MX390537B - Imidazolonilquinolinas y el uso de las mismas como inhibidores de cinasa atm - Google Patents

Imidazolonilquinolinas y el uso de las mismas como inhibidores de cinasa atm

Info

Publication number
MX390537B
MX390537B MX2020011558A MX2020011558A MX390537B MX 390537 B MX390537 B MX 390537B MX 2020011558 A MX2020011558 A MX 2020011558A MX 2020011558 A MX2020011558 A MX 2020011558A MX 390537 B MX390537 B MX 390537B
Authority
MX
Mexico
Prior art keywords
kinase inhibitors
imidazolonylquinolines
atm kinase
atm
het1
Prior art date
Application number
MX2020011558A
Other languages
English (en)
Spanish (es)
Other versions
MX2020011558A (es
Inventor
Kai Schiemann
Thomas Fuchss
Original Assignee
Merck Patent Gmbh
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 Merck Patent Gmbh filed Critical Merck Patent Gmbh
Publication of MX2020011558A publication Critical patent/MX2020011558A/es
Publication of MX390537B publication Critical patent/MX390537B/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
    • A61K31/4375Heterocyclic 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 six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • 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
    • A61K31/33Heterocyclic 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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
MX2020011558A 2015-04-02 2016-03-31 Imidazolonilquinolinas y el uso de las mismas como inhibidores de cinasa atm MX390537B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP15000968 2015-04-02
PCT/EP2016/000542 WO2016155884A1 (de) 2015-04-02 2016-03-31 Imidazolonylchinoline und deren verwendung als atm kinase inhibitoren

Publications (2)

Publication Number Publication Date
MX2020011558A MX2020011558A (es) 2022-03-09
MX390537B true MX390537B (es) 2025-03-20

Family

ID=52814780

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2020011558A MX390537B (es) 2015-04-02 2016-03-31 Imidazolonilquinolinas y el uso de las mismas como inhibidores de cinasa atm
MX2017012613A MX376947B (es) 2015-04-02 2016-03-31 Imidazolonilquinolinas y el uso de las mismas como inhibidores de cinasa atm.

Family Applications After (1)

Application Number Title Priority Date Filing Date
MX2017012613A MX376947B (es) 2015-04-02 2016-03-31 Imidazolonilquinolinas y el uso de las mismas como inhibidores de cinasa atm.

Country Status (23)

