andrographolide-14-laurate | 1201658-84-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: andrographolide-14-laurate
• 英文别名: 14-lauroyl andrographolide；[(3S,4E)-4-[2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-5-oxooxolan-3-yl] dodecanoate
• CAS: 1201658-84-5
• 化学式: C₃₂H₅₂O₆
• 分子量: 532.761
• InChiKey: DBCAGMDIEVUVOA-GBCAECJPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.9
• 重原子数：
  38
• 可旋转键数：
  15
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.81
• 拓扑面积：
  93.1
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  (3S,4E)-4-[2-[(4aR,6aS,7R,10aS,10bR)-Decahydro-3,3,6a,10b-tetramethyl-8-methylene-1H-naphtho[2,1-d][1,3]dioxin-7-yl]ethylidene]tetrahydro-5-oxo-3-furanyl dodecanoate 在 水 、 溶剂黄146 作用下， 反应 0.5h， 以38.7%的产率得到andrographolide-14-laurate
  参考文献：
  名称：

  Design, synthesis and antibacterial activity of novel andrographolide derivatives

  摘要：

  A series of andrographolide derivatives were synthesized through a facile condensation reaction with different carboxylic acids. The new compounds were characterized and screened for their antibacterial activities. A number of the new compounds significantly reduced bacterial quorum sensing virulence factors production in Pseudomonas aeruginosa, essential for pathogenesis. Compound 11b showed the best activity among all the new compounds. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.04.094

文献信息

• Regioselective and efficient enzymatic synthesis of antimicrobial andrographolide derivatives
  作者：Harshal S. Patil、Dipesh D. Jadhav、Ajay Paul、Fayaj A. Mulani、Shrikant J. Karegaonkar、Hirekodathakallu V. Thulasiram

  DOI：10.1016/j.bmcl.2018.01.007

  日期：2018.4

  Labdane diterpene andrographolide (1) is a major constituent of Andrographis paniculata and known to exhibit wide spectrum of biological activities. In this study, regioselective monoesters of (1) have been synthesized by using Amano lipase AK (Pseudomonas fluorescens) as a biocatalyst. Amano lipase AK was able to execute highly efficient esterification of hydroxyl group attached to C-14 carbon of

  拉丹烷二萜穿心莲内酯（1）是穿心莲的主要成分，已知具有广泛的生物活性。在这项研究中，通过使用Amano脂肪酶AK（荧光假单胞菌）作为生物催化剂合成了（1）的区域选择性单酯。在酰基供体的存在下，Amano脂肪酶AK能够对与（1）的C-14碳相连的羟基进行高效酯化。在各种合成的衍生物中，包括两种新化合物，如穿心莲内酯-14-丙酸酯（3）和穿心莲内酯-14-己酸酯（5）显示出对金黄色葡萄球菌的抗菌活性。最低抑菌浓度（MIC）较低，分别为4 µg / mL和16 µg / mL。此外，如FITC摄取和SEM成像研究所示，它们在各自的MIC处显示出较低的溶血活性，并且细菌细胞膜的通透性增加。
• Enzymatic synthesis and antibacterial activity of andrographolide derivatives
  作者：Zhi-Gang Chen、Quan Zhu、Min-Hua Zong、Zhen-Xin Gu、Yong-Bin Han

  DOI：10.1016/j.procbio.2011.05.011

  日期：2011.8

  A series of andrographolide derivatives have been synthesized through enzymatic acylation reactions. Immobilized Candida antarctica lipase B (Novozym 435) was found to be a useful biocatalyst for the 35-gram scale syntheses of these acylated derivatives, and the biocatalyst displayed excellent regioselectivity and high operational stability during the transformation. The 14-substituted andrographolide derivative was the sole detectable product from each acylation reaction. The acylated andrographolides showed antibacterial activity against representative Gram-positive and Gram-negative bacteria [with minimal inhibitory concentrations (MICs) as low as 4 mu g/mL], whereas andrographolide exhibited no such activity. Chain length of acyl moiety on the lactone-ring at the C-14 position plays an important role in determining the potency of the antibacterial activity. These results indicate an enzymatic modification was not only facile and green, but an effective method for the preparation of an andrographolide monoester. (C) 2011 Elsevier Ltd. All rights reserved.
• Design, synthesis and antibacterial activity of novel andrographolide derivatives
  作者：Zhongli Wang、Pei Yu、Gaoxiao Zhang、Lipeng Xu、Dingyuan Wang、Liang Wang、Xiangping Zeng、Yuqiang Wang

  DOI：10.1016/j.bmc.2010.04.094

  日期：2010.6.15

  A series of andrographolide derivatives were synthesized through a facile condensation reaction with different carboxylic acids. The new compounds were characterized and screened for their antibacterial activities. A number of the new compounds significantly reduced bacterial quorum sensing virulence factors production in Pseudomonas aeruginosa, essential for pathogenesis. Compound 11b showed the best activity among all the new compounds. (C) 2010 Elsevier Ltd. All rights reserved.