SV2018005655A - "derivados de 8-[6-[3-(amino)propoxi]-3-piridil]1-isopropilimidazo[4,5-c]quinolin-2-ona como moduladores selectivos de la cinasa de la ataxia telangiectasia mutada (atm) para el tratamiento del cancer" - Google Patents
"derivados de 8-[6-[3-(amino)propoxi]-3-piridil]1-isopropilimidazo[4,5-c]quinolin-2-ona como moduladores selectivos de la cinasa de la ataxia telangiectasia mutada (atm) para el tratamiento del cancer"Info
- Publication number
- SV2018005655A SV2018005655A SV2018005655A SV2018005655A SV2018005655A SV 2018005655 A SV2018005655 A SV 2018005655A SV 2018005655 A SV2018005655 A SV 2018005655A SV 2018005655 A SV2018005655 A SV 2018005655A SV 2018005655 A SV2018005655 A SV 2018005655A
- Authority
- SV
- El Salvador
- Prior art keywords
- quinolin
- atm
- compounds
- ona
- cancer
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
LA MEMORIA DESCRIPTIVA SE REFIERE EN GENERAL A COMPUESTOS DE FÓRMULA (I): (VER FORMULA) Y SALES FARMACÉUTICAMENTE ACEPTABLES DE ESTOS, DONDE R1, R2, R3, R4 Y R5 TIENEN CUALQUIERA DE LOS SIGNIFICADOS DEFINIDOS EN LA PRESENTE. LA MEMORIA DESCRIPTIVA TAMBIÉN SE REFIERE AL USO DE COMPUESTOS DE FÓRMULA (I) Y SALES DE ESTOS PARA TRATAR O PREVENIR UNA ENFERMEDAD MEDIADA POR ATM, INCLUIDO EL CÁNCER. LA MEMORIA DESCRIPTIVA SE REFIERE ADEMÁS A COMPOSICIONES FARMACÉUTICAS QUE COMPRENDEN COMPUESTOS DE TIPO IMIDAZO[4,5-C]QUINOLIN-2-ONA SUSTITUIDOS Y SALES FARMACÉUTICAMENTE ACEPTABLES DE ESTOS; KITS QUE COMPRENDEN TALES COMPUESTOS Y SALES; MÉTODOS DE PRODUCCIÓN DE TALES COMPUESTOS Y SALES; E INTERMEDIOS ÚTILES EN TAL PRODUCCIÓN
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1516504.6A GB201516504D0 (en) | 2015-09-17 | 2015-09-17 | Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer |
Publications (1)
Publication Number | Publication Date |
---|---|
SV2018005655A true SV2018005655A (es) | 2018-04-27 |
Family
ID=54544418
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SV2018005655A SV2018005655A (es) | 2015-09-17 | 2018-03-16 | "derivados de 8-[6-[3-(amino)propoxi]-3-piridil]1-isopropilimidazo[4,5-c]quinolin-2-ona como moduladores selectivos de la cinasa de la ataxia telangiectasia mutada (atm) para el tratamiento del cancer" |
Country Status (37)
Country | Link |
---|---|
US (5) | US9856255B2 (es) |
EP (2) | EP3683220B1 (es) |
JP (1) | JP6605130B2 (es) |
KR (2) | KR102028848B1 (es) |
CN (1) | CN108137576B (es) |
AR (1) | AR106053A1 (es) |
AU (1) | AU2016323399B2 (es) |
BR (1) | BR112018004325B1 (es) |
CA (1) | CA2997399C (es) |
CL (1) | CL2018000677A1 (es) |
CO (1) | CO2018002829A2 (es) |
CR (1) | CR20180172A (es) |
CY (1) | CY1124680T1 (es) |
DK (2) | DK3683220T3 (es) |
DO (1) | DOP2018000065A (es) |
EA (1) | EA033284B1 (es) |
ES (2) | ES2920876T3 (es) |
GB (1) | GB201516504D0 (es) |
HK (2) | HK1255408A1 (es) |
HR (1) | HRP20210149T1 (es) |
HU (2) | HUE053066T2 (es) |
IL (1) | IL257847B (es) |
LT (1) | LT3350180T (es) |
MX (1) | MX2018003186A (es) |
