2-naphthaldehyde-N-(4,7-dichloro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)hydrazone | 1201799-28-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2-naphthaldehyde-N-(4,7-dichloro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)hydrazone
• CAS: 1201799-28-1
• 化学式: C₁₉H₁₁Cl₂N₃O
• 分子量: 368.222
• InChiKey: YBGSVSGWAOOCES-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
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• 重原子数：
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• 可旋转键数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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文献信息

• Khan, Khalid Mohammed; Khan, Momin; Ali, Muhammad, Journal of the Chemical Society of Pakistan, 2013, vol. 35, # 3, p. 987 - 993
  作者：Khan, Khalid Mohammed、Khan, Momin、Ali, Muhammad、Qadir, Muhammad Irfan、Perveen, Shahnaz、Karim, Aneela、Choudhary, Muhammad Iqbal

  DOI：——

  日期：——
• Khan, Momin; Khan, Khalid Mohammed; Rahim, Fazal, Journal of the Chemical Society of Pakistan, 2015, vol. 37, # 3, p. 520 - 526
  作者：Khan, Momin、Khan, Khalid Mohammed、Rahim, Fazal、Samreen、Perveen, Shahnaz、Karim, Aneela、Imtiazuddin、Choudhary, Muhammad Iqbal

  DOI：——

  日期：——
• Synthesis of bis-Schiff bases of isatins and their antiglycation activity
  作者：Khalid Mohammed Khan、Momin Khan、Muhammad Ali、Muhammad Taha、Saima Rasheed、Shahnaz Perveen、M. Iqbal Choudhary

  DOI：10.1016/j.bmc.2009.09.028

  日期：2009.11

  Bis-Schiff bases 1-27 have been synthesized and their in vitro antiglycation potential has been evaluated. Compounds 21 (IC50 = 243.95 +/- 4.59 mu M), 20 (IC50 = 257.61 +/- 5.63 mu M), and 7 (IC50 = 291.14 +/- 2.53 mu M) showed an excellent antiglycation activity better than the standard (rutin, IC50 = 294.46 +/- 1.50 mu M). This study has identified a series of potential molecules as antiglycation agents. A structure-activity relationship has been studied, and all the compounds were characterized by spectroscopic techniques. (C) 2009 Elsevier Ltd. All rights reserved.
• N-Acylpolyamine inhibitors of HDM2 and HDMX binding to p53
  作者：Ryo Hayashi、Deyun Wang、Toshiaki Hara、Jaclyn A. Iera、Stewart R. Durell、Daniel H. Appella

  DOI：10.1016/j.bmc.2009.10.032

  日期：2009.12

  Selective inhibition of protein-protein interactions important for cellular processes could lead to the development of new therapies against disease. In the area of cancer, overexpression of the proteins human double minute 2 (HDM2) and its homolog HDMX has been linked to tumor aggressiveness. Both HDM2 and HDMX bind to p53 and prevent cell cycle arrest or apoptosis in damaged cells. Developing a strategy to simultaneously prevent the binding of both HDM2 and HDMX to p53 is an essential feature of inhibitors to restore p53 activity in a number of different cancers. Inhibition of protein-protein interactions with synthetic molecules is an emerging area of research that requires new inhibitors tailored to mimic the types of interfaces between proteins. Our strategy to create inhibitors of protein-protein interactions is to develop a non-natural scaffold that may be used as a starting point to identify important molecular components necessary for inhibition. In this study, we report an N-acylpolyamine (NAPA) scaffold that supports numerous sidechains in a compact atomic arrangement. NAPAs were constructed by a series of reductive aminations between amino acid derivatives followed by acylation at the resulting secondary amine. An optimized NAPA was able to equally inhibit the association of both HDM2 and HDMX with p53. Our results demonstrate some of the challenges associated with targeting multiple protein-protein interactions involved in overlapping cellular processes. Published by Elsevier Ltd.