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8-异戊基-7-甲氧基-2H-色烯-2-酮 | 6619-22-3

中文名称
8-异戊基-7-甲氧基-2H-色烯-2-酮
中文别名
——
英文名称
8-isopentyl-7-methoxy-2H-chromen-2-one
英文别名
8-isopentyl-7-methoxy-coumarin;8-Isopentyl-7-methoxy-cumarin;7-Methoxy-8-(3-methylbutyl)-cumarin;Dihydroosthol;2H-1-Benzopyran-2-one, 7-methoxy-8-(3-methylbutyl)-;7-methoxy-8-(3-methylbutyl)chromen-2-one
8-异戊基-7-甲氧基-2H-色烯-2-酮化学式
CAS
6619-22-3
化学式
C15H18O3
mdl
——
分子量
246.306
InChiKey
JUCKDULTLYEHAA-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

物化性质

  • 保留指数:
    2333.8

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    8-异戊基-7-甲氧基-2H-色烯-2-酮三溴化硼 作用下, 以 二氯甲烷 为溶剂, 以69%的产率得到8-isopentyl-7-hydroxy-2H-chromen-2-one
    参考文献:
    名称:
    Identification and structure-activity relationship studies of osthol, a cytotoxic principle from Cnidium monnieri
    摘要:
    Osthol (1) was isolated from the fruit of Cnidium monnieri as a cytotoxic principle. Its structure-activity relationship study reveals that the 3,4-olefinic bond is essential for its cytotoxic activity, and the prenyl (C-5) unit attached at the 8 position enhances the cytotoxicity. Analogues 7 and 8 that have a longer alkoxy unit at the 7 position showed ten times higher cytotoxicity than 1. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/0960-894x(96)00315-0
  • 作为产物:
    参考文献:
    名称:
    Butenandt; Marten, Justus Liebigs Annalen der Chemie, 1932, vol. 495, p. 187,202
    摘要:
    DOI:
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文献信息

  • Spaeth; Galinovsky, Chemische Berichte, 1937, vol. 70, p. 235,238
    作者:Spaeth、Galinovsky
    DOI:——
    日期:——
  • Synthesis and evaluation of aliphatic-chain hydroxamates capped with osthole derivatives as histone deacetylase inhibitors
    作者:Wei-Jan Huang、Ching-Chow Chen、Shi-Wei Chao、Chia-Chun Yu、Chen-Yui Yang、Jih-Hwa Guh、Yun-Chieh Lin、Chiao-I. Kuo、Ping Yang、Chung-I. Chang
    DOI:10.1016/j.ejmech.2011.06.002
    日期:2011.9
    Our previous studies have demonstrated that osthole, a Chinese herbal compound, could be incorporated into the hydroxycinnamide scaffold of LBH-589, a potent HDAC inhibitor, as an effective hydrophobic cap; the resulting compounds showed significant potency against several HDAC isoforms. Here, we presented a series of osthole derivatives fused with the aliphatic-hydroxamate core of suberoylanilide hydroxamic acid (SAHA), a clinically-approved HDAC inhibitor. Several compounds showed potent activity against nuclear HDACs. Further assays against individual HDAC isoforms revealed that some compounds showed not only SAHA-like activity towards HDAC1, -4 and -6, they inhibited HDAC8 by log difference than SAHA and thus exhibited a broader HDAC inhibition spectrum. Among them, compound 6g showed potent antiproliferative effect on several human cancer cell lines. (C) 2011 Elsevier Masson SAS. All rights reserved.
  • Discovery of novel osthole derivatives as potential anti-breast cancer treatment
    作者:Lisha You、Rui An、Xinhong Wang、Yimin Li
    DOI:10.1016/j.bmcl.2010.10.027
    日期:2010.12
    Osthole, an ingredient of Traditional Chinese Medicine (TCM) from natural product Cnidium monnieri (L.) Cusson, was used as a lead compound for structural modification. A series of osthole derivatives bearing aryl substituents at 3-position of coumarin, has been prepared and evaluated for their growth inhibitory activity against human breast cancer cell lines MCF-7 and MDA-MB-231. Interestingly, some derivatives exhibited good inhibition, among them compound 8e was found to be the most potent compound with IC50 values of 0.24 mu M, 0.31 mu M against MCF-7 and MDA-MB-231, respectively, which was improved more than 100-folds compared with its parent compound osthole. (C) 2010 Elsevier Ltd. All rights reserved.
  • Injustice in forensic psychiatry: the Scott-Moncrieff hypothesis revisited
    作者:Philip Sugarman、Ashmesh Roychowdhury
    DOI:10.1080/09585180050142660
    日期:2000.1
    Scott-Moncrieff (1993) argued that key decision-making in forensic psychiatry may be biased against the individual by false or misleading information presented in reports. We examined this by comparing accounts of incidents and other problems in reports to the mental health review tribunal, with contemporaneous records. In a regional secure unit a significant discrepancy was found, particularly in the reporting of aggressive behaviour. The authors argue that reliance on verbal accounts and inadequate contemporaneous notekeeping are more likely explanations than true bias, but accept Scott-Moncrieff's recommendation of proper investigation of incidents in hospital.
  • Synthesis of 8-Isoamyl-7-methoxycoumarin (Dihydro-osthol)
    作者:H. L. Haller、Fred Acree
    DOI:10.1021/ja01321a051
    日期:1934.6
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