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3-{N-[(adenosin-5'-yloxy)(hydroxy)phosphoryl]-S-methylsulfonimidoyl}propanoic acid | 1401207-22-4

中文名称
——
中文别名
——
英文名称
3-{N-[(adenosin-5'-yloxy)(hydroxy)phosphoryl]-S-methylsulfonimidoyl}propanoic acid
英文别名
3-[N-[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]-S-methylsulfonimidoyl]propanoic acid
3-{N-[(adenosin-5'-yloxy)(hydroxy)phosphoryl]-S-methylsulfonimidoyl}propanoic acid化学式
CAS
1401207-22-4
化学式
C14H21N6O9PS
mdl
——
分子量
480.395
InChiKey
WUQSAXAFWFRXAL-DWNRMBSWSA-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):
    -3.1
  • 重原子数:
    31
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    241
  • 氢给体数:
    5
  • 氢受体数:
    14

反应信息

  • 作为产物:
    描述:
    3-{N-[(2',3'-O-isopropylideneadenosin-5'-yloxy)phosphoryl]-S-methylsulfonimidoyl}propanoic acid bis-morpholine salt 在 三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 以1.23 g的产率得到3-{N-[(adenosin-5'-yloxy)(hydroxy)phosphoryl]-S-methylsulfonimidoyl}propanoic acid
    参考文献:
    名称:
    A sulfoximine-based inhibitor of human asparagine synthetase kills l-asparaginase-resistant leukemia cells
    摘要:
    An adenylated sulfoximine transition-state analogue 1, which inhibits human asparagine synthetase (hASNS) with nanomolar potency, has been reported to suppress the proliferation of an L-asparagine amidohydrolase (ASNase)-resistant MOLT-4 leukemia cell line (MOLT-4R) when L-asparagine is depleted in the medium. We now report the synthesis and biological activity of two new sulfoximine analogues of 1 that have been studied as part of systematic efforts to identify compounds with improved cell permeability and/or metabolic stability. One of these new analogues, an amino sulfoximine 5 having no net charge at cellular pH, is a better hASNS inhibitor (K*(I) = 8 nM) than 1 and suppresses proliferation of MOLT-4R cells at 10-fold lower concentration (IC50 = 0.1 mM). More importantly, and in contrast to the lead compound 1, the presence of sulfoximine 5 at concentrations above 0.25 mM causes the death of MOLT-4R cells even when ASNase is absent in the culture medium. The amino sulfoximine 5 exhibits different dose-response behavior when incubated with an ASNase-sensitive MOLT-4 cell line (MOLT-4S), supporting the hypothesis that sulfoximine 5 exerts its effect by inhibiting hASNS in the cell. Our work provides further evidence for the idea that hASNS represents a chemotherapeutic target for the treatment of leukemia, and perhaps other cancers, including those of the prostate. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2012.07.047
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