JP4527408B2 - ムスカリン性アンタゴニスト - Google Patents

ムスカリン性アンタゴニスト Download PDF

Info

Publication number
JP4527408B2
JP4527408B2 JP2003587783A JP2003587783A JP4527408B2 JP 4527408 B2 JP4527408 B2 JP 4527408B2 JP 2003587783 A JP2003587783 A JP 2003587783A JP 2003587783 A JP2003587783 A JP 2003587783A JP 4527408 B2 JP4527408 B2 JP 4527408B2
Authority
JP
Japan
Prior art keywords
compound
alkyl
group
mmol
formula
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
JP2003587783A
Other languages
English (en)
Japanese (ja)
Other versions
JP2006507220A5 (OSRAM
JP2006507220A (ja
Inventor
クレイグ ディー. ボイル,
ウィリアム ジェイ. グリーンリー,
サミュエル チャカラマンニル,
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Sharp and Dohme LLC
Original Assignee
Schering Corp
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 Schering Corp filed Critical Schering Corp
Publication of JP2006507220A publication Critical patent/JP2006507220A/ja
Publication of JP2006507220A5 publication Critical patent/JP2006507220A5/ja
Application granted granted Critical
Publication of JP4527408B2 publication Critical patent/JP4527408B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/20Spiro-condensed ring systems
    • 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
    • A61P25/28Drugs 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
    • 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
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/96Sulfur atom

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
JP2003587783A 2002-04-26 2003-04-24 ムスカリン性アンタゴニスト Expired - Fee Related JP4527408B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US37609302P 2002-04-26 2002-04-26
PCT/US2003/012694 WO2003091220A1 (en) 2002-04-26 2003-04-24 Muscarinic antagonists

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2009285736A Division JP2010059213A (ja) 2002-04-26 2009-12-16 ムスカリン性アンタゴニスト

Publications (3)

Publication Number Publication Date
JP2006507220A JP2006507220A (ja) 2006-03-02
JP2006507220A5 JP2006507220A5 (OSRAM) 2006-05-25
JP4527408B2 true JP4527408B2 (ja) 2010-08-18

Family

ID=29270760

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2003587783A Expired - Fee Related JP4527408B2 (ja) 2002-04-26 2003-04-24 ムスカリン性アンタゴニスト
JP2009285736A Withdrawn JP2010059213A (ja) 2002-04-26 2009-12-16 ムスカリン性アンタゴニスト

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2009285736A Withdrawn JP2010059213A (ja) 2002-04-26 2009-12-16 ムスカリン性アンタゴニスト

Country Status (11)

Country Link
US (1) US6890936B2 (OSRAM)
EP (1) EP1499596B1 (OSRAM)
JP (2) JP4527408B2 (OSRAM)
CN (1) CN1649845A (OSRAM)
AT (1) ATE413388T1 (OSRAM)
AU (1) AU2003228674A1 (OSRAM)
CA (1) CA2484217A1 (OSRAM)
DE (1) DE60324544D1 (OSRAM)
ES (1) ES2315494T3 (OSRAM)
MX (1) MXPA04010552A (OSRAM)
WO (1) WO2003091220A1 (OSRAM)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GEP20094705B (en) 2003-04-24 2009-06-10 Incyte Corp Aza spiro alkane derivatives as inhibitors of metalloproteases
CA2579820A1 (en) * 2004-09-20 2006-03-30 Targacept, Inc. Azaspiroalkene and azapiroalkane compounds with nicotinic cholinergic receptor activity
US7678363B2 (en) 2005-08-26 2010-03-16 Braincells Inc Methods of treating psychiatric conditions comprising administration of muscarinic agents in combination with SSRIs
AU2007299920A1 (en) * 2006-09-19 2008-03-27 Braincells, Inc. PPAR Mediated Modulation of Neurogenesis
WO2008036846A2 (en) * 2006-09-22 2008-03-27 Braincells, Inc. Combination comprising an hmg-coa reductase inhibitor and a second neurogenic agent for treating a nervous system disorder and increasing neurogenesis
US20080108574A1 (en) * 2006-09-27 2008-05-08 Braincells, Inc. Melanocortin receptor mediated modulation of neurogenesis
JP5379692B2 (ja) 2006-11-09 2013-12-25 プロビオドルグ エージー 潰瘍、癌及び他の疾患の治療のためのグルタミニルシクラーゼの阻害薬としての3−ヒドロキシ−1,5−ジヒドロ−ピロール−2−オン誘導体
SI2091948T1 (sl) 2006-11-30 2012-07-31 Probiodrug Ag Novi inhibitorji glutaminil ciklaze
ZA200905537B (en) 2007-03-01 2010-10-27 Probiodrug Ag New use of glutaminyl cyclase inhibitors
EP2865670B1 (en) 2007-04-18 2017-01-11 Probiodrug AG Thiourea derivatives as glutaminyl cyclase inhibitors
TW200902007A (en) * 2007-05-25 2009-01-16 Astrazeneca Ab Spirocyclopropyl piperidine derivatives
US20100130477A1 (en) * 2008-11-25 2010-05-27 Astrazeneca Ab Spirocyclobutyl Piperidine Derivatives
EP2475428B1 (en) 2009-09-11 2015-07-01 Probiodrug AG Heterocylcic derivatives as inhibitors of glutaminyl cyclase
CN109662964A (zh) 2010-02-09 2019-04-23 约翰斯.霍普金斯大学 用于改善认知功能的方法和组合物
WO2011107530A2 (en) 2010-03-03 2011-09-09 Probiodrug Ag Novel inhibitors
BR112012022478B1 (pt) 2010-03-10 2021-09-21 Probiodrug Ag Inibidores heterocíclicos de glutaminil ciclase (qc, ec 2.3.2.5), seu processo de preparação, e composição farmacêutica
JP5945532B2 (ja) 2010-04-21 2016-07-05 プロビオドルグ エージー グルタミニルシクラーゼの阻害剤としてのベンゾイミダゾール誘導体
US20110281853A1 (en) 2010-05-12 2011-11-17 Rishi Arora Compositions and methods for treating or preventing atrial fibrillation
ES2570167T3 (es) 2011-03-16 2016-05-17 Probiodrug Ag Derivados de benzimidazol como inhibidores de glutaminil ciclasa
JP6440625B2 (ja) 2012-11-14 2018-12-19 ザ・ジョンズ・ホプキンス・ユニバーシティー 精神分裂病を処置するための方法および組成物
CN105142623A (zh) 2013-03-15 2015-12-09 艾吉因生物股份有限公司 用于改善认知功能的方法和组合物
WO2014144663A1 (en) 2013-03-15 2014-09-18 The Johns Hopkins University Methods and compositions for improving cognitive function
DK3212637T3 (da) * 2014-10-31 2021-07-12 Indivior Uk Ltd Dopamin-d3-receptorantagonistforbindelser
NZ738682A (en) 2015-05-22 2022-01-28 Agenebio Inc Extended release pharmaceutical compositions of levetiracetam
WO2019014427A1 (en) * 2017-07-12 2019-01-17 Vanderbilt University ANTAGONISTS OF THE MUSCARINIC RECEPTOR OF ACETYLCHOLINE M4
EP3461819B1 (en) 2017-09-29 2020-05-27 Probiodrug AG Inhibitors of glutaminyl cyclase
US11325896B2 (en) 2017-12-20 2022-05-10 Vanderbilt University Antagonists of the muscarinic acetylcholine receptor M4
TWI767148B (zh) * 2018-10-10 2022-06-11 美商弗瑪治療公司 抑制脂肪酸合成酶(fasn)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04225953A (ja) * 1990-05-07 1992-08-14 Shionogi & Co Ltd スピロ ジベンゾスベラン誘導体
GB9309422D0 (en) * 1993-05-07 1993-06-23 Res Inst Medicine Chem Chemical compounds
WO1999032489A1 (en) * 1997-12-23 1999-07-01 Alcon Laboratories, Inc. Muscarinic agents and use thereof to treat glaucoma, myopia and various other conditions
EP1386920A4 (en) * 2001-04-20 2005-09-14 Banyu Pharma Co Ltd benzimidazolone derivatives

