Convergent approach to water soluble camptothecin derivatives
- 5 October 1995
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 5 (19) , 2189-2194
- https://doi.org/10.1016/0960-894x(95)00354-v
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Synthesis and Antitumor Activity of 20(S)-Camptothecin Derivatives: A-Ring Modified and 7,10-Disubstituted Camptothecins.CHEMICAL & PHARMACEUTICAL BULLETIN, 1991
- Synthesis of water-soluble (aminoalkyl)camptothecin analogs: inhibition of topoisomerase I and antitumor activityJournal of Medicinal Chemistry, 1991
- DNA Topoisomerase I—Targeted Chemotherapy of Human Colon Cancer in XenograftsScience, 1989
- Therapeutic efficacy of human recombinant interleukin-2 (TGP-3) alone or in combination with cyclophosphamide and immunocompetent cells in allogeneic, semi-syngeneic, and syngeneic murine tumorsCancer Immunology, Immunotherapy, 1989
- Tetrahedron report number 105Tetrahedron, 1981
- Plant antitumor agents. 18. Synthesis and biological activity of camptothecin analogsJournal of Medicinal Chemistry, 1980
- Nucleophilic character of alkyl radicals—IITetrahedron, 1970
- Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata1,2Journal of the American Chemical Society, 1966