MY (1) | MY195669A (es) |
NI (1) | NI201800033A (es) |
PE (1) | PE20181078A1 (es) |
PH (1) | PH12018500532A1 (es) |
PL (2) | PL3683220T3 (es) |
PT (2) | PT3683220T (es) |
RS (1) | RS61435B1 (es) |
SI (1) | SI3350180T1 (es) |
SV (1) | SV2018005655A (es) |
TN (1) | TN2018000078A1 (es) |
TW (2) | TWI762109B (es) |
WO (1) | WO2017046216A1 (es) |
ZA (1) | ZA202209171B (es) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB201516504D0 (en) * | 2015-09-17 | 2015-11-04 | Astrazeneca Ab | Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer |
GB201608227D0 (en) * | 2016-05-11 | 2016-06-22 | Astrazeneca Ab | Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer |
JOP20190209A1 (ar) * | 2017-03-16 | 2019-09-12 | Astrazeneca Ab | مركبات إيميدازو [ 4، 5-c ] كينولين-2-أون ديوترومية واستخدامها في علاج السرطان |
CN111344293A (zh) | 2017-09-20 | 2020-06-26 | 阿斯利康(瑞典)有限公司 | 1,3-二氢咪唑并[4,5-c]噌啉-2-酮化合物及其在治疗癌症中的用途 |
WO2020052688A1 (en) | 2018-09-14 | 2020-03-19 | Suzhou Zanrong Pharma Limited | 1-ISOPROPYL-3-METHYL-8- (PYRIDIN-3-YL) -1, 3-DIHYDRO-2H-IMIDAZO [4, 5-c] CINNOLIN-2-ONE AS SELECTIVE MODULATORS OF ATAXIA TELANGIECTASIA MUTATED (ATM) KINASE AND USES THEREOF |
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 |
JP7407298B2 (ja) * | 2020-03-04 | 2023-12-28 | ファロス・アイバイオ・カンパニー・リミテッド | 2,3,5-置換されたチオフェン化合物の卵巣癌の予防、改善または治療用途 |
WO2021260580A1 (en) | 2020-06-24 | 2021-12-30 | Astrazeneca Uk Limited | Combination of antibody-drug conjugate and atm inhibitor |
CA3194102A1 (en) * | 2020-09-28 | 2022-03-31 | Chuanwu ZHAO | A class of fused ring compounds, and preparation and use thereof |
EP3992191A1 (en) | 2020-11-03 | 2022-05-04 | Deutsches Krebsforschungszentrum | Imidazo[4,5-c]quinoline compounds and their use as atm kinase inhibitors |
WO2022125614A1 (en) * | 2020-12-09 | 2022-06-16 | Stingray Therapeutics, Inc. | Phosphonates as inhibitors of enpp1 and cdnp |
WO2022193166A1 (en) * | 2021-03-17 | 2022-09-22 | Suzhou Zanrong Pharma Limited | Selective modulators of ataxia telangiectasia mutated (atm) kinase and uses thereof |
CN115304598B (zh) * | 2021-08-25 | 2024-05-31 | 石药集团中奇制药技术(石家庄)有限公司 | 一种杂环类化合物及其制备方法和用途 |
GB202114704D0 (en) | 2021-10-14 | 2021-12-01 | Univ Birmingham | ATM inhibition |
IL314381A (en) * | 2022-01-26 | 2024-09-01 | Chia Tai Tianqing Pharmaceutical Group Co Ltd | A compound containing a hydrazino group |
AU2022452885A1 (en) * | 2022-04-11 | 2024-09-05 | Wei Zhong | Substituted 1-(3,3-difluoropiperidin-4-yl)-imidazo[4,5-c] quinolin-2-one derivative crystal form, salt crystal form, preparation method and application |
Family Cites Families (92)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2094139A1 (en) | 1990-10-22 | 1992-04-23 | Frederick W. Wassmundt | Aryl and heteroaryl compounds having anti-retrovirus activity |
TW301607B (es) | 1993-03-09 | 1997-04-01 | Takeda Pharm Industry Co Ltd | |
GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
