Evidence map›Paper›PMID 42631357›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Molecular Basis for Activation to Inhibition Switching in Kv7.2 Channel Modulators.

Tania Ciaglia, Giusy Carleo, Zhenni Yang, Francesca Di Matteo, Federica De Rosa, Gerardina Smaldone, Zhao-Bing Gao, Marco D'Alì, Rita Turcio, Demin Ma and 11 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 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

21 authors.

Tania CiagliaDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0000-0002-6592-4373
Giusy CarleoDepartment of Neuroscience, Reproductive Sciences and Dentistry, Section of Pharmacology, University of Naples Federico II, Naples, Italy.ORCID https://orcid.org/0009-0009-7908-4369
Zhenni YangNanhu Brain-Computer Interface Institute, Hangzhou, Zhejiang, China.ORCID https://orcid.org/0009-0002-1837-2788
Francesca Di MatteoDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0000-0002-9907-6472
Federica De RosaDepartment of Neuroscience, Reproductive Sciences and Dentistry, Section of Pharmacology, University of Naples Federico II, Naples, Italy.
Gerardina SmaldoneDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0000-0003-1380-9717
Zhao-Bing GaoState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Pudong, Shanghai, China.ORCID https://orcid.org/0000-0001-8931-5508
Marco D'AlìDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences (CHIBIOFARAM), University of Messina, Viale Ferdinando Stagno d'Alcontres 31, Messina, Italy.ORCID https://orcid.org/0009-0007-2225-2996
Rita TurcioDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0009-0005-1145-4942
Demin MaNanhu Brain-Computer Interface Institute, Hangzhou, Zhejiang, China.
Veronica Di SarnoDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0000-0002-1397-5240
Nannan SuDepartment of Neurology of the Fourth Affiliated Hospital, Center For Membrane Receptors and Brain Medicine, School of Medicine, Zhejiang University, Hangzhou, China.
Salvatore Vincenzo GiofrèDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences (CHIBIOFARAM), University of Messina, Viale Ferdinando Stagno d'Alcontres 31, Messina, Italy.ORCID https://orcid.org/0000-0002-3117-587X
Giacomo PepeDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0000-0002-7561-2023
Pietro CampigliaDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0000-0002-1069-2181
Alessia BertaminoDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0000-0002-5482-6276
Francesco MiceliDepartment of Neuroscience, Reproductive Sciences and Dentistry, Section of Pharmacology, University of Naples Federico II, Naples, Italy.ORCID https://orcid.org/0000-0002-5393-1402
Jiangtao GuoNanhu Brain-Computer Interface Institute, Hangzhou, Zhejiang, China.
Nunzio IraciDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences (CHIBIOFARAM), University of Messina, Viale Ferdinando Stagno d'Alcontres 31, Messina, Italy.ORCID https://orcid.org/0000-0002-1359-8684
Carmine OstacoloDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.ORCID https://orcid.org/0000-0003-3715-8680
Maurizio TaglialatelaDepartment of Neuroscience, Reproductive Sciences and Dentistry, Section of Pharmacology, University of Naples Federico II, Naples, Italy.ORCID https://orcid.org/0000-0002-8202-0560

Funding

European Rare Disease Research allianceEuropean Union-Next Generation EU, Mission 4, Component 2 CUP E63C22002170007K.C. Wong Education FoundationMinistero della SaluteMOE Frontier Science Center for Brain Science & Brain-Machine Integration, Zhejiang UniversityNational Key R&D Program of China 2025YFC3409700National Natural Science Foundation of China 32371204National Natural Science Foundation of China 32421001Regione Campania
6 · The paper itself

Abstract

Kv7 voltage-gated potassium channels play a critical role in controlling electrical properties of excitable tissues. Neuronally-expressed Kv7 channels are involved in both common and rare neuropsychiatric disorders, ranging from epilepsy to depression and neurodegenerative diseases; thus, they represent attractive therapeutic targets. However, no Kv7 modulator is currently available for clinical use. Improved knowledge of the functional and structural determinants responsible for ligand-induced Kv7 channel modulation is likely to fill this gap. In the present work, we describe the cryo-electron microscopy structures of human Kv7.2 channels in complex with two retigabine analogues: compound 60 (c60), which we previously described as a Kv7 activator with improved pharmacokinetic and pharmacodynamic properties, and the newly designed compound 106 (c106), which acts as a potent Kv7 blocker. Although both compounds occupy the same pocket at the S5-S6 interface in the pore domain, docking and molecular dynamics simulations and electrophysiological experiments revealed that the opposite functional behavior is due to their differential interaction, involving the L307 residue. Thus, we herein provide novel mechanistic insights into the molecular mechanisms governing Kv7 channel modulation by exogenous ligands which may prove useful to target Kv7 channels with more potent and selective modulators.

Indexed as

CarbamatesKCNQ2 Potassium ChannelPhenylenediaminesPotassium Channel BlockersCryoelectron MicroscopyHumansMolecular Docking SimulationMolecular Dynamics SimulationCarbamatesezogabineKCNQ2 Potassium ChannelPhenylenediaminesPotassium Channel BlockersCryo‐EMdrug discoveryelectrophysiologyKv7 channels modulatorsmolecular modelling

Identifiers

PMID42631357
PMCPMC13653627

What OpenQuestion holds

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Registered trials

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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.