[go: up one dir, main page]

CR20240045A - Compuestos que inhiben la isoforma alfa de pi3k y métodos para tratar el cáncer - Google Patents

Compuestos que inhiben la isoforma alfa de pi3k y métodos para tratar el cáncer

Info

Publication number
CR20240045A
CR20240045A CR20240045A CR20240045A CR20240045A CR 20240045 A CR20240045 A CR 20240045A CR 20240045 A CR20240045 A CR 20240045A CR 20240045 A CR20240045 A CR 20240045A CR 20240045 A CR20240045 A CR 20240045A
Authority
CR
Costa Rica
Prior art keywords
pi3k
inhibit
methods
compounds
treating cancer
Prior art date
Application number
CR20240045A
Other languages
English (en)
Inventor
Jean Jr David St
Original Assignee
Scorpion 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
Publication date
Application filed by Scorpion Therapeutics Inc filed Critical Scorpion Therapeutics Inc
Publication of CR20240045A publication Critical patent/CR20240045A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32Nitrogen atom
    • 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
    • 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
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • C07D405/02Heterocyclic 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 two hetero rings
    • C07D405/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Esta descripción proporciona compuestos de la Fórmula (I) y sales farmacéuticamente aceptables de estos, que inhiben la isoforma alfa (PI3Ka) de la fosfatidilinositol 4,5-bisfosfato 3-quinasa (PI3K). Estas entidades químicas son útiles, por ejemplo, para tratar una afección, enfermedad o trastorno en el que el aumento (por ejemplo, excesivo) de la activación de PI3Ka contribuye a la patología y/o a los síntomas y/o a la progresión de la afección, enfermedad o trastorno (por ejemplo, cáncer) en un sujeto (por ejemplo, un ser humano). Esta descripción también proporciona composiciones que contienen la misma, así como también métodos de uso y fabricación de la misma.
CR20240045A 2021-08-09 2022-08-08 Compuestos que inhiben la isoforma alfa de pi3k y métodos para tratar el cáncer CR20240045A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US202163231156P 2021-08-09 2021-08-09
PCT/US2022/039674 WO2023018636A1 (en) 2021-08-09 2022-08-08 Compounds that inhibit pi3k isoform alpha and methods for treating cancer

Publications (1)

Publication Number Publication Date
CR20240045A true CR20240045A (es) 2024-02-20

Family

ID=83188497

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20240045A CR20240045A (es) 2021-08-09 2022-08-08 Compuestos que inhiben la isoforma alfa de pi3k y métodos para tratar el cáncer

Country Status (17)

Country Link
US (1) US20240343728A1 (es)
EP (1) EP4363414A1 (es)
JP (1) JP2024533975A (es)
KR (1) KR20240051953A (es)
CN (1) CN118159534A (es)
AU (1) AU2022325819A1 (es)
CA (1) CA3227902A1 (es)
CL (1) CL2024000327A1 (es)
CO (1) CO2024000448A2 (es)
CR (1) CR20240045A (es)
DO (1) DOP2024000019A (es)
EC (1) ECSP24008488A (es)
IL (1) IL310588A (es)
MA (1) MA63885B1 (es)
MX (1) MX2024000708A (es)
PE (1) PE20240652A1 (es)
WO (1) WO2023018636A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024097721A1 (en) 2022-11-02 2024-05-10 Petra Pharma Corporation Targeting allosteric and orthosteric pockets of phosphoinositide 3-kinase (pi3k) for the treatment of disease
WO2024233256A1 (en) 2023-05-05 2024-11-14 Eli Lilly And Company Imlunestrant or salts thereof for use in treating and preventing central nervous system (cns) metastases in subjects having er+ breast cancer
WO2025036439A1 (en) * 2023-08-16 2025-02-20 Laekna Pharmaceutical Ningbo Co., Ltd. Multicyclic compounds and their use as pi3k alpha inhibitors

