Phytochemical Name : Jerantinine A

Properties Information
PhytoCAT-ID PhytoCAT-659
Phytochemical name or plant extracts Jerantinine A
PMID 28198434
Literature evidence Jerantinine A (JA) is a novel indole alkaloid which displays potent anti-proliferative activities against human cancer cell lines by inhibiting tubulin polymerization and inducing G2/M cell cycle arrest.
IUPAC name methyl (1R,12R,19S)-12-ethyl-4-hydroxy-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate
Phytochemicals’ class or type of plant extracts Alkaloid
Source of phytochemicals or plant Extracts Tabernaemontana corymbosa
Geographical availability Bangladesh, Borneo, Cambodia, China South-Central, China Southeast, Hainan, Laos, Lesser Sunda Is., Malaya, Myanmar, Sumatera, Thailand, Vietnam
Plant parts Leaves
Other cancers Breast cancer
Target gene or protein SF3B1, SF3B3
Gene or Protein evidence Using a combined pooled-genome wide shRNA library screen and global proteomic profiling, we showed that JA targets the spliceosome by up-regulating SF3B1 and SF3B3 protein in breast cancer cells.
Target pathways NA
IC50 0.72 ± 0.18 μM against T47D 0.86 ± 0.09 μM against MDA-MB-468 1.22 ± 0.15 μM against MCF-7
Potency Jerantinine A (JA) is a novel indole alkaloid which displays potent anti-proliferative activities against human cancer cell lines by inhibiting tubulin polymerization and inducing G2/M cell cycle arrest.
Cell line/ mice model MCF-7, MDA-MB-468, T47D, MCF-10A
Additional information  Further analyses showed that JA stabilizes endogenous SF3B1 protein in breast cancer cells and induced dissociation of the protein from the nucleosome complex. Together, these results demonstrate that JA exerts its antitumor activity by targeting SF3B1 and SF3B3 in addition to its reported targeting of tubulin polymerization.
PubChem ID 25112179
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:60466167-2
Safety NA