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(R)-2-Benzyloxycarbonylamino-4,4-dimethoxy-2-naphthalen-2-ylmethyl-butyric acid methyl ester | 847020-77-3

中文名称
——
中文别名
——
英文名称
(R)-2-Benzyloxycarbonylamino-4,4-dimethoxy-2-naphthalen-2-ylmethyl-butyric acid methyl ester
英文别名
——
(R)-2-Benzyloxycarbonylamino-4,4-dimethoxy-2-naphthalen-2-ylmethyl-butyric acid methyl ester化学式
CAS
847020-77-3
化学式
C26H29NO6
mdl
——
分子量
451.519
InChiKey
SXFDOEUWFFGYPG-AREMUKBSSA-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):
    4.23
  • 重原子数:
    33.0
  • 可旋转键数:
    10.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    83.09
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Design, Synthesis, and Binding Affinities of Pyrrolinone-Based Somatostatin Mimetics
    摘要:
    Tetrapyrrolinone somatostatin (SRIF) mimetics (cf. 1), based on a heterochiral (D,L-Mixed) pyrrolinone scaffold, were designed, synthesized, and evaluated for biological activity. The iterative synthetic sequence, incorporating the requisite functionalized coded and noncoded amino acid side chains, comprised a longest linear synthetic sequence of 23 steps. Binding affinities at two somatostatin receptor subtypes (hsst 4 and 5) reveal micromolar activity, demonstrating that the D,L-Mixed pyrrolinone scaffold can be employed to generate functional mimetics of peptide beta-turns.
    DOI:
    10.1021/ol0476974
  • 作为产物:
    参考文献:
    名称:
    Design, Synthesis, and Binding Affinities of Pyrrolinone-Based Somatostatin Mimetics
    摘要:
    Tetrapyrrolinone somatostatin (SRIF) mimetics (cf. 1), based on a heterochiral (D,L-Mixed) pyrrolinone scaffold, were designed, synthesized, and evaluated for biological activity. The iterative synthetic sequence, incorporating the requisite functionalized coded and noncoded amino acid side chains, comprised a longest linear synthetic sequence of 23 steps. Binding affinities at two somatostatin receptor subtypes (hsst 4 and 5) reveal micromolar activity, demonstrating that the D,L-Mixed pyrrolinone scaffold can be employed to generate functional mimetics of peptide beta-turns.
    DOI:
    10.1021/ol0476974
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