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1-{2-[(1S)-amino-2-methylpropyl]-4-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]piperazine | 956035-71-5

中文名称
——
中文别名
——
英文名称
1-{2-[(1S)-amino-2-methylpropyl]-4-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]piperazine
英文别名
(2R)-1-[4-[2-[(1S)-1-amino-2-methylpropyl]-4-methylphenyl]piperazin-1-yl]-3-(4-chlorophenyl)-2-methylpropan-1-one
1-{2-[(1S)-amino-2-methylpropyl]-4-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]piperazine化学式
CAS
956035-71-5
化学式
C25H34ClN3O
mdl
——
分子量
428.017
InChiKey
IMYWIXVEAKDSQK-DVECYGJZSA-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):
    5
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    49.6
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1-{2-[(1S)-amino-2-methylpropyl]-4-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]piperazineBoc-beta-丙氨酸碳酸氢钠1-羟基苯并三唑1-(3-二甲基氨基丙基)-3-乙基碳二亚胺三氟乙酸 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 生成 1-{2-[(1S)-(aminopropionyl)amino-2-methylpropyl]-4-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]piperazine
    参考文献:
    名称:
    Discovery of 1-{2-[(1S)-(3-Dimethylamino-propionyl)amino-2-methylpropyl]-4-methyl-phenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)-propionyl]piperazine as an Orally Active Antagonist of the Melanocortin-4 Receptor for the Potential Treatment of Cachexia
    摘要:
    A potent and Selective antagonist of the melanocortin-4 receptor, 1-{2-[(IS)-(3-dimethylaminopropionyl)amino-2-methylpropyl}-6-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]pip- erazine (10d), was identified from a series piperazinebenzylamine attached with a N,N-dimethyl-beta-alanine side chain. This compound possessed high water solubility and exhibited good metabolic profiles. In animals, 10d showed moderate to good oral bioavailability and promoted food intake in tumor-bearing mice after oral administration.
    DOI:
    10.1021/jm070806a
  • 作为产物:
    描述:
    1-{2-[(1S)-(S-tert-butylsulfinyl)amino-(2-methylpropyl)]-4-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]piperazine 在 盐酸 作用下, 以 甲醇乙醚 为溶剂, 反应 1.0h, 生成 1-{2-[(1S)-amino-2-methylpropyl]-4-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]piperazine
    参考文献:
    名称:
    Discovery of 1-{2-[(1S)-(3-Dimethylamino-propionyl)amino-2-methylpropyl]-4-methyl-phenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)-propionyl]piperazine as an Orally Active Antagonist of the Melanocortin-4 Receptor for the Potential Treatment of Cachexia
    摘要:
    A potent and Selective antagonist of the melanocortin-4 receptor, 1-{2-[(IS)-(3-dimethylaminopropionyl)amino-2-methylpropyl}-6-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]pip- erazine (10d), was identified from a series piperazinebenzylamine attached with a N,N-dimethyl-beta-alanine side chain. This compound possessed high water solubility and exhibited good metabolic profiles. In animals, 10d showed moderate to good oral bioavailability and promoted food intake in tumor-bearing mice after oral administration.
    DOI:
    10.1021/jm070806a
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文献信息

  • Discovery of 1-{2-[(1<i>S</i>)-(3-Dimethylamino-propionyl)amino-2-methylpropyl]-4-methyl-phenyl}-4-[(2<i>R</i>)-methyl-3-(4-chlorophenyl)-propionyl]piperazine as an Orally Active Antagonist of the Melanocortin-4 Receptor for the Potential Treatment of Cachexia
    作者:Chen、Wanlong Jiang、Fabio Tucci、Joe A. Tran、Beth A. Fleck、Sam R. Hoare、Margaret Joppa、Stacy Markison、Jenny Wen、Yang Sai、Michael Johns、Ajay Madan、Takung Chen、Caroline W. Chen、Dragan Marinkovic、Melissa Arellano、John Saunders、Alan C. Foster
    DOI:10.1021/jm070806a
    日期:2007.11.1
    A potent and Selective antagonist of the melanocortin-4 receptor, 1-2-[(IS)-(3-dimethylaminopropionyl)amino-2-methylpropyl}-6-methylphenyl}-4-[(2R)-methyl-3-(4-chlorophenyl)propionyl]pip- erazine (10d), was identified from a series piperazinebenzylamine attached with a N,N-dimethyl-beta-alanine side chain. This compound possessed high water solubility and exhibited good metabolic profiles. In animals, 10d showed moderate to good oral bioavailability and promoted food intake in tumor-bearing mice after oral administration.
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