Country Link
US (5) US10457677B2 (https=)
EP (3) EP3868761B1 (https=)
JP (2) JP6791873B2 (https=)
KR (2) KR102652052B1 (https=)
CN (3) CN107889488B (https=)
AU (4) AU2016239270B2 (https=)
BR (1) BR122019005502B1 (https=)
DK (2) DK3277681T3 (https=)
ES (3) ES2880626T3 (https=)
HR (2) HRP20191396T1 (https=)
HU (2) HUE054745T2 (https=)
IL (3) IL254714B (https=)
LT (2) LT3277681T (https=)
MX (2) MX390537B (https=)
PL (2) PL3560924T3 (https=)
PT (2) PT3277681T (https=)
RS (2) RS62082B1 (https=)
RU (1) RU2743343C2 (https=)
SG (2) SG10202002181UA (https=)
SI (2) SI3277681T1 (https=)
TR (1) TR201911244T4 (https=)
WO (1) WO2016155884A1 (https=)
ZA (1) ZA201707423B (https=)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RS62082B1 (sr) * 2015-04-02 2021-08-31 Merck Patent Gmbh Imidazolonilhinolini i njihova primena kao inhibitora atm kinaze
GB201516504D0 (en) 2015-09-17 2015-11-04 Astrazeneca Ab Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer
GB201519406D0 (en) * 2015-11-03 2015-12-16 Astrazeneca Ab Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer
CN110312717B (zh) * 2017-02-27 2022-04-12 上海瑛派药业有限公司 取代的稠合杂芳三环化合物作为激酶抑制剂及其应用
JOP20190209A1 (ar) * 2017-03-16 2019-09-12 Astrazeneca Ab مركبات إيميدازو [ 4، 5-c ] كينولين-2-أون ديوترومية واستخدامها في علاج السرطان
MX2020007442A (es) 2018-01-12 2020-09-14 Prolynx Llc Protocolo para minimizar la toxicidad de dosificaciones de combinacion y agente formador de imagen para verificacion.
EP3765019A1 (en) 2018-03-14 2021-01-20 Merck Patent GmbH Compounds and uses thereof to treat tumors in a subject
FI3904350T3 (fi) 2018-04-12 2023-11-15 Bayer Ag N-(syklopropyylimetyyli)-5-(metyylisulfonyyli)-n-{1-[1-(pyrimidin-2-yyli)-1h-1,2,4-triatsol-5-yyli]etyyli}bentsamidijohdannaisia ja vastaavia pyridiinikarboksamidijohdannaisia tuholaistorjunta-aineina
WO2019201283A1 (en) * 2018-04-20 2019-10-24 Xrad Therapeutics, Inc. Dual atm and dna-pk inhibitors for use in anti-tumor therapy
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
GB201814487D0 (en) * 2018-09-06 2018-10-24 Cycle Pharmaceuticals Ltd Cancer
CN109045042A (zh) * 2018-09-21 2018-12-21 上海交通大学医学院附属上海儿童医学中心 Atm抑制剂在制备抑制急性淋巴细胞性白血病复发的药物中的应用
CN112771045B (zh) * 2018-09-30 2022-04-19 南京明德新药研发有限公司 喹啉并吡咯烷-2-酮类衍生物及其应用
RS65518B1 (sr) 2019-03-27 2024-06-28 Merck Patent Gmbh Jedinjenja imidazolonilhinolina i njihova terapijska upotreba
ES3008232T3 (en) * 2019-07-30 2025-03-21 Xrad Therapeutics Inc Dual atm and dna-pk inhibitors for use in anti-tumor therapy
WO2021084124A1 (en) 2019-11-01 2021-05-06 Ares Trading S.A. COMBINED INHIBITION OF PD-1, TGFβ AND ATM TOGETHER WITH RADIOTHERAPY FOR THE TREATMENT OF CANCER
JP7727627B2 (ja) * 2019-12-04 2025-08-21 シーエイチディーアイ ファウンデーション,インコーポレーテッド Atmキナーゼ阻害剤及び組成物並びにそれらの使用の方法
WO2021139814A1 (zh) * 2020-01-09 2021-07-15 南京明德新药研发有限公司 喹啉并咪唑类化合物及其应用
CN115380031A (zh) * 2020-03-30 2022-11-22 南京明德新药研发有限公司 作为atm抑制剂的喹啉并吡咯烷-2-酮类化合物的晶型及其应用
IL299178A (en) * 2020-06-18 2023-02-01 Merck Patent Gmbh Atm inhibitors for use in treatment of viral infections
US20230256110A1 (en) 2020-06-24 2023-08-17 Astrazeneca Uk Limited Combination of antibody-drug conjugate and atm inhibitor
MX2023002792A (es) 2020-09-18 2023-03-16 Merck Patent Gmbh Preparacion farmaceutica.
EP4142710B1 (en) 2020-09-21 2024-01-31 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
CN115232122B (zh) * 2021-04-23 2024-05-31 石药集团中奇制药技术(石家庄)有限公司 炔类化合物及其制备和应用
CN115716829B (zh) * 2022-11-13 2024-05-31 药康众拓(江苏)医药科技有限公司 一种喹啉并咪唑酮联氘代吡唑类化合物及其应用
AU2023385854A1 (en) 2022-11-23 2025-06-12 Forward Therapeutics, Inc. MODULATORS OF TNF-α ACTIVITY
WO2025157979A1 (en) 2024-01-26 2025-07-31 Merck Patent Gmbh Synthesis route for preparing 8-(1,3-dimethyl-1h-pyrazol-4-yl)-1-(sa)-(3-fluoro-5-methoxy-pyridin-4-yl)-7-methoxy-3-methyl-1,3-dihydro-imidazo[4,5-c]quinolin-2-one
WO2025212627A1 (en) 2024-04-03 2025-10-09 Forward Therapeutics, Inc. Modulators of tnf-alpha activity
WO2025217307A1 (en) 2024-04-09 2025-10-16 Revolution Medicines, Inc. Methods for predicting response to a ras(on) inhibitor and combination therapies
TW202547461A (zh) 2024-05-17 2025-12-16 美商銳新醫藥公司 Ras抑制劑
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors
WO2026072904A2 (en) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions and methods for treating lung cancer

