Bioorthogonal chemistry for prodrug activation in vivo

Q Fu, S Shen, P Sun, Z Gu, Y Bai, X Wang… - Chemical Society …, 2023 - pubs.rsc.org
Prodrugs have emerged as a major strategy for addressing clinical challenges by improving
drug pharmacokinetics, reducing toxicity, and enhancing treatment efficacy. The emergence …

Click and release: bioorthogonal approaches to “on-demand” activation of prodrugs

X Ji, Z Pan, B Yu, LK De La Cruz, Y Zheng… - Chemical Society …, 2019 - pubs.rsc.org
Prodrug approaches represent an excellent solution to certain pharmaceutical issues
commonly encountered in the drug discovery and development process. Along this line, the …

Supramolecular prodrugs based on host–guest interactions

WC Geng, JL Sessler, DS Guo - Chemical Society Reviews, 2020 - pubs.rsc.org
Classic prodrug strategies rely on covalent modification of active drugs to provide systems
with superior pharmacokinetic properties than the parent drug and facilitate administration …

General Strategy for Integrated Bioorthogonal Prodrugs: Pt(II)-Triggered Depropargylation Enables Controllable Drug Activation In Vivo

T Sun, T Lv, J Wu, M Zhu, Y Fei, J Zhu… - Journal of Medicinal …, 2020 - ACS Publications
Bioorthogonal decaging reactions for controllable drug activation within complex biological
systems are highly desirable yet extremely challenging. Herein, we find a new class of Pt (II) …

The expanding role of prodrugs in contemporary drug design and development

J Rautio, NA Meanwell, L Di… - Nature reviews drug …, 2018 - nature.com
Prodrugs are molecules with little or no pharmacological activity that are converted to the
active parent drug in vivo by enzymatic or chemical reactions or by a combination of the two …

Towards the next generation of biomedicines by site-selective conjugation

QY Hu, F Berti, R Adamo - Chemical Society Reviews, 2016 - pubs.rsc.org
Bioconjugates represent an emerging class of medicines, which offer therapeutic
opportunities overtaking those of the individual components. Many novel bioconjugates …

Emerging strategies in stimuli-responsive prodrug nanosystems for cancer therapy

C Ding, C Chen, X Zeng, H Chen, Y Zhao - ACS nano, 2022 - ACS Publications
Prodrugs are chemically modified drug molecules that are inactive before administration.
After administration, they are converted in situ to parent drugs and induce the mechanism of …

Prodrugs: design and clinical applications

J Rautio, H Kumpulainen, T Heimbach… - Nature reviews Drug …, 2008 - nature.com
Prodrugs are bioreversible derivatives of drug molecules that undergo an enzymatic and/or
chemical transformation in vivo to release the active parent drug, which can then exert the …

Making smart drugs smarter: The importance of linker chemistry in targeted drug delivery

X Yang, Z Pan, MR Choudhury, Z Yuan… - Medicinal research …, 2020 - Wiley Online Library
Smart drugs, such as antibody‐drug conjugates, for targeted therapy rely on the ability to
deliver a warhead to the desired location and to achieve activation at the same site. Thus …

Current prodrug design for drug discovery

PW Hsieh, CF Hung, JY Fang - Current pharmaceutical design, 2009 - ingentaconnect.com
Prodrugs are inactive compounds which are metabolized either chemically or enzymatically
in a controlled or predictable manner to the parent active drug inside the body. Prodrugs can …