Evidence map›Paper›PMID 42074025›Full record

ReviewInternational journal of molecular sciences2026

Kinetic Analysis of Irreversible Covalent Enzyme Inhibitors and Its Use in Drug Design.

Jean Chaudière

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. 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

1 author.

Jean ChaudièreCNRS, IMS, UMR 5218, University of Bordeaux, 33405 Talence, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Irreversible covalent enzyme inhibitors, including targeted covalent inhibitors (TCIs) and mechanism-based enzyme inhibitors (MBEIs), play an increasingly important role in drug discovery. Their pharmacological behavior is governed by intrinsic inactivation parameters, typically described by the inactivation constant K

Indexed as

Drug DesignEnzyme InhibitorsEnzymesHumansKineticsEnzyme InhibitorsEnzymesdrug designenzyme inactivationirreversible inhibitionkinetic mechanismmechanism-based enzyme inhibitorpartition ratiosuicide substratetargeted covalent inhibitor

Identifiers

PMID42074025
PMCPMC13116466

What OpenQuestion holds

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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.