RAPTA-C (Ru(eta6-p-cymene)Cl2(pta)) acts as an anti-cancer and anti-angiogenic agent. RAPTA-C exhibits anti-metastatic, anti-angiogenic, and anti-tumoral activities through protein and histone-deoxyribonucleic acid alterations. RAPTA-C exhibits cell growth inhibition by triggering G(2)/M phase arrest in cancer cells. RAPTA-C also enhances the levels of p53 and triggers the mitochondrial Apoptotic pathway, resulting in cytochrome C release and caspase-9 activation. RAPTA-C reduces the growth of tumors with the inhibition of angiogenesis in a ovarian carcinoma model[1][2][3].
Molekulargewicht:
460.32
Reinheit:
99.30
CAS Nummer:
[372948-28-2]
Formel:
C16H23Cl2N3PRu
Target-Kategorie:
Apoptosis,Caspase
Anwendungsbeschreibung:
MCE Product type: Reference compound
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