[go: up one dir, main page]

MX341368B - Inhibidores de la cinasa del punto de control 1 para potenciar agentes dañinos del adn. - Google Patents

Inhibidores de la cinasa del punto de control 1 para potenciar agentes dañinos del adn.

Info

Publication number
MX341368B
MX341368B MX2011010675A MX2011010675A MX341368B MX 341368 B MX341368 B MX 341368B MX 2011010675 A MX2011010675 A MX 2011010675A MX 2011010675 A MX2011010675 A MX 2011010675A MX 341368 B MX341368 B MX 341368B
Authority
MX
Mexico
Prior art keywords
inhibitors
dna damaging
damaging agents
checkpoint kinase
potentiating
Prior art date
Application number
MX2011010675A
Other languages
English (en)
Other versions
MX2011010675A (es
Inventor
Michael J Humphries
Shannon L Winski
Original Assignee
Array Biopharma 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 Array Biopharma Inc * filed Critical Array Biopharma Inc *
Publication of MX2011010675A publication Critical patent/MX2011010675A/es
Publication of MX341368B publication Critical patent/MX341368B/es

Links

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
    • A61K31/4353Heterocyclic 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
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0053Mouth and digestive tract, i.e. intraoral and peroral administration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Nutrition Science (AREA)
  • Physiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Se proporciona un inhibidor de CHK 1 para administración a un paciente con cáncer para potenciar un agente dañino de ADN.
MX2011010675A 2009-04-11 2010-04-09 Inhibidores de la cinasa del punto de control 1 para potenciar agentes dañinos del adn. MX341368B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16856309P 2009-04-11 2009-04-11
PCT/US2010/030634 WO2010118390A1 (en) 2009-04-11 2010-04-09 Checkpoint kinase 1 inhibitors for potentiating dna damaging agents

Publications (2)

Publication Number Publication Date
MX2011010675A MX2011010675A (es) 2012-03-16
MX341368B true MX341368B (es) 2016-08-17

Family

ID=42651200

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2011010675A MX341368B (es) 2009-04-11 2010-04-09 Inhibidores de la cinasa del punto de control 1 para potenciar agentes dañinos del adn.

Country Status (15)

Country Link
EP (1) EP2416773B1 (es)
JP (2) JP5805071B2 (es)
KR (1) KR101676062B1 (es)
CN (1) CN102612365B (es)
AU (1) AU2010233122B2 (es)
BR (1) BRPI1013920A2 (es)
CA (1) CA2758300C (es)
ES (1) ES2608656T3 (es)
IL (1) IL215709A (es)
MX (1) MX341368B (es)
NZ (1) NZ596125A (es)
RU (1) RU2567044C2 (es)
SG (3) SG10201900212QA (es)
WO (1) WO2010118390A1 (es)
ZA (1) ZA201108273B (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2242755B1 (en) 2008-01-08 2012-09-12 Array Biopharma, Inc. Pyrrolopyridines as kinase inhibitors
ES2392014T3 (es) 2008-01-09 2012-12-03 Array Biopharma, Inc. Pirazolopiridinas como inhibidores de la cinasa
US8481557B2 (en) 2009-04-11 2013-07-09 Array Biopharma Inc. Method of treatment using checkpoint kinase 1 inhibitors
GB201008005D0 (en) 2010-05-13 2010-06-30 Sentinel Oncology Ltd Pharmaceutical compounds
EP2640386B1 (en) 2010-11-16 2017-01-18 Array Biopharma Inc. Combination of checkpoint kinase 1 inhibitors and wee 1 kinase inhibitors
GB201119799D0 (en) 2011-11-16 2011-12-28 Sentinel Oncology Ltd Pharmaceutical compounds
JP6606428B2 (ja) 2013-10-11 2019-11-13 国立大学法人 東京医科歯科大学 脊髄小脳変性症を予防又は治療するための薬剤
GB201402277D0 (en) 2014-02-10 2014-03-26 Sentinel Oncology Ltd Pharmaceutical compounds
EP3461480A1 (en) 2017-09-27 2019-04-03 Onxeo Combination of a dna damage response cell cycle checkpoint inhibitors and belinostat for treating cancer
TW202043198A (zh) * 2019-01-17 2020-12-01 美商Ifm Due有限公司 用於治療與sting活性相關之病況的化合物及組合物
KR102285996B1 (ko) * 2019-08-08 2021-08-05 차의과학대학교 산학협력단 혈관신생을 억제하는 데 사용하기 위한 조성물 및 그 용도
WO2021113661A1 (en) 2019-12-05 2021-06-10 Seagen Inc. Amorphous and polymorphic form of a specific chk1 inhibitor
GB202107924D0 (en) 2021-06-03 2021-07-21 Sentinel Oncology Ltd A pharmaceutical salt
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025080946A2 (en) 2023-10-12 2025-04-17 Revolution Medicines, Inc. Ras inhibitors

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003028724A1 (en) * 2001-10-04 2003-04-10 Smithkline Beecham Corporation Chk1 kinase inhibitors
US20070185013A1 (en) * 2003-09-17 2007-08-09 Icos Corporation Use of chk1 inhibitors to control cell proliferation
UY29177A1 (es) * 2004-10-25 2006-05-31 Astex Therapeutics Ltd Derivados sustituidos de purina, purinona y deazapurina, composiciones que los contienen métodos para su preparación y sus usos
KR20080100838A (ko) * 2006-04-04 2008-11-19 화이자 프로덕츠 인코포레이티드 (2r,z)-2-아미노-2-사이클로헥실-n-(5-(1-메틸-1h-피라졸-4-일)-1-옥소-2,6-다이하이드로-1h-[1,2]다이아제피노[4,5,6-cd]인돌-8-일)아세트아미드의 복합 요법
WO2008063558A2 (en) * 2006-11-17 2008-05-29 Schering Corporation Combination of an inhibitor of dna polymerase-alpha and an inhibitor of a checkpoint kinase for proliferative disorders
AR071717A1 (es) * 2008-05-13 2010-07-07 Array Biopharma Inc Pirrolo[2,3-b]piridinas inhibidoras de quinasas chk1 y chk2,composiciones farmaceuticas que las contienen,proceso para prepararlas y uso de las mismas en el tratamiento y prevencion del cancer.

Also Published As

Publication number Publication date
SG175242A1 (en) 2011-11-28
AU2010233122B2 (en) 2015-09-17
RU2011145773A (ru) 2013-05-20
AU2010233122A1 (en) 2011-11-24
BRPI1013920A2 (pt) 2016-04-05
EP2416773A1 (en) 2012-02-15
IL215709A (en) 2017-06-29
WO2010118390A1 (en) 2010-10-14
MX2011010675A (es) 2012-03-16
CA2758300A1 (en) 2010-10-14
NZ596125A (en) 2012-08-31
CA2758300C (en) 2017-07-25
ZA201108273B (en) 2013-07-31
ES2608656T3 (es) 2017-04-12
SG10201404012RA (en) 2014-09-26
CN102612365A (zh) 2012-07-25
EP2416773B1 (en) 2016-09-28
JP2014198741A (ja) 2014-10-23
KR101676062B1 (ko) 2016-11-14
SG10201900212QA (en) 2019-02-27
IL215709A0 (en) 2012-01-31
KR20120004523A (ko) 2012-01-12
RU2567044C2 (ru) 2015-10-27
JP5805071B2 (ja) 2015-11-04
CN102612365B (zh) 2017-04-12
JP2012523435A (ja) 2012-10-04

Similar Documents

Publication Publication Date Title
MX341368B (es) Inhibidores de la cinasa del punto de control 1 para potenciar agentes dañinos del adn.
TN2013000508A1 (en) Combination therapy comprising a cdk4/6 inhibitor and a pi3k inhibitor for use in the treatment of cancer
TN2009000400A1 (en) Methods of treating cancer using pyridopyrimidininone inhibitors of pi3k alpha
EP1962839A4 (en) ADMINISTRATION OF A MNTOR INHIBITOR FOR THE TREATMENT OF PATIENTS WITH CANCER
UA115320C2 (uk) Інгібітори кінази
UA98141C2 (ru) Способы лечения с применением хинаксолиновых ингибиторов pi3k-альфа
UY33498A (es) Combinaciones de inhibidores de quinasas para el tratamiento de cancer
JO2885B1 (en) Protein kinase inhibitors
UA106748C2 (uk) Похідні проліну як інгібітори катепсину
JO3073B1 (ar) مثبطات ثنائية ملتحمة ثلاثية الحلقة ل cdk 4/6 و flt3
AU2012214029A8 (en) Rorgammat inhibitors
EA201070237A1 (ru) Четвертичные опиоидные карбоксамиды
ECSP099436A (es) Acilaminopirazoles como inhibidores de fgfr
MX343669B (es) Combinacion de inhibidores de la cinasa de control 1 inhibidores de la cinasa wee 1.
PH12012502129A1 (en) New combination therapy in treatment of oncological and fibrotic diseases
MX2011011733A (es) Inhiibidores de dihidroorotato deshidrogenasa como compuestos virostaticos.
ECSP11011136A (es) Compuestos útiles para inhibir chk1
WO2009127669A3 (en) Ido inhibitors and therapeutic uses thereof
IN2012DN00765A (es)
SG10201810575WA (en) Treatment of prostate cancer with tor kinase inhibitors
MX2015012386A (es) Inhibidores de la cinasa cdk9.
MX2009010483A (es) 5-oxoisoxazoles como inhibidores de lipasas y fosfolipasas.
ES2530755T3 (es) Terapia de combinación para el tratamiento del cáncer
WO2011038924A3 (en) Proteasome inhibitors for treating cancer
EP1891082A4 (en) NEW INHIBITORS OF PYRUVATE KINASE AS THERAPEUTIC AGENTS AGAINST CANCER

Legal Events

Date Code Title Description
FG Grant or registration