Phytochemical Name : Camalexin

Properties Information
PhytoCAT-ID PhytoCAT-184
Phytochemical name or plant extracts Camalexin
PMID 23179315
Literature evidence In conclusion, camalexin is more potent in aggressive prostate cancer cells that express high ROS levels, and this phytoalexin has a strong potential as a novel therapeutic agent for the treatment of especially metastatic prostate cancer.
IUPAC name 2-(1H-indol-3-yl)-1,3-thiazole
Phytochemicals’ class or type of plant extracts Indole phytoalexin
Source of phytochemicals or plant Extracts Arabidopsis thaliana
Geographical availability Afghanistan, Albania, Algeria, Altay, Austria, Azores, Baleares, Baltic States, Belarus, Belgium, Bulgaria, Canary Is., Cape Verde, Central European Russia, China North-Central, China South-Central, China Southeast, Corse, Cyprus, Czechoslovakia, Denmark, Djibouti, East Aegean Is., East European Russia, East Himalaya, Eritrea, Ethiopia, Finland, France, Germany, Great Britain, Greece, Hungary, Iran, Ireland, Italy, Japan, Kazakhstan, Kenya, Kirgizstan, Korea, Krasnoyarsk, Kriti, Krym, Lebanon-Syria, Libya, Madeira, Mongolia, Morocco, Nepal, Netherlands, North Caucasus, North European Russia, Northwest European Russia, Norway, Pakistan, Palestine, Poland, Portugal, Romania, Rwanda, Sardegna, Saudi Arabia, Sicilia, Somalia, South European Russia, Spain, Sudan, Sweden, Switzerland, Tadzhikistan, Tanzania, Tibet, Transcaucasus, Tunisia, Turkey, Turkey-in-Europe, Tuva, Uganda, Ukraine, Uzbekistan, West Himalaya, West Siberia, Xinjiang, Yugoslavia, Zaïre
Plant parts NA
Other cancers Breast cancer, Prostate cancer
Target gene or protein NA
Gene or Protein evidence NA
Target pathways NA
IC50 NA
Potency This compound has been researched predominantly with regard to plant chemical defense mechanisms, and has been shown to exert cytostatic/cytotoxic effects on the human protozoan pathogen Trypanosoma cruzi [31] and on the human breast cancer cell line SKBr3, where it displays higher potency than the traditional anticancer agents cisplatin and melphalan
Cell line/ mice model SKBR-3, PREC
Additional information  This compound has been researched predominantly with regard to plant chemical defense mechanisms, and has been shown to exert cytostatic/cytotoxic effects on the human protozoan pathogen Trypanosoma cruzi and on the human breast cancer cell line SKBr3, where it displays higher potency than the traditional anticancer agents cisplatin and melphalan
PubChem ID 636970
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:277970-1
Safety NA