NZ330868A (en) | 1996-02-13 | 2000-01-28 | Zeneca Ltd | 4-phenoxy, phenylthio or phenylamino substituted quinazoline derivatives ane medicaments useful as VEGF inhibitors |
ES2169355T3 (es) | 1996-03-05 | 2002-07-01 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina. |
GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
US6632823B1 (en) | 1997-12-22 | 2003-10-14 | Merck & Co., Inc. | Substituted pyridine compounds useful as modulators of acetylcholine receptors |
EP1107759A1 (en) | 1998-08-03 | 2001-06-20 | Basf Corporation | Pyridinones for the treatment of sexual dysfunction |
CA2362401A1 (en) | 1999-02-04 | 2000-08-10 | Paul Fleming | G-protein coupled heptahelical receptor binding compounds and methods of use thereof |
US20020151712A1 (en) | 1999-09-14 | 2002-10-17 | Nan-Horng Lin | 3-pyrrolidinyloxy-3'-pyridyl ether compounds useful for controlling chemical synaptic transmission |
AU2002213467A1 (en) | 2000-10-11 | 2002-04-22 | Chemocentryx, Inc. | Modulation of ccr4 function |
WO2002030357A2 (en) | 2000-10-11 | 2002-04-18 | Chemocentryx, Inc. | Compounds and methods for modulating ccr4 function |
EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
AU2002303156A1 (en) | 2001-03-23 | 2002-10-08 | Bethesda Pharmaceuticals, Inc. | Design and synthesis of optimized ligands for ppar |
JP2002293745A (ja) | 2001-03-29 | 2002-10-09 | St Marianna Univ School Of Medicine | 慢性関節リウマチ治療剤 |
WO2003084997A1 (en) | 2001-04-10 | 2003-10-16 | Transtech Pharma, Inc. | Probes, systems and methods for drug discovery |
WO2002087618A1 (fr) | 2001-04-27 | 2002-11-07 | Takeda Chemical Industries, Ltd. | Methode de prevention et de traitement du cancer |
WO2002094264A1 (en) | 2001-05-23 | 2002-11-28 | Tularik Inc. | Ccr4 antagonists |
EP1270535A3 (de) | 2001-06-20 | 2004-02-18 | Clariant GmbH | Verfahren zur Herstellung von substituierten aromatischen Verbindungen |
JP4082888B2 (ja) | 2001-10-17 | 2008-04-30 | 広栄化学工業株式会社 | ビアリール化合物の製造法 |
AU2003214873A1 (en) | 2002-01-18 | 2003-09-02 | Ceretek Llc | Methods of treating conditions associated with an edg receptor |
JP4167848B2 (ja) | 2002-04-10 | 2008-10-22 | 広栄化学工業株式会社 | ビアリール化合物の製造法 |
GB0211649D0 (en) | 2002-05-21 | 2002-07-03 | Novartis Ag | Organic compounds |
WO2004007472A1 (ja) | 2002-07-10 | 2004-01-22 | Ono Pharmaceutical Co., Ltd. | Ccr4アンタゴニストおよびその医薬用途 |
EP1542948A4 (en) | 2002-08-23 | 2008-12-17 | Univ Connecticut | NEW BIPHENYL AND BIPHENYLENE CANNABINOIDS |
JP2006511460A (ja) | 2002-08-23 | 2006-04-06 | ユニバーシティ オブ コネチカット | 治療適応を持つケトカンナビノイド |
EP1599475A2 (en) * | 2003-03-06 | 2005-11-30 | Eisai Co., Ltd. | Jnk inhibitors |
US20070105959A1 (en) | 2003-03-11 | 2007-05-10 | Shinya Kusuda | Cynnamyl alcohol derivative compounds and drugs containing the compounds as active ingredient |
WO2004113258A1 (ja) | 2003-06-20 | 2004-12-29 | Shionogi & Co., Ltd. | 炭素−炭素結合生成反応 |
WO2005023771A1 (ja) | 2003-09-05 | 2005-03-17 | Ono Pharmaceutical Co., Ltd. | ケモカインレセプターアンタゴニストおよびその医薬用途 |
