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18-methoxy-16(13->14)abeo-18a-homo-ent-halima-1(10),14,18a(18)Z-triene | 946052-01-3

中文名称
——
中文别名
——
英文名称
18-methoxy-16(13->14)abeo-18a-homo-ent-halima-1(10),14,18a(18)Z-triene
英文别名
——
18-methoxy-16(13->14)abeo-18a-homo-ent-halima-1(10),14,18a(18)Z-triene化学式
CAS
946052-01-3
化学式
C22H36O
mdl
——
分子量
316.527
InChiKey
AMMUCOOSUFFHNZ-NGHPPWEISA-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

反应信息

  • 作为反应物:
    描述:
    18-methoxy-16(13->14)abeo-18a-homo-ent-halima-1(10),14,18a(18)Z-triene对甲苯磺酸 作用下, 以 丙酮 为溶剂, 反应 3.0h, 以91%的产率得到16(13->14)abeo-18a-homo-ent-halima-1(10),14-dien-18-al
    参考文献:
    名称:
    Synthesis of novel antitumoural analogues of dysidiolide from ent-halimic acid
    摘要:
    Several sesterterpenolides analogues of dysidiolide have been synthesized and their in vitro antitumoural activity against human HeLa, A549, HT-29 and HL-60 carcinoma cells is presented. The proliferation inhibition data showed a significant antitumour activity of the compounds 1b, 2a, 2b, 3a, 3b, 4a, 4b, 5, inhibiting proliferation of distinct cancer cell types with an IC50 in the low micromolar range. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.06.007
  • 作为产物:
    描述:
    16(13->14)abeo-ent-halima-1(10),14-dien-18-al 、 甲氧基甲基三苯基氯化膦sodium hexamethyldisilazane 作用下, 以 四氢呋喃 为溶剂, 反应 1.5h, 以91%的产率得到18-methoxy-16(13->14)abeo-18a-homo-ent-halima-1(10),14,18a(18)Z-triene
    参考文献:
    名称:
    Synthesis of novel antitumoural analogues of dysidiolide from ent-halimic acid
    摘要:
    Several sesterterpenolides analogues of dysidiolide have been synthesized and their in vitro antitumoural activity against human HeLa, A549, HT-29 and HL-60 carcinoma cells is presented. The proliferation inhibition data showed a significant antitumour activity of the compounds 1b, 2a, 2b, 3a, 3b, 4a, 4b, 5, inhibiting proliferation of distinct cancer cell types with an IC50 in the low micromolar range. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.06.007
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