Computational comparison of microtubule-stabilising agents laulimalide and peloruside with taxol and colchicine
- 1 October 2004
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 14 (19) , 4825-4829
- https://doi.org/10.1016/j.bmcl.2004.07.053
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- The Solid State, Solution and Tubulin-Bound Conformations of Agents that Promote Microtubule StabilizationCurrent Medicinal Chemistry - Anti-Cancer Agents, 2012
- Design and Total Synthesis of a Superior Family of Epothilone Analogues, which Eliminate Xenograft Tumors to a Nonrelapsable StateAngewandte Chemie International Edition in English, 2003
- The High‐Resolution Solution Structure of Epothilone A Bound to Tubulin: An Understanding of the Structure–Activity Relationships for a Powerful Class of Antitumor AgentsAngewandte Chemie International Edition in English, 2003
- Novel molecules that interact with microtubules and have functional activity similar to Taxol™Drug Discovery Today, 2001
- The Epothilones, Eleutherobins, and Related Types of MoleculesCurrent Pharmaceutical Design, 2001
- Microtubule-stabilizing agents: a growing class of important anticancer drugsCurrent Opinion in Chemical Biology, 2001
- Structural Insights into Microtubule FunctionAnnual Review of Biophysics, 2001
- How Taxol® stabilises microtubule structureChemistry & Biology, 1999
- Chemical Biology of EpothilonesAngewandte Chemie International Edition in English, 1998
- Phase II Trial of Taxol, an Active Drug in the Treatment of Metastatic Breast CancerJNCI Journal of the National Cancer Institute, 1991