JP2009506069A - ムスカリン性受容体調節による神経発生 - Google Patents

ムスカリン性受容体調節による神経発生 Download PDF

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JP2009506069A
JP2009506069A JP2008528217A JP2008528217A JP2009506069A JP 2009506069 A JP2009506069 A JP 2009506069A JP 2008528217 A JP2008528217 A JP 2008528217A JP 2008528217 A JP2008528217 A JP 2008528217A JP 2009506069 A JP2009506069 A JP 2009506069A
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cas
agent
muscarinic
neurogenesis
receptor
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JP2009506069A5 (enExample
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バーロー,カロリー
エー. カーター,トッド
アイ. ロラン,キム
シー. ピレス,ジャミーソン
モース,アンドリュー
ジトニック,ダナ
トロイナー,カイ
ブロードヘッド,アレックス
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ブレインセルス,インコーポレイティド
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • AHUMAN NECESSITIES
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    • A61K31/325Carbamic acids; Thiocarbamic acids; Anhydrides or salts thereof
    • AHUMAN NECESSITIES
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    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • AHUMAN NECESSITIES
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    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
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    • A61K31/47Quinolines; Isoquinolines
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
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  • Pharmacology & Pharmacy (AREA)
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  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Addiction (AREA)
  • Pain & Pain Management (AREA)
  • Anesthesiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
JP2008528217A 2005-08-26 2006-08-25 ムスカリン性受容体調節による神経発生 Pending JP2009506069A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US71184605P 2005-08-26 2005-08-26
US72712705P 2005-10-14 2005-10-14
US73813305P 2005-11-17 2005-11-17
US80382606P 2006-06-02 2006-06-02
PCT/US2006/033299 WO2007025177A2 (en) 2005-08-26 2006-08-25 Neurogenesis by muscarinic receptor modulation

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JP2009506069A true JP2009506069A (ja) 2009-02-12
JP2009506069A5 JP2009506069A5 (enExample) 2009-09-17

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US (2) US7678363B2 (enExample)
EP (3) EP1928437A2 (enExample)
JP (1) JP2009506069A (enExample)
AU (1) AU2006282896A1 (enExample)
CA (1) CA2620333A1 (enExample)
WO (1) WO2007025177A2 (enExample)

Cited By (1)

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JP2017531043A (ja) * 2014-10-20 2017-10-19 アナベックス ライフ サイエンシズ コーポレイション 抗発作治療のためのa19−144、a2−73およびある特定の抗コリンエステラーゼ阻害剤、組成物および方法

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