JP2005170939A (ja) | 2003-11-20 | 2005-06-30 | Takeda Chem Ind Ltd | 糖尿病の予防・治療剤 |
RU2006121646A (ru) | 2003-11-21 | 2008-01-10 | Новартис АГ (CH) | Производные 1h-имидазохинолина в качестве ингибиторов протеинкиназы |
WO2006038594A1 (ja) | 2004-10-04 | 2006-04-13 | Ono Pharmaceutical Co., Ltd. | N型カルシウムチャネル阻害薬 |
WO2006064757A1 (ja) | 2004-12-13 | 2006-06-22 | Ono Pharmaceutical Co., Ltd. | アミノカルボン酸誘導体およびその医薬用途 |
GB0510390D0 (en) * | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
US20070032522A1 (en) | 2005-07-01 | 2007-02-08 | Kumar Dange V | Antiviral agents |
US20090306035A1 (en) | 2005-08-26 | 2009-12-10 | Emory University | Compounds and Methods for modulating the Silencing of a Polynucleotide of Interest |
JO3598B1 (ar) | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني |
JP2009023986A (ja) | 2006-11-08 | 2009-02-05 | Pharma Ip | 抗癌剤としてのビアリール誘導体 |
CL2008000191A1 (es) | 2007-01-25 | 2008-08-22 | Astrazeneca Ab | Compuestos derivados de 4-amino-cinnotina-3-carboxamida; inhibidores de csf-1r quinasa; su proceso de preparacion; y su uso para tratar el cancer. |
ES2733822T3 (es) | 2007-02-20 | 2019-12-03 | Novartis Ag | Imidazoquinolinas como inhibidores duales de lípido quinasa y mTOR |
US20080221128A1 (en) | 2007-03-07 | 2008-09-11 | Christian Gege | Metalloprotease inhibitors containing a squaramide moiety |
US8039505B2 (en) | 2007-04-11 | 2011-10-18 | University Of Utah Research Foundation | Compounds for modulating T-cells |
PE20090717A1 (es) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | Derivados de quinolina como inhibidores de la pi3 quinasa |
US7928111B2 (en) | 2007-06-08 | 2011-04-19 | Senomyx, Inc. | Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors |
US9321730B2 (en) | 2007-08-21 | 2016-04-26 | The Hong Kong Polytechnic University | Method of making and administering quinoline derivatives as anti-cancer agents |
EP2276488A1 (en) | 2008-03-26 | 2011-01-26 | Novartis AG | 5imidazoquinolines and pyrimidine derivatives as potent modulators of vegf-driven angiogenic processes |
KR20110029161A (ko) | 2008-07-01 | 2011-03-22 | 제넨테크, 인크. | Mek 키나제 억제제로서의 비시클릭 헤테로사이클 |
WO2010007756A1 (ja) | 2008-07-14 | 2010-01-21 | 塩野義製薬株式会社 | Ttk阻害作用を有するピリジン誘導体 |
CA2735932C (en) | 2008-09-30 | 2013-07-09 | Pfizer Inc. | Imidazo[1,5]naphthyridine compounds, their pharmaceutical use and compositions |
EP2376495A4 (en) | 2008-12-08 | 2012-10-31 | Vm Pharma Llc | COMPOSITIONS OF PROTEIN RECEPTOR TYROSINE KINASE INHIBITORS |
US20120093917A1 (en) | 2009-04-02 | 2012-04-19 | Robert Hromas | Metnase and intnase inhibitors and their use in treating cancer |
TW201041888A (en) | 2009-05-06 | 2010-12-01 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
UA106074C2 (uk) * | 2009-06-04 | 2014-07-25 | Новартіс Аг | ПОХІДНІ 1H-ІМІДАЗО[4,5-c]ХІНОЛІНОНУ |
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 |
