MX2009014247A - Compuestos heterociclicos utiles como inhibidores de mk2. - Google Patents

Compuestos heterociclicos utiles como inhibidores de mk2.

Info

Publication number
MX2009014247A
MX2009014247A MX2009014247A MX2009014247A MX2009014247A MX 2009014247 A MX2009014247 A MX 2009014247A MX 2009014247 A MX2009014247 A MX 2009014247A MX 2009014247 A MX2009014247 A MX 2009014247A MX 2009014247 A MX2009014247 A MX 2009014247A
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MX
Mexico
Prior art keywords
inhibitors
heterocyclic compounds
compounds useful
ways
symbols
Prior art date
Application number
MX2009014247A
Other languages
English (en)
Inventor
Achim Schlapbach
Guido Koch
Laszlo Revesz
Original Assignee
Novartis Ag
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.)
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Publication date
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of MX2009014247A publication Critical patent/MX2009014247A/es

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    • 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
    • C07D471/12Heterocyclic 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 three hetero rings
    • C07D471/14Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P19/04Drugs for skeletal disorders for non-specific disorders of the connective tissue
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P9/00Drugs for disorders of the cardiovascular system
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    • 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
    • C07D471/12Heterocyclic 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 three hetero rings
    • C07D471/20Spiro-condensed systems
    • 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
    • C07D471/22Heterocyclic 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 systems contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/22Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/22Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
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  • Neurology (AREA)
  • Pulmonology (AREA)
  • Biomedical Technology (AREA)
  • Rheumatology (AREA)
  • Diabetes (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hematology (AREA)
  • Dermatology (AREA)
  • Neurosurgery (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
  • Virology (AREA)
  • Urology & Nephrology (AREA)
  • Communicable Diseases (AREA)
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  • Tropical Medicine & Parasitology (AREA)
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Abstract

La presente invención describe compuestos tetracíclicos de la fórmula (lA) o (!B): (ver fórmulas (IA) e (IB)) en donde los símbolos R, X, A, Y, R2, R3 y D son como se definen en la memoria descriptiva, su uso en el tratamiento de ciertas enfermedades, por ejemplo, dependientes de la actividad de MK-2 o TNF, y sus formas de fabricación.
MX2009014247A 2007-07-16 2008-07-14 Compuestos heterociclicos utiles como inhibidores de mk2. MX2009014247A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP07112549 2007-07-16
PCT/EP2008/059158 WO2009010488A1 (en) 2007-07-16 2008-07-14 Heterocyclic compounds useful as mk2 inhibitors

Publications (1)

Publication Number Publication Date
MX2009014247A true MX2009014247A (es) 2010-01-28

Family

ID=38792023

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009014247A MX2009014247A (es) 2007-07-16 2008-07-14 Compuestos heterociclicos utiles como inhibidores de mk2.

Country Status (15)

Country Link
US (2) US7838674B2 (es)
EP (1) EP2178874A1 (es)
JP (1) JP2010533674A (es)
KR (1) KR20100031619A (es)
CN (1) CN101687869A (es)
AR (1) AR067535A1 (es)
AU (1) AU2008277676A1 (es)
BR (1) BRPI0814426A2 (es)
CA (1) CA2693904A1 (es)
CL (1) CL2008002073A1 (es)
EA (1) EA201000100A1 (es)
MX (1) MX2009014247A (es)
PE (1) PE20090480A1 (es)
TW (1) TW200904818A (es)
WO (1) WO2009010488A1 (es)

