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5-(4-acetyl[1,4]diazepan-1-yl)pentanoic acid | 1272842-91-7

中文名称
——
中文别名
——
英文名称
5-(4-acetyl[1,4]diazepan-1-yl)pentanoic acid
英文别名
5-(4-acetyl-1,4-diazepan-1-yl)pentanoic acid
5-(4-acetyl[1,4]diazepan-1-yl)pentanoic acid化学式
CAS
1272842-91-7
化学式
C12H22N2O3
mdl
——
分子量
242.318
InChiKey
ARMHOIKXPJNVLB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -2.2
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    60.8
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    5-(4-甲氧基苯)-1H-咪唑-2-胺5-(4-acetyl[1,4]diazepan-1-yl)pentanoic acidN,N'-羰基二咪唑 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 12.0h, 以14%的产率得到5-(4-acetyl[1,4]diazepan-1-yl)pentanoic acid [5-(4-methoxyphenyl)-1H-imidazol-2-yl]amide
    参考文献:
    名称:
    Discovery of a Novel Alpha-7 Nicotinic Acetylcholine Receptor Agonist Series and Characterization of the Potent, Selective, and Orally Efficacious Agonist 5-(4-Acetyl[1,4]diazepan-1-yl)pentanoic Acid [5-(4-Methoxyphenyl)-1H-pyrazol-3-yl] Amide (SEN15924, WAY-361789)
    摘要:
    Alpha-7 nicotinic acetylcholine receptors (alpha 7 nAChR) are implicated in the modulation of many cognitive functions such as attention, working memory, and episodic memory. For this reason, alpha 7 nAChR agonists represent promising therapeutic candidates for the treatment of cognitive impairment associated with Alzheimer's disease (AD) and schizophrenia. A medicinal chemistry effort, around our previously reported chemical series, permitted the discovery of a novel class of alpha 7 nAChR agonists with improved selectivity, in particular against the alpha 3 receptor subtype and better ADME profile. The exploration of this series led to the identification of 5-(4-acetyl[1,4]diazepan-1-yl)pentanoic acid [5-(4-methoxyphenyl)-1H-pyrazol-3-yl] amide (25, SEN15924, WAY-361789), a novel, full agonist of the alpha 7 nAChR that was evaluated in vitro and in vivo. Compound 25 proved to be potent and selective, and it demonstrated a fair pharmacokinetic profile accompanied by efficacy in rodent behavioral cognition models (novel object recognition and auditory sensory gating).
    DOI:
    10.1021/jm300247y
  • 作为产物:
    描述:
    1-乙酰基-1H-1,4-二氮杂庚烷 在 sodium hydroxide 作用下, 以 甲苯 为溶剂, 反应 26.0h, 生成 5-(4-acetyl[1,4]diazepan-1-yl)pentanoic acid
    参考文献:
    名称:
    Discovery of a Novel Alpha-7 Nicotinic Acetylcholine Receptor Agonist Series and Characterization of the Potent, Selective, and Orally Efficacious Agonist 5-(4-Acetyl[1,4]diazepan-1-yl)pentanoic Acid [5-(4-Methoxyphenyl)-1H-pyrazol-3-yl] Amide (SEN15924, WAY-361789)
    摘要:
    Alpha-7 nicotinic acetylcholine receptors (alpha 7 nAChR) are implicated in the modulation of many cognitive functions such as attention, working memory, and episodic memory. For this reason, alpha 7 nAChR agonists represent promising therapeutic candidates for the treatment of cognitive impairment associated with Alzheimer's disease (AD) and schizophrenia. A medicinal chemistry effort, around our previously reported chemical series, permitted the discovery of a novel class of alpha 7 nAChR agonists with improved selectivity, in particular against the alpha 3 receptor subtype and better ADME profile. The exploration of this series led to the identification of 5-(4-acetyl[1,4]diazepan-1-yl)pentanoic acid [5-(4-methoxyphenyl)-1H-pyrazol-3-yl] amide (25, SEN15924, WAY-361789), a novel, full agonist of the alpha 7 nAChR that was evaluated in vitro and in vivo. Compound 25 proved to be potent and selective, and it demonstrated a fair pharmacokinetic profile accompanied by efficacy in rodent behavioral cognition models (novel object recognition and auditory sensory gating).