RU2015104301A (ru) | 2009-09-28 | 2015-11-10 | Ф.Хоффманн-Ля Рош Аг | Бензоксепиновые ингибиторы р13 и способы применения |
GB0919423D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
CN102199152A (zh) | 2010-03-25 | 2011-09-28 | 高大新 | 杂环咪唑类磷脂激酶抑制剂 |
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 |
AR082499A1 (es) | 2010-08-23 | 2012-12-12 | Gruenenthal Gmbh | Compuestos utiles para trastornos del sistema nervioso, inflamatorios, estomacales y como analgesicos |
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 |
AR083267A1 (es) | 2010-10-04 | 2013-02-13 | Novartis Ag | Combinaciones farmaceuticas |
SG190210A1 (en) | 2010-12-03 | 2013-06-28 | Novartis Ag | Pharmaceutical compositions |
BR112013013837A2 (pt) | 2010-12-06 | 2016-09-13 | Piramal Entpr Ltd | derivados de substituição de imidazoquinolina |
WO2012083866A1 (en) | 2010-12-22 | 2012-06-28 | The Hong Kong Polytechnic University | Quinoline derivatives as anti-cancer agents |
TWI450891B (zh) | 2010-12-29 | 2014-09-01 | Dev Center Biotechnology | 新穎微管蛋白抑制劑 |
JO3003B1 (ar) * | 2011-01-14 | 2016-09-05 | Lilly Co Eli | مركب أيميدازو [4، 5 -c ] كينولين-2- واحد واستخدامه كمثبط كيناز PI3/mtor |
EP2694678A2 (en) | 2011-04-04 | 2014-02-12 | Netherland Cancer Institute | Methods and compositions for predicting resistance to anticancer treatment |
CN103917525B (zh) | 2011-05-23 | 2016-08-17 | 依兰制药公司 | Lrrk2激酶活性的抑制剂 |
WO2012162635A1 (en) | 2011-05-26 | 2012-11-29 | Sunovion Pharmaceuticals Inc. | Metabotropic glutamate receptors 5 modulators and methods of use thereof |
WO2013022740A2 (en) | 2011-08-05 | 2013-02-14 | Corning Incorporated | Gpr35 ligands and the uses thereof |
JP6042060B2 (ja) | 2011-09-26 | 2016-12-14 | サノフイ | ピラゾロキノリノン誘導体、その調製および治療上の使用 |
WO2013070659A1 (en) | 2011-11-07 | 2013-05-16 | Sunovion Pharmaceuticals Inc. | Modulators of opioid receptors and methods of use thereof |
WO2013074965A1 (en) | 2011-11-16 | 2013-05-23 | Microbiotix, Inc. | Aminoalkyl phenol ether inhibitors of influenza a virus |
WO2013157018A1 (en) | 2012-04-18 | 2013-10-24 | Indian Institute Of Technology Madras | A process for the preparation of the core structure in quinolone and napthyridone class of antibiotics |
WO2013184621A1 (en) | 2012-06-06 | 2013-12-12 | Novartis Ag | Combination of a 17 -alpha -hydroxylase (c17, 20 - lyase) inhibitor and a specific pi-3k inhibitor for treating a tumor disease |
CN110664816A (zh) | 2012-06-07 | 2020-01-10 | 佐治亚州立大学研究基金会公司 | Seca抑制剂以及其制备和使用方法 |
WO2013192367A1 (en) | 2012-06-22 | 2013-12-27 | Novartis Ag | Neuroendocrine tumor treatment |
KR102245985B1 (ko) | 2012-08-16 | 2021-04-30 | 노파르티스 아게 | Pi3k 억제제와 c-met 억제제의 조합물 |
WO2014031872A2 (en) | 2012-08-23 | 2014-02-27 | The Broad Institute, Inc. | Small molecule inhibitors for treating parasitic infections |
US9713612B2 (en) | 2013-03-12 | 2017-07-25 | Curegenix, Inc. | Compounds for treatment of cancer |
GB201309180D0 (en) | 2013-05-21 | 2013-07-03 | Ucl Business Plc | Compounds and Their Uses |
