Evidence map›Paper›PMID 37955299›Full record

ReviewJournal of enzyme inhibition and medicinal chemistry2023

Recent progress in discovery of novel AAK1 inhibitors: from pain therapy to potential anti-viral agents.

Ying-Hui Yuan, Nian-Dong Mao, Ji-Long Duan, Hang Zhang, Carmen Garrido, Frédéric Lirussi, Yuan Gao, Tian Xie, Xiang-Yang Ye

Abstract readReview
In one paragraph

Review in Journal of enzyme inhibition and medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. 7-azaindole as privileged scaffold: Advances in drug design and structural modification.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Review
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  11. Pain Signaling by GPCRs and RTKs.Trends in pharmacological sciences · 2025
    Review
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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

9 authors.

Ying-Hui YuanSchool of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Nian-Dong MaoSchool of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Ji-Long DuanSchool of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Hang ZhangKey Laboratory of Elemene Class Anti-Cancer Chinese Medicines; Engineering Laboratory of Development and Application of Traditional Chinese Medicines; Collaborative Innovation Center of Traditional Chinese Medicines of Zhejiang Province, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Carmen GarridoINSERM UMR 1231, Labex LipSTIC, University of Bourgogne, Dijon, France.
Frédéric LirussiINSERM UMR 1231, Labex LipSTIC, University of Bourgogne, Dijon, France.
Yuan GaoSchool of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Tian XieSchool of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Xiang-Yang YeSchool of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adaptor associated kinase 1 (AAK1), a member of the Ark1/Prk1 family of Ser/Thr kinases, is a specific key kinase regulating Thr156 phosphorylation at the μ2 subunit of the adapter complex-2 (AP-2) protein. Due to their important biological functions, AAK1 systems have been validated in clinics for neuropathic pain therapy, and are being explored as potential therapeutic targets for diseases caused by various viruses such as Hepatitis C (HCV), Dengue, Ebola, and COVID-19 viruses and for amyotrophic lateral sclerosis (ALS). Centreing on the advances of drug discovery programs in this field up to 2023, AAK1 inhibitors are discussed from the aspects of the structure-based rational molecular design, pharmacology, toxicology and synthetic routes for the compounds of interest in this review. The aim is to provide the medicinal chemistry community with up-to-date information and to accelerate the drug discovery programs in the field of AAK1 small molecule inhibitors.

Indexed as

Antiviral AgentsProtein Serine-Threonine KinasesHumansPainPhosphorylationAAK1 protein, humanAntiviral AgentsProtein Serine-Threonine KinasesAdaptor associated kinase 1 (AAK1)inhibitormedicinal chemistrytherapeutic application

Identifiers

PMID37955299
PMCPMC10653628

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.