    DOI:
    10.1021/jm300247y
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文献信息

  • [EN] SYNTHESIS OF PYRAZOLES<br/>[FR] SYNTHÈSE DE PYRAZOLES
    申请人:WYETH CORP
    公开号:WO2009091832A1
    公开(公告)日:2009-07-23
    The present invention provides methods of making HCl salts, and methods of using them to modulate alpha7 nicotinic acetylcholine receptors and/or to treat any of a variety of disorders, diseases, and conditions. Provided compounds can affect, among other things, neurological, psychiatric and/or inflammatory system.
    本发明提供了制备HCl盐的方法,以及利用它们调节α7烟碱乙酰胆碱受体和/或治疗各种疾病、疾病和症状的方法。所提供的化合物可以影响神经系统、精神病和/或炎症系统等方面。
  • [EN] ALPHA7 NICOTINIC ACETYLCHOLINE RECEPTOR INHIBITORS<br/>[FR] INHIBITEURS DE RÉCEPTEURS NICOTINIQUES ALPHA-7 DE L'ACÉTYLCHOLINE
    申请人:WYETH CORP
    公开号:WO2010009290A1
    公开(公告)日:2010-01-21
    The present invention provides compounds and compositions, methods of making them, and methods of using them to modulate α7 nicotinic acetylcholine receptors and/or to treat any of a variety of disorders, diseases, and conditions. Provided compounds can affect, among other things, neurological, psychiatric and/or inflammatory systems.
    本发明提供了化合物和组合物,制备它们的方法,以及利用它们调节α7烟碱乙酰胆碱受体和/或治疗各种疾病、疾病和症状的方法。所提供的化合物可以影响神经系统、精神病学和/或炎症系统等方面。
  • COMPOUND FORMS AND USES THEREOF
    申请人:Mirmehrabi Mahmoud
    公开号:US20090181953A1
    公开(公告)日:2009-07-16
    The present invention provides, among other things, forms of a compound of formula 1. In some embodiments, the present invention provides salt forms and/or crystal forms. In some embodiments, the present invention provides solid forms. The present invention also provides methods of making and using provided forms.
    本发明提供了化合物的一种形式,其化学式为1。在一些实施方式中,本发明提供盐形式和/或晶体形式。在一些实施方式中,本发明提供固体形式。本发明还提供了制备和使用所提供形式的方法。
  • COMPOUNDS USEFUL AS ALPHA7 NICOTINIC ACETYLCHOLINE RECEPTOR AGONISTS
    申请人:Haydar Simon N.
    公开号:US20090181952A1
    公开(公告)日:2009-07-16
    The present invention provides compounds and compositions, and methods of using them to modulate α7 nicotinic acetylcholine receptors and/or to treat any of a variety of disorders, diseases, and conditions. Provided compounds can affect, among other things, neurological, psychiatric and/or inflammatory systems.
    本发明提供了化合物和组合物,以及使用它们调节α7烟碱性乙酰胆碱受体和/或治疗各种紊乱、疾病和情况的方法。所提供的化合物可以影响神经系统、精神疾病和/或炎症系统等方面。
  • SYNTHESIS OF PYRAZOLES
    申请人:Chew Warren
    公开号:US20090264648A1
    公开(公告)日:2009-10-22
    The present invention provides compounds and compositions, methods of making them, and methods of using them to modulate α7 nicotinic acetylcholine receptors and/or to treat any of a variety of disorders, diseases, and conditions. Provided compounds can affect, among other things, neurological, psychiatric and/or inflammatory system.
    本发明提供了化合物和组合物,制备方法以及使用方法,用于调节α7尼古丁乙酰胆碱受体和/或治疗各种疾病、疾病和情况。提供的化合物可以影响神经、精神和/或炎症系统等方面。
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