Phytochemical Name : Perillic acid

Properties Information
PhytoCAT-ID PhytoCAT-126
Phytochemical name or plant extracts Perillic acid
PMID 9824849
Literature evidence Monoterpenes inhibit cell growth, cell cycle progression, and cyclin D1 gene expression in human breast cancer cell lines.
IUPAC name 4-prop-1-en-2-ylcyclohexene-1-carboxylic acid
Phytochemicals’ class or type of plant extracts Monoterpene
Source of phytochemicals or plant Extracts Perilla frutescens
Geographical availability Assam, Bangladesh, China South-Central, China Southeast, East Himalaya, India, Japan, Jawa, Khabarovsk, Korea, Laos, Myanmar, Nepal, Primorye, Taiwan, Thailand, Vietnam, West Himalaya
Plant parts NA
Other cancers Breast cancer
Target gene or protein Cyclin D1 mRNA
Gene or Protein evidence Finally, we showed that the effects of limonene-related monoterpenes on cell proliferation and cell cycle progression were preceded by a decrease in cyclin D1 mRNA levels.
Target pathways NA
IC50 NA
Potency To a lesser extent, perillic acid affected MCF-7 cell growth, which was reduced by 16% at 50 ^M and by 66% at 3 mM. MDA-MB231 cell growth was only slightly affected by perillic acid, which reduced cell proliferation by 26% at a concentration of 3 mM. In the least-sensitive MDA-MB-231 cells, a maximum decrease in proliferation of 32% was observed after seven days of treatment with 3 mM perillic acid.
Cell line/ mice model T47D, MCF-7, MDA-MB-231
Additional information  Sensitivity of breast cancer cell lines to monoterpenes was in the following order: T-47D > MCF-7 > MDA-MB-231. Growth inhibition induced by perillyl alcohol and perillic acid was associated with a fall in the proportion of cells in the S phase and an accumulation of cells in the G1 phase of the cell cycle.
PubChem ID 1256
Additional PMIDs 7987974 7587953 9824849
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:190343-2
Safety NA