Biocompatible strategies for peptide macrocyclisation

J He, P Ghosh, C Nitsche - Chemical Science, 2024 - pubs.rsc.org
Peptides are increasingly important drug candidates, offering numerous advantages over
conventional small molecules. However, they face significant challenges related to stability …

A biocompatible, highly efficient click reaction and its applications

Y Yuan, G Liang - Organic & Biomolecular Chemistry, 2014 - pubs.rsc.org
Herein, we review the development, optimization, applications and potential prospects of a
novel click reaction based on the condensation reaction between 2-cyanobenzothiazole …

Biocompatible macrocyclization between cysteine and 2-cyanopyridine generates stable peptide inhibitors

C Nitsche, H Onagi, JP Quek, G Otting, D Luo… - Organic …, 2019 - ACS Publications
Peptides featuring an N-terminal cysteine residue and the unnatural amino acid 3-(2-cyano-
4-pyridyl) alanine (Cpa) cyclize spontaneously in aqueous solution at neutral pH. Cpa is …

An Efficient, Site‐Selective and Spontaneous Peptide Macrocyclisation During in vitro Translation

M Liu, R Yoshisada, A Amedi… - … A European Journal, 2023 - Wiley Online Library
Macrocyclisation provides a means of stabilising the conformation of peptides, often
resulting in improved stability, selectivity, affinity, and cell permeability. In this work, a new …

Scope and limitations of the nicking enzyme amplification reaction for the synthesis of base-modified oligonucleotides and primers for PCR

P Ménová, V Raindlova, M Hocek - Bioconjugate chemistry, 2013 - ACS Publications
Enzymatic synthesis of short (10–22 nt) base-modified oligonucleotides (ONs) was
developed by nicking enzyme amplification reaction (NEAR) using Vent (exo-) polymerase …

Deoxynucleoside triphosphates bearing histamine, carboxylic acid, and hydroxyl residues–synthesis and biochemical characterization

M Hollenstein - Organic & biomolecular chemistry, 2013 - pubs.rsc.org
Modified nucleoside triphosphates (dAHsTP, dUPOHTP, and dCValTP) bearing imidazole,
hydroxyl, and carboxylic acid residues connected to the purine and pyrimidine bases …

Post-synthesis DNA modifications using a trans-cyclooctene click handle

K Wang, D Wang, K Ji, W Chen, Y Zheng… - Organic & …, 2015 - pubs.rsc.org
Post-synthesis DNA modification is a very useful method for DNA functionalization. This is
achieved by using a modified NTP, which has a handle for further modifications, replacing …

N, S-double labeling of N-terminal cysteines via an alternative conjugation pathway with 2-cyanobenzothiazole

W Wang, J Gao - The Journal of Organic Chemistry, 2019 - ACS Publications
Conjugation of 2-cyanobenzothiazole (CBT) with N-terminal cysteines (NCys) typically gives
a luciferin product. We herein report an alternative reaction pathway leading to an N …

Post-modification of 2-formylthiophene based heterocyclic azo dyes

D Xu, Z Li, YX Peng, J Geng, HF Qian, W Huang - Dyes and Pigments, 2016 - Elsevier
In order to further adjust the π-conjugated system, solubility and electronic spectrum of 2-
amino-3-cyano-4-chloro-5-formylthiophene based blue colored heterocyclic blue azo dyes …

Applications of CBT-Cys click reaction: Past, present, and future

M Zhang, G Liang - Science China Chemistry, 2018 - Springer
Herein, we review the development, applications and potential prospects of CBT-Cys click
reaction. This click condensation reaction is based on the condensation reaction between 2 …