Evidence map›Paper›PMID 38931004›Full record

ReviewMolecules (Basel, Switzerland)2024

KCNT1 Channel Blockers: A Medicinal Chemistry Perspective.

Francesca Di Matteo, Francesca Mancuso, Rita Turcio, Tania Ciaglia, Claudio Stagno, Carla Di Chio, Pietro Campiglia, Alessia Bertamino, Salvatore Vincenzo Giofrè, Carmine Ostacolo and 1 more

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

11 authors.

Francesca Di MatteoDepartment of Pharmacy, University of Salerno, Via G. Paolo II, 84084 Fisciano, Italy.ORCID 0000-0002-9907-6472
Francesca MancusoDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences (CHIBIOFARAM), University of Messina, Viale F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0002-2209-957X
Rita TurcioDepartment of Pharmacy, University of Salerno, Via G. Paolo II, 84084 Fisciano, Italy.
Tania CiagliaDepartment of Pharmacy, University of Salerno, Via G. Paolo II, 84084 Fisciano, Italy.ORCID 0000-0002-6592-4373
Claudio StagnoDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences (CHIBIOFARAM), University of Messina, Viale F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0002-7994-8253
Carla Di ChioDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences (CHIBIOFARAM), University of Messina, Viale F. Stagno d'Alcontres 31, 98166 Messina, Italy.
Pietro CampigliaDepartment of Pharmacy, University of Salerno, Via G. Paolo II, 84084 Fisciano, Italy.ORCID 0000-0002-1069-2181
Alessia BertaminoDepartment of Pharmacy, University of Salerno, Via G. Paolo II, 84084 Fisciano, Italy.
Salvatore Vincenzo GiofrèDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences (CHIBIOFARAM), University of Messina, Viale F. Stagno d'Alcontres 31, 98166 Messina, Italy.
Carmine OstacoloDepartment of Pharmacy, University of Salerno, Via G. Paolo II, 84084 Fisciano, Italy.ORCID 0000-0003-3715-8680
Nunzio IraciDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences (CHIBIOFARAM), University of Messina, Viale F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0002-1359-8684

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Potassium channels have recently emerged as suitable target for the treatment of epileptic diseases. Among potassium channels, KCNT1 channels are the most widely characterized as responsible for several epileptic and developmental encephalopathies. Nevertheless, the medicinal chemistry of KCNT1 blockers is underdeveloped so far. In the present review, we describe and analyse the papers addressing the issue of KCNT1 blockers' development and identification, also evidencing the pros and the cons of the scientific approaches therein described. After a short introduction describing the epileptic diseases and the structure-function of potassium channels, we provide an extensive overview of the chemotypes described so far as KCNT1 blockers, and the scientific approaches used for their identification.

Indexed as

Chemistry, PharmaceuticalEpilepsyPotassium Channel BlockersAnimalsAnticonvulsantsHumansNerve Tissue ProteinsPotassium Channels, Sodium-ActivatedPotassium Channels, Tandem Pore DomainPotassium Channels, Voltage-GatedStructure-Activity RelationshipAnticonvulsantsKCNT1 protein, humanNerve Tissue ProteinsPotassium Channel BlockersPotassium Channels, Sodium-ActivatedPotassium Channels, Tandem Pore DomainPotassium Channels, Voltage-Gatedepileptic encephalopathiesKCNT1 blockers’ identificationKCNT1 potassium channelmedicinal chemistry campaigns

Identifiers

PMID38931004
PMCPMC11206332

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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.