First Generation Design, Synthesis, and Evaluation of Azepine-based Cryptophycin Analogues
Overview
Chemistry
Affiliations
[structure: see text] Azepine-based cryptophycin mimics (+)-4 and (+)-5 have been designed and synthesized. Biological evaluation revealed modest in vitro activity against several human tumor cell lines, thereby supporting the utility of novel scaffolds for the design and synthesis of cryptophycin analogues.
Jin R, Wu B, Bian K, Yu J, Dai J, Zuo Y Nat Commun. 2022; 13(1):7035.
PMID: 36396652 PMC: 9672039. DOI: 10.1038/s41467-022-34841-1.
Tubulin Inhibitor-Based Antibody-Drug Conjugates for Cancer Therapy.
Chen H, Lin Z, Arnst K, Miller D, Li W Molecules. 2017; 22(8).
PMID: 28763044 PMC: 6152078. DOI: 10.3390/molecules22081281.
Exploring privileged structures: the combinatorial synthesis of cyclic peptides.
Horton D, Bourne G, Smythe M Mol Divers. 2003; 5(4):289-304.
PMID: 12549678 DOI: 10.1023/a:1021365402751.
Exploring privileged structures: the combinatorial synthesis of cyclic peptides.
Horton D, Bourne G, Smythe M J Comput Aided Mol Des. 2002; 16(5-6):415-30.
PMID: 12489688 DOI: 10.1023/a:1020863921840.