Evidence map›Paper›PMID 38833124›Full record

ReviewMolecular diversity2025

A survey of isatin hybrids