916151-03-6Relevant academic research and scientific papers
Design and synthesis of novel dehydroepiandrosterone analogues as potent antiproliferative agents
Huang, Xing,Shen, Qing-Kun,Zhang, Hong-Jian,Li, Jia-Li,Tian, Yu-Shun,Quan, Zhe-Shan
, (2018/09/12)
The aim of the present study was to determine the cytotoxic effects of a series of novel dehydroepiandrosterone derivatives containing triazole at the C16 position on human cancer cells. The cancer cells used in the present study were A549, Hel
AZOLE COMPOUNDS USED AS TUBERCULOSTATIC AND LEISHMANICIDE AGENTS
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Page/Page column 34-35, (2008/06/13)
This invention refers to new 1, 2, 3-triazole and imidazole compounds included in the families of compounds represented by general formula VIII (see formula VIII) where: X is an atom of "C" or "N"; where X is "N" the radicals do triazole ring are represen
Synthesis, tuberculosis inhibitory activity, and SAR study of N-substituted-phenyl-1,2,3-triazole derivatives
Costa, Marilia S.,Boechat, Nubia,Rangel, Erica A.,da Silva, Fernando de C.,de Souza, Alessandra M.T.,Rodrigues, Carlos R.,Castro, Helena C.,Junior, Ivan N.,Lourenco, Maria Cristina S.,Wardell, Solange M.S.V.,Ferreira, Vitor F.
, p. 8644 - 8653 (2008/02/08)
The aim of this work was to describe the synthesis, the in vitro anti-Mycobacterium tuberculosis profile, and the structure-activity relationship (SAR) study of new N-substituted-phenyl-1,2,3-triazole-4-carbaldehydes (3a-l). The reactions of aromatic amin
