Properties | Information | |
---|---|---|
PhytoCAT-ID | PhytoCAT-1883 | |
Phytochemical name or plant extracts | Boldine | |
PMID | 27611982 | |
Literature evidence | Exposure to boldine decreased bromodeoxyuridine incorporation and histone H3 phosphorylation but did not induce apoptosis. | |
IUPAC name | (6aS)-1,10-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,9-diol | |
Phytochemicals’ class or type of plant extracts | Alkaloid | |
Source of phytochemicals or plant Extracts | Lindera umbellata | |
Geographical availability | Japan | |
Plant parts | NA | |
Other cancers | Breast cancer | |
Target gene or protein | p38, ERK, JNK | |
Gene or Protein evidence | Boldine treatment resulted in p38, ERK, and JNK activation in the mitogen-activated protein kinase pathway in a dose-dependent manner. | |
Target pathways | NA | |
IC50 | NA | |
Potency | Boldine was cytotoxic to MCF-7 cells and reduced their viability and proliferation in vitro. | |
Cell line/ mice model | MCF-7, MDA-MB-231, Tumor-bearing mice | |
Additional information | There was neither antagonism nor synergism between boldine and doxorubicin, except a possible synergism of i. p. boldine 90 mg/kg combined with doxorubicin when compared with doxorubicin alone.Boldine was cytotoxic to MCF-7 cells and reduced their viability and proliferation in vitro. Exposure to boldine decreased bromodeoxyuridine incorporation and histone H3 phosphorylation but did not induce apoptosis. | |
PubChem ID | 10154 | |
Additional PMIDs | 25746354 | |
Additional sources of information | https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:465469-1 | |
Safety | NA |