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o-NBS-N(Me)-(D)-Trp-NH2 | 514844-44-1

中文名称
——
中文别名
——
英文名称
o-NBS-N(Me)-(D)-Trp-NH2
英文别名
——
o-NBS-N(Me)-(D)-Trp-NH2化学式
CAS
514844-44-1
化学式
C18H18N4O5S
mdl
——
分子量
402.431
InChiKey
RJMPLQGUSDKMIA-MRXNPFEDSA-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):
    1.79
  • 重原子数:
    28.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    139.4
  • 氢给体数:
    2.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    o-NBS-N(Me)-(D)-Trp-NH2potassium carbonate苯硫酚 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 生成 N(Me)-(D)-Trp-NH2
    参考文献:
    名称:
    New Active Series of Growth Hormone Secretagogues
    摘要:
    New growth hormone secretagogue (GHS) analogues were synthesized and evaluated for growth hormone releasing activity. This series derived from EP-51389 is based on a gem-diamino structure. Compounds that exhibited higher in vivo GH-releasing potency than hexarelin in rat (subcutaneous administration) were then tested per os in beagle dogs and for their binding affinity to human pituitary GHS receptors and to hGHS-R 1a. Compound 7 (JMV 1843, H-Aib-(D)-Trp-(D)-gTrp-formyl) showed high potency in these tests and was selected for clinical studies.(1)
    DOI:
    10.1021/jm020985q
  • 作为产物:
    描述:
    D-tryptophan amidepotassium carbonate三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.25h, 生成 o-NBS-N(Me)-(D)-Trp-NH2
    参考文献:
    名称:
    New Active Series of Growth Hormone Secretagogues
    摘要:
    New growth hormone secretagogue (GHS) analogues were synthesized and evaluated for growth hormone releasing activity. This series derived from EP-51389 is based on a gem-diamino structure. Compounds that exhibited higher in vivo GH-releasing potency than hexarelin in rat (subcutaneous administration) were then tested per os in beagle dogs and for their binding affinity to human pituitary GHS receptors and to hGHS-R 1a. Compound 7 (JMV 1843, H-Aib-(D)-Trp-(D)-gTrp-formyl) showed high potency in these tests and was selected for clinical studies.(1)
    DOI:
    10.1021/jm020985q
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