Cyclic peptide drugs approved in the last two decades (2001–2021)

H Zhang, S Chen - RSC Chemical Biology, 2022 - pubs.rsc.org
In contrast to the major families of small molecules and antibodies, cyclic peptides, as a
family of synthesizable macromolecules, have distinct biochemical and therapeutic …

Macrocyclic peptides as drug candidates: recent progress and remaining challenges

AA Vinogradov, Y Yin, H Suga - Journal of the American Chemical …, 2019 - ACS Publications
Peptides as a therapeutic modality attract much attention due to their synthetic accessibility,
high degree of specific binding, and the ability to target protein surfaces traditionally …

New modalities for challenging targets in drug discovery

E Valeur, SM Guéret, H Adihou… - Angewandte Chemie …, 2017 - Wiley Online Library
Our ever‐increasing understanding of biological systems is providing a range of exciting
novel biological targets, whose modulation may enable novel therapeutic options for many …

Constraining cyclic peptides to mimic protein structure motifs

TA Hill, NE Shepherd, F Diness… - Angewandte Chemie …, 2014 - Wiley Online Library
Many proteins exert their biological activities through small exposed surface regions called
epitopes that are folded peptides of well‐defined three‐dimensional structures. Short …

Methods for generating and screening libraries of genetically encoded cyclic peptides in drug discovery

C Sohrabi, A Foster, A Tavassoli - Nature Reviews Chemistry, 2020 - nature.com
Drug discovery has traditionally focused on using libraries of small molecules to identify
therapeutic drugs, but new modalities, especially libraries of genetically encoded cyclic …

Peptide therapeutics: targeting the undruggable space

N Tsomaia - European journal of medicinal chemistry, 2015 - Elsevier
Rapid advancements in genomics have brought a better understanding of molecular
mechanisms for various pathologies and identified a number of highly attractive target …

[HTML][HTML] Challenges and opportunities for non-antibody scaffold drugs

R Vazquez-Lombardi, TG Phan, C Zimmermann… - Drug discovery today, 2015 - Elsevier
Highlights•Non-antibody scaffold drugs are a promising new class of biologics drugs.•The
first candidate scaffolds are now moving into clinical development and practice.•Challenges …

Phage selection of cyclic peptides for application in research and drug development

K Deyle, XD Kong, C Heinis - Accounts of chemical research, 2017 - ACS Publications
Conspectus Cyclic peptides can bind to protein targets with high affinities and selectivities,
which makes them an attractive modality for the development of research reagents and …

Therapeutics targeting the fibrinolytic system

H Lin, L Xu, S Yu, W Hong, M Huang… - Experimental & molecular …, 2020 - nature.com
The function of the fibrinolytic system was first identified to dissolve fibrin to maintain
vascular patency. Connections between the fibrinolytic system and many other physiological …

Druggable protein–protein interactions–from hot spots to hot segments

N London, B Raveh, O Schueler-Furman - Current opinion in chemical …, 2013 - Elsevier
Highlights•PPIs that are dominated by a continuous epitope are amenable for inhibition.•A
significant share of PPIs contains such 'hot segments'.•Peptide-based inhibitors are obvious …