A series of 3-methyl-2-phenyl-1H-indoles was prepared and investigated for antiproliferative activity on three human tumor cell lines, HeLa, A2780, and MSTO-211H, and some structure-activity relationships were drawn up. The GI(50) values of the most potent compounds (32 and 33) were lower than 5 mu M in all tested cell lines. For the most biologically relevant derivatives, the effect on human DNA topoisomerase II relaxation activity was investigated, which highlighted the good correlation between the antiproliferative effect and topoisomerase II inhibition. The most potent derivative, 32, was shown to induce the apoptosis pathway. The obtained results highlight 3-methyl-2-phenyl-1H-indole as a promising scaffold for further optimization of ...
A series of novel indole derivatives containing α-aminophosphonate moieties were synthesized as anti...
Heterocyclic rings are recognized as key components of many natural, semi-synthetic and synthetic mo...
Novel benzo[30,20:5,6]thiopyrano[3,2-b]indol-10(11H)-ones 1a-v were synthesized and evaluated for th...
A series of 3-methyl-2-phenyl-1H-indoles was prepared and investigated for antiproliferative activit...
A series of 3-methyl-2-phenyl-1H-indoles was prepared and investigated for antiproliferative activit...
Inhibition of microtubule function using tubulin targeting agents has received growing attention in ...
Inhibition of microtubule function using tubulin targeting agents has received growing attention in ...
Inhibition of microtubule function using tubulin targeting agents has received growing attention in ...
Inhibition of microtubule function using tubulin targeting agents has received growing attention in ...
A convenient synthesis of indolin-2-ones substituted in the 3 position by an aminomethylene group be...
One new indolocarbazole, 3-hydroxy-K252d (3), together with the recently reported 3-hydroxyholyrine ...
We designed 39 new 2-phenylindole derivatives as potential anticancer agents bearing the 3,4,5-trime...
The synthesis and antitumor activity of new E-3-(2-chloro-3-indolylmethylene)1,3-dihydroindol-2-ones...
Objective: The present work aimed to synthesize some new 1, 3-diheterocyles indolyl derivatives and ...
The synthesis and biological evaluation of a series of novel heterocyclic indole derivatives is desc...
A series of novel indole derivatives containing α-aminophosphonate moieties were synthesized as anti...
Heterocyclic rings are recognized as key components of many natural, semi-synthetic and synthetic mo...
Novel benzo[30,20:5,6]thiopyrano[3,2-b]indol-10(11H)-ones 1a-v were synthesized and evaluated for th...
A series of 3-methyl-2-phenyl-1H-indoles was prepared and investigated for antiproliferative activit...
A series of 3-methyl-2-phenyl-1H-indoles was prepared and investigated for antiproliferative activit...
Inhibition of microtubule function using tubulin targeting agents has received growing attention in ...
Inhibition of microtubule function using tubulin targeting agents has received growing attention in ...
Inhibition of microtubule function using tubulin targeting agents has received growing attention in ...
Inhibition of microtubule function using tubulin targeting agents has received growing attention in ...
A convenient synthesis of indolin-2-ones substituted in the 3 position by an aminomethylene group be...
One new indolocarbazole, 3-hydroxy-K252d (3), together with the recently reported 3-hydroxyholyrine ...
We designed 39 new 2-phenylindole derivatives as potential anticancer agents bearing the 3,4,5-trime...
The synthesis and antitumor activity of new E-3-(2-chloro-3-indolylmethylene)1,3-dihydroindol-2-ones...
Objective: The present work aimed to synthesize some new 1, 3-diheterocyles indolyl derivatives and ...
The synthesis and biological evaluation of a series of novel heterocyclic indole derivatives is desc...
A series of novel indole derivatives containing α-aminophosphonate moieties were synthesized as anti...
Heterocyclic rings are recognized as key components of many natural, semi-synthetic and synthetic mo...
Novel benzo[30,20:5,6]thiopyrano[3,2-b]indol-10(11H)-ones 1a-v were synthesized and evaluated for th...