ATE475650T1 - Positive allosterische chinolon-m1- rezeptormodulatoren - Google Patents

Positive allosterische chinolon-m1- rezeptormodulatoren

Info

Publication number
ATE475650T1
ATE475650T1 AT06838942T AT06838942T ATE475650T1 AT E475650 T1 ATE475650 T1 AT E475650T1 AT 06838942 T AT06838942 T AT 06838942T AT 06838942 T AT06838942 T AT 06838942T AT E475650 T1 ATE475650 T1 AT E475650T1
Authority
AT
Austria
Prior art keywords
positive allosteric
quinolone
compounds
receptor
receptor modulators
Prior art date
Application number
AT06838942T
Other languages
English (en)
Inventor
William Shipe
Craig Lindsley
David Hallett
Original Assignee
Merck Sharp & Dohme
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 Sharp & Dohme filed Critical Merck Sharp & Dohme
Application granted granted Critical
Publication of ATE475650T1 publication Critical patent/ATE475650T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D215/54Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
    • C07D215/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20Oxygen atoms
    • C07D215/22Oxygen atoms attached in position 2 or 4
    • C07D215/233Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04JMULTIPLEX COMMUNICATION
    • H04J3/00Time-division multiplex systems
    • H04J3/02Details
    • H04J3/06Synchronising arrangements
    • H04J3/0635Clock or time synchronisation in a network
    • H04J3/0638Clock or time synchronisation among nodes; Internode synchronisation
    • H04J3/0658Clock or time synchronisation among packet nodes
    • H04J3/0661Clock or time synchronisation among packet nodes using timestamps
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04LTRANSMISSION OF DIGITAL INFORMATION, e.g. TELEGRAPHIC COMMUNICATION
    • H04L63/00Network architectures or network communication protocols for network security
    • H04L63/14Network architectures or network communication protocols for network security for detecting or protecting against malicious traffic
    • H04L63/1441Countermeasures against malicious traffic
    • H04L63/1458Denial of Service
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04LTRANSMISSION OF DIGITAL INFORMATION, e.g. TELEGRAPHIC COMMUNICATION
    • H04L63/00Network architectures or network communication protocols for network security
    • H04L63/12Applying verification of the received information
    • H04L63/123Applying verification of the received information received data contents, e.g. message integrity

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Computer Security & Cryptography (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)
  • Computer Networks & Wireless Communication (AREA)
  • Signal Processing (AREA)
  • General Engineering & Computer Science (AREA)
  • Computer Hardware Design (AREA)
  • Computing Systems (AREA)
  • Anesthesiology (AREA)
  • Pain & Pain Management (AREA)
  • Psychology (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Data Exchanges In Wide-Area Networks (AREA)
  • Control Of Eletrric Generators (AREA)
  • Steroid Compounds (AREA)
AT06838942T 2005-12-05 2006-12-04 Positive allosterische chinolon-m1- rezeptormodulatoren ATE475650T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US74223405P 2005-12-05 2005-12-05
US78927206P 2006-04-04 2006-04-04
PCT/US2006/046262 WO2007067489A1 (en) 2005-12-05 2006-12-04 Quinolone m1 receptor positive allosteric modulators

Publications (1)

Publication Number Publication Date
ATE475650T1 true ATE475650T1 (de) 2010-08-15

Family

ID=37963841

Family Applications (1)

Application Number Title Priority Date Filing Date
AT06838942T ATE475650T1 (de) 2005-12-05 2006-12-04 Positive allosterische chinolon-m1- rezeptormodulatoren

Country Status (9)

