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8-(Chloromethyl)-5-hydroxy-4-propyl-8,9-dihydropyrano[2,3-h]chromene-2,10-dione | 1207064-79-6

中文名称
——
中文别名
——
英文名称
8-(Chloromethyl)-5-hydroxy-4-propyl-8,9-dihydropyrano[2,3-h]chromene-2,10-dione
英文别名
——
8-(Chloromethyl)-5-hydroxy-4-propyl-8,9-dihydropyrano[2,3-h]chromene-2,10-dione化学式
CAS
1207064-79-6
化学式
C16H15ClO5
mdl
——
分子量
322.745
InChiKey
BQLUJKIZMQVOJP-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):
    2.6
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    72.8
  • 氢给体数:
    1
  • 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:
    1,1-二乙氧基-3-甲基-2-丁烯8-(Chloromethyl)-5-hydroxy-4-propyl-8,9-dihydropyrano[2,3-h]chromene-2,10-dione吡啶 作用下, 以 甲苯 为溶剂, 反应 1.5h, 以79%的产率得到10-chloromethyl-11-demethyl-12-oxo-calanolide A
    参考文献:
    名称:
    Highly Suppressing Wild-Type HIV-1 and Y181C Mutant HIV-1 Strains by 10-Chloromethyl-11-demethyl-12-oxo-calanolide A with Druggable Profile
    摘要:
    We herein report a new compound: 10-chloromethyl-11-demethyl-12-oxo-calanolide A (20, EC50 = 7.4 nM, St = 1417), which demonstrates a druggable profile with 32.7% oral bioavailability in rat, tolerated oral single dose toxicity in mice, and especially the feature of highly efficient suppression of the wild-type HIV-1 and Y181C mutant HIV-1 at an EC50 = 7.4 nM and EC50 = 0.46 nM, respectively.
    DOI:
    10.1021/jm901653e
  • 作为产物:
    描述:
    8-(4-chlorobut-2-enoyl)-5,7-dihydroxy-4-propylchromen-2-one 在 sodium acetate 作用下, 以 乙醇 为溶剂, 反应 5.0h, 以75%的产率得到8-(Chloromethyl)-5-hydroxy-4-propyl-8,9-dihydropyrano[2,3-h]chromene-2,10-dione
    参考文献:
    名称:
    Highly Suppressing Wild-Type HIV-1 and Y181C Mutant HIV-1 Strains by 10-Chloromethyl-11-demethyl-12-oxo-calanolide A with Druggable Profile
    摘要:
    We herein report a new compound: 10-chloromethyl-11-demethyl-12-oxo-calanolide A (20, EC50 = 7.4 nM, St = 1417), which demonstrates a druggable profile with 32.7% oral bioavailability in rat, tolerated oral single dose toxicity in mice, and especially the feature of highly efficient suppression of the wild-type HIV-1 and Y181C mutant HIV-1 at an EC50 = 7.4 nM and EC50 = 0.46 nM, respectively.
    DOI:
    10.1021/jm901653e
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文献信息

  • Highly Suppressing Wild-Type HIV-1 and Y181C Mutant HIV-1 Strains by 10-Chloromethyl-11-demethyl-12-oxo-calanolide A with Druggable Profile
    作者:Hai Xue、Xiaofan Lu、Purong Zheng、Li Liu、Chunyan Han、Jinping Hu、Zijie Liu、Tao Ma、Yan Li、Lin Wang、Zhiwei Chen、Gang Liu
    DOI:10.1021/jm901653e
    日期:2010.2.11
    We herein report a new compound: 10-chloromethyl-11-demethyl-12-oxo-calanolide A (20, EC50 = 7.4 nM, St = 1417), which demonstrates a druggable profile with 32.7% oral bioavailability in rat, tolerated oral single dose toxicity in mice, and especially the feature of highly efficient suppression of the wild-type HIV-1 and Y181C mutant HIV-1 at an EC50 = 7.4 nM and EC50 = 0.46 nM, respectively.
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