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α-ethylene-δ-lactone | 90292-27-6

中文名称
——
中文别名
——
英文名称
α-ethylene-δ-lactone
英文别名
Lacton-hexadien-(1,5)-carbonsaeure-(3);3-Ethenyloxan-2-one
α-ethylene-δ-lactone化学式
CAS
90292-27-6
化学式
C7H10O2
mdl
——
分子量
126.155
InChiKey
VRGMVOYHYVNOMI-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):
    1.4
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    (E)-ethylidene-5-pentanolide甲醇 为溶剂, 反应 6.5h, 以70%的产率得到α-ethylene-δ-lactone
    参考文献:
    名称:
    A Convenient Synthesis of α-Vinyl-lactones by Photo-Deconjugation of α,β-Unsaturated γ- or δ-Lactones
    摘要:
    DOI:
    10.1055/s-1983-30609
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文献信息

  • Linear polyester and semi-linear glycidol polymer systems: formulation and synthesis of novel monomers and macromolecular structures
    申请人:Vanderbilt University
    公开号:US10610598B2
    公开(公告)日:2020-04-07
    Disclosed herein are glycidol-based polymers, nanoparticles, and methods related thereto useful for drug delivery. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    本文公开了用于给药的缩水甘油基聚合物、纳米颗粒及其相关方法。本摘要旨在作为在特定技术领域进行搜索的扫描工具,并非对本发明的限制。
  • .alpha.-Spirocyclopentyl- and .alpha.-spirocyclopropyl-.gamma.-butyrolactones: conformationally constrained derivatives of anticonvulsant and convulsant .alpha.,.alpha.-disubstituted .gamma.-butyrolactones
    作者:Eileen M. Peterson、Kun Xu、Katherine D. Holland、Ann C. McKeon、Steven M. Rothman、James A. Ferrendelli、Douglas F. Covey
    DOI:10.1021/jm00028a011
    日期:1994.1
    To further study the putative gamma-butyrolactone site of the GABA(A)/chloride channel complex, constrained derivatives of convulsant and anticonvulsant alpha,alpha-disubstituted gamma-butyrolactones (alpha-spirocyclopropyl- and alpha-spirocyclopentyl-gamma-butyrolactones) were synthesized and evaluated biologically. Most of the spirocyclopropyl agents were anticonvulsants when tested against pentylenetetrazole-induced seizures in mice. These agents effectively displaced (35)[S]-tert-butylbicyclophosphorothionate ((35)[S] -TBPS), a ligand for the picrotoxin binding site of the GABA(A)/chloride channel, from rat neuronal membranes and affected the GABA-mediated current in hippocampal neurons. The monomethyl-substituted spirocyclopropyl agent with a methyl group cis to the carbonyl (15) potentiates GABA-induced current whereas the trans derivative (16) blocks the current. The only anticonvulsant in the spirocyclopentyl series was the unsubstituted spirocyclopentyl compound 2. All the other substituted spirocyclopentyl targets were inactive in vivo at the highest dose tested except for convulsant 9, which has a trans 2,5-dimethyl-substituted cyclopentyl ring. All the spirocyclopentyl derivatives displaced (35)[S]-TBPS from rat neuronal membranes very effectively, and they also all potentiated GABA-induced chloride current except for convulsant 9 which blocked the current. From the data obtained in this investigation, it appears that when the volume occupied above and below the lactone ring is as large as that occupied by spirocyclopentyl agent 9, convulsant activity is observed. Groups with less volume in these areas either are inactive in the behavioral test or have anticonvulsant activity. When bound to the GABA(A)/chloride channel, the larger molecules may stabilize the closed state of the channel whereas the smaller molecules may stabilize the open state.
  • HENIN, F.;MORTEZAEI, R.;PETE, J. -P., SYNTHESIS, BRD, 1983, N 12, 1019-1021
    作者:HENIN, F.、MORTEZAEI, R.、PETE, J. -P.
    DOI:——
    日期:——
  • Linear Polyester and Semi-Linear Glycidol Polymer Systems: Formulation and Synthesis of Novel Monomers and Macromolecular Structures
    申请人:Vanderbilt University
    公开号:US20160206743A1
    公开(公告)日:2016-07-21
    Disclosed herein are glycidol-based polymers, nanoparticles, and methods related thereto useful for drug delivery. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
  • US9161983B2
    申请人:——
    公开号:US9161983B2
    公开(公告)日:2015-10-20
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