HUE024426T2 - Imidazo[4,5-c]kinolin-2-on vegyület és alkalmazása P13 kináz/mTOR kettõs inhibitorként - Google Patents

Imidazo[4,5-c]kinolin-2-on vegyület és alkalmazása P13 kináz/mTOR kettõs inhibitorként Download PDF

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Publication number
HUE024426T2
HUE024426T2 HUE12701207A HUE12701207A HUE024426T2 HU E024426 T2 HUE024426 T2 HU E024426T2 HU E12701207 A HUE12701207 A HU E12701207A HU E12701207 A HUE12701207 A HU E12701207A HU E024426 T2 HUE024426 T2 HU E024426T2
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HU
Hungary
Prior art keywords
cancer
compound
add
imidazo
quinolin
Prior art date
Application number
HUE12701207A
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English (en)
Inventor
David Anthony Barda
Mary Margaret Mader
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 HUE024426T2 publication Critical patent/HUE024426T2/hu

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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
    • A61K31/47Quinolines; 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

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  • 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)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Claims (6)

  1. és -^feaíma^ása P13 kínáz/mTGR kettes inhibitorként Szabadalmi igénypontok 1 ^agyőiét, maly a 8-p-|l-hidrokí»1“mailatil|pidbió^Íll-1-l2S)^2-ma^x|prcspli]-3~fnet!Í- í,3* dihiöFor2H4$yázo^^ vagy gyógy ászai slag e l fogad h ató sója.
  2. 2. Az 1. Igénypont szerinti vegyütei, mely a metökip?öpi|-3“meii- 1 jirdiNdFo-SB-irnidazp^S-sl^
  3. 3. A :2, Igénypont szánni vegyiét, mely a 8~|5-( 1-hidroxi-1 “metllel0pindin'3-il]~1~ps>2~ metokiprdpi|-3-melít-1 J^diNid:ro~2H-lmld:azD|4,S-elklnöiín-2-Qn kristályos formája, melynek röntgen-diffrakciós spektrumában 28 ± 0.2 érték mellei, 8.5? értéknél, és 9.06. 15.93, 18.29, éSi 18.8? közül egy vagy több értéknél jslenkezük jellemző maximum.
  4. 4. Gyógyászati készítmény, mely az 1-3, igénypontok bármelyike szerinti vegyilétet vágy-sóját és egy gyögyszerészeíüeg elfogadható hordozót, hígitószert vagy kötőanyagot tartalmaz.
  5. 5. Az 1-3. igénypontok bármelyike szerinti vegyöSet vagy sója terápiában történő alkalmazásra.
  6. 6. Az 1-3. igénypontok bármelyike szerinti vegyüieívagy sója rák kezelésében történi alkalmazásra. T, Vegyülő! a 8, Igénypont szerinti alkalmazásra, ahol a rák hólyagrák, vastagbélrák, gyomorrok, fej és nyak rák, NSCLC, mellrák, melanoma, petefészekrák, hasnyáimlrigyrák, prosztatarák, glioblastoma, tüdőrák:, veserák, szarkóma, hemafopoíetícus és lymphoid szövet fák, GNG rak, nyak! rák, endometrium rák,; májirak, bőrrák, gyomorrák, pajzsmirigyrák, felső légúti rák, és feégy^reze&rák.
HUE12701207A 2011-01-14 2012-01-11 Imidazo[4,5-c]kinolin-2-on vegyület és alkalmazása P13 kináz/mTOR kettõs inhibitorként HUE024426T2 (hu)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number Publication Date
HUE024426T2 true HUE024426T2 (hu) 2016-01-28

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
HUE12701207A HUE024426T2 (hu) 2011-01-14 2012-01-11 Imidazo[4,5-c]kinolin-2-on vegyület és alkalmazása P13 kináz/mTOR kettõs inhibitorként

Country Status (39)

Country Link
US (2) US8440829B2 (hu)
EP (1) EP2663564B1 (hu)
JP (1) JP5891247B2 (hu)
KR (1) KR101561360B1 (hu)
CN (1) CN103282364B (hu)
AR (1) AR084551A1 (hu)
AU (1) AU2012205619B2 (hu)
BR (1) BR112013017672A2 (hu)
CA (1) CA2824760C (hu)
CL (1) CL2013002005A1 (hu)
CO (1) CO6731133A2 (hu)
CR (1) CR20130289A (hu)
CY (1) CY1116007T1 (hu)
DK (1) DK2663564T3 (hu)
DO (1) DOP2013000158A (hu)
EA (1) EA022163B1 (hu)
EC (1) ECSP13012764A (hu)
ES (1) ES2531891T3 (hu)
GT (1) GT201300180A (hu)
HK (1) HK1188454A1 (hu)
HR (1) HRP20150135T1 (hu)
HU (1) HUE024426T2 (hu)
IL (1) IL227165A (hu)
JO (1) JO3003B1 (hu)
ME (1) ME02019B (hu)
MX (1) MX2013008185A (hu)
MY (1) MY164705A (hu)
PE (1) PE20140864A1 (hu)
PL (1) PL2663564T3 (hu)
PT (1) PT2663564E (hu)
RS (1) RS53828B1 (hu)
SG (1) SG191744A1 (hu)
SI (1) SI2663564T1 (hu)
SV (1) SV2013004496A (hu)
TN (1) TN2013000237A1 (hu)
TW (1) TWI518086B (hu)
UA (1) UA109921C2 (hu)
WO (1) WO2012097039A1 (hu)
ZA (1) ZA201304757B (hu)

Families Citing this family (22)