Country Link
US (1) US8389545B2 (de)
EP (1) EP1963271B1 (de)
JP (1) JP5192389B2 (de)
AT (1) ATE475650T1 (de)
AU (1) AU2006322045A1 (de)
CA (1) CA2631917A1 (de)
DE (1) DE602006015851D1 (de)
TW (1) TW200840814A (de)
WO (2) WO2007067489A1 (de)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008002621A2 (en) 2006-06-28 2008-01-03 Merck & Co., Inc. Benzyl-substituted quinolone m1 receptor positive allosteric modulators
CA2711487A1 (en) * 2008-01-25 2009-07-30 Merck Sharp & Dohme Corp. Quinolizidinone m1 receptor positive allosteric modulators
EP2252299B1 (de) * 2008-02-15 2014-03-19 Merck Sharp & Dohme Corp. Kondensierte pyridon-m1-rezeptor-positive allosterische modulatoren
EP2268280B1 (de) * 2008-03-21 2013-04-24 Merck Sharp & Dohme Corp. Positive allosterische Chinolizidinon-M1-Rezeptor-Modulatoren
AU2009241392A1 (en) 2008-05-01 2009-11-05 Merck Sharp & Dohme Corp. 4-oxo-1,4-dihydroquinoline M1 receptor positive allosteric modulators
EP2312949B1 (de) * 2008-08-12 2013-08-28 Merck Sharp & Dohme Corp. Positive allosterische n-heterozyklische m1-rezeptormodulatoren
US8278453B2 (en) 2008-10-06 2012-10-02 Merck Sharp & Dohme Corp. Quinolizidinone M1 receptor positive allosteric modulators
WO2010047990A1 (en) 2008-10-23 2010-04-29 Merck Sharp & Dohme Corp. Fused heterocyclic m1 receptor positive allosteric modulators
CA2750708A1 (en) * 2009-02-23 2010-08-26 Merck Sharp & Dohme Corp. Pyrazolo [4,3-c] cinnolin-3-one m1 receptor positive allosteric modulators
WO2010123716A1 (en) * 2009-04-20 2010-10-28 Merck Sharp & Dohme Corp. Heterocyclic fused cinnoline m1 receptor positive allosteric modulators
WO2011041143A1 (en) * 2009-10-01 2011-04-07 Merck Sharp & Dohme Corp. HETEROCYCLIC-FUSED PYRAZOLO[4,3-c]PYRIDIN-3-ONE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
WO2011062853A1 (en) * 2009-11-20 2011-05-26 Merck Sharp & Dohme Corp. Quinolizidinone carboxamide m1 receptor positive allosteric modulators
KR101494059B1 (ko) 2009-12-17 2015-02-16 머크 샤프 앤드 돔 코포레이션 퀴놀린 아미드 m1 수용체 양성 알로스테릭 조절제
WO2011137049A1 (en) 2010-04-30 2011-11-03 Merck Sharp & Dohme Corp. Heterocyclic quinolizine derived m1 receptor positive allosteric modulators
WO2011159554A1 (en) * 2010-06-15 2011-12-22 Merck Sharp & Dohme Corp. Tetrahydroquinoline amide m1 receptor positive allosteric modulators
WO2011159553A1 (en) 2010-06-15 2011-12-22 Merck Sharp & Dohme Corp. Heterocyclic fused phenanthrolinone m1 receptor positive allosteric modulators
WO2012003147A1 (en) 2010-07-01 2012-01-05 Merck Sharp & Dohme Corp. Isoindolone m1 receptor positive allosteric modulators
WO2012158475A1 (en) 2011-05-17 2012-11-22 Merck Sharp & Dohme Corp. N-linked lactam m1 receptor positive allosteric modulators
US8940765B2 (en) 2011-05-17 2015-01-27 Merck Sharp & Dohme Corp. N-linked quinolineamide M1 receptor positive allosteric modulators
US9284312B2 (en) 2011-05-17 2016-03-15 Merck Sharp & Dohme Corp. N-methyl tetrahydroquinoline M1 receptor positive allosteric modulators
US9586964B2 (en) 2011-10-28 2017-03-07 Vanderbilt University Substituted 2-(4-heterocyclylbenzyl)isoindolin-1-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M1
WO2013071201A1 (en) 2011-11-11 2013-05-16 Vanderbilt University Substituted benzylspiroindolin-2-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m1
US9029563B2 (en) 2012-01-06 2015-05-12 Vanderbilt University Substituted 1-benzylindolin-2-one analogs as positive allosteric modulators of muscarinic acetylcholine M1 receptors
WO2013106795A1 (en) * 2012-01-12 2013-07-18 Vanderbilt University Substituted 4-(1h~pyrazol-4.yl)benzyl analogues as positive allosteric modulators of machr m1 receptors
JP6211509B2 (ja) 2012-03-02 2017-10-11 武田薬品工業株式会社 複素環化合物およびその用途
JP6211530B2 (ja) 2012-11-19 2017-10-11 武田薬品工業株式会社 含窒素複素環化合物
AU2016276139B2 (en) 2015-06-08 2018-07-19 Suven Life Sciences Limited Muscarinic M1 receptor positive allosteric modulators
BR112017026561A2 (pt) * 2015-06-09 2018-08-14 Bayer Pharma Aktiengesellschaft moduladores alostéricos positivos do receptor muscarínico m2
WO2017042643A1 (en) 2015-09-10 2017-03-16 Suven Life Sciences Limited Fluoroindole derivatives as muscarinic m1 receptor positive allosteric modulators
WO2017155816A1 (en) * 2016-03-09 2017-09-14 Merck Sharp & Dohme Corp. Quinazoline compounds useful as m1 receptor positive allosteric modulators
US11523858B2 (en) 2017-08-11 2022-12-13 Bradley D. Vilims System and method for RF ablation with generated images of ablated tissue lesions
CN111018778B (zh) * 2019-12-30 2020-11-06 杭州师范大学 一种喹诺酮类衍生物及其制备方法和应用
US20250064833A1 (en) 2021-12-13 2025-02-27 Sage Therapeutics, Inc. Combination of muscarinic receptor positive modulators and nmda positive allosteric modulators

