Podocarpusflavone A


CAS No. : 22136-74-9

22136-74-9
Price and Availability of CAS No. : 22136-74-9
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Cat. No. : HY-N2198
M.Wt: 552.48
Formula: C31H20O10
Purity: >98 %
Solubility: DMSO : 50 mg/mL (ultrasonic)
Introduction of 22136-74-9 :

Podocarpusflavone A is a biflavonoid present in the leaves of Podocarpus henkelii, with anti-tumor, topoisomerase I inhibitory, antibacterial and antifungal activities. Podocarpusflavone A exhibits antibacterial activity against Enterococcus faecalis and Pseudomonas aeruginosa. Podocarpusflavone A shows weak activity against fungal pathogens. Podocarpusflavone A targets topoisomerase I and induces cell cycle arrest and apoptosis in MCF-7 cells. Podocarpusflavone A can be used for studies on cancer, bacterial and fungal infections[1][2]. In Vitro:Podocarpusflavone A (PFA) (Serial two-fold dilutions from an initial 1 mg/mL; 12-24 h) shows broad-spectrum bactericidal activity against Enterococcus faecalis and Pseudomonas aeruginosa (MIC = 60 μg/mL), with weaker activity against Staphylococcus aureus (MIC = 130 μg/mL) and Escherichia coli (MIC = 250 μg/mL)[1].
Podocarpusflavone A (Serial two-fold dilutions from an initial 1 mg/mL; 24-48 h) exhibits weak antifungal activity against Candida albicans and Aspergillus fumigatus (MIC = 250 μg/mL) and Cryptococcus neoformans (MIC = 130 μg/mL) at 24 h and 48 h incubation[1].
Podocarpusflavone A (CC50 threshold of 1000 μg/mL; MIC values as measured in antibacterial and antifungal assays) has favorable selective antimicrobial activity (SI > 15) against Enterococcus faecalis and Pseudomonas aeruginosa, with lower selectivity against other tested bacterial and fungal pathogens[1].
Podocarpusflavone A (PF) (1-40 µM; 72 h) shows potent antiproliferative activity against KB, MCF-7, DLD and HEp-2 tumor cell lines with ED50 values of 4.67 µg/mL, 15.17 µg/mL, 4.95 µg/mL and 10.87 µg/mL[2].

Podocarpusflavone A (20-40 µg/mL; 24 h) induces cell cycle arrest at sub-G1/S phase and triggers apoptosis in MCF-7 cells[2].
Podocarpusflavone A shows moderate Topoisomerase I inhibitory activity with an IC50 value of 65.98 µg/mL[2].

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