洋芹酸 | 7731-10-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 洋芹酸
• 英文名称: 4,7-dimethoxybenzo[d][1,3]dioxole-5-carboxylic acid
• 英文别名: apiole acid；apiolic acid；4,7-dimethoxy-benzo[1,3]dioxole-5-carboxylic acid；4,7-Dimethoxy-benzo[1,3]dioxol-5-carbonsaeure；2,5-dimethoxy-3,4-methylenedioxybenzoate；2,5-Dimethoxy-3,4-methylendioxybenzoesaeure；4,7-Dimethoxy-1,3-benzodioxole-5-carboxylic acid
• CAS: 7731-10-4
• 化学式: C₁₀H₁₀O₆
• mdl: MFCD09261480
• 分子量: 226.186
• InChiKey: XEZGWUNLELQKOP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  74.2
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  洋芹酸 在 氯化亚砜 、 sodium hydride 作用下， 以 四氢呋喃 、 mineral oil 为溶剂， 反应 1.5h， 生成 2-(4-methoxyphenyl)-3-oxo-3-(2,5-dimethoxy-3,4-methylenedioxyphenyl)propanenitrile
  参考文献：
  名称：

  cis-Restricted 3-Aminopyrazole Analogues of Combretastatins: Synthesis from Plant Polyalkoxybenzenes and Biological Evaluation in the Cytotoxicity and Phenotypic Sea Urchin Embryo Assays

  摘要：

  We have synthesized a series of novel cis-restricted 4,5-polyalkoxydiaryl-3-aminopyrazole analogues of combretastatins via short synthetic sequences using building blocks isolated from dill and parsley seed extracts. The resulting compounds were tested in vivo in the phenotypic sea urchin embryo assay to reveal their antimitotic and antitubulin effects. The most potent aminopyrazole, 14a, altered embryonic cell division at 10 nM concentration, exhibiting microtubule-destabilizing properties. Compounds 12a and 14a displayed pronounced cytotoxicity in the NCI60 anticancer drug screen, with the ability to inhibit growth of multidrug-resistant cancer cells.

  DOI：

  10.1021/np400310m
• 作为产物：
  描述：

  洋芹脑 在 过氧化脲素 、 臭氧 、 potassium hydroxide 作用下， 以 吡啶 、 甲醇 、 氯仿 为溶剂， 反应 2.17h， 生成 洋芹酸
  参考文献：
  名称：

  Dill and parsley seed extracts in scale up synthesis of aminopolyalkoxybenzenes – beneficial synthons for fused nitrogen polyalkoxyheterocycles

  摘要：

  Ecologically friendly transformation of readily accessible plant allylpolyalkoxybenzenes to hardly available aminotetraalkoxybenzenes has been developed. The efficacy of hydrogenation stage is substantially increased by the application of highly porous ceramic block Pd-catalysts featuring a large surface area, low hydraulic resistance, significant thermal and mechanical stabililty, multiple cycling and easy regeneration.

  DOI：

  10.1016/j.mencom.2016.01.026

文献信息

• 3-(5-)-Amino-o-diarylisoxazoles: Regioselective synthesis and antitubulin activity
  作者：Dmitry V. Tsyganov、Victor N. Khrustalev、Leonid D. Konyushkin、Mikhail M. Raihstat、Sergei I. Firgang、Roman V. Semenov、Alex S. Kiselyov、Marina N. Semenova、Victor V. Semenov

  DOI：10.1016/j.ejmech.2013.12.006

  日期：2014.2

  materials for the synthetic scheme were easily available from plant extracts. The targeted molecules were further tested in the phenotypic sea urchin embryo assay to identify compounds with antimitotic microtubule destabilizing activity. Structure–activity relationship studies suggested that the structural features essential for potent antiproliferative activity include: 1) 5-aminoisoxazole bridge linking

