[HTML][HTML] Recent applications of retro-inverso peptides

N Doti, M Mardirossian, A Sandomenico… - International Journal of …, 2021 - mdpi.com
Natural and de novo designed peptides are gaining an ever-growing interest as drugs
against several diseases. Their use is however limited by the intrinsic low bioavailability and …

Peptide and protein mimetics by retro and retroinverso analogs

J Rai - Chemical biology & drug design, 2019 - Wiley Online Library
Retroinverso analog of a natural polypeptide can sometimes mimic the structure and
function of the natural peptide. The additional advantage of using retroinverso analog is that …

Recent developments in retro peptides and proteins—an ongoing topochemical exploration

M Chorev, M Goodman - Trends in biotechnology, 1995 - cell.com
Main-chain peptidomimetics based on peptide-bond reversal and inversion of chirality
represent important structural alterations for peptides and proteins, and are highly significant …

The design, synthesis and application of stereochemical and directional peptide isomers: a critical review

PM Fischer - Current Protein and Peptide Science, 2003 - ingentaconnect.com
Physiological processes are regulated to a large extent by physical and chemical
interactions between polypeptides. Although many small molecules have been discovered …

[HTML][HTML] Immunosilencing peptides by stereochemical inversion and sequence reversal: retro-D-peptides

P Arranz-Gibert, S Ciudad, J Seco, J García, E Giralt… - Scientific Reports, 2018 - nature.com
Peptides are experiencing a new era in medical research, finding applications ranging from
therapeutics to vaccines. In spite of the promising properties of peptide pharmaceuticals …

A dozen years of retro-inverso peptidomimetics

M Chorev, M Goodman - Accounts of chemical research, 1993 - ACS Publications
Twelve years ago we published an Account in which we presented a stereochemical
analysis of cyclic and linear retro-peptide systems. 1 We postulated that reversal of peptide …

Protease‐resistant peptide design—empowering nature's fragile warriors against HIV

MT Weinstock, JN Francis, JS Redman… - Peptide Science, 2012 - Wiley Online Library
Peptides have great potential as therapeutic agents, but their use is often limited by
susceptibility to proteolysis and their resulting in vivo fragility. In this review, we focus on …

Method to generate highly stable D-amino acid analogs of bioactive helical peptides using a mirror image of the entire PDB

M Garton, S Nim, TA Stone, KE Wang… - Proceedings of the …, 2018 - National Acad Sciences
Biologics are a rapidly growing class of therapeutics with many advantages over traditional
small molecule drugs. A major obstacle to their development is that proteins and peptides …

Stereoselective synthesis of conformationally constrained reverse turn dipeptide mimetics

W Qiu, X Gu, VA Soloshonok, MD Carducci, VJ Hruby - Tetrahedron Letters, 2001 - Elsevier
Peptide side chains play critical roles in the event of molecular recognition. In order to study
the bioactive conformation of parent peptides, a concise and straightforward five-step …

[HTML][HTML] Non-Canonical Amino Acids as Building Blocks for Peptidomimetics: Structure, Function, and Applications

TG Castro, M Melle-Franco, CEA Sousa… - Biomolecules, 2023 - mdpi.com
This review provides a fresh overview of non-canonical amino acids and their applications in
the design of peptidomimetics. Non-canonical amino acids appear widely distributed in …