Bridging Converts a Noncytotoxic nor-Paclitaxel Derivative to a Cytotoxic Analogue by Constraining It to the T-Taxol Conformation
- 1 August 2006
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 8 (18) , 3983-3986
- https://doi.org/10.1021/ol061438s
Abstract
The synthesis of the bridged A-nor-paclitaxel 4 has been achieved from paclitaxel in a key test of the T-Taxol conformational hypothesis. Although the unbridged A-nor-paclitaxel 3 is essentially noncytotoxic, the bridged analogue 4 is strongly cytotoxic. This result provides strong evidence for the T-Taxol conformation as the bioactive tubulin-binding conformation of paclitaxel.Keywords
This publication has 32 references indexed in Scilit:
- The T-Taxol ConformationJournal of Medicinal Chemistry, 2006
- Design, synthesis and biological activity of novel C2-C3′ N-Linked macrocyclic taxoidsBioorganic & Medicinal Chemistry Letters, 2002
- Refined structure of αβ-tubulin at 3.5 Å resolution 1 1Edited by I. A. WilsonJournal of Molecular Biology, 2001
- Enantiopure fluorine-containing taxoids: potent anticancer agents and versatile probes for biomedical problemsJournal of Fluorine Chemistry, 1999
- Synthesis and Biological Evaluation of 2-Acyl Analogues of Paclitaxel (Taxol)Journal of Medicinal Chemistry, 1998
- Parametrized Models of Aqueous Free Energies of Solvation Based on Pairwise Descreening of Solute Atomic Charges from a Dielectric MediumThe Journal of Physical Chemistry, 1996
- NMR and molecular modeling study of active and inactive taxol analogues in aqueous and nonaqueous solutionCanadian Journal of Chemistry, 1994
- This and that: sequential theories for stomach cancer and the multiple applications of isotopic ratiosTrends in Pharmacological Sciences, 1992
- Promotion of microtubule assembly in vitro by taxolNature, 1979
- Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reactionBiochemical Pharmacology, 1973