Synthesis and biological activities of NB-506 analogues modified at the glucose group

This publication has 11 references indexed in Scilit:

• Synthesis and biological activities of NB-506 analogues: Effects of the positions of two hydroxyl groups at the indole rings
  Bioorganic & Medicinal Chemistry Letters, 1999
• In vivo Anti‐tumor Activity of a Novel Indolocarbazole Compound, J‐107088, on Murine and Human Tumors Transplanted into Mice
  Japanese Journal of Cancer Research, 1999
• Synthesis and biological activities of topoisomerase I inhibitors, 6-N-amino analogues of NB-506
  Bioorganic & Medicinal Chemistry Letters, 1999
• Sequence-selective DNA cleavage by a topoisomerase I poison, NB-506
  International Journal of Cancer, 1998
• Synthesis of Dissymmetric Indolocarbazole Glycosides Using the Mitsunobu Reaction at the Glycosylation Step
  Tetrahedron, 1997
• Synthesis of NB-506, A new anticancer agent
  Tetrahedron, 1997
• Targeted Disruption of the Mouse Topoisomerase I Gene by Camptothecin Selection
  Molecular and Cellular Biology, 1996
• Practical synthesis of indolopyrrolocarbazoles
  Tetrahedron, 1996
• A new antitumor substance, BE-13793C, produced by a streptomycete. Taxonomy, fermentation, isolation, structure determination and biological activity.
  The Journal of Antibiotics, 1991
• Antigenic determinants of Salmonella serogroups A and D1.Synthesis of trisaccharide glycosides for use as artificial antigens
  Carbohydrate Research, 1982