* 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
EA201891005A1 (ru) 2015-12-15 2018-12-28 Эли Лилли Энд Компани Комбинированная терапия рака
US10722484B2 (en) 2016-03-09 2020-07-28 K-Gen, Inc. Methods of cancer treatment
RU2754452C2 (ru) * 2016-04-12 2021-09-02 Эли Лилли Энд Компани Комбинированная терапия ингибиторами notch и pi3k/mtor для применения в лечении рака
AU2017249078B2 (en) 2016-04-12 2022-10-20 Eli Lilly And Company Combination therapy with notch and CDK4/6 inhibitors for the treatment of cancer
AU2017268187A1 (en) 2016-05-20 2018-11-29 Eli Lilly And Company Combination therapy with notch and PD-1 or PD-L1 inhibitors
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
JP2020507605A (ja) 2017-02-17 2020-03-12 フレッド ハッチンソン キャンサー リサーチ センター Bcma関連癌および自己免疫疾患の治療のための併用療法
WO2019157516A1 (en) 2018-02-12 2019-08-15 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
FI3813946T3 (fi) 2018-06-15 2024-06-25 Janssen Pharmaceutica Nv Rapamysiinianalogeja ja niiden käyttötapoja
WO2020081329A1 (en) * 2018-10-18 2020-04-23 Camp4 Therapeutics Corporation Methods and compositions for modulating pcsk9 and angptl3 expression
US11819476B2 (en) 2019-12-05 2023-11-21 Janssen Pharmaceutica Nv Rapamycin analogs and uses thereof
WO2022060377A1 (en) * 2020-09-21 2022-03-24 Wei Zhong Substituted 1-(3,3-difluoropiperidin-4-yl)-imidazo[4,5-c] quinolin-2-one compounds with blood-brain barrier penetrable capability
EP3992191A1 (en) 2020-11-03 2022-05-04 Deutsches Krebsforschungszentrum Imidazo[4,5-c]quinoline compounds and their use as atm kinase inhibitors

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
WO2005054237A1 (en) 2003-11-21 2005-06-16 Novartis Ag 1h-imidazoquinoline derivatives as protein kinase inhibitors
US8158794B2 (en) * 2005-02-23 2012-04-17 3M Innovative Properties Company Hydroxyalkyl substituted imidazoquinoline compounds and methods
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
AU2006311871B2 (en) 2005-11-04 2011-03-03 3M Innovative Properties Company Hydroxy and alkoxy substituted 1H-imidazoquinolines and methods
WO2007106854A2 (en) 2006-03-15 2007-09-20 Coley Pharmaceutical Group, Inc. Hydroxy and alkoxy substituted 1h-imidazonaphthyridines and methods
CA2735932C (en) * 2008-09-30 2013-07-09 Pfizer Inc. Imidazo[1,5]naphthyridine compounds, their pharmaceutical use and compositions
WO2010139747A1 (en) 2009-06-04 2010-12-09 Novartis Ag 1H-IMIDAZO[4, 5-c]QUINOLINONE COMPOUNDS, USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES
EP2438064A1 (en) 2009-06-04 2012-04-11 Novartis AG 1H-IMIDAZO[4,5-c]QUINOLINONE DERIVATIVES
EP2448937B1 (en) * 2009-06-30 2014-04-09 Piramal Enterprises Limited Imidazo[4,5-c]quinoline derivatives and their use in the treatment of tumours and/or inflammations
CN103402520A (zh) * 2010-12-06 2013-11-20 皮拉马尔企业有限公司 具有取代基的咪唑并喹啉衍生物
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
PT2663564E (pt) 2015-02-24
KR20130116302A (ko) 2013-10-23
TW201307343A (zh) 2013-02-16
MX2013008185A (es) 2013-08-21
US20130237562A1 (en) 2013-09-12
ME02019B (me) 2015-05-20
SG191744A1 (en) 2013-08-30
EA201390823A1 (ru) 2013-12-30
SV2013004496A (es) 2017-11-07
EA022163B1 (ru) 2015-11-30
JP5891247B2 (ja) 2016-03-22
CA2824760C (en) 2016-03-15
AU2012205619A1 (en) 2013-06-27
KR101561360B1 (ko) 2015-10-16
AR084551A1 (es) 2013-05-22
HK1188454A1 (en) 2014-05-02
WO2012097039A1 (en) 2012-07-19
TN2013000237A1 (en) 2014-11-10
BR112013017672A2 (pt) 2018-09-18
CN103282364A (zh) 2013-09-04
UA109921C2 (uk) 2015-10-26
ECSP13012764A (es) 2013-09-30
TWI518086B (zh) 2016-01-21
RS53828B1 (en) 2015-06-30
DK2663564T3 (en) 2015-01-12
MY164705A (en) 2018-01-30
CN103282364B (zh) 2015-06-17
EP2663564A1 (en) 2013-11-20
EP2663564B1 (en) 2014-12-17
PE20140864A1 (es) 2014-07-19
ZA201304757B (en) 2014-12-23
US20120184577A1 (en) 2012-07-19
US8658668B2 (en) 2014-02-25
DOP2013000158A (es) 2013-11-30
IL227165A (en) 2016-06-30
NZ611541A (en) 2015-02-27
JP2014502638A (ja) 2014-02-03
US8440829B2 (en) 2013-05-14
HRP20150135T1 (en) 2015-03-13
JO3003B1 (ar) 2016-09-05
CO6731133A2 (es) 2013-08-15
CA2824760A1 (en) 2012-07-19
CY1116007T1 (el) 2017-01-25
ES2531891T3 (es) 2015-03-20
CR20130289A (es) 2013-10-07
CL2013002005A1 (es) 2013-12-27
PL2663564T3 (pl) 2015-05-29
AU2012205619B2 (en) 2015-05-21
GT201300180A (es) 2014-04-08
SI2663564T1 (sl) 2015-01-30

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