arildone | 56219-53-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: arildone
• 英文别名: 4-[6-(4-Methoxyphenoxy)hexyl]-3,5-heptanedione；4-[6-(4-Methoxyphenoxy)hexyl]heptane-3,5-dione
• CAS: 56219-53-5
• 化学式: C₂₀H₃₀O₄
• 分子量: 334.456
• InChiKey: QAFRZMLZDAPVGI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  24
• 可旋转键数：
  13
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  arildone 在 肼 作用下， 以 乙醇 为溶剂， 以22%的产率得到3,5-diethyl-4-[6-(4-methoxy-phenoxy)-hexyl]-1H-pyrazole
  参考文献：
  名称：

  一些4-[（（芳氧基）烷基）吡唑的合成和抗疱疹活性。

  摘要：

  DOI：

  10.1021/jm00138a018
• 作为产物：
  描述：

  1-[(6-溴己基)氧基]-4-甲氧基苯 生成 arildone
  参考文献：
  名称：

  Aryloxyalkyl diketones

  摘要：

  烷氧基烷基二酮和酮酯是一种有用的杀虫剂和抗病毒剂，可以从烷氧基烷基卤代物和二酮或酮酯的碱金属烯醇盐，或者从卤代烷基-二酮和酚的碱金属盐制备而成。

  公开号：

  US04031246A1

文献信息

• Antiviral activity of some .beta.-diketones. 1. Aryl alkyl diketones. In vitro activity against both RNA and DNA viruses
  作者：Guy D. Diana、U. Joseph Salvador、Ethel S. Zalay、Robert E. Johnson、Joseph C. Collins、David Johnson、William B. Hinshaw、Roman R. Lorenz、William H. Thielking、Francis Pancic

  DOI：10.1021/jm00216a003

  日期：1977.6

  The discovery that 4-[3-ethyl-6-[(3,4-methylenedioxy)phenyl]-3-hexenyl]-3,5-heptanedione (40) exhibited an in vitro inhibitory effect against equine rhinovirus led to a structure--activity study to establish the criteria for optimum activity. Modification of the bridge included removal of the ethyl group and reduction of the double bond. The heptanedione was replaced with hexanedione and pentanedione with a minimal effect. The effect of replacing the heptanedione with beta-keto esters and monoketones was also investigated. Maintaining the hexamethylene bridge and heptanedione, the methylenedioxy group was replaced with various substitutents. In general, most substituents did not adversely affect activity particularly against equine rhinovirus although there was some variation in activity against herpesvirus. Strongly hydrophilic groups significantly reduced activity. Finally, the effect of varying the length of the alkyl bridge was examined in the 4-hydroxyphenyl series, where peak activity was attained with n = 8.
• Ellipticine derivatives with an affinity to the estrogen receptor. An approach to develop intercalating drugs with a specific effect on the hormone-dependent breast cancer
  作者：Alain Delbarre、Robert Oberlin、Bernard P. Roques、Jean Louis Borgna、Henri Rochefort、Jean Bernard Le Pecq、Alain Jacquemin-Sablon

  DOI：10.1021/jm00383a011

  日期：1985.6

  In order to obtain breast tumor directed agents, we have prepared mixed compounds using estradiol or (E)-clomiphene as specific vectors of the breast tissue and a DNA intercalator from the ellipticine series as the cytotoxic agent. Among the newly synthesized ellipticine derivatives, only the 2-[3-aza-5-(3,17 beta-dihydroxy-1,3,5-estratrien-17 alpha-yl)-4-oxopentamethylene]ellipticinium bromide shows the desired properties, DNA intercalation and affinity for estrogen receptor. Competition experiments with estradiol on the hormone-dependent human MCF-7 breast cancer cell line demonstrate that a transport by the estrogen receptor system is not involved in the antitumor activity of derivative 24.
• DIANA, G. D.;CARABATEAS, P. M.;WILLIAMS, G. L.;PANCIC, F.;STEINBERG, B. A+, J. MED. CHEM., 1981, 24, N 6, 731-735
  作者：DIANA, G. D.、CARABATEAS, P. M.、WILLIAMS, G. L.、PANCIC, F.、STEINBERG, B. A+

  DOI：——

  日期：——
• DIANA, G. D.;MCKINLAY, M. A.;BRISSON, C. J.;ZALAY, E. S.;MIRALLES, J. V.;+, J. MED. CHEM., 1985, 28, N 6, 748-752
  作者：DIANA, G. D.、MCKINLAY, M. A.、BRISSON, C. J.、ZALAY, E. S.、MIRALLES, J. V.、+

  DOI：——

  日期：——
• Synthesis and antiherpetic activity of some 4-[(aryloxy)alkyl]pyrazoles
  作者：Guy D. Diana、Philip M. Carabateas、Gordon L. Williams、Francis Pancic、Bernard A. Steinberg

  DOI：10.1021/jm00138a018

  日期：1981.6