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α-(2-isopropenyl)-γ-butyrolactone | 68344-94-5

中文名称
——
中文别名
——
英文名称
α-(2-isopropenyl)-γ-butyrolactone
英文别名
3-isopropenyl-dihydro-furan-2-one;3-(Prop-1-en-2-yl)oxolan-2-one;3-prop-1-en-2-yloxolan-2-one
α-(2-isopropenyl)-γ-butyrolactone化学式
CAS
68344-94-5
化学式
C7H10O2
mdl
——
分子量
126.155
InChiKey
HYFDSKYCHSENQM-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):
    1.6
  • 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

点击查看最新优质反应信息

文献信息

  • .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:——
  • A Convenient Synthesis of α-Vinyl-lactones by Photo-Deconjugation of α,β-Unsaturated γ- or δ-Lactones
    作者:Françoise Hénin、Reza Mortezaei、Jean-Pierre Pete
    DOI:10.1055/s-1983-30609
    日期:——
  • Cyclopropane-Fused <i>N</i>-Heterocycles via Aza-Heck-Triggered C(sp<sup>3</sup>)–H Functionalization Cascades
    作者:Changcheng Jing、Benjamin T. Jones、Ross J. Adams、John F. Bower
    DOI:10.1021/jacs.2c08304
    日期:2022.9.21
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