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6221335B1 (en) * 1994-03-25 2001-04-24 Isotechnika, Inc. Method of using deuterated calcium channel blockers
PT1104760E (pt) * 1999-12-03 2003-06-30 Pfizer Prod Inc Compostos de sulfamoil-heteroarilpirazole como agentes analgesicos e anti-inflamatorios
GB0211649D0 (en) 2002-05-21 2002-07-03 Novartis Ag Organic compounds
PL1879893T3 (pl) 2005-03-21 2010-11-30 Ferrer Int Sposób otrzymywania podstawionych w pozycji 1, związków 1H-imidazo[4,5-c]chinolino-4-aminowych i związki pośrednie
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
EP1934201A1 (en) * 2005-10-06 2008-06-25 Auspex Pharmaceuticals Inc. Deuterated inhibitors of gastric h+, k+-atpase with enhanced therapeutic properties
US7750168B2 (en) * 2006-02-10 2010-07-06 Sigma-Aldrich Co. Stabilized deuteroborane-tetrahydrofuran complex
AU2008218806B2 (en) 2007-02-20 2011-12-01 Novartis Ag Imidazoquinolines as dual lipid kinase and mTOR inhibitors
KR20100126553A (ko) 2008-03-26 2010-12-01 노파르티스 아게 Vegf-유도성 혈관신생 과정의 유력한 조절제로서의 이미다조퀴놀린 및 피리미딘 유도체
CN104592231A (zh) 2008-06-10 2015-05-06 Abbvie公司 新的三环化合物
CN102170873B (zh) 2008-10-01 2014-07-30 诺华股份有限公司 用于治疗与hedgehog通路有关的病症的smoothened拮抗
JP2012528829A (ja) 2009-06-04 2012-11-15 ノバルティス アーゲー 1H−イミダゾ[4,5−c]キノリノン化合物
AU2010255727B2 (en) * 2009-06-04 2013-02-28 Novartis Ag 1H-imidazo[4,5-c]quinolinone derivatives
GB0919423D0 (en) * 2009-11-05 2009-12-23 Glaxosmithkline Llc Novel compounds
BR112012022868A2 (pt) * 2010-03-16 2018-06-05 Merck Patent Gmbh morfolinilquinazolinas
AU2011273931B2 (en) * 2010-06-28 2015-04-23 Merck Patent Gmbh 2,4- diaryl - substituted [1,8] naphthyridines as kinase inhibitors for use against cancer
CN102372711B (zh) 2010-08-18 2014-09-17 山东轩竹医药科技有限公司 咪唑并喹啉类PI3K和mTOR双重抑制剂
DE102010035744A1 (de) * 2010-08-28 2012-03-01 Merck Patent Gmbh Imidazolonylchinoline
CN102399218A (zh) 2010-09-16 2012-04-04 和记黄埔医药(上海)有限公司 一类并合三杂环及其作为pi3k抑制剂的用途
WO2012075253A2 (en) 2010-12-03 2012-06-07 Novartis Ag Pharmaceutical compositions
CN103012398B (zh) 2011-09-19 2015-10-14 上海恒瑞医药有限公司 咪唑并喹啉类衍生物及其可药用盐、其制备方法及其在医药上的应用
US9879003B2 (en) 2012-04-11 2018-01-30 Dana-Farber Cancer Institute, Inc. Host targeted inhibitors of dengue virus and other viruses
RU2014154009A (ru) 2012-06-06 2016-08-10 Новартис Аг Комбинация ингибитора 17-альфа-гидроксилазы (с17,20-лиазы) и специфического ингибитора pi-3k для лечения онкологического заболевания
NO2714752T3 (https=) * 2014-05-08 2018-04-21
RS62082B1 (sr) 2015-04-02 2021-08-31 Merck Patent Gmbh Imidazolonilhinolini i njihova primena kao inhibitora atm kinaze

