18812-25-4Relevant academic research and scientific papers
Design, synthesis and biological evaluation of novel compounds with conjugated structure as anti-tumor agents
Su, Hong,Nebbioso, Angela,Carafa, Vincenzo,Chen, Yadong,Yang, Bo,Altucci, Lucia,You, Qidong
, p. 7992 - 8002 (2008/12/23)
A series of hydroxamic acids with conjugated structure was designed and synthesized to explore the possible HDAC subtype selectivity by testing these compounds against recombinant human HDAC1 and HDAC4. The most selective compound resulted 5a, with a SI of 11.9. The enzymatic inhibitory activity of these conjugated compounds was relatively weak; however, some of these compounds showed significant effect in inducing apoptosis. Moreover, the anti-proliferative activity in cancer cells resulted quite promising, especially in the HCT119 cell line.
SYNTHETIC ANALOGUES OF PROSTAGLANDINS F2α AND E2
Kozmik, Vaclav,Palecek, Jaroslav
, p. 138 - 148 (2007/10/02)
The synthesis of new derivatives of prostaglandins F2α and E2 XIIa,b - XVa,b and XXa,b - XXIIIa,b containing the furan or thiophene nucleus in the upper chain has been accomplished starting from -(+/-)-hexahydro-5-hydr