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Publication number Priority date Publication date Assignee Title
US8494544B2 (en) * 2009-12-03 2013-07-23 Osocad Remote Limited Liability Company Method, apparatus and computer program to perform location specific information retrieval using a gesture-controlled handheld mobile device
CN104710423A (zh) * 2009-12-14 2015-06-17 默沙东有限责任公司 Mk2抑制剂
AU2014277711B2 (en) * 2009-12-14 2016-10-27 Merck Sharp & Dohme B.V. MK2 inhibitors
US20120065195A1 (en) 2010-03-31 2012-03-15 Clark Christopher T Compounds for treating neurodegenerative diseases
EP2619181A1 (en) 2010-09-23 2013-07-31 Syngenta Participations AG Novel microbiocides
ES2602791T3 (es) * 2011-01-26 2017-02-22 Nerviano Medical Sciences S.R.L. Derivados de pirrolo tricíclicos, proceso para su preparación y su uso como inhibidores de cinasa
JP5925808B2 (ja) * 2011-01-26 2016-05-25 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ 三環式誘導体、これらの調製方法およびこれらのキナーゼ阻害剤としての使用
WO2012117021A2 (en) 2011-03-03 2012-09-07 Syngenta Participations Ag Novel microbiocidal oxime ethers
BR112013028895A2 (pt) 2011-05-10 2016-08-09 Bayer Ip Gmbh (tio)carbonilamidinas bicíclicas
WO2013092460A1 (en) 2011-12-20 2013-06-27 Syngenta Participations Ag Cyclic bisoxime microbicides
EP2641901A1 (en) 2012-03-22 2013-09-25 Syngenta Participations AG. Novel microbiocides
KR101561330B1 (ko) 2012-09-19 2015-10-16 주식회사 두산 인돌로인돌계 유기 발광 화합물 및 이를 이용한 유기 전계 발광 소자
CN102936216B (zh) * 2012-12-05 2015-03-04 南京药石药物研发有限公司 7,9-二氧代-2,6-氮杂-螺[3.5]壬-2-甲酸叔丁酯及其中间体的制备方法
NO2953942T3 (es) 2013-02-06 2018-03-24
KR20210091832A (ko) * 2013-03-15 2021-07-22 셀젠 카르 엘엘씨 Mk2 억제제 및 이의 용도
MA40534B1 (fr) 2014-09-17 2021-04-30 Celgene Car Llc Inhibiteurs de mk2 et leurs utilisations
CN105348263B (zh) * 2015-12-15 2018-03-23 乐普药业股份有限公司 一种达比加群酯中间体的制备方法
EA201992153A1 (ru) 2016-10-05 2020-02-25 Зе Глобал Эллайенс Фо Тб Драг Девелопмент, Инк. Гетероарилтрифторборатные соединения для лечения микобактериальных инфекций
MX2019010642A (es) 2017-03-16 2019-10-17 Celgene Car Llc Inhibidores de cinasa activada por mitogeno 2 (mk2), sintesis de los mismos, e intermediarios de los mismos.
US11230551B2 (en) 2017-03-16 2022-01-25 Celgene Car Llc Deuterated analogs of MK2 inhibitors and uses thereof
US11098057B2 (en) 2017-03-16 2021-08-24 Celgene Car Llc 9,10,11,12-tetrahydro-8H-[1,4]diazepino[5′,6′:4,5]thieno[3,2-F]quinolin-8-one compounds and uses thereof
US11124525B2 (en) 2017-03-16 2021-09-21 Celgene Car Llc Heteroaryl compounds useful as MK2 inhibitors
AU2018236286B2 (en) 2017-03-16 2022-02-17 Bristol-Myers Squibb Company Forms and compositions of a MK2 inhibitor
CN107383026B (zh) * 2017-06-29 2019-04-30 武汉药明康德新药开发有限公司 一种7-羟甲基-2,5-二氮杂螺[3,4]辛烷-2-甲酸叔丁酯的合成方法
CN109336890B (zh) * 2018-11-17 2020-03-20 重庆文理学院 一种吲唑类衍生物的合成方法及抗肿瘤应用
CN109678879A (zh) * 2019-02-27 2019-04-26 陕西科技大学 一种苯并噻吩并吡喃酮类化合物及其合成方法
CN109678878A (zh) * 2019-02-27 2019-04-26 陕西科技大学 一种苯并噻吩并香豆素类化合物及其合成方法
CN110563726A (zh) * 2019-07-23 2019-12-13 上海合全药业股份有限公司 叔丁基-7,9-二氧亚基-2,6-二氮杂螺[4.5]癸烷-2-甲酸基酯的制备方法
WO2023025298A1 (zh) * 2021-08-27 2023-03-02 瑞石生物医药有限公司 喹啉并呋喃衍生物及其用途

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WO2003070236A2 (en) * 2002-02-19 2003-08-28 Pharmacia Italia S.P.A. Tricyclic pyrazole derivatives, process for their preparation and their use as antitumor agents
EP1572682A4 (en) * 2002-12-20 2008-01-23 Pharmacia Corp ACYCLIC PYRAZOLE COMPOUNDS

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Publication number Publication date
AR067535A1 (es) 2009-10-14
BRPI0814426A2 (pt) 2015-01-06
CL2008002073A1 (es) 2009-02-20
KR20100031619A (ko) 2010-03-23
CN101687869A (zh) 2010-03-31
TW200904818A (en) 2009-02-01
AU2008277676A1 (en) 2009-01-22
US20090098218A1 (en) 2009-04-16
JP2010533674A (ja) 2010-10-28
US7838674B2 (en) 2010-11-23
WO2009010488A1 (en) 2009-01-22
PE20090480A1 (es) 2009-05-24
EA201000100A1 (ru) 2010-08-30
US20120022030A1 (en) 2012-01-26
CA2693904A1 (en) 2009-01-22
EP2178874A1 (en) 2010-04-28

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