Synthesis and antiproliferative activity of substituted benzopyranoisoindoles: A new class of cytotoxic compounds
摘要:
A series of novel aminosubstituted benzopyranoisoindoles possessing structural analogy to an active nitracrine metabolite are reported, The compounds exhibited interesting cytotoxic activity against a panel of cell lines, which was maximized by the presence of both 1-dialkylaminoethyl and 3-nitro substituents. (c) 2006 Elsevier Ltd. All rights reserved.
Synthesis and antiproliferative activity of substituted benzopyranoisoindoles: A new class of cytotoxic compounds
作者:Christiana Hadjipavlou、Ioannis K. Kostakis、Nicole Pouli、Panagiotis Marakos、Harris Pratsinis、Dimitris Kletsas
DOI:10.1016/j.bmcl.2006.06.074
日期:2006.9
A series of novel aminosubstituted benzopyranoisoindoles possessing structural analogy to an active nitracrine metabolite are reported, The compounds exhibited interesting cytotoxic activity against a panel of cell lines, which was maximized by the presence of both 1-dialkylaminoethyl and 3-nitro substituents. (c) 2006 Elsevier Ltd. All rights reserved.
Synthesis, spectroscopic and computational evaluation of a xanthene-based fluorogenic derivatization reagent for the determination of primary amines
作者:Amalia D. Kalampaliki、Steve Vincent、Suman Mallick、Hoang-Ngoan Le、Guillaume Barnoin、Yogesh W. More、Alain Burger、Yannis Dotsikas、Evagelos Gikas、Benoît Y. Michel、Ioannis K. Kostakis
DOI:10.1016/j.dyepig.2021.109798
日期:2021.12
concentration range. Here, we report the design, synthesis and photophysical characterization of a fluorogenic derivatization reagent with exclusive selectivity for primaryamines. This xanthene-based dye owns an exacerbated fluorogenic character making the derivatized amine absorbing in yellow and emitting in the vermilion edge. In addition to being fluorogenic, this derivatization method also has