SANC00479



Cephalostatin 3




C55H76N2O11




941.2




10472152




116199-49-6




2D Image 3D View


    • C[C@H]1[C@H]2CC=C3[C@]2(CO[C@]14[C@@H]([C@@H](C(O4)(C)C)C)O)C(=O)C[C@]5([C@H]3CC[C@@H]6[C@@]5(CC7=C(C6)N=C8C[C@]9([C@@H](CC[C@@H]1[C@@H]9C[C@H]([C@]2(C1=C[C@H]1[C@@]2([C@@H]([C@@]2(O1)[C@@H](C[C@@](O2)(C)CO)O)C)O)C)O)CC8=N7)C)C)O

    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. (1988) Isolation and Structure of the Hemichordate Cell Growth Inhibitors Cephalostatins 2, 3, and 4


  • Alkaloid

  • Cephalostatin

  • Steroid

  • Steroids and steroid derivatives (Classyfire)


    • None Recorded

  • Cephalodiscus gilchristi

  • Anticancer