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PE20152007A1 - Entidades quimicas - Google Patents

Entidades quimicas

Info

Publication number
PE20152007A1
PE20152007A1 PE2015001900A PE2015001900A PE20152007A1 PE 20152007 A1 PE20152007 A1 PE 20152007A1 PE 2015001900 A PE2015001900 A PE 2015001900A PE 2015001900 A PE2015001900 A PE 2015001900A PE 20152007 A1 PE20152007 A1 PE 20152007A1
Authority
PE
Peru
Prior art keywords
heteroaryl
aryl
compounds
treatment
chemical entities
Prior art date
Application number
PE2015001900A
Other languages
English (en)
Inventor
Munoz David Alvaro Cebrian
Soler Maria Nieto
Oliver Renner
Contreras Andres Joaquin Lopez
Busto Carmen Varela
Costa Matilde Murga
Aristegui Sonsoles Rodriguez
Lazaro Luis Ignacio Toledo
Ferreira Maria Del Rosario Rico
Aparicio Carmen Blanco
Fernandez Joaquin Pastor
Gonzalez Sonia Martinez
Ruiz Oscar Fernandez-Capetillo
Original Assignee
Fundacion Ct De Investigaciones Oncologicas Carlos Iii
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=48013903&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20152007(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Fundacion Ct De Investigaciones Oncologicas Carlos Iii filed Critical Fundacion Ct De Investigaciones Oncologicas Carlos Iii
Publication of PE20152007A1 publication Critical patent/PE20152007A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/14Ortho-condensed systems
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53831,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • 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
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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

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)
  • Bioinformatics & Cheminformatics (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Steroid Compounds (AREA)

Abstract

Referida a compuestos triciclicos de formula (I), en donde R1 es arilo o heteroarilo, R2 es NR3S=2R3, alquilo, cicloalquilo, arilo o heteroarilo y m es 1 o 2; asi como a sus sales, solvatos y estereoisomeros farmaceuticamente aceptables de los mismos. Estos compuestos son inhibidores de cinasa de ataxia telangiectasia mutada y relacionada con Rad3 (ATR) y son potencialmente utiles en el tratamiento del cancer, principalmente de pulmon, prostata, melanoma, ovario, mama, endometrio, entre otros. Tambien esta referida a composiciones farmaceuticas, productos de combinacion y procedimientos de tratamiento que usan estas composiciones
PE2015001900A 2013-03-15 2014-03-14 Entidades quimicas PE20152007A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP13382089 2013-03-15

Publications (1)

Publication Number Publication Date
PE20152007A1 true PE20152007A1 (es) 2016-02-04

Family

ID=48013903

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2015001900A PE20152007A1 (es) 2013-03-15 2014-03-14 Entidades quimicas

Country Status (31)

Country Link
US (1) US9453031B2 (es)
EP (1) EP2970332B1 (es)
JP (1) JP6379115B2 (es)
KR (1) KR102206318B1 (es)
CN (1) CN105051047B (es)
AR (1) AR095443A1 (es)
AU (1) AU2014229735B2 (es)
BR (1) BR112015023060B1 (es)
CA (1) CA2904768C (es)
CL (1) CL2015002591A1 (es)
CY (1) CY1120619T1 (es)
DK (1) DK2970332T3 (es)
EA (1) EA029771B1 (es)
ES (1) ES2670674T3 (es)
HR (1) HRP20180839T1 (es)
HU (1) HUE037685T2 (es)
IL (1) IL240708B (es)
LT (1) LT2970332T (es)
MX (1) MX368056B (es)
NO (1) NO2970332T3 (es)
NZ (1) NZ711038A (es)
PE (1) PE20152007A1 (es)
PH (1) PH12015502159B1 (es)
PL (1) PL2970332T3 (es)
PT (1) PT2970332T (es)
RS (1) RS57216B1 (es)
SG (1) SG11201507555PA (es)
SI (1) SI2970332T1 (es)
TW (1) TWI557131B (es)
UA (1) UA118261C2 (es)
WO (1) WO2014140644A1 (es)

Families Citing this family (18)

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ES2649156T3 (es) 2013-01-14 2018-01-10 Incyte Holdings Corporation Compuestos bicíclicos de carboxamida aromática útiles como inhibidores de quinasas Pim
TW201932456A (zh) 2013-01-15 2019-08-16 美商英塞特控股公司 適用作pim激酶抑制劑之噻唑甲醯胺及吡啶甲醯胺化合物
MX2016002367A (es) 2013-08-23 2016-10-28 Incyte Corp Compuestos de carboxamida de furo y tienopiridina utiles como inhibidores de cinasas pim.
WO2016010897A1 (en) 2014-07-14 2016-01-21 Incyte Corporation Bicyclic heteroaromatic carboxamide compounds useful as pim kinase inhibitors
US9580418B2 (en) 2014-07-14 2017-02-28 Incyte Corporation Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors
WO2016112374A2 (en) * 2015-01-09 2016-07-14 The General Hospital Corporation Treating cancer using inhibitors of ataxia-telangiectasia mutated and rad3-related (atr)
US9540347B2 (en) 2015-05-29 2017-01-10 Incyte Corporation Pyridineamine compounds useful as Pim kinase inhibitors
TWI734699B (zh) 2015-09-09 2021-08-01 美商英塞特公司 Pim激酶抑制劑之鹽
US9920032B2 (en) 2015-10-02 2018-03-20 Incyte Corporation Heterocyclic compounds useful as pim kinase inhibitors
US10570149B2 (en) 2016-05-24 2020-02-25 Merck Patent Gmbh Tricyclic heterocylic derivatives
US10596161B2 (en) 2017-12-08 2020-03-24 Incyte Corporation Low dose combination therapy for treatment of myeloproliferative neoplasms
IL276489B2 (en) * 2018-02-07 2024-09-01 Shijiazhuang Sagacity New Drug Dev Company Ltd Atr inhibitor and application thereof
WO2020094084A1 (zh) * 2018-11-07 2020-05-14 南京明德新药研发有限公司 作为ret抑制剂的三并环衍生物
CN113004303A (zh) * 2019-12-18 2021-06-22 江苏恒瑞医药股份有限公司 嘧啶并噁嗪类三环衍生物、其制备方法及其在医药上的应用
WO2021143821A1 (zh) * 2020-01-17 2021-07-22 江苏恒瑞医药股份有限公司 稠合杂芳基类衍生物、其制备方法及其在医药上的应用
WO2022078480A1 (zh) 2020-10-16 2022-04-21 上海迪诺医药科技有限公司 三杂环衍生物、其药物组合物及应用
CN115466258A (zh) * 2021-06-11 2022-12-13 成都苑东生物制药股份有限公司 Atr抑制剂及其用途
CN115286645A (zh) * 2022-08-16 2022-11-04 南京雷正医药科技有限公司 三环杂环衍生物及其药物组合物和用途