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 |
JP2016540773A (ja) * | 2013-12-06 | 2016-12-28 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Atrキナーゼの阻害剤として有用な化合物 |
NO2714752T3 (es) * | 2014-05-08 | 2018-04-21 | ||
GB201409044D0 (en) | 2014-05-21 | 2014-07-02 | Ucl Business Plc | New compounds |
RS62082B1 (sr) | 2015-04-02 | 2021-08-31 | Merck Patent Gmbh | Imidazolonilhinolini i njihova primena kao inhibitora atm kinaze |
CN104876912B (zh) | 2015-04-08 | 2017-07-21 | 苏州云轩医药科技有限公司 | Wnt信号通路抑制剂及其应用 |
US10858316B2 (en) | 2015-07-10 | 2020-12-08 | University Of Maryland, Baltimore | Small molecule inhibitors of the MCL-1 oncoprotein and uses thereof |
GB201516504D0 (en) * | 2015-09-17 | 2015-11-04 | Astrazeneca Ab | Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer |
US10781218B2 (en) | 2016-03-16 | 2020-09-22 | Kura Oncology, Inc. | Substituted inhibitors of menin-MLL and methods of use |
-
2015
- 2015-09-17 GB GBGB1516504.6A patent/GB201516504D0/en not_active Ceased
-
2016
- 2016-09-14 TW TW109145998A patent/TWI762109B/zh active
- 2016-09-14 TW TW105129931A patent/TWI714631B/zh active
- 2016-09-15 PT PT201561727T patent/PT3683220T/pt unknown
- 2016-09-15 HU HUE16770461A patent/HUE053066T2/hu unknown
- 2016-09-15 DK DK20156172.7T patent/DK3683220T3/da active
- 2016-09-15 LT LTEP16770461.8T patent/LT3350180T/lt unknown
- 2016-09-15 BR BR112018004325-7A patent/BR112018004325B1/pt active IP Right Grant
- 2016-09-15 MX MX2018003186A patent/MX2018003186A/es unknown
- 2016-09-15 PL PL20156172.7T patent/PL3683220T3/pl unknown
- 2016-09-15 CN CN201680052951.0A patent/CN108137576B/zh active Active
- 2016-09-15 PL PL16770461T patent/PL3350180T3/pl unknown
- 2016-09-15 EP EP20156172.7A patent/EP3683220B1/en active Active
- 2016-09-15 SI SI201631074T patent/SI3350180T1/sl unknown
- 2016-09-15 TN TNP/2018/000078A patent/TN2018000078A1/en unknown
- 2016-09-15 ES ES20156172T patent/ES2920876T3/es active Active
- 2016-09-15 KR KR1020187010323A patent/KR102028848B1/ko active IP Right Grant
- 2016-09-15 HU HUE20156172A patent/HUE058884T2/hu unknown
- 2016-09-15 EP EP16770461.8A patent/EP3350180B1/en active Active
- 2016-09-15 ES ES16770461T patent/ES2853924T3/es active Active
- 2016-09-15 AU AU2016323399A patent/AU2016323399B2/en active Active
- 2016-09-15 CR CR20180172A patent/CR20180172A/es unknown
- 2016-09-15 JP JP2018513812A patent/JP6605130B2/ja active Active
- 2016-09-15 MY MYPI2018701049A patent/MY195669A/en unknown
- 2016-09-15 PT PT167704618T patent/PT3350180T/pt unknown
- 2016-09-15 RS RS20210170A patent/RS61435B1/sr unknown
- 2016-09-15 CA CA2997399A patent/CA2997399C/en active Active
- 2016-09-15 PE PE2018000343A patent/PE20181078A1/es unknown
- 2016-09-15 KR KR1020197028342A patent/KR102469153B1/ko active IP Right Grant
- 2016-09-15 WO PCT/EP2016/071782 patent/WO2017046216A1/en active Application Filing
- 2016-09-15 DK DK16770461.8T patent/DK3350180T3/da active
