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((S)-4-(11-aminoundecanamido)cyclopent-1-en-1-yl)(butyl)phosphinic acid | 1425330-58-0

中文名称
——
中文别名
——
英文名称
((S)-4-(11-aminoundecanamido)cyclopent-1-en-1-yl)(butyl)phosphinic acid
英文别名
——
((S)-4-(11-aminoundecanamido)cyclopent-1-en-1-yl)(butyl)phosphinic acid化学式
CAS
1425330-58-0
化学式
C20H39N2O3P
mdl
——
分子量
386.515
InChiKey
QTVRCQOGQHEFFH-SFHVURJKSA-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):
    4.69
  • 重原子数:
    26.0
  • 可旋转键数:
    15.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.85
  • 拓扑面积:
    92.42
  • 氢给体数:
    3.0
  • 氢受体数:
    3.0

上下游信息

  • 下游产品
    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:
    ((S)-4-(11-aminoundecanamido)cyclopent-1-en-1-yl)(butyl)phosphinic acid2-(甲基氨基)-苯甲酸 2,5-二氧代-1-吡咯烷基酯碳酸氢钠 作用下, 以 四氢呋喃乙二醇二甲醚 为溶剂, 反应 16.0h, 以81%的产率得到((S)-4-(11-(2-(methylamino)benzamido)undecanamido)cyclopent-1-en-1-yl)(butyl)phosphinic acid
    参考文献:
    名称:
    Design, Synthesis, and Pharmacological Evaluation of Fluorescent and Biotinylated Antagonists of ρ1 GABAC Receptors
    摘要:
    The rho(1) GABA(C) receptor is a ligand-gated chloride ion channel that shows promise as a therapeutic target for myopia, sleep disorders, memory and learning facilitation, and anxiety-related disorders. As such, there is a need for molecular probes to understand the role GABA(C) receptors play in physiological and pathological processes. To date, no labeled (either radioactive or fluorescent) GABA(C) selective ligand has been developed that can act as a marker for GABA(C) receptor visualization and localization studies. Herein, we report a series of fluorescent ligands containing different-sized linkers and fluorophores based around (S)-4-ACPBPA [(4-aminocyclopenten-1-yl)-butylphosphinic acid], a selective GABA(C) antagonist. One of these conjugates, (S)-4-ACPBPA-C5-BODIPY (13), displayed moderate potency (IC50 = 58.61 mu M) and selectivity (>100 times) for rho(1) over alpha(1)beta(2)gamma(2L) GABA(A) receptors. These conjugates are novel lead agents for the development of more potent and selective fluorescent probes for studying the localization and function of GABA(C) receptors in living cells.
    DOI:
    10.1021/ml300476v
  • 作为产物:
    参考文献:
    名称:
    Design, Synthesis, and Pharmacological Evaluation of Fluorescent and Biotinylated Antagonists of ρ1 GABAC Receptors
    摘要:
    The rho(1) GABA(C) receptor is a ligand-gated chloride ion channel that shows promise as a therapeutic target for myopia, sleep disorders, memory and learning facilitation, and anxiety-related disorders. As such, there is a need for molecular probes to understand the role GABA(C) receptors play in physiological and pathological processes. To date, no labeled (either radioactive or fluorescent) GABA(C) selective ligand has been developed that can act as a marker for GABA(C) receptor visualization and localization studies. Herein, we report a series of fluorescent ligands containing different-sized linkers and fluorophores based around (S)-4-ACPBPA [(4-aminocyclopenten-1-yl)-butylphosphinic acid], a selective GABA(C) antagonist. One of these conjugates, (S)-4-ACPBPA-C5-BODIPY (13), displayed moderate potency (IC50 = 58.61 mu M) and selectivity (>100 times) for rho(1) over alpha(1)beta(2)gamma(2L) GABA(A) receptors. These conjugates are novel lead agents for the development of more potent and selective fluorescent probes for studying the localization and function of GABA(C) receptors in living cells.
    DOI:
    10.1021/ml300476v
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