Properties |
Information |
PhytoCAT-ID |
PhytoCAT-1197 |
Phytochemical name or plant extracts |
Tragopogon porrifolius extract |
PMID |
31879598 |
Literature evidence |
The antioxidant activity evaluated using the DPPH radical scavenging, thiobarbituric acid and reducing power methods. |
IUPAC name |
NA |
Phytochemicals’ class or type of plant extracts |
Ethanolic extract |
Source of phytochemicals or plant Extracts |
Tragopogon porrifolius |
|
Geographical availability |
Albania, Algeria, Baleares, Baltic States, Bulgaria, Canary Is., Corse, Czechoslovakia, East Aegean Is., France, Great Britain, Greece, Italy, Kriti, Libya, Morocco, Portugal, Romania, Sardegna, Saudi Arabia, Sicilia, Spain, Tunisia, Turkey, Turkey-in-Europe, Ukraine, West Himalaya, Yugoslavia |
Plant parts |
Leaves |
Other cancers |
Breast cancer |
Target gene or protein |
CAT |
Gene or Protein evidence |
Also, in the CCl4-treated groups (VI, VII, and VIII), the extract raised the CAT levels by 72, 124, and 222%, respectively, compared to the control group. |
Target pathways |
NA |
IC50 |
0.0625 mg/mL against MDA-MB-231 |
Potency |
Both extracts also exhibited significant anticancer effect on MDA-MB-231 breast cancer cells. |
Cell line/ mice model |
MDA-MB-231 |
Additional information |
T.
porrifolius exhibited higher α-glucosidase inhibitory activity, and both extract showed strong α-amylase inhibition activity compared to reference drug acarbose.
T.
porrifolius and P.
cognatum ethanolic extracts exhibited antimicrobial activity in the concentration range of 0.039-2.5 mg/ml. |
PubChem ID |
NA |
Additional PMIDs |
25694787 |
Additional sources of information |
https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:256109-1 |
Safety |
NA |