Also Published As

Publication number Publication date
WO2003091220A1 (en) 2003-11-06
ES2315494T3 (es) 2009-04-01
DE60324544D1 (de) 2008-12-18
JP2006507220A (ja) 2006-03-02
US20040067972A1 (en) 2004-04-08
CN1649845A (zh) 2005-08-03
US6890936B2 (en) 2005-05-10
AU2003228674A1 (en) 2003-11-10
EP1499596B1 (en) 2008-11-05
HK1068136A1 (en) 2005-04-22
CA2484217A1 (en) 2003-11-06
ATE413388T1 (de) 2008-11-15
JP2010059213A (ja) 2010-03-18
EP1499596A1 (en) 2005-01-26
MXPA04010552A (es) 2005-01-25

Similar Documents

Publication Publication Date Title
JP4527408B2 (ja) ムスカリン性アンタゴニスト
JP4448134B2 (ja) ベンズアミド置換基を有する環状アミンbase−1阻害剤
AU688120B2 (en) New piperidine compounds, process for their preparation and the pharmaceutical compositions which contain them
EP2010506B1 (en) Diazepan derivatives modulators of chemokine receptors
JP2009155350A (ja) ムスカリン性アンタゴニストとしてのピペリジン化合物
EP1870405A1 (en) Carbonylated (Aza)cyclohexanes as dopamine D3 receptor ligands
JP2004512324A (ja) Nmda受容体拮抗剤としてのアミド誘導体
AU9206798A (en) Pyrrolidine and piperidine modulators of chemokine receptor activity
JP2009167218A (ja) Mchアンタゴニストおよび肥満治療でのそれらの使用
HRP20000495A2 (en) N-acyl cyclic amine derivatives
JP2006502181A (ja) 5−ht4レセプターアゴニストとしてのイミダゾピリジン化合物
ZA200700329B (en) New heterocyclic carboxylic acid amide derivatives
CN101925383A (zh) 甲酰胺化合物及其作为趋化因子受体激动剂的应用
KR101567116B1 (ko) Nk1 수용체 길항제로서의 5-[5-[2-(3,5-비스(트리플루오로메틸)페닐)-2-메틸프로파노일메틸아미노]-4-(4-플루오로-2-메틸페닐)]-2-피리디닐-2-알킬-프롤린아미드
US6916822B2 (en) Phenoxyalkylamine derivatives useful as opioid δ receptor agonists
ZA200700322B (en) New benzoyl urea derivatives
JP4605801B2 (ja) 肥満治療用のmchアンタゴニスト
DE69529790T2 (de) Imidazolin-Derivate, deren Herstellung und deren Verwendung als Tachykinin-Rezeptor Antagonisten
US20090029979A1 (en) 5-htx modulators
JP2007521286A5 (OSRAM)
HK1068136B (en) Muscarinic antagonists
JPWO2005030722A1 (ja) N−置換−n−(4−ピペリジニル)アミド誘導体
EP1910316B1 (en) Substituted triazole derivatives and their use as neurokinin 3 receptor antagonists

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20060324

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20060324

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20090917

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20091216

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20100527

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20100603

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130611

Year of fee payment: 3

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

LAPS Cancellation because of no payment of annual fees