Development of a nitroreductase-dependent theranostic payload for antibody-drug conjugate

Z Su, F Xie, X Xu, L Liu, D Xiao, X Zhou, S Li - Bioorganic Chemistry, 2022 - Elsevier
Antibody-drug conjugates are gradually revolutionizing anticancer therapy. Payload is one
of the most crucial components of ADC for high antitumor activity. However, there is no direct …

Anisamide-modified dual-responsive drug delivery system with MRI capacity for cancer targeting therapy

W Yao, C Liu, N Wang, H Zhou, H Chen… - Journal of Molecular …, 2021 - Elsevier
The targeting dual-responsive intelligent drug delivery system has been employed for
cancer treatment as a positive strategy. Herein, we synthesized anisamide-modified …

Kinetics improvement of protease-mediated formation of pyronin dyes

S Debieu, A Romieu - Tetrahedron Letters, 2018 - Elsevier
A fluorescent probe for protease sensing and based on the “covalent-assembly” principle is
reported. The basic rational for this unusual class of chemodosimeters proposed by the …

A novel one-and two-photon fluorescent probe induced by light for selective imaging of Cys in living cells and tissues

Y Ma, Y Zhao, L Xia, J Huang, Y Gu, P Wang - Analytica Chimica Acta, 2018 - Elsevier
A novel one-and two-photon fluorescent probe based on a photoreaction was developed for
the detection of cysteine (Cys). After it was reacted with Cys and illuminated by light, a strong …

Fluorogenic Enzyme-Triggered Domino Reactions Producing Quinoxalin-2(1H)-one-based Heterocycles

G Dejouy, K Renault, Q Bonnin, A Chevalier… - Organic …, 2020 - ACS Publications
A simple and effective biocompatible domino reaction triggered by a model protease and
leading to the formation of strongly fluorescent quinoxalin-2 (1 H)-one N-heterocycles is …

Development of Photoremovable Linkers as a Novel Strategy to Improve the Pharmacokinetics of Drug Conjugates and Their Potential Application in Antibody–Drug …

AN Johan, Y Li - Pharmaceuticals, 2022 - mdpi.com
Although there have been extensive research and progress on the discovery of anticancer
drug over the years, the application of these drugs as stand-alone therapy has been limited …

Revisiting the Chemistry and Photophysics of 3‐(N‐Methylpyridinium‐4‐yl)Coumarins for Designing “Covalent‐Assembly” and “Molecular Disassembly” Fluorescent …

V Gaumerd, K Renault, P Renard… - ChemPhotoChem, 2024 - Wiley Online Library
The constant need for high‐performance aniline‐or phenol‐based fluorophores suitable for
the construction of activity‐based fluorescent probes, led us to study both synthesis and …

Design and synthesis of gene-directed caged cyclic nucleotides exhibiting cell type selectivity

AZ Suzuki, T Sakano, H Sasaki, R Watahiki… - Chemical …, 2021 - pubs.rsc.org
We designed a new caging group that can be photoactivated only in the presence of a non-
endogenous enzyme when exposed to 405 nm light. Because cells or tissues can be …

Strategies for using nanoprobes to perceive and treat cancer activity: a review

B Kang, A Kukreja, D Song, YM Huh… - Journal of biological …, 2017 - Springer
Nanomedicine has seen a significant increase in research on stimuli-responsive activatable
nanoprobes for tumor-specific delivery and diagnosis. The tumor microenvironment has …

Photoactivatable o-Hydroxycinnamic Platforms for Bioimaging and Therapeutic Release: Miniperspective

A Gupta, A Gautam, PK Sasmal - Journal of Medicinal Chemistry, 2022 - ACS Publications
Photoactivatable or photoremovable protecting groups (PPGs) have become a powerful
material and gained enormous interest in the field of biomedical applications. PPGs have …