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diethyl (4-(((3S)-3-methyl-4-(((phenylmethyl)oxy)carbonyl)-1-piperazinyl)methyl)phenyl)propanedioate | 923565-69-9

中文名称
——
中文别名
——
英文名称
diethyl (4-(((3S)-3-methyl-4-(((phenylmethyl)oxy)carbonyl)-1-piperazinyl)methyl)phenyl)propanedioate
英文别名
Diethyl {4-[((3S)-3-methyl-4-{[(phenylmethyl)oxy]carbonyl}-1-piperazinyl)methyl]phenyl}propanedioate;diethyl 2-[4-[[(3S)-3-methyl-4-phenylmethoxycarbonylpiperazin-1-yl]methyl]phenyl]propanedioate
diethyl (4-(((3S)-3-methyl-4-(((phenylmethyl)oxy)carbonyl)-1-piperazinyl)methyl)phenyl)propanedioate化学式
CAS
923565-69-9
化学式
C27H34N2O6
mdl
——
分子量
482.577
InChiKey
MNIGFFWRAFYZQA-FQEVSTJZSA-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):
    4
  • 重原子数:
    35
  • 可旋转键数:
    12
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    85.4
  • 氢给体数:
    0
  • 氢受体数:
    7

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:
    diethyl (4-(((3S)-3-methyl-4-(((phenylmethyl)oxy)carbonyl)-1-piperazinyl)methyl)phenyl)propanedioatesodium hydroxide 作用下, 以 1,4-二氧六环 为溶剂, 反应 2.0h, 以84%的产率得到(4-(((3S)-3-methyl-4-(((phenylmethyl)oxy)carbonyl)-1-piperazinyl)methyl)phenyl)acetic acid
    参考文献:
    名称:
    Discovery of N-(3-Fluorophenyl)-1-[(4-([(3S)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine (GSK962040), the First Small Molecule Motilin Receptor Agonist Clinical Candidate
    摘要:
    N-(3-Fluorophenyl)-1-[(4-([(3S)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine 12 (GSK962040) is a novel small molecule motilin receptor agonist. It possesses excellent activity at the recombinant human motilin receptor and also at the native rabbit motilin receptor where its agonist activity results in potentiation of the amplitude of neuronal-mediated contractions of isolated gastric antrum, tissue. Compound 12 also possesses highly promising pharmacokinetic profiles in both rat and dog, and these results, in combination with further profiling in human native tissue and an in vivo model of gastrointestinal transit in the rabbit, have led to its selection as a candidate for further development.
    DOI:
    10.1021/jm801332q
  • 作为产物:
    描述:
    phenylmethyl (2S)-4-((4-bromophenyl)methyl)-2-methyl-1-piperazinecarboxylate丙二酸二乙酯potassium phosphate 、 palladium diacetate 、 2-二-叔丁基磷-2'-甲基联苯 作用下, 以 1,4-二氧六环 为溶剂, 以60%的产率得到diethyl (4-(((3S)-3-methyl-4-(((phenylmethyl)oxy)carbonyl)-1-piperazinyl)methyl)phenyl)propanedioate
    参考文献:
    名称:
    Discovery of N-(3-Fluorophenyl)-1-[(4-([(3S)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine (GSK962040), the First Small Molecule Motilin Receptor Agonist Clinical Candidate
    摘要:
    N-(3-Fluorophenyl)-1-[(4-([(3S)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine 12 (GSK962040) is a novel small molecule motilin receptor agonist. It possesses excellent activity at the recombinant human motilin receptor and also at the native rabbit motilin receptor where its agonist activity results in potentiation of the amplitude of neuronal-mediated contractions of isolated gastric antrum, tissue. Compound 12 also possesses highly promising pharmacokinetic profiles in both rat and dog, and these results, in combination with further profiling in human native tissue and an in vivo model of gastrointestinal transit in the rabbit, have led to its selection as a candidate for further development.
    DOI:
    10.1021/jm801332q
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文献信息

  • BENZYLPIPERAZINE DERIVATIVES AND THEIR MEDICAL USE
    申请人:Johnson Christopher Norbert
    公开号:US20090054456A1
    公开(公告)日:2009-02-26
    The present invention relates to novel benzylpiperazine derivatives such as compounds of formula (I), which have activity as agonists of the GPR38 receptor and the use of such compounds or pharmaceutical compositions thereof in the treatment of gastrointestinal disorders.
    本发明涉及新型苄基哌嗪衍生物,如公式(I)化合物,其具有作为GPR38受体激动剂的活性,以及在治疗胃肠道疾病中使用这些化合物或其制剂的药物组合物。
  • COMPOUNDS
    申请人:Glaxo Group Limited
    公开号:US20130317041A1
    公开(公告)日:2013-11-28
    The present invention relates to benzylpiperazine derivatives such as compounds of formula (I), which have activity as agonists of the GPR38 receptor and the use of such compounds or pharmaceutical compositions thereof in the preparation of medicaments suitable for the treatment of gastrointestinal disorders.
    本发明涉及苄基哌嗪衍生物,例如公式(I)的化合物,它们具有作为GPR38受体激动剂的活性,以及使用这些化合物或其制剂在制备适用于治疗胃肠道疾病的药物中的用途。
  • Benzylpiperazine derivatives and their medical use
    申请人:Johnson Christopher Norbert
    公开号:US08536182B2
    公开(公告)日:2013-09-17
    The present invention relates to novel benzylpiperazine derivatives such as compounds of formula (I), which have activity as agonists of the GPR38 receptor and the use of such compounds or pharmaceutical compositions thereof in the treatment of gastrointestinal disorders.
    本发明涉及新型苯基哌嗪衍生物,如式(I)化合物,具有作为GPR38受体激动剂的活性,以及这些化合物或其药物组合物在治疗胃肠道疾病中的应用。
  • WO2007/12479
    申请人:——
    公开号:——
    公开(公告)日:——
  • Discovery of <i>N</i>-(3-Fluorophenyl)-1-[(4-([(3<i>S</i>)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine (GSK962040), the First Small Molecule Motilin Receptor Agonist Clinical Candidate
    作者:Susan M. Westaway、Samantha L. Brown、Stephen C. M. Fell、Christopher N. Johnson、David T. MacPherson、Darren J. Mitchell、James W. Myatt、Steven J. Stanway、Jon T. Seal、Geoffrey Stemp、Mervyn Thompson、Kirk Lawless、Fiona McKay、Alison I. Muir、Jonathan M. Barford、Chermaine Cluff、Sadhia R. Mahmood、Kim L. Matthews、Shiyam Mohamed、Beverley Smith、Alexander J. Stevens、Victoria J. Bolton、Emma M. Jarvie、Gareth J. Sanger
    DOI:10.1021/jm801332q
    日期:2009.2.26
    N-(3-Fluorophenyl)-1-[(4-([(3S)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine 12 (GSK962040) is a novel small molecule motilin receptor agonist. It possesses excellent activity at the recombinant human motilin receptor and also at the native rabbit motilin receptor where its agonist activity results in potentiation of the amplitude of neuronal-mediated contractions of isolated gastric antrum, tissue. Compound 12 also possesses highly promising pharmacokinetic profiles in both rat and dog, and these results, in combination with further profiling in human native tissue and an in vivo model of gastrointestinal transit in the rabbit, have led to its selection as a candidate for further development.
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