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6-[1,3]dioxolan-2-yl-4-oxo-hexanoic acid methyl ester | 816432-05-0

中文名称
——
中文别名
——
英文名称
6-[1,3]dioxolan-2-yl-4-oxo-hexanoic acid methyl ester
英文别名
methyl 6-(2,5-dioxolanyl)-4-oxohexanoate;Methyl 6-(1,3-dioxolan-2-yl)-4-oxohexanoate
6-[1,3]dioxolan-2-yl-4-oxo-hexanoic acid methyl ester化学式
CAS
816432-05-0
化学式
C10H16O5
mdl
——
分子量
216.234
InChiKey
YOTXYSDQCJTFPO-UHFFFAOYSA-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):
    -0.4
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    61.8
  • 氢给体数:
    0
  • 氢受体数:
    5

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:
    6-[1,3]dioxolan-2-yl-4-oxo-hexanoic acid methyl ester溶剂黄146 作用下, 以 为溶剂, 反应 5.0h, 以87%的产率得到methyl 4,7-dioxoheptanoate
    参考文献:
    名称:
    Synthesis and structural characterization of carboxyethylpyrrole-modified proteins: mediators of age-related macular degeneration
    摘要:
    Protein modifications in which the e-amino group of lysyl residues is incorporated into a 2-(omega-carboxy-ethyl)pyrrole (CEP) are mediators of age-related macular degeneration (AMD). They promote both angiogenesis into the retina ('wet AMD') and geographic retinal atrophy ('dry AMD'). Blood levels of CEPs are biomarkers for clinical prognosis of the disease. To enable mechanistic studies of their role in promoting AMD, for example, through the activation of B- and T-cells, interaction with receptors, or binding with complement proteins, we developed an efficient synthesis of CEP derivatives, that is especially effective for proteins. The structures of tryptic peptides derived from CEP-modified proteins were also determined. A key finding is that 4,7-dioxoheptanoic acid 9-fluorenylmethyl ester reacts with primary amines to provide 9-fluorenylmethyl esters of CEP-modified proteins that can be deprotected in situ with 1,8-diazabicyclo[5.4.0]undec-7-ene without causing protein denaturation. The introduction of multiple CEP-modifications with a wide variety of CEP: protein ratios is readily achieved using this strategy. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.09.009
  • 作为产物:
    描述:
    2-(2-溴乙基)-1,3-二恶烷丁二酸单甲酯酰氯magnesium 作用下, 以 四氢呋喃 为溶剂, 以60%的产率得到6-[1,3]dioxolan-2-yl-4-oxo-hexanoic acid methyl ester
    参考文献:
    名称:
    Synthesis and structural characterization of carboxyethylpyrrole-modified proteins: mediators of age-related macular degeneration
    摘要:
    Protein modifications in which the e-amino group of lysyl residues is incorporated into a 2-(omega-carboxy-ethyl)pyrrole (CEP) are mediators of age-related macular degeneration (AMD). They promote both angiogenesis into the retina ('wet AMD') and geographic retinal atrophy ('dry AMD'). Blood levels of CEPs are biomarkers for clinical prognosis of the disease. To enable mechanistic studies of their role in promoting AMD, for example, through the activation of B- and T-cells, interaction with receptors, or binding with complement proteins, we developed an efficient synthesis of CEP derivatives, that is especially effective for proteins. The structures of tryptic peptides derived from CEP-modified proteins were also determined. A key finding is that 4,7-dioxoheptanoic acid 9-fluorenylmethyl ester reacts with primary amines to provide 9-fluorenylmethyl esters of CEP-modified proteins that can be deprotected in situ with 1,8-diazabicyclo[5.4.0]undec-7-ene without causing protein denaturation. The introduction of multiple CEP-modifications with a wide variety of CEP: protein ratios is readily achieved using this strategy. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.09.009
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文献信息

  • Diagnostic methods for age related macular degeneration
    申请人:——
    公开号:US20040265924A1
    公开(公告)日:2004-12-30
    Diagnostic methods for identifying a test subject who has or is at risk of developing age-related macular degeneration (AMD) or an analogous disease associated with oxidation of DHA-containing lipids are provided. In one aspect, the methods comprise: assaying for the presence of elevated levels of 2-(&ohgr;-carboxyethyl) pyrrole (CEP) adducts in a bodily fluid which has been obtained from the test subject. In a preferred embodiment, such methods comprise providing an antibody that is immunospecific for CEP, contacting a bodily fluid from the subject with the anti-CEP antibody, and assaying for the formation of a complex between the antibody and an antigen in the sample. In another aspect, the methods comprise assaying for the presence of elevated levels of an antibody that binds to or is immunospecific for a CEP adduct in the bodily fluid of the test subject. The present invention also relates to CEP protein and peptide adducts, an antibody reactive with a CEP adduct and a diagnostic kit comprising such antibody.
  • DIAGNOSTIC METHODS FOR AGE RELATED MACULAR DEGENERATION
    申请人:Hollyfield Joe G.
    公开号:US20080160505A1
    公开(公告)日:2008-07-03
    Diagnostic methods for identifying a test subject who has or is at risk of developing age-related macular degeneration (AMD) or an analogous disease associated with oxidation of DHA-containing lipids are provided. In one aspect, the methods comprise: assaying for the presence of elevated levels of 2-(ω-carboxyethyl) pyrrole (CEP) adducts in a bodily fluid which has been obtained from the test subject. In a preferred embodiment, such methods comprise providing an antibody that is immunospecific for CEP, contacting a bodily fluid from the subject with the anti-CEP antibody, and assaying for the formation of a complex between the antibody and an antigen in the sample. In another aspect, the methods comprise assaying for the presence of elevated levels of an antibody that binds to or is immunospecific for a CEP adduct in the bodily fluid of the test subject. The present invention also relates to CEP protein and peptide adducts, an antibody reactive with a CEP adduct and a diagnostic kit comprising such antibody.
  • US7172874B2
    申请人:——
    公开号:US7172874B2
    公开(公告)日:2007-02-06
  • US7341839B2
    申请人:——
    公开号:US7341839B2
    公开(公告)日:2008-03-11
  • US7560257B2
    申请人:——
    公开号:US7560257B2
    公开(公告)日:2009-07-14
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