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methyl cyclopentyl(3-methoxyphenethyl)carbamate | 1260224-81-4

中文名称
——
中文别名
——
英文名称
methyl cyclopentyl(3-methoxyphenethyl)carbamate
英文别名
methyl N-cyclopentyl-N-[2-(3-methoxyphenyl)ethyl]carbamate
methyl cyclopentyl(3-methoxyphenethyl)carbamate化学式
CAS
1260224-81-4
化学式
C16H23NO3
mdl
——
分子量
277.364
InChiKey
BASSKWOMSDZKKK-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):
    3.3
  • 重原子数:
    20
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    参考文献:
    名称:
    Design and Synthesis of an Orally Active Metabotropic Glutamate Receptor Subtype-2 (mGluR2) Positive Allosteric Modulator (PAM) That Decreases Cocaine Self-Administration in Rats
    摘要:
    The modification of 3'((2-cyclopentyl-6,7-dimethyl-1-oxo-2,3-dihydro-1 H-inden-5-yloxy)methyl)biphenyl 4-carboxylic acid (BINA, 1) by incorporating heteroatoms into the structure and replacing the cyclopentyl moiety led to the development of new mGluR2 positive allosteric modulators (PAMs) with optimized potency and superior druglike properties These analogues are more potent than 1 in vitro and are highly selective for mGluR2 vs other mGluR subtypes They have significantly improved pharmacokinetic (PK) properties, with excellent oral bioavailability and brain penetration The benzisothiazol-3-one derivative 14 decreased cocaine self-administration in rats, providing proof-of-concept for the use of mGluR2 PAMs for the treatment of cocaine dependence
    DOI:
    10.1021/jm1012165
  • 作为产物:
    描述:
    3-甲氧基苯乙胺三乙胺 作用下, 以 乙醚乙腈 为溶剂, 反应 0.17h, 生成 methyl cyclopentyl(3-methoxyphenethyl)carbamate
    参考文献:
    名称:
    Design and Synthesis of an Orally Active Metabotropic Glutamate Receptor Subtype-2 (mGluR2) Positive Allosteric Modulator (PAM) That Decreases Cocaine Self-Administration in Rats
    摘要:
    The modification of 3'((2-cyclopentyl-6,7-dimethyl-1-oxo-2,3-dihydro-1 H-inden-5-yloxy)methyl)biphenyl 4-carboxylic acid (BINA, 1) by incorporating heteroatoms into the structure and replacing the cyclopentyl moiety led to the development of new mGluR2 positive allosteric modulators (PAMs) with optimized potency and superior druglike properties These analogues are more potent than 1 in vitro and are highly selective for mGluR2 vs other mGluR subtypes They have significantly improved pharmacokinetic (PK) properties, with excellent oral bioavailability and brain penetration The benzisothiazol-3-one derivative 14 decreased cocaine self-administration in rats, providing proof-of-concept for the use of mGluR2 PAMs for the treatment of cocaine dependence
    DOI:
    10.1021/jm1012165
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文献信息

  • POSITIVE ALLOSTERIC MODULATORS OF GROUP II MGLURS
    申请人:Cosford Nicholas D. P.
    公开号:US20120071503A1
    公开(公告)日:2012-03-22
    The disclosure provides compounds and compositions, and methods of using these compounds and compositions, as positive allosteric modulators of the metabotropic glutamate subtype 2 (mGlu2) receptor, and for treating CNS disorders associated with the mGlu2 receptor including schizophrenia, anxiety, addiction, e.g. cocaine addiction, nicotine addiction, and the like.
    本公开提供化合物和组合物,以及使用这些化合物和组合物的方法,作为代谢型谷酸亚型2(mGlu2)受体的正向变构调节剂,并用于治疗与mGlu2受体相关的中枢神经系统疾病,包括精神分裂症、焦虑症、成瘾等,例如可卡因成瘾、尼古丁成瘾等。
  • Positive allosteric modulators of group II mGluRs
    申请人:Cosford Nicholas D. P.
    公开号:US08748632B2
    公开(公告)日:2014-06-10
    The disclosure provides compounds and compositions, and methods of using these compounds and compositions, as positive allosteric modulators of the metabotropic glutamate subtype 2 (mGlu2) receptor, and for treating CNS disorders associated with the mGlu2 receptor including schizophrenia, anxiety, addiction, e.g. cocaine addiction, nicotine addiction, and the like.
    该披露提供了化合物和组合物,以及使用这些化合物和组合物的方法,作为代谢型谷酸亚型2(mGlu2)受体的正向变构调节剂,并用于治疗与mGlu2受体相关的中枢神经系统疾病,包括精神分裂症、焦虑、成瘾,例如可卡因成瘾、尼古丁成瘾等。
  • US8748632B2
    申请人:——
    公开号:US8748632B2
    公开(公告)日:2014-06-10
  • [EN] POSITIVE ALLOSTERIC MODULATORS OF GROUP II MGLURS<br/>[FR] MODULATEURS ALLOSTÉRIQUES POSITIFS DE MGLURS DE TYPE 2
    申请人:SANFORD BURNHAM MED RES INST
    公开号:WO2011116356A2
    公开(公告)日:2011-09-22
    The disclosure provides compounds and compositions, and methods of using these compounds and compositions, as positive ailosteric modulators of the melabotropic glutamatc subtype 2 (mGlu2) receptor, and for treating CNS disorders associated with the mGlu2 receptor including schizophrenia, anxiety, addiction, e.g. cocaine addiction, nicotine addiction, and the like.
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