Phytochemical Name : Artemisinin

Properties Information
PhytoCAT-ID PhytoCAT-1325
Phytochemical name or plant extracts Artemisinin
PMID 32862573
Literature evidence DAPI and comet assays revealed that artemisinin induced powerful apoptotic effects, triggering significant dose-dependent DNA damage.
IUPAC name (1R,4S,5R,8S,9R,12S,13R)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadecan-10-one
Phytochemicals’ class or type of plant extracts Sesquiterpene lactone
Source of phytochemicals or plant Extracts Artemisia annua
Geographical availability Afghanistan, Algeria, Altay, Amur, Borneo, Bulgaria, Buryatiya, Central European Rus, China North-Central, China South-Central, China Southeast, Chita, Cyprus, East European Russia, East Himalaya, Egypt, Greece, Hainan, India, Inner Mongolia, Iran, Iraq, Irkutsk, Japan, Jawa, Kazakhstan, Khabarovsk, Kirgizstan, Korea, Krasnoyarsk, Krym, Lebanon-Syria, Lesser Sunda Is., Libya, Malaya, Maluku, Manchuria, Mongolia, Morocco, Myanmar, Nepal, North Caucasus, Northwest European R, Pakistan, Philippines, Primorye, Qinghai, Romania, South European Russi, Sulawesi, Sumatera, Tadzhikistan, Taiwan, Tibet, Transcaucasus, Tunisia, Turkey, Turkey-in-Europe, Turkmenistan, Tuva, Uzbekistan, Vietnam, West Himalaya, Western Sahara, Xinjiang
Plant parts NA
Other cancers Breast cancer, Prostate cancer, Lung cancer, Colorectal cancer, Cervical cancer
Target gene or protein CDK4, Cyclin-B1, Cyclin D1, Cyclin E, ER , miR-34a ,TSP50
Gene or Protein evidence Artemsinin and artesunate increased miR-34a expression in a dose-dependent manner correlating with down-regulation of the miR-34a target gene, CDK4. Artemisinin strongly downregulated ERalpha protein and transcripts without altering expression or activity of ERbeta. 25-methoxyl-dammarane-3?, 12?, 20-triol and artemisinin synergistically inhibit MDA-MB-231 cell proliferation through downregulation of testes-specific protease 50 (TSP50) expression.The molecule also targeted G2/M phase cell cycle along with targeting some key cell cycle related proteins including cyclin-B1, cyclin D1 and cyclin E.
Target pathways NA
IC50 NA
Potency NA
Cell line/ mice model MCF-7, MDA-MB-231, P-388, A-549, HT-29, KB
Additional information  Effectively blocks estrogen-stimulated cell cycle progression in MCF-7 cells Artemisinin and the pure antiestrogen fulvestrant exhibit cooperative reduction of ERalpha protein levels and enhanced G(1) cell cycle arrest Induces autophagy in MDA-MB-231 cisplatin-resistant human breast cancer cells by creating autophagosomes and autophagic vacuoles, and targets G2/M phase cell cycle along with key cell cycle related proteins including cyclin-B1, cyclin D1 and cyclin E 70 % 25-methoxyl-dammarane-3?, 12?, 20-triol and 30 % artemisinin, inhibit the TSP50-3'-UTR reporter activity and the expression of TSP50, inhibit MDA-MB-231 cell proliferation and induce cell cycle arrest. Could inhibit tumor growth in a xenograft model of breast cancer (IN VIVO) Artemisinin derivatives decrease expression and secretion of the angiogenic growth factor pleiotrophin by the cancer cells themselves, and inhibit angiogenesis in vivo and endothelial cell growth in vitro Shows strong anticancer effects in MDA-MB-231 cisplatin-resistant cancer cells by triggering apoptosis and autophagy and G2/M phase arrest Increases miR-34a expression correlating with down-regulation of the miR-34a target gene, CDK4
PubChem ID 68827
Additional PMIDs 18784357 8134418 32862573 25789847 25705665 32149317 25209896 31132755 27039397 27478545 27448920 28549888
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:304416-2
Safety NA