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US5583024A (en) 1985-12-02 1996-12-10 The Regents Of The University Of California Recombinant expression of Coleoptera luciferase
AU3427093A (en) * 1992-01-15 1993-08-03 E.I. Du Pont De Nemours And Company Bridged heterocyclic fungicides
JPH08336393A (ja) 1995-04-13 1996-12-24 Mitsubishi Chem Corp 光学活性なγ−置換−β−ヒドロキシ酪酸エステルの製造法
US20020192228A1 (en) 1997-02-12 2002-12-19 Samir M. Hanash Protein markers for lung cancer and use thereof
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
US6602677B1 (en) 1997-09-19 2003-08-05 Promega Corporation Thermostable luciferases and methods of production
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
PL205557B1 (pl) 1999-02-10 2010-05-31 Astrazeneca Ab Pochodne indolu
AU769222B2 (en) 1999-11-05 2004-01-22 Genzyme Corporation Quinazoline derivatives as VEGF inhibitors
MY130363A (en) 2000-02-15 2007-06-29 Sugen Inc "pyrrole substituted 2-indolinone protein kinase inhibitors"
BR0111230A (pt) 2000-05-31 2003-06-10 Astrazeneca Ab Composto, e, uso e processo para a preparação do mesmo
UA73993C2 (uk) 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
BR0112224A (pt) 2000-07-07 2003-06-10 Angiogene Pharm Ltd Composto, composição farmacêutica, uso de um composto ou de um sal, solvato ou pró-droga farmaceuticamente aceitável do mesmo, e, processo para preparar um composto
SK52003A3 (en) 2000-07-07 2003-07-01 Angiogene Pharm Ltd Colchinol derivatives as angiogenesis inhibitors, method for their preparation and pharmaceutical composition comprising the same
US8735411B2 (en) * 2006-10-02 2014-05-27 Abbvie Inc. Macrocyclic benzofused pyrimidine derivatives
CA2667960A1 (en) * 2006-10-30 2008-05-08 Novartis Ag Imidazopyridazines as pi3k lipid kinase inhibitors
AR066477A1 (es) * 2007-05-09 2009-08-19 Novartis Ag Imidazopiridazinas sustituidas como inhibidores de cinasa de lipido
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Also Published As

Publication number Publication date
CL2015002591A1 (es) 2016-02-05
HRP20180839T1 (hr) 2018-06-29
AR095443A1 (es) 2015-10-14
MX368056B (es) 2019-09-18
EA029771B1 (ru) 2018-05-31
LT2970332T (lt) 2018-06-11
WO2014140644A1 (en) 2014-09-18
HUE037685T2 (hu) 2018-09-28
JP2016510803A (ja) 2016-04-11
EA201591781A1 (ru) 2016-02-29
SI2970332T1 (en) 2018-06-29
NO2970332T3 (es) 2018-07-28
CA2904768A1 (en) 2014-09-18
UA118261C2 (uk) 2018-12-26
KR20150129741A (ko) 2015-11-20
CA2904768C (en) 2021-07-27
PL2970332T3 (pl) 2018-08-31
KR102206318B1 (ko) 2021-01-25
CY1120619T1 (el) 2019-12-11
BR112015023060A2 (pt) 2017-07-18
IL240708B (en) 2019-08-29
IL240708A0 (en) 2015-10-29
NZ711038A (en) 2020-02-28
MX2015011549A (es) 2016-05-31
PH12015502159A1 (en) 2016-01-25
EP2970332B1 (en) 2018-02-28
US9453031B2 (en) 2016-09-27
US20160024112A1 (en) 2016-01-28
CN105051047A (zh) 2015-11-11
ES2670674T3 (es) 2018-05-31
PH12015502159B1 (en) 2016-01-25
RS57216B1 (sr) 2018-07-31
CN105051047B (zh) 2017-12-15
AU2014229735A1 (en) 2015-09-03
TW201446772A (zh) 2014-12-16
BR112015023060B1 (pt) 2022-07-05
EP2970332A1 (en) 2016-01-20
DK2970332T3 (en) 2018-05-22
SG11201507555PA (en) 2015-10-29
JP6379115B2 (ja) 2018-08-22
PT2970332T (pt) 2018-05-25
AU2014229735B2 (en) 2018-08-09
HK1215021A1 (en) 2016-08-12
TWI557131B (zh) 2016-11-11

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