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AC-42 | 244291-63-2

中文名称
——
中文别名
——
英文名称
AC-42
英文别名
4-n-Butyl-1-[4-(2-methylphenyl)-4-oxo-1-butyl]piperidine;4-(4-Butylpiperidin-1-yl)-1-(2-methylphenyl)butan-1-one
AC-42化学式
CAS
244291-63-2
化学式
C20H31NO
mdl
——
分子量
301.472
InChiKey
ANTKBACNWQHQJE-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

物化性质

  • 沸点:
    427.5±28.0 °C(Predicted)
  • 密度:
    0.958±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.2
  • 重原子数:
    22
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    4-(4-n-丁基哌啶-1-基)丁腈2-碘苯甲醚sodium hydroxide硫酸 作用下, 以 四氢呋喃乙醚 为溶剂, 以26%的产率得到AC-42
    参考文献:
    名称:
    Compounds with activity on muscarinic receptors
    摘要:
    提供了化合物和方法,用于缓解或治疗需要改变肌胆碱m1受体活性以产生益处的疾病或状况。在该方法中,向需要此类治疗的患者施用有效量的选择性肌胆碱m1激动剂化合物。
    公开号:
    US06528529B1
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文献信息

  • COMPOUNDS WITH ACTIVITY ON MUSCARINIC RECEPTORS
    申请人:Brann Mark
    公开号:US20080108618A1
    公开(公告)日:2008-05-08
    Compounds and methods are provided for the alleviation or treatment of diseases or conditions in which modification of muscarinic m1 receptor activity has a beneficial effect. In the method, a therapeutically effective amount of a selective muscarinic m1 agonist compound is administered to a patient in need of such treatment.
    提供了化合物和方法,用于缓解或治疗改变毒蕈碱受体m1活性有益影响的疾病或状况。在该方法中,向需要此类治疗的患者施用选择性毒蕈碱受体m1激动剂化合物的治疗有效量。
  • SCREENING METHOD
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP3627152A1
    公开(公告)日:2020-03-25
    The present invention provides a useful and efficient screening method for finding a cholinergic muscarinic M1 receptor positive allosteric modulator (M1PAM) with reduced cholinergic side effects. The present invention also provides a method for treating Alzheimer's disease and the like, a method for reducing cholinergic side effects, and the like which use M1PAM selected by the screening method and having a low α value, or the M1PAM and an acetylcholinesterase inhibitor.
    本发明提供了一种有用且高效的筛选方法,用于寻找具有降低胆碱能副作用的胆碱能毒蕈碱 M1 受体正性异位调节剂(M1PAM)。本发明还提供了一种治疗阿尔茨海默病等疾病的方法、一种减少胆碱能副作用的方法等,这些方法使用了通过筛选方法选出的具有低α值的M1PAM,或M1PAM乙酰胆碱酯酶抑制剂
  • MUSCARINIC COMBINATION AND ITS USE FOR COMBATING HYPOCHOLINERGIC DISORDERS OF THE CENTRAL NERVOUS SYSTEM
    申请人:Chase Pharmaceuticals Corporation
    公开号:EP4019018A1
    公开(公告)日:2022-06-29
    A combination of a muscarinic cholinergic receptor agonist with a non-anticholinergic antiemetic agent, and the optional addition of an acetyl choline esterase inhibitor, for the treatment of hypocholinergic disorder of the central nervous system.
    一种毒蕈碱类胆碱能受体激动剂与非抗胆碱能止吐药的复方制剂,并可选择添加乙酰胆碱酯酶抑制剂,用于治疗中枢神经系统的低胆碱能紊乱。
  • Muscarinic combinations and their use for combating hypocholinergic disorders of the central nervous system
    申请人:Chase Pharmaceuticals Corporation
    公开号:US10307409B2
    公开(公告)日:2019-06-04
    A combination of a muscarinic cholinergic receptor agonist, a non-anticholinergic antiemetic agent and a non-selective, peripheral anticholinergic agent for the treatment of hypocholinergic disorders of the central nervous system.
    一种毒蕈碱胆碱能受体激动剂、一种非抗胆碱能止吐药和一种非选择性外周抗胆碱能药的复方制剂,用于治疗中枢神经系统的低胆碱能紊乱。
  • Oxybutynin transdermal therapeutic system muscarinic agonist combination
    申请人:CHASE PHARMACEUTICALS CORPORATION
    公开号:US10596139B2
    公开(公告)日:2020-03-24
    Pharmaceutical compositions and combinations containing a muscarinic receptor antagonist, such as oxybutynin in a transdermal therapeutic system, and a muscarinic receptor agonist, optionally with an acetyl cholinesterase inhibitor, and methods of using the same for treatment of hypocholinergic disorders of the central nervous system such as Alzheimer type dementia. The respective pharmaceutical compositions and combinations of the present invention allow for safe administration of high doses of muscarinic receptor agonist, and improved efficacy of the muscarinic receptor agonist for treatment of hypocholinergic disorders of the central nervous system. The pharmaceutical compositions and combinations also allow for a maximum supply of acetylcholine to the central nervous system, when an acetyl cholinesterase inhibitor is used in combination with a muscarinic receptor antagonist and a muscarinic receptor agonist.
    含有毒蕈碱受体拮抗剂(如透皮治疗系统中的奥昔布宁)和毒蕈碱受体激动剂(可选择与乙酰胆碱酯酶抑制剂一起使用)的药物组合物和组合物,以及使用这些药物组合物和组合物治疗中枢神经系统低胆碱能疾病(如阿尔茨海默型痴呆症)的方法。本发明的各种药物组合物和组合物可以安全地施用大剂量毒蕈碱受体激动剂,并提高毒蕈碱受体激动剂治疗中枢神经系统低胆碱能疾病的疗效。当乙酰胆碱酯酶抑制剂与毒蕈碱受体拮抗剂和毒蕈碱受体激动剂联合使用时,本发明的药物组合物和复方制剂还能最大限度地向中枢神经系统提供乙酰胆碱
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