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11,12-dimethoxy-8,9-dihydro-7H-5-oxa-benzo[6,7]cyclohepta[1,2-a]naphthalen-6-one | 1609188-61-5

中文名称
——
中文别名
——
英文名称
11,12-dimethoxy-8,9-dihydro-7H-5-oxa-benzo[6,7]cyclohepta[1,2-a]naphthalen-6-one
英文别名
4,5-Dimethoxy-13-oxatetracyclo[9.8.0.02,7.014,19]nonadeca-1(11),2,4,6,14,16,18-heptaen-12-one;4,5-dimethoxy-13-oxatetracyclo[9.8.0.02,7.014,19]nonadeca-1(11),2,4,6,14,16,18-heptaen-12-one
11,12-dimethoxy-8,9-dihydro-7H-5-oxa-benzo[6,7]cyclohepta[1,2-a]naphthalen-6-one化学式
CAS
1609188-61-5
化学式
C20H18O4
mdl
——
分子量
322.361
InChiKey
VIDURUICZGSUEJ-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):
    3.9
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    5-苯基戊酸 在 aluminum (III) chloride 、 sodium chlorite氯化亚砜四丁基溴化铵双氧水 、 palladium diacetate 、 potassium carbonate三氯氧磷 作用下, 以 aq. phosphate buffer 、 二氯甲烷乙腈 为溶剂, 反应 12.5h, 生成 11,12-dimethoxy-8,9-dihydro-7H-5-oxa-benzo[6,7]cyclohepta[1,2-a]naphthalen-6-one
    参考文献:
    名称:
    新型苯并亚砜香豆素基团的合成及其作为潜在抗癌药的评价
    摘要:
    合成了一系列新颖的带有苯并亚砜的香豆素部分5a – c,并通过分析和光谱(FT-IR,1 H NMR,13 C NMR,HRMS)研究了它们的结构。评价了新合成的化合物对四种人类癌细胞系A549(人类肺泡腺癌细胞系),HeLa(人类宫颈癌细胞系),MDA-MB-231(人类乳腺腺癌细胞系),MCF-7的细胞毒性。 (人类乳腺腺癌细胞系)和正常细胞系HEK293(人类胚胎肾细胞系)。化合物5a对IC 50表现出有希望的细胞毒性对所有癌细胞系(如A549,HeLa,MCF-7和MDA-MB-231)的Mp值范围为3.35至16.79μM,而化合物5c对HeLa和MDA-MB-231的细胞毒性显着,IC 50值为6.72和4.87 , 分别。
    DOI:
    10.1016/j.ejmech.2014.04.015
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文献信息

  • Synthesis of novel building blocks of benzosuberone bearing coumarin moieties and their evaluation as potential anticancer agents
    作者:Bandi Yadagiri、Uma Devi Holagunda、Rajashaker Bantu、Lingaiah Nagarapu、C. Ganesh Kumar、Sujitha Pombala、B. Sridhar
    DOI:10.1016/j.ejmech.2014.04.015
    日期:2014.5
    A series of novel benzosuberone bearing coumarin moieties 5a–c have been synthesized and their structures were determined by analytical and spectral (FT-IR, 1H NMR, 13C NMR, HRMS) studies. The newly synthesized compounds were evaluated for their cytotoxicity against four human cancer cell lines, A549 (Human alveolar adenocarcinoma cell line), HeLa (Human cervical cancer cell line), MDA-MB-231 (Human
    合成了一系列新颖的带有苯并亚砜的香豆素部分5a – c,并通过分析和光谱(FT-IR,1 H NMR,13 C NMR,HRMS)研究了它们的结构。评价了新合成的化合物对四种人类癌细胞系A549(人类肺泡腺癌细胞系),HeLa(人类宫颈癌细胞系),MDA-MB-231(人类乳腺腺癌细胞系),MCF-7的细胞毒性。 (人类乳腺腺癌细胞系)和正常细胞系HEK293(人类胚胎肾细胞系)。化合物5a对IC 50表现出有希望的细胞毒性对所有癌细胞系(如A549,HeLa,MCF-7和MDA-MB-231)的Mp值范围为3.35至16.79μM,而化合物5c对HeLa和MDA-MB-231的细胞毒性显着,IC 50值为6.72和4.87 , 分别。
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同类化合物

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