AR084551A1 - COMPUESTO DE IMIDAZO[4,5-C]QUINOLIN-2-ONA COMO INHIBIDOR DUAL DE mTOR/CINASA PI3 - Google Patents

COMPUESTO DE IMIDAZO[4,5-C]QUINOLIN-2-ONA COMO INHIBIDOR DUAL DE mTOR/CINASA PI3

Info

Publication number
AR084551A1
AR084551A1 ARP110104894A ARP110104894A AR084551A1 AR 084551 A1 AR084551 A1 AR 084551A1 AR P110104894 A ARP110104894 A AR P110104894A AR P110104894 A ARP110104894 A AR P110104894A AR 084551 A1 AR084551 A1 AR 084551A1
Authority
AR
Argentina
Prior art keywords
mtor
quinolin
cinasa
ona
dual inhibitor
Prior art date
Application number
ARP110104894A
Other languages
English (en)
Spanish (es)
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of AR084551A1 publication Critical patent/AR084551A1/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
    • A61K31/47Quinolines; 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
    • 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
    • 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

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
ARP110104894A 2011-01-14 2011-12-22 COMPUESTO DE IMIDAZO[4,5-C]QUINOLIN-2-ONA COMO INHIBIDOR DUAL DE mTOR/CINASA PI3 AR084551A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161432958P 2011-01-14 2011-01-14

Publications (1)

Publication Number Publication Date
AR084551A1 true AR084551A1 (es) 2013-05-22

Family

ID=45531593

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP110104894A AR084551A1 (es) 2011-01-14 2011-12-22 COMPUESTO DE IMIDAZO[4,5-C]QUINOLIN-2-ONA COMO INHIBIDOR DUAL DE mTOR/CINASA PI3

Country Status (39)

