EMAC2105 | 949912-63-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: EMAC2105
• CAS: 949912-63-4
• 化学式: C₁₆H₁₈BrN₃S
• 分子量: 364.309
• InChiKey: DOBCKAARTRJCGF-UHFFFAOYSA-N

反应信息

• 作为产物：
  描述：

  2-methylcyclohexanone thiosemicarbazone 在 1-(4-bromophenyl)-2-haloethan-1-one 作用下， 以 水 为溶剂， 反应 48.0h， 以77%的产率得到EMAC2105
  参考文献：
  名称：

  Exploring the thiazole scaffold for the identification of new agents for the treatment of fluconazole resistant Candida

  摘要：

  Cyclohexyliden- and 2-methylcyclohexyliden-hydrazo-4-arylthiazoles were synthesized and tested as antifungal agents. All compounds exhibited minimal inhibitory concentration (MIC) values comparable with those of fluconazole (FLC). Moreover, some compounds showed fungicidal activity at low concentration. Worth noting five out of nine compounds were active towards Candida albicans 25 FLC resistant isolated from clinical specimens. The cellular toxicity was evaluated and none of the compounds is toxic at the MIC. On the basis of our data we can conclude that these derivatives are promising agents for the treatment of resistant C. albicans.

  DOI：

  10.3109/14756366.2015.1113171

文献信息

• Synthesis and in vitro activity of 2-thiazolylhydrazone derivatives compared with the activity of clotrimazole against clinical isolates of Candida spp.
  作者：Franco Chimenti、Bruna Bizzarri、Elias Maccioni、Daniela Secci、Adriana Bolasco、Rossella Fioravanti、Paola Chimenti、Arianna Granese、Simone Carradori、Daniela Rivanera、Daniela Lilli、Alessandra Zicari、Simona Distinto

  DOI：10.1016/j.bmcl.2007.05.078

  日期：2007.8

  In this paper, we report on the synthesis of a novel series of 2-thiazolylhydrazone derivatives and the influence of the substituents on the thiazole ring on antifungal activity. All synthesized compounds were screened for their in vitro activities against 22 clinical isolates of Candida spp., representing six different species, compared to clotrimazole as a reference compound. Some of the tested compounds were found to possess significant antifungal activity when compared to clotrimazole, in particular compound 14 which exhibited higher potency against most of the Candida spp. considered. The compounds that were most active as anti-Candida agents were also Submitted to cytotoxic screening by the Trypan Blue dye exclusion assay and in general they were shown to induce low cytotoxic effects. (c) 2007 Elsevier Ltd. All rights reserved.