Properties | Information | |
---|---|---|
PhytoCAT-ID | PhytoCAT-1970 | |
Phytochemical name or plant extracts | Atranorin | |
PMID | 20837130 | |
Literature evidence | One of the ways for searching for potentially new anti-cancer drugs is the testing of various naturally synthesized compounds. | |
IUPAC name | (3-hydroxy-4-methoxycarbonyl-2,5-dimethylphenyl) 3-formyl-2,4-dihydroxy-6-methylbenzoate | |
Phytochemicals’ class or type of plant extracts | Depside | |
Source of phytochemicals or plant Extracts | Stereocaulon alpinum | |
Geographical availability | NA | |
Plant parts | Lichen | |
Other cancers | Breast cancer, Cervical cancer, Liver cancer, Ovarian cancer, Leukemia | |
Target gene or protein | NA | |
Gene or Protein evidence | NA | |
Target pathways | NA | |
IC50 | >200 μM against MCF-7 and SK-BR-3 | |
Potency | Our study reports on the sensitivity of up to nine human cancer cell lines (A2780, HeLa, MCF-7, SK-BR-3, HT-29, HCT-116 p53(+/+), HCT-116 p53(-/-), HL-60 and Jurkat) to the anti-proliferative/cytotoxic effects of four typical secondary metabolites of lichens (parietin, atranorin, usnic acid and gyrophoric acid). | |
Cell line/ mice model | A2780, HeLa, MCF-7, SKBR-3, HT-29, HCT-116 p53(+/+), HCT-116 p53(-/-), HL-60 and Jurkat | |
Additional information | NA | |
PubChem ID | 68066 | |
Additional PMIDs | 15784343 | |
Additional sources of information | NA | |
Safety | NA |