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1175836A (en) 1977-09-20 1984-10-09 Marcel Pesson Production of 1,4-dihydroquinoline-3-carboxylic acid derivatives
JPS5845426B2 (ja) 1978-09-29 1983-10-08 杏林製薬株式会社 置換キノリンカルボン酸誘導体
US4914110A (en) * 1984-05-11 1990-04-03 Societe De Conseils De Recherches Et D'applications Scientifiques Quinoline derivatives, their preparation and therapeutic compositions containing the same
US4623650A (en) 1984-12-06 1986-11-18 Pfizer Inc. Antibiotic derivatives of 7-phenyl-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids
JPS61218584A (ja) 1985-03-23 1986-09-29 Hokuriku Seiyaku Co Ltd キノリン−3−カルボン酸誘導体
JP2831000B2 (ja) * 1988-03-03 1998-12-02 大日本製薬株式会社 (2−アミノベンゾイル)酢酸エステル誘導体
FR2674247B1 (fr) 1991-03-19 1993-07-16 Bouchara Sa Nouvelles quinolones fluorees, leur procede de preparation et les compositions pharmaceutiques en renfermant.
FR2675144B1 (fr) 1991-04-10 1995-06-16 Bouchara Sa Nouvelles quinolones difluorees - leur procede de preparation et les compositions pharmaceutiques en renfermant.
TW301607B (de) 1993-03-09 1997-04-01 Takeda Pharm Industry Co Ltd
WO1997040846A1 (en) 1996-04-30 1997-11-06 Takeda Chemical Industries, Ltd. COMBINED USE OF GnRH AGONIST AND ANTAGONIST
JP2000103707A (ja) * 1998-09-28 2000-04-11 Permachem Asia Ltd 工業用殺菌剤
US6583153B2 (en) 2000-12-12 2003-06-24 Ortho-Mcneil Pharmaceutical, Inc. 7-heterocyclyl quinoline and thieno[2,3-b]yridine derivatives useful as antagonists of gonadotropin releasing hormone
DE10108271A1 (de) 2001-02-21 2002-08-22 Schering Ag Chinolin-, Isochinolin- und Phthalazinderivate als Antagonisten des Gonadotropin freisetzenden Hormons
SE0101256D0 (sv) * 2001-04-06 2001-04-06 A & Science Invest Ab Treatment of low back pain
CN1652784A (zh) * 2002-05-14 2005-08-10 加利福尼亚大学董事会 取代的喹诺酮羧酸、它们的衍生物、作用部位、以及其用途
TW200418829A (en) 2003-02-14 2004-10-01 Avanir Pharmaceutics Inhibitors of macrophage migration inhibitory factor and methods for identifying the same
MXPA06000675A (es) 2003-07-24 2006-04-19 Astellas Pharma Inc Derivado de quinolona o sal del mismo.
US7498341B2 (en) 2004-01-31 2009-03-03 Sanofi Aventis Deutschland Gmbh Heterocyclically substituted 7-amino-4-quinolone-3-carboxylic acid derivatives, process for their preparation and their use as medicaments
WO2005087759A1 (en) 2004-03-10 2005-09-22 The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services Qiunolin-4-ones as inhibitors of retroviral integrase for the treatment of hiv, aids and aids related complex (arc)
EP2522670A1 (de) * 2004-04-07 2012-11-14 Takeda Pharmaceutical Company Limited Heterozyklische CRF-Rezeptor-Antagonisten
JP2006117555A (ja) 2004-10-20 2006-05-11 Kyorin Pharmaceut Co Ltd 1−トリフルオロメチル−4−キノロンカルボン酸誘導体
JP4858683B2 (ja) 2005-01-20 2012-01-18 アステラス製薬株式会社 キノロン誘導体又はその塩の製造法
JP2008094720A (ja) 2005-01-20 2008-04-24 Astellas Pharma Inc キノロン誘導体のプロドラッグ又はその塩
JP4853824B2 (ja) 2005-01-20 2012-01-11 アステラス製薬株式会社 キノロン誘導体を有効成分とする医薬組成物

