539856-46-7Relevant academic research and scientific papers
SYNTHESIS OF DUOCARMYCIN ANALOGUES
-
, (2016/12/22)
A novel Fmoc protected duocarmycin subunit of formula (I) and utilisation as a reagent in solid phase protein synthesis methodology. Also provided is a novel method of solid phase peptide synthesis, and in particular a method for the production of novel i
Solid-Phase Synthesis of Duocarmycin Analogues and the Effect of C-Terminal Substitution on Biological Activity
Stephenson, Michael J.,Howell, Lesley A.,O'Connell, Maria A.,Fox, Keith R.,Adcock, Claire,Kingston, Jenny,Sheldrake, Helen,Pors, Klaus,Collingwood, Stephen P.,Searcey, Mark
, p. 9454 - 9457 (2015/10/12)
The duocarmycins are potent antitumor agents with potential for use in the development of antibody-drug conjugates (ADCs) as well as being clinical candidates in their own right. In this article, we describe the synthesis of a duocarmycin monomer (DSA) th
A concise and efficient synthesis of seco-duocarmycin SA
Tietze, Lutz F.,Haunert, Frank,Feuerstein, Tim,Herzig, Tobias
, p. 562 - 566 (2007/10/03)
A short and efficient synthesis of seco-duocarmycin SA (3), a highly potent cytostatic agent and direct precursor of the natural product duocarmycin SA (1), has been achieved. Starting from commercially available 2-methoxy-4-nitroaniline (4) the synthetic
