Justicidin B inhibits the growth of the pathogenic fungi Aspergillus fumigatus (MIC ≥ 1 μg/mL), Aspergillus flavus (MIC ≥ 12 μg/mL), and Candida albicans (MIC ≥ 4 μg/mL), but is not effective against Cryptococcus neoformans and Blastoschizomyces capitatus[1].
Justicidin B also exhibits strong activity against the trypomastigote form of Trypanosoma brucei rhodesiense (IC50 = 0.2 μg/mL) and moderate activity against Trypanosoma cruzi (IC500 = 2.6 μg/mL)[1].
Justicidin B shows cytotoxic activity and induction of apoptosis in MDA-MB-231 and MCF-7 breast cancer derived cell lines. The 24 h treatment of both cell lines increased the level of apoptotic DNA fragmentation. Exposure of MDA-MB-231 cells with Justicidin B leads to concentration dependent decrease in the expression of NFkB; whereas the treatment of MCF-7, is consistent with strong increase in the expression of this transcription factor[2].
References:
[1]. Jürg Gertsch, et al. Antifungal, antiprotozoal, cytotoxic and piscicidal properties of Justicidin B and a new arylnaphthalide lignan from Phyllanthus piscatorum. Planta Med. 2003 May;69(5):420-4.
[2]. G Momekov, et al. Effect of justicidin B - a potent cytotoxic and pro-apoptotic arylnaphtalene lignan on human breast cancer-derived cell lines. Neoplasma. 2011;58(4):320-5.
[3]. Iliana Ionkova, et al. Linum narbonense: A new valuable tool for biotechnological production of a potent anticancer lignan Justicidine B. Pharmacogn Mag. 2013 Jan;9(33):39-44.
















