Wang Shifa

TL;DR: A series of new N-substituted 1H-dibenzo[a,c]carbazole derivatives synthesized from dehydroabietic acid displayed pronounced antimicrobial activity against tested strains with low MIC values and exhibited potent inhibitory activity comparable to reference drugs amikacin and ketoconazole.

TL;DR: A series of new 1H-benzo[d]imidazole derivatives of dehydroabietic acid were designed and synthesized as potent antitumor agents and showed significant cytotoxic activities against two hepatocarcinoma cells and reduced cytotoxicity against noncancerous human hepatocyte (LO2).

TL;DR: A series of new quinoxaline derivatives of dehydroabietic acid (DAA) were designed and synthesized as potential antitumor agents and confirmed that compound 4b could induce the apoptosis of SMMC-7721 cells in a dose-dependent manner.

TL;DR: In this article, the authors have shown that Nitrogen-containing heterocyclic compounds are pharmaceutically acceptable salt of the dehydroabietic acid benzimidazole derivatives and have good antitumor bioactivity.