (es) 2020-01-06
CR20190503A (es) 2020-02-28
WO2018187506A1 (en) 2018-10-11
ES2992084T3 (es) 2024-12-09
AR111407A1 (es) 2019-07-10
EP3606519B1 (en) 2024-06-05
TWI779022B (zh) 2022-10-01
ECSP19078393A (es) 2019-12-27
AU2018250217B2 (en) 2022-05-19
US20210087167A1 (en) 2021-03-25
CN110730661B (zh) 2023-06-13
CN110730661A (zh) 2020-01-24
CL2019002810A1 (es) 2020-03-27
PL3606519T3 (pl) 2024-10-28
SI3606519T1 (sl) 2024-10-30
HUE068103T2 (hu) 2024-12-28
EA201992299A1 (ru) 2020-03-26
MX2019012013A (es) 2019-12-18
DOP2019000255A (es) 2019-12-15
AU2018250217A1 (en) 2019-11-07
IL269711B (en) 2021-12-01
CO2019011708A2 (es) 2020-01-17
US10150755B2 (en) 2018-12-11
RU2019134679A (ru) 2021-05-05
BR112019021021A2 (pt) 2020-05-05
EP3606519A1 (en) 2020-02-12
FI3606519T3 (fi) 2024-08-09
PH12019502288A1 (en) 2020-07-13

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