Also Published As

Publication number Publication date
US8389545B2 (en) 2013-03-05
WO2007100366A2 (en) 2007-09-07
WO2007100366A3 (en) 2007-11-29
CA2631917A1 (en) 2007-06-14
AU2006322045A1 (en) 2007-06-14
JP2009518309A (ja) 2009-05-07
WO2007067489A1 (en) 2007-06-14
JP5192389B2 (ja) 2013-05-08
TW200840814A (en) 2008-10-16
US20100317692A1 (en) 2010-12-16
EP1963271B1 (de) 2010-07-28
DE602006015851D1 (de) 2010-09-09
EP1963271A1 (de) 2008-09-03

Similar Documents

Publication Publication Date Title
ATE475650T1 (de) Positive allosterische chinolon-m1- rezeptormodulatoren
ATE530544T1 (de) Benzyl-substituierte positive allosterische chinolon-m1-rezeptormodulatoren
TN2011000209A1 (en) Aryl methyl benzoquinazolinone m1 receptor positive allosteric modulators
TN2012000231A1 (en) Quinoline amide m1 receptor positive allosteric modulators
BR0316350A (pt) Diaminotriazóis úteis como inibidores de proteìna cinases
EP2582676A4 (de) Positive allosterische tetrahydrochinolin-amid-m1-rezeptormodulatoren
MX2012002583A (es) Moduladores de piranil aril metil benzoquinazolinona alostericos positivos del receptor m1.
TW200728305A (en) Spiropiperidine beta-sectetase inhibitors for the treatment of alzheimer's disease
EA200901373A1 (ru) Аминогетероциклические соединения
CY1110965T1 (el) Επιπροσθετες ετεροπολυκυκλικες ενωσεις και η χρηση τους ως ανταγωνιστες μεταβολοτροπικου υποδοχεα γλουταμικου
EA201071245A1 (ru) Новые терапевтические подходы для лечения болезни альцгеймера и связанных нарушений посредством модулирования реакции клеток на стресс
TW200716546A (en) Oxindole compounds and their uses as therapeutic agents
ATE396973T1 (de) Benzylether- und benzylamino-beta-sekretase- hemmer zur behandlung von alzheimer-krankheit
EA200700489A1 (ru) Новые бензоконденсированные гетероарилсульфамидные производные, полезные в качестве противоконвульсивных средств
EA200971107A1 (ru) Катехоламиновые производные, полезные для лечения болезни паркинсона
CY1111070T1 (el) Παραγωγα 2-αμινο-κουιναζολινης χρησιμα ως αναστολεις της β-σεκρετασης (bace)
TW200800976A (en) New compounds for the treatment of neurological, psychiatric or pain disorders
ATE517861T1 (de) Benzylether und benzylaminoverbindungen als inhibitoren von beta-secretase zur behandlung von alzheimer-krankheit
EA200600971A1 (ru) Применение замещённых 2 - аминотетралинов для профилактического лечения болезни паркинсона
DE602006006712D1 (de) Thiazolylpiperidin-derivate nützlich als h3 rezeptor modulatoren
ATE552257T1 (de) Positive allosterische chinolizidinon-m1- rezeptormodulatoren
EA200600071A1 (ru) Производные n-фенилпиперазина и способы профилактики или лечения заболеваний, связанных с 5ht-рецептором
ATE538796T1 (de) Piperidin- und pyrrolidin-beta-secretase-hemmer zur behandlung von alzheimer-krankheit
WO2009117283A3 (en) Quinolizidinone m1 receptor positive allosteric modulators
EA200801302A1 (ru) Композиции и способы лечения нарушений цнс

Legal Events

Date Code Title Description
RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties