Kulandasamy, R., Adhikari, A.V. and Stables, J.P. (2009) A New Class of Anticonvulsants Possessing 6 Hz Activity: 3,4-Dialkyloxy Thiophenebishydrazones. European Journal of Medicinal Chemistry, 44, 4376-4384.
http://dx.doi.org/10.1016/j.ejmech.2009.05.026

has been cited by the following article:

• TITLE: The Synthesis and Cytotoxicity of Novel Thiophene Derivatives Derived from 2-(4-Oxo-4,4-Dihydrothiazol-2-yl) Acetonitrile

  AUTHORS: Eman M. Samir, Amr S. Abouzied, Faten I. Hamed

  KEYWORDS: Thiazole, Cyclopentanone, Thiophene, Hydrazide, Cytotoxicity

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.6 No.2, May 19, 2016

  ABSTRACT: The reaction of the 2-(4-oxo-4,4-dihydrothiazol-2-yl)acetonitrile 1 with cyaclopentanone (2) afforded the condensed product 3. The latter underwent a series of heterocyclizations through its reaction with different reagents. Moreover, compound 1 underwent the Gewald’s thiophene to afford compounds 15 and 17. The reaction of either hydrazine hydrate or phenylhydrazine with compound 17 gave the hydrazide derivatives 19a and 19b, respectively. The cytotoxicity of the newly synthesized products was measured towards the three cancer cell lines MCF-7, NCI-H460 and SF-268. The study showed that compounds 3, 5, 9c, 11, 13a, 13c, 17 and 19b were the most active compounds towards the three cancer cell lines.