- 2016-09-15 EA EA201890650A patent/EA033284B1/ru not_active IP Right Cessation
- 2016-09-16 AR ARP160102832A patent/AR106053A1/es active IP Right Grant
- 2016-09-16 US US15/267,398 patent/US9856255B2/en active Active
-
2017
- 2017-11-27 US US15/822,617 patent/US10457679B2/en active Active
-
2018
- 2018-02-26 NI NI201800033A patent/NI201800033A/es unknown
- 2018-03-04 IL IL257847A patent/IL257847B/en active IP Right Grant
- 2018-03-06 DO DO2018000065A patent/DOP2018000065A/es unknown
- 2018-03-12 PH PH12018500532A patent/PH12018500532A1/en unknown
- 2018-03-14 CL CL2018000677A patent/CL2018000677A1/es unknown
- 2018-03-16 SV SV2018005655A patent/SV2018005655A/es unknown
- 2018-03-16 CO CONC2018/0002829A patent/CO2018002829A2/es unknown
- 2018-11-15 HK HK18114571.8A patent/HK1255408A1/zh unknown
- 2018-12-27 HK HK18116623.1A patent/HK1257413A1/zh unknown
-
2019
- 2019-09-27 US US16/584,996 patent/US10882858B2/en active Active
-
2020
- 2020-12-01 US US17/108,117 patent/US11613539B2/en active Active
-
2021
- 2021-01-29 HR HRP20210149TT patent/HRP20210149T1/hr unknown
- 2021-02-11 CY CY20211100117T patent/CY1124680T1/el unknown
-
2022
- 2022-08-16 ZA ZA2022/09171A patent/ZA202209171B/en unknown
-
2023
- 2023-02-21 US US18/171,735 patent/US20230286981A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SV2018005655A (es) | "derivados de 8-[6-[3-(amino)propoxi]-3-piridil]1-isopropilimidazo[4,5-c]quinolin-2-ona como moduladores selectivos de la cinasa de la ataxia telangiectasia mutada (atm) para el tratamiento del cancer" | |
SV2018005663A (es) | Compuestos de imidazo [4,5-c] quinolin-2-ona y su uso en el tratamiento del cancer | |
SV2018005680A (es) | Compuestos de imidazo [4,5-c] quinolin- 2-ona y su uso en el tratamiento del cancer | |
CL2019001714A1 (es) | Compuestos de amino-triazolopiridina y su uso en el tratamiento del cáncer. | |
DOP2016000281A (es) | Compuestos de imidazo[4,5-c]quinolin-2-ona y su uso para tratar cáncer | |
CL2017001426A1 (es) | Nuevos compuestos de 5-amino-6h-tiazolo[4,5-d]pirimidin-2,7-diona 3-sustituidos para el tratamiento y profilaxis de infecciones virales. | |
CO2018004857A2 (es) | Derivados de dihidroimidazopirazinona usados en el tratamiento del cáncer | |
CR20150472A (es) | USO DE DERIVADOS DE PIRAZOLOPIRIMIDINA PARA EL TRATAMIENTO DE TRANSTORNOS RELACIONADOS CON LA PI3Kd | |
AR100431A1 (es) | Compuestos de pladienolida piridina y métodos de uso | |
AR108461A1 (es) | Compuestos imidazo[4,5-c]quinolin-2-ona y su uso en el tratamiento del cáncer | |
NI201600176A (es) | Compuestos de 1, 3, 4 - tiadiazol y uso de los mismos para el tratamiento del cáncer. | |
CL2019002900A1 (es) | Análogos de benzoazepina como agentes inhibidores de la tirosina cinasa de bruton. | |
CL2019002527A1 (es) | Compuestos de tipo imidazo[4,5-c]quinolin-2-ona deuterados y su uso en el tratamiento del cáncer. | |
CO2018010951A2 (es) | Compuestos de cinnolin-4-amina y su uso en el tratamiento del cáncer |