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2408773A2 (en) * 2009-03-20 2012-01-25 Amgen, Inc Inhibitors of pi3 kinase
DE102009043260A1 (de) * 2009-09-28 2011-04-28 Merck Patent Gmbh Pyridinyl-imidazolonderivate
BR112017000132A2 (pt) * 2014-07-04 2018-01-09 Lupin Ltd composto, composição farmacêutica e método de tratamento ou prevenção de uma doença responsiva à inibição da atividade de pi3k
TWI601732B (zh) * 2015-07-02 2017-10-11 赫孚孟拉羅股份公司 苯并氧氮呯噁唑啶酮化合物及其用途
WO2017221272A1 (en) * 2016-06-23 2017-12-28 Sun Pharmaceutical Industries Limited Process for the preparation of idelalisib
WO2021001431A1 (en) * 2019-07-02 2021-01-07 INSERM (Institut National de la Santé et de la Recherche Médicale) Use of pi3ka-selective inhibitors for treating metastatic disease in patients suffering from pancreatic cancer

Also Published As

Publication number Publication date
CO2024000448A2 (es) 2024-02-15
JP2024533975A (ja) 2024-09-18
CA3227902A1 (en) 2023-02-16
IL310588A (en) 2024-04-01
CL2024000327A1 (es) 2024-08-09
WO2023018636A1 (en) 2023-02-16
CN118159534A (zh) 2024-06-07
AU2022325819A1 (en) 2024-02-29
PE20240652A1 (es) 2024-04-04
MA63885A1 (fr) 2024-09-30
EP4363414A1 (en) 2024-05-08
MA63885B1 (fr) 2025-01-31
ECSP24008488A (es) 2024-05-31
MX2024000708A (es) 2024-02-08
DOP2024000019A (es) 2024-03-15
KR20240051953A (ko) 2024-04-22
US20240343728A1 (en) 2024-10-17

Similar Documents

Publication Publication Date Title
DOP2023000271A (es) Derivados de la urea que pueden ser utilizados para tratar el cáncer
DOP2024000019A (es) Compuestos que inhiben la isoforma alfa de pi3k y métodos para tratar el cáncer
ECSP22087539A (es) Inhibidores de kras tricíclicos fusionados
CO2019008932A2 (es) Imidazo-quinolinas sustituidas como moduladores de nlrp3
DOP2019000020A (es) Compuestos de tiazolo-piridina sustituida como inhibidores de malt1
UY38742A (es) Compuestos de 2,3,5-pyrazolo[1,5-a]pirimidina trisustituida
CL2019001079A1 (es) Métodos para usar indazol-3-carboxamidas y su uso como inhibidores de la vía de señalización de wnt/b-catenina.
GT200500325A (es) Pirazolo-pirimidinas 1,4-sustituidas como inhibidores de quinasa
CL2022002919A1 (es) Aminotiazoles sustituidos como inhibidores de dgkzeta para la activación inmune
UY29093A1 (es) Derivados de 4-oxo-3. 4-dihidroquinazolin-6-carboxamida, inhibidores de b-raf, composiciones que los contienen, procesos de preparación y aplicaiones.
MX2013002713A (es) Imidazopiridazinas sustituidas.
UY30094A1 (es) Compuestos químicos
CO2023010023A2 (es) Inhibidores de cdk2 y métodos de uso de los mismos
CL2021003568A1 (es) Compuestos heteroaromáticos como inhibidores de vanina (divisional de solicitud n° 202101198)
CL2020001107A1 (es) Novedosos derivados de pirazolo-pirrolo-pirimidina como inhibidores de p2x3.
AR117844A1 (es) Derivados de tiazolopiridina como antagonistas del receptor de adenosina
ES2164899T3 (es) Uso de alcaloides de la clase lamellarina en metodos de tratamiento.
UY39061A (es) Inhibidores macrocíclicos de rip2-cinasa
UY39819A (es) Métodos para tratar el cáncer
MX2018008157A (es) Alfa-amino esteres de derivado de hidroxipropiltiazolidin carboxamida, y formas de sales y polimorfos cristalinos de estos.
AR126147A1 (es) Derivados de urea para tratar el cáncer
PE20181450A1 (es) Compuestos de 1,3,4-tiadiazol y su uso en el tratamiento del cancer
UY31812A (es) Derivados de cinolina como inhibidores de csf-1
DOP2022000203A (es) 3-fenoxiazetidin-1-il-pirazinas sustituidas con actividad antagonista gpr52
CR20240216A (es) Derivados de naftiridinona para el tratamiento de una enfermedad o un trastorno