  已经验证了被聚烷氧基芳基药效基团取代的5-氨基-和3-氨基二芳基异恶唑的区域选择性合成。合成方案的起始原料很容易从植物提取物中获得。在表型海胆胚胎试验中进一步测试了目标分子，以鉴定具有抗有丝分裂微管去稳定活性的化合物。结构与活性之间的关系研究表明，有效的抗增殖活性必不可少的结构特征包括：1）5-氨基异恶唑桥联双芳基取代基（环A和B）；2）未取代的5-氨基；3）3,4,5-甲氧基取代的苯和4-甲氧基苯的药效基团分别作为环A和B。
• Synthesis and antiproliferative activity of conformationally restricted 1,2,3-triazole analogues of combretastatins in the sea urchin embryo model and against human cancer cell lines
  作者：Dmitry V. Demchuk、Alexander V. Samet、Natalia B. Chernysheva、Vladimir I. Ushkarov、Galina A. Stashina、Leonid D. Konyushkin、Mikhail M. Raihstat、Sergei I. Firgang、Alex A. Philchenkov、Michael P. Zavelevich、Ludmila M. Kuiava、Vasyl F. Chekhun、Dmitry Yu. Blokhin、Alex S. Kiselyov、Marina N. Semenova、Victor V. Semenov

  DOI：10.1016/j.bmc.2013.12.015

  日期：2014.1

  microtubule destabilizing agents using the sea urchin embryo model. Structure–activity relationship studies identified compounds substituted with 3,4,5-trimethoxyphenyl and 3,4-methylenedioxy-5-methoxyphenyl ring A and 4-methoxyphenyl ring B as potent antiproliferative agents with high cytotoxicity against a panel of human cancer cell lines including multi-drug resistant cells. 4,5-Diaryl-1,2,3-triazoles (C–C

  合成了康普他汀A4的一系列1,5-二芳基-和4,5-二芳基-1,2,3-三唑衍生物，并使用海胆胚胎模型评估其作为抗有丝分裂微管去稳定剂。 结构-活性关系研究确定了被3,4,5-三甲氧基苯基和3,4-亚甲二氧基-5-甲氧基苯基环A和4-甲氧基苯基环B取代的化合物是有效的抗增殖剂，对一组人类癌细胞系具有高细胞毒性，包括多药耐药细胞。发现4,5-二芳基-1,2,3-三唑类化合物（CC几何形状）比各自的1,5-二芳基-1,2,3-三唑类化合物（NC几何形状）活性高得多。化合物10ad'通过胱天蛋白酶2/3/9激活和抗凋亡蛋白XIAP的下调诱导人T白血病Jurkat细胞中的G 2 / M细胞周期停滞和凋亡。有丝分裂灾难已被评估为另一种可能的细胞死亡模式。
• Reprint of: Antiproliferative activity of the Antrodia camphorata secondary metabolite 4,7-dimethoxy-5-methylbenzo[d][1,3]dioxole and analogues
  作者：Sing Yee Yeung、Matthew J. Piggott

  DOI：10.1016/j.fitote.2018.04.001

  日期：2018.4

  secondary metabolite, 4,7-dimethoxy-5-methylbenzo[d][1,3]dioxole, have been reported to possess promising anticancer activity. In this work the natural product and analogues bearing more polar substituents were synthesised and assessed for antiproliferative activity in the NCI-60 screen. Although each compound inhibited the growth of some cell lines at 10μM, none had sufficient activity to warrant

  据报道，传统中药真菌樟脑樟及其次级代谢产物4,7-二甲氧基-5-甲基苯并[d] [1,3]二恶唑均具有良好的抗癌活性。在这项工作中，合成了带有更多极性取代基的天然产物和类似物，并在NCI-60筛选中评估了其抗增殖活性。尽管每种化合物均以10μM抑制某些细胞系的生长，但没有一种具有足够的活性值得进一步研究。
• Synthesis of Antimitotic Polyalkoxyphenyl Derivatives of Combretastatin Using Plant Allylpolyalkoxybenzenes
  作者：Victor V. Semenov、Alex S. Kiselyov、Ilia Y. Titov、Irina K. Sagamanova、Natalie N. Ikizalp、Natalia B. Chernysheva、Dmitry V. Tsyganov、Leonid D. Konyushkin、Sergei I. Firgang、Roman V. Semenov、Irina B. Karmanova、Mikhail M. Raihstat、Marina N. Semenova

  DOI：10.1021/np1004278

  日期：2010.11.29
• 303. Derivatives of 1 : 2 : 3 : 4-tetrahydroxybenzene. Part V. The synthesis of parsley apiole and derivatives
  作者：Wilson Baker、R. I. Savage

  DOI：10.1039/jr9380001602

  日期：——