Also Published As

Publication number Publication date
ES2741853T3 (es) 2020-02-12
AU2016239270A1 (en) 2017-11-16
JP2021046403A (ja) 2021-03-25
BR112017020941A2 (pt) 2018-07-10
US20230203034A1 (en) 2023-06-29
AU2025200385A1 (en) 2025-02-13
HUE045477T2 (hu) 2019-12-30
HUE054745T2 (hu) 2021-09-28
DK3560924T3 (da) 2021-06-28
US11608338B2 (en) 2023-03-21
ES2880626T3 (es) 2021-11-25
RS59139B1 (sr) 2019-09-30
US20210198257A1 (en) 2021-07-01
NZ774407A (en) 2024-09-27
SI3277681T1 (sl) 2019-09-30
PL3560924T3 (pl) 2021-10-11
AU2020204241B2 (en) 2022-11-17
SG10202002181UA (en) 2020-05-28
LT3560924T (lt) 2021-08-25
RU2743343C2 (ru) 2021-02-17
BR122019005502B1 (pt) 2024-02-27
US20190211013A1 (en) 2019-07-11
CN111747952A (zh) 2020-10-09
HRP20210981T1 (hr) 2021-09-17
WO2016155884A1 (de) 2016-10-06
RU2017138100A (ru) 2019-05-08
CN111689963A (zh) 2020-09-22
NZ736641A (en) 2024-09-27
MX2017012613A (es) 2018-01-24
US10745399B2 (en) 2020-08-18
SI3560924T1 (sl) 2021-08-31
ZA201707423B (en) 2021-05-26
CN107889488B (zh) 2020-08-11
LT3277681T (lt) 2019-08-12
MX2020011558A (es) 2022-03-09
HRP20191396T1 (hr) 2019-11-01
RU2017138100A3 (https=) 2019-10-04
KR102652052B1 (ko) 2024-03-27
EP3277681B1 (de) 2019-05-08
IL254714A0 (en) 2017-11-30
KR20170132323A (ko) 2017-12-01
JP2018510191A (ja) 2018-04-12
IL254714B (en) 2020-01-30
EP3560924B1 (de) 2021-03-31
EP3277681A1 (de) 2018-02-07
AU2016239270B2 (en) 2020-03-26
SG11201708065QA (en) 2017-10-30
TR201911244T4 (tr) 2019-08-21
IL271494A (en) 2020-02-27
JP6791873B2 (ja) 2020-11-25
IL282584A (en) 2021-06-30
AU2020204241A1 (en) 2020-07-16
US10457677B2 (en) 2019-10-29
CN107889488A (zh) 2018-04-06
US10975075B2 (en) 2021-04-13
MX376947B (es) 2025-03-07
JP7111790B2 (ja) 2022-08-02
AU2022256215A1 (en) 2022-11-24
US20200325137A1 (en) 2020-10-15
DK3277681T3 (da) 2019-07-29
IL271494B (en) 2021-05-31
KR20240044525A (ko) 2024-04-04
EP3560924A1 (de) 2019-10-30
PT3277681T (pt) 2019-08-20
ES2946507T3 (es) 2023-07-20
IL282584B (en) 2021-12-01
EP3868761A1 (de) 2021-08-25
EP3868761B1 (de) 2023-03-01
RS62082B1 (sr) 2021-08-31
US20180072715A1 (en) 2018-03-15
CA2981365A1 (en) 2016-10-06
PT3560924T (pt) 2021-07-02
PL3277681T3 (pl) 2019-10-31

Similar Documents

Publication Publication Date Title
MX390537B (es) Imidazolonilquinolinas y el uso de las mismas como inhibidores de cinasa atm
CY1121831T1 (el) Παραγωγα θειενο [2,3-c] πυρρολ-4-ονης ως αναστολεις της erk
CY1123626T1 (el) Ετεροκυκλικοι αναστολεις πρωτεϊνικης κινασης
CL2015001985A1 (es) Compuestos de tiazolcarboxamidas y piridinacarboxamida, inhibidores de quinasa pim.
MX384948B (es) Derivados de carbonucleósidos sustituidos útiles como agentes antineoplásicos.
CO2018000631A2 (es) Compuestos bicíclicos como inhibidores de atx
MX390348B (es) Compuestos de benzimidazol como inhibidores de c-kit
CO2018000668A2 (es) Nuevos compuestos bicíclicos como inhibidores duales de atx/ca
CL2015002932A1 (es) Inhibidores de proteína quinasa
CO2017011754A2 (es) Amidas heterocíclicas como inhibidores de quinasa
CL2019001993A1 (es) Inhibidores selectivos de jak1.
CL2019002609A1 (es) Compuestos heterocíclicos útiles como inhibidores dobles atx/ca.
MX381160B (es) Agonistas del receptor de apelina y metodos de uso.
CL2015002194A1 (es) Inhbidores de erk y sus usos
ECSP17016797A (es) Indazoles sustituidos con benzilo como inhibidores de bub1
CR20180374A (es) Compuestos heterocíclicos como inmunomoduladores
CL2016000150A1 (es) Compuestos y composiciones como inhibidores de la mek
EA202090291A3 (ru) Производные бипиразола в качестве ингибиторов jak
MX371312B (es) Pirazolil-ureas como inhibidores de quinasas.
UY35643A (es) Nuevos compuestos útiles como nematicidas, sus composiciones y métodos de uso
CL2016001840A1 (es) Compuestos derivados de pirimidinas fusionadas como inhibidores del complejo p97; composicion farmaceutica y uso en el tratamiento del cancer.
MX2018008362A (es) Derivados de quinolin-2-ona.
MX381487B (es) Ciertos inhibidores de la proteina quinasa.
MX2017004600A (es) Compuestos de aminopurina sustituida, composiciones del mismo, y metodos de tratamiento con los mismos.
CL2018001171A1 (es) Compuestos de imidazo[4,5-c]quinolin-2-ona y su uso en el tratamiento del cáncer