Properties |
Information |
PhytoCAT-ID |
PhytoCAT-602 |
Phytochemical name or plant extracts |
6,7-di-O-acetylsinococuline (FK-3000) |
PMID |
25823424 |
Literature evidence |
These studies demonstrate that FK-3000, isolated from S. delavayi Diels., is a promising, pathway-specific anticancer agent that exhibits low toxicity. |
IUPAC name |
[(1S,9S,12S,13S)-12-acetyloxy-3-hydroxy-4,11-dimethoxy-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,10-tetraen-13-yl] acetate |
Phytochemicals’ class or type of plant extracts |
Alkaloid |
Source of phytochemicals or plant Extracts |
Stephania delavayi |
|
Geographical availability |
China South-Central, Myanmar |
Plant parts |
NA |
Other cancers |
Breast cancer, Prostate cancer, Colon cancer |
Target gene or protein |
NF-kB, COX-2, cyclin B, p-CDC2 |
Gene or Protein evidence |
FK-3000 suppressed NF-kB nuclear translocation, decreased NF-kB phosphorylation, and decreased COX-2 protein expression.
Conclusively FK-3000 exerts its antiproliferative effect through two pathways: i) G2/M cell cycle arrest via downregulation of cyclin B and phospho-CDC2 by p38 MAPK phosphorylation and CDC25B dephosphorylation, and ii) p38 MAPK-independent induction of apoptosis. |
Target pathways |
NF-kB-COX-2 pathway |
IC50 |
0.52 µg/ml against MDA-MB-231
0.77 µg/ml against MCF-7
|
Potency |
The FK-3000 half maximal inhibitory concentration (IC50) in MDA-MB-231 breast carcinoma cells at 48 h was 0.52 µg/ml and it induced apoptosis in a dose- and time-dependent manner. |
Cell line/ mice model |
MDA-MB-231 xenografted mice, MCF-7, MDA-MB-231, PC-3, HT-29 |
Additional information |
The tumor size was smallest in the co-treatment group, indicating that FK-3000 may have a synergistic effect with Taxol.
FK-3000 treatment showed no adverse effects on blood cell counts, serum protein levels, or pathology. |
PubChem ID |
9823255 |
Additional PMIDs |
25384584 |
Additional sources of information |
https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:581412-1 |
Safety |
These studies demonstrate that FK-3000, isolated from S. delavayi Diels., is a promising, pathway-specific anticancer agent that exhibits low toxicity. |