SANC00491



Cephalostatin 17




C54H74N2O10




911.17




170591-44-3




2D Image 3D View


    • O=C1C([H])([H])[C@]7(O[H])[C@@]([H])(C2=C([H])C([H])([H])[C@@]3([H])[C@]([H])(C([H])([H])[H])[C@]4(OC([H])([H])[C@@]123)OC(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[C@]4([H])O[H])C([H])([H])C([H])([H])[C@@]6([H])C([H])([H])c5nc%13c(nc5C([H])([H])[C@]67C([H])([H])[H])C([H])([H])[C@]%12([H])C([H])([H])C([H])([H])[C@@]%11([H])C%10=C([H])[C@@]9([H])O[C@]8(OC(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[C@]8([H])O[H])[C@@]([H])(C([H])([H])[H])[C@@]9(O[H])[C@@]%10(C([H])([H])[H])[C@@]([H])(O[H])C([H])([H])[C@]%11([H])[C@@]%12(C([H])([H])[H])C%13([H])[H]

    O=C1CC2C(CCC3Cc4nc5c(nc4CC32)CC2CCC3C4=CC6OC7(CCCO7)CC6C4CCC3C2C5)C2=CCC3CC4(CCCO4)OCC123
    C1CCOCC1
    C1CCCCC1
    C=C1CCCC2CCCCC12
    O=C1CC2C(CCC3Cc4nc5c(nc4CC32)CC2CCC3C4=CC6OC7(CCCO7)CC6C4CCC3C2C5)C2=CCC3CCOCC123
    C1CCC2CCCCC2C1



  • Moser & Rudi (2008) Review of Cytotoxic Cephalostatins and Ritterazines: Isolation and Synthesis

  • Pettit et al. (1995) Antineoplastic agents. Part 292. Isolation and structure of the exceptional pterobranchia human cancer inhibitors cephalostatins 16 and 17


  • Alkaloid

  • Cephalostatin

  • Steroid

  • Steroids and steroid derivatives (Classyfire)


    • None Recorded

  • Cephalodiscus gilchristi

  • Anticancer