Exploring macrocyclization strategies to design novel octreotate-based radioconjugates-Reference-Cited by-同舟云学术

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Exploring macrocyclization strategies to design novel octreotate-based radioconjugates

Published:2024-07 Issue: Volume:145 Page:155162
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Chapeau Dylan^ORCID,Iroidis Angelos,Beckman Savanne,Seimbille Yann

Publisher

Elsevier BV

Reference34 articles.

1. The current state of peptide drug discovery: back to the future?;Henninot;J. Med. Chem.,2017

2. Stapled peptides-a useful improvement for peptide-based drugs;Moiola;Molecules,2019

3. Activation of apoptosis in vivo by a hydrocarbon-stapled BH3 helix;Walensky;Science,1979

4. Towards understanding cell penetration by stapled peptides;Chu;Medchemcomm,2015

5. Cu I -catalyzed azide – alkyne intramolecular i -to- (i + 4) side-chain-to-side- chain cyclization promotes the formation of helix-like secondary structures;Scrima;Eur. J. Org. Chem.,2010

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