Properties | Information | |
---|---|---|
PhytoCAT-ID | PhytoCAT-537 | |
Phytochemical name or plant extracts | Diallyl disulphide | |
PMID | 23163853 | |
Literature evidence | Histone deacetylation inhibitors (HDACi) are known to suppress cancer growth and induce apoptosis in cancer cells. | |
IUPAC name | 3-(prop-2-enyldisulfanyl)prop-1-ene | |
Phytochemicals’ class or type of plant extracts | Organosulfur | |
Source of phytochemicals or plant Extracts | Allium vineale | |
Geographical availability | Albania, Algeria, Austria, Baleares, Baltic States, Belarus, Belgium, Bulgaria, Corse, Czechoslovakia, Denmark, Finland, France, Germany, Great Britain, Greece, Hungary, Iran, Ireland, Italy, Krym, Lebanon-Syria, Morocco, Netherlands, Norway, Poland, Portugal, Romania, Sardegna, Sicilia, Spain, Sweden, Switzerland, Transcaucasus, Turkey, Turkey-in-Europe, Ukraine, Yugoslavia | |
Plant parts | Bulb | |
Other cancers | Breast cancer | |
Target gene or protein | Bax, Bcl-2, Bcl-w, Bcl-xL | |
Gene or Protein evidence | Further studies revealed that DADS modulates the cellular levels of Bax, Bcl-2, Bcl-xL, and Bcl-w in a dose-dependent manner, suggesting the involvement of Bcl-2 family proteins in DADS induced apoptosis. | |
Target pathways | NA | |
IC50 | NA | |
Potency | The data thus indicate that the HDACi properties of DADS may be responsible for the induction of apoptosis in breast cancer cells. | |
Cell line/ mice model | MCF-7 | |
Additional information | Here it is shown that DADS has HDACi properties in MCF-7 cells as it lowers the removal of an acetyl group from an acetylated substrate and induces histone-4 (H4) hyper-acetylation. | |
PubChem ID | 16590 | |
Additional PMIDs | 15827557 | |
Additional sources of information | https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:529111-1 | |
Safety | NA |