Country Link
US (2) US8440829B2 (https=)
EP (1) EP2663564B1 (https=)
JP (1) JP5891247B2 (https=)
KR (1) KR101561360B1 (https=)
CN (1) CN103282364B (https=)
AR (1) AR084551A1 (https=)
AU (1) AU2012205619B2 (https=)
BR (1) BR112013017672A2 (https=)
CA (1) CA2824760C (https=)
CL (1) CL2013002005A1 (https=)
CO (1) CO6731133A2 (https=)
CR (1) CR20130289A (https=)
CY (1) CY1116007T1 (https=)
DK (1) DK2663564T3 (https=)
DO (1) DOP2013000158A (https=)
EA (1) EA022163B1 (https=)
EC (1) ECSP13012764A (https=)
ES (1) ES2531891T3 (https=)
GT (1) GT201300180A (https=)
HR (1) HRP20150135T1 (https=)
HU (1) HUE024426T2 (https=)
IL (1) IL227165A (https=)
JO (1) JO3003B1 (https=)
ME (1) ME02019B (https=)
MX (1) MX2013008185A (https=)
MY (1) MY164705A (https=)
PE (1) PE20140864A1 (https=)
PH (1) PH12013501493A1 (https=)
PL (1) PL2663564T3 (https=)
PT (1) PT2663564E (https=)
RS (1) RS53828B1 (https=)
SG (1) SG191744A1 (https=)
SI (1) SI2663564T1 (https=)
SV (1) SV2013004496A (https=)
TN (1) TN2013000237A1 (https=)
TW (1) TWI518086B (https=)
UA (1) UA109921C2 (https=)
WO (1) WO2012097039A1 (https=)
ZA (1) ZA201304757B (https=)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO3003B1 (ar) 2011-01-14 2016-09-05 Lilly Co Eli مركب أيميدازو [4، 5 -c ] كينولين-2- واحد واستخدامه كمثبط كيناز PI3/mtor
US9050345B2 (en) 2013-03-11 2015-06-09 Bristol-Myers Squibb Company Pyrrolotriazines as potassium ion channel inhibitors
US20160264570A1 (en) * 2013-11-15 2016-09-15 The United States Of America, As Represented By The Secretary, Department Of Health And Human Serv Method of blocking transmission of malarial parasite
TWI609687B (zh) 2015-04-14 2018-01-01 美國禮來大藥廠 平滑肌肉瘤之標靶性治療
TW201703769A (zh) 2015-05-08 2017-02-01 美國禮來大藥廠 用於癌症的組合療法
GB201516504D0 (en) * 2015-09-17 2015-11-04 Astrazeneca Ab Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer
HK1254687A1 (zh) * 2015-12-15 2019-07-26 Eli Lilly And Company 用於癌症的联合疗法
US10722484B2 (en) 2016-03-09 2020-07-28 K-Gen, Inc. Methods of cancer treatment
WO2017180385A1 (en) * 2016-04-12 2017-10-19 Eli Lilly And Company Combination therapy with notch and pi3k/mtor inhibitors for use in treating cancer
ES2881801T3 (es) * 2016-04-12 2021-11-30 Lilly Co Eli Terapia de combinación con inhibidores de Notch y CDK4/6 para su uso en el tratamiento de cáncer de pulmón
MA45025A (fr) 2016-05-20 2019-03-27 Lilly Co Eli Traitement d'association utilisant des inhibiteurs de notch et de pd-1 ou pd-l1
WO2018017410A1 (en) 2016-07-22 2018-01-25 Eli Lilly And Company Combination therapy of abemaciclib and a pi3 kinase/mtor dual inhibitor for use in the treatment of breast cancer
WO2018063873A1 (en) 2016-09-27 2018-04-05 Eli Lilly And Company Combination therapy of abemaciclib and a pi3 kinase/mtor dual inhibitor for use in the treatment of pancreatic cancer
US11376259B2 (en) 2016-10-12 2022-07-05 Eli Lilly And Company Targeted treatment of mature T-cell lymphoma
IL268349B2 (en) 2017-02-17 2024-08-01 Hutchinson Fred Cancer Res Combination therapies for treatment of bcma-related cancers and autoimmune disorders
SG11202003427XA (en) 2017-11-06 2020-05-28 Juno Therapeutics Inc Combination of a cell therapy and a gamma secretase inhibitor
US10596165B2 (en) 2018-02-12 2020-03-24 resTORbio, Inc. Combination therapies
CN110386932A (zh) 2018-04-20 2019-10-29 艾科思莱德制药公司 用于抗肿瘤疗法中的双重atm和dna-pk抑制剂
IL314362A (en) 2018-06-15 2024-09-01 Janssen Pharmaceutica Nv Rapamycin analogs and their uses
WO2020081329A1 (en) * 2018-10-18 2020-04-23 Camp4 Therapeutics Corporation Methods and compositions for modulating pcsk9 and angptl3 expression
KR20220128345A (ko) 2019-12-05 2022-09-20 아나쿠리아 테라퓨틱스, 인코포레이티드 라파마이신 유사체 및 이의 용도
ES2974742T3 (es) * 2020-09-21 2024-07-01 Wei Zhong Compuestos de 1-(3,3-difluoropiperidin-4-il)-imidazo[4,5-c]quinolin-2-ona sustituidos con capacidad de penetración en la barrera hematoencefálica
EP3992191A1 (en) 2020-11-03 2022-05-04 Deutsches Krebsforschungszentrum Imidazo[4,5-c]quinoline compounds and their use as atm kinase inhibitors
MX2024007790A (es) 2021-12-22 2024-09-06 Camp4 Therapeutics Corp Modulación de la transcripción génica utilizando oligonucleótidos antisentido dirigidos a arn reguladores.

