Phytochemical Name : Delcosine

Properties Information
PhytoCAT-ID PhytoCAT-721
Phytochemical name or plant extracts Delcosine
PMID 31222559
Literature evidence These acylated alkaloid derivatives caused accumulation of TNBC cells at sub-G1 within 24 h. 1-Acylation of 1 appears to be critical for producing antiproliferative activity in this alkaloid class and a means to provide promising new leads for further development into antitumor agents.
IUPAC name (2R,3R,4S,5S,6S,8R,9R,10R,13S,16S,17R,18S)-11-ethyl-6,13,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol
Phytochemicals’ class or type of plant extracts Diterpenoid alkaloid
Source of phytochemicals or plant Extracts Aconitum barbatum Aconitum napellus Aconitum yesoense
Geographical availability Altay, Amur, Buryatiya, China North-Central, China Southeast, Chita, Inner Mongolia, Irkutsk, Kazakhstan, Khabarovsk, Korea, Krasnoyarsk, Manchuria, Mongolia, Tuva, West Siberia, Xinjiang, Yakutskiya ,,,,Most of Europe, including Britain, east to N. W. Asia and the Himalayas,,, Hokkaido, Japan
Plant parts Root
Other cancers Breast cancer, Lung cancer, Prostate cancer, Cervical cancer
Target gene or protein NA
Gene or Protein evidence NA
Target pathways NA
IC50 NA
Potency Among the tested alkaloids, C19-diterpenoid (e.g., lipojesaconitine, delcosine and delpheline derivatives) and C20-diterpenoid (e.g., kobusine and pseudokobusine derivatives) alkaloids exhibited significant cytotoxic activity and, thus, provide promising new leads for further development as antitumor agents.
Cell line/ mice model MCF-7, MDA-MB-231, A549, DU145,KB
Additional information  NA
PubChem ID 441725
Additional PMIDs 31234546
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:707190-1
Safety NA