Evidence map›Paper›PMID 38553420›Full record

ReviewChemMedChem2024

Autocleaving Bonds for Better Drugs.

Jiaqi Guo, Annabelle Chang, Bing Xu

Abstract readReview
In one paragraph

Review in ChemMedChem, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jiaqi GuoDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, MA, 02454, USA.ORCID https://orcid.org/0000-0002-0254-0401
Annabelle ChangDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, MA, 02454, USA.
Bing XuDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, MA, 02454, USA.ORCID https://orcid.org/0000-0002-4639-387X

Funding

Subcellular Enzyme-instructed self-assembly for molecular anticancer nanomedicinesR01CA142746 · NCI · BRANDEIS UNIVERSITY · PI Bing Xu · 2010 to 2026
$6.4M
National Science Foundation NSF DMR-2011846NCI NIH HHS NIH CA142746NCI NIH HHS R01 CA142746
6 · The paper itself

Abstract

While bond formation has historically been the mainstay of medicinal chemistry, the phenomenon of bond cleavage has received less focus. However, the success of numerous oral medications demonstrates the importance of controlled cleavage in prodrugs to achieve desired therapeutic outcomes. Nevertheless, effective strategies to control this cleavage remain limited. This concept article introduces a novel approach: employing peptides as conjugates to drugs to modulate the hydrolysis of these conjugates and enhance drug efficacy. The article begins by briefly outlining common prodrug strategies, followed by a few representative examples of how peptides can be leveraged to control the autohydrolysis of peptide-conjugated prodrugs for bacterial and cancer cell inhibition. Finally, it provides a brief outlook on the future potential of this promising new research direction in molecular medicine.

Indexed as

Antineoplastic AgentsPeptidesProdrugsAnti-Bacterial AgentsHumansHydrolysisMolecular StructureAnti-Bacterial AgentsAntineoplastic AgentsPeptidesProdrugsautohydrolysisbond cleavagediglycinepeptideprodrug

Identifiers

PMID38553420
PMCPMC11219257

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.