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0211649D0 (en) 2002-05-21 2002-07-03 Novartis Ag Organic compounds
AR046845A1 (es) * 2003-11-21 2005-12-28 Novartis Ag Derivados de 1h-imidazo[4,5-c]quinolina para tratamiento de enfermedades dependientes de las proteino-quinasas
DE602004014969D1 (de) 2003-11-21 2008-08-21 Novartis Ag 1h-imidazochinolinderivate als proteinkinaseinhibitoren
CA2598656A1 (en) * 2005-02-23 2006-08-31 Coley Pharmaceutical Group, Inc. Hydroxyalkyl substituted imidazoquinoline compounds and methods
GB0510390D0 (en) * 2005-05-20 2005-06-29 Novartis Ag Organic compounds
KR20080083270A (ko) 2005-11-04 2008-09-17 콜레이 파마시티컬 그룹, 인코포레이티드 하이드록시 및 알콕시 치환된 1에이치 이미다조퀴놀린 및방법
WO2007106854A2 (en) 2006-03-15 2007-09-20 Coley Pharmaceutical Group, Inc. Hydroxy and alkoxy substituted 1h-imidazonaphthyridines and methods
WO2010038165A1 (en) 2008-09-30 2010-04-08 Pfizer Inc. Imidazo[1,5]naphthyridine compounds, their pharmaceutical use and compositions
CN102803259A (zh) * 2009-06-04 2012-11-28 诺瓦提斯公司 用于治疗增殖性疾病的1H-咪唑并[4,5-c]喹啉酮化合物
NZ596487A (en) 2009-06-04 2012-11-30 Novartis Ag 1H-IMIDAZO[4,5-c]QUINOLINONE DERIVATIVES AND THE USE THEREOF AS PI3K INHIBITORS
AU2009349135A1 (en) * 2009-06-30 2012-02-16 Piramal Enterprises Limited Imidazo [4,5-c]quinoline derivatives and their use in the treatment of tumors and/or inflammation
JP2014504286A (ja) * 2010-12-06 2014-02-20 ピラマル エンタープライジーズ リミテッド 置換イミダゾキノリン誘導体
JO3003B1 (ar) 2011-01-14 2016-09-05 Lilly Co Eli مركب أيميدازو [4، 5 -c ] كينولين-2- واحد واستخدامه كمثبط كيناز PI3/mtor

Also Published As

Publication number Publication date
KR20130116302A (ko) 2013-10-23
EA022163B1 (ru) 2015-11-30
ECSP13012764A (es) 2013-09-30
EP2663564A1 (en) 2013-11-20
SV2013004496A (es) 2017-11-07
CO6731133A2 (es) 2013-08-15
NZ611541A (en) 2015-02-27
AU2012205619A1 (en) 2013-06-27
DK2663564T3 (en) 2015-01-12
CL2013002005A1 (es) 2013-12-27
US8658668B2 (en) 2014-02-25
CY1116007T1 (el) 2017-01-25
CA2824760A1 (en) 2012-07-19
PH12013501493A1 (en) 2021-06-02
DOP2013000158A (es) 2013-11-30
EP2663564B1 (en) 2014-12-17
PT2663564E (pt) 2015-02-24
WO2012097039A1 (en) 2012-07-19
SI2663564T1 (sl) 2015-01-30
MY164705A (en) 2018-01-30
US20130237562A1 (en) 2013-09-12
ME02019B (me) 2015-05-20
KR101561360B1 (ko) 2015-10-16
MX2013008185A (es) 2013-08-21
ZA201304757B (en) 2014-12-23
HUE024426T2 (en) 2016-01-28
CR20130289A (es) 2013-10-07
SG191744A1 (en) 2013-08-30
TWI518086B (zh) 2016-01-21
PE20140864A1 (es) 2014-07-19
HK1188454A1 (en) 2014-05-02
IL227165A (en) 2016-06-30
TW201307343A (zh) 2013-02-16
CA2824760C (en) 2016-03-15
HRP20150135T1 (xx) 2015-03-13
GT201300180A (es) 2014-04-08
TN2013000237A1 (en) 2014-11-10
EA201390823A1 (ru) 2013-12-30
US20120184577A1 (en) 2012-07-19
CN103282364A (zh) 2013-09-04
PL2663564T3 (pl) 2015-05-29
JO3003B1 (ar) 2016-09-05
RS53828B1 (sr) 2015-06-30
US8440829B2 (en) 2013-05-14
CN103282364B (zh) 2015-06-17
ES2531891T3 (es) 2015-03-20
BR112013017672A2 (pt) 2018-09-18
AU2012205619B2 (en) 2015-05-21
UA109921C2 (uk) 2015-10-26
JP5891247B2 (ja) 2016-03-22
JP2014502638A (ja) 2014-02-03

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