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(E)-4,8-dimethyl-3,7-nonadienylphosphonic acid | 537696-69-8

中文名称
——
中文别名
——
英文名称
(E)-4,8-dimethyl-3,7-nonadienylphosphonic acid
英文别名
(E)-4,8-dimethylnona-3,7-dienylphosphonic acid;[(3E)-4,8-dimethylnona-3,7-dienyl]phosphonic acid
(E)-4,8-dimethyl-3,7-nonadienylphosphonic acid化学式
CAS
537696-69-8
化学式
C11H21O3P
mdl
——
分子量
232.26
InChiKey
WBTJFOQXJPYXSO-DHZHZOJOSA-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

物化性质

  • 沸点:
    386.6±52.0 °C(Predicted)
  • 密度:
    1.074±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    15
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 氢受体数:
    3

上下游信息

  • 上游原料
    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:
    氯磷酸二苯酯(E)-4,8-dimethyl-3,7-nonadienylphosphonic acid三正丁胺 作用下, 以 甲醇四氢呋喃 为溶剂, 反应 2.5h, 生成
    参考文献:
    名称:
    Synthesis of Prenyl Pyrophosphonates as New Potent Phosphoantigens Inducing Selective Activation of Human Vγ9Vδ2 T Lymphocytes
    摘要:
    gamma9delta2T cells represent the most abundant population of human blood gammadeltaT lymphocytes. They produce and promote strong cytotoxic activity against many pathogens that are implicated in several human infectious diseases. Their activation requires their exposure to small phosphorus-containing antigens in the family of prenyl pyrophosphates and their related biosynthetic precursors such as isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP), which are naturally occurring metabolites in mycobacteria and several other microbial pathogens. The broad specificity in the recognition of these molecules by the T-lymphocyte population expressing a Vgamma9Vdelta2 cell receptor might facilitate their manipulation by designing small potent synthetic agonist ligands. In this paper, we describe the synthesis and the biological evaluation of new pyrophosphonate compounds as new isosteric analogues of natural prenyl pyrophosphates. Several prenyl and alkenyl pyrophosphonate with different chain lengths and degrees of insaturation (24-28, 48-50, and 64-66) were tested as well as the alkoxymethylpyrophosphonic analogue of IPP (compound 76) as its closest isostere. Several of them appeared to be better activators of Vgamma9Vdelta2 T cell proliferation than IPP. These results open the perspective of a potential use of isoprenoides pyrophosphonates as specific immunoregulatory molecules.
    DOI:
    10.1021/jm049861z
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis of Prenyl Pyrophosphonates as New Potent Phosphoantigens Inducing Selective Activation of Human Vγ9Vδ2 T Lymphocytes
    摘要:
    gamma9delta2T cells represent the most abundant population of human blood gammadeltaT lymphocytes. They produce and promote strong cytotoxic activity against many pathogens that are implicated in several human infectious diseases. Their activation requires their exposure to small phosphorus-containing antigens in the family of prenyl pyrophosphates and their related biosynthetic precursors such as isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP), which are naturally occurring metabolites in mycobacteria and several other microbial pathogens. The broad specificity in the recognition of these molecules by the T-lymphocyte population expressing a Vgamma9Vdelta2 cell receptor might facilitate their manipulation by designing small potent synthetic agonist ligands. In this paper, we describe the synthesis and the biological evaluation of new pyrophosphonate compounds as new isosteric analogues of natural prenyl pyrophosphates. Several prenyl and alkenyl pyrophosphonate with different chain lengths and degrees of insaturation (24-28, 48-50, and 64-66) were tested as well as the alkoxymethylpyrophosphonic analogue of IPP (compound 76) as its closest isostere. Several of them appeared to be better activators of Vgamma9Vdelta2 T cell proliferation than IPP. These results open the perspective of a potential use of isoprenoides pyrophosphonates as specific immunoregulatory molecules.
    DOI:
    10.1021/jm049861z
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文献信息

  • Phosphonates useful as modulators of t $g(g)9$g(d)2 lymphocyte activity
    申请人:Montero Jean-Louis
    公开号:US20060241087A1
    公开(公告)日:2006-10-26
    The invention concerns novel phosphonate derivatives, preparation method, use thereof as ligands modulating T γ9δ2 lymphocyte activity and pharmaceutical compositions comprising them.
    这项发明涉及新型膦酸酯衍生物,其制备方法,以及将其用作调节T γ9δ2淋巴细胞活性的配体和包含它们的药物组合物。
  • [EN] PHOSPHONATES USEFUL AS MODULATORS OF T DOLLAR G(G)9 DOLLAR G(D)2 LYMPHOCYTE ACTIVITY<br/>[FR] PHOSPHONATES UTILES COMME MODULATEURS DE L'ACTIVITE DES LYMPHOCYTES t-GAMMA-9-DELTA-2
    申请人:MAYOLY SPINDLER LAB
    公开号:WO2003050128A1
    公开(公告)日:2003-06-19
    L'invention se rapporte à de nouveaux dérivés phosphonate, à leur procédé de préparation, à leur utilisation comme ligands modulateurs des lymphocytes T Ϝ9δ2 et aux compositions pharmaceutiques les comprenant.
    该发明涉及新的膦酸酯衍生物,其制备方法,其作为调节T细胞Ϝ9δ2的配体的用途以及包含它们的制药组合物。
  • Phosphonates useful as modulators of T-gamma-9-delta-2 activity
    申请人:Montero Jean-Louis
    公开号:US20100204184A1
    公开(公告)日:2010-08-12
    The invention concerns novel phosphonate derivatives, preparation method, use thereof as ligands modulating T γ9δ2 lymphocyte activity and pharmaceutical compositions comprising them.
    这项发明涉及新型膦酸盐衍生物、其制备方法,以及将其用作调节T γ9δ2淋巴细胞活性的配体和包含它们的制药组合物。
  • PHOSPHONATES UTILES COMME MODULATEURS DE L'ACTIVITE DES LYMPHOCYTES T-GAMMA-9-DELTA-2
    申请人:Laboratoire Mayoly Spindler
    公开号:EP1453840A1
    公开(公告)日:2004-09-08
  • US8017596B2
    申请人:——
    公开号:US8017596B2
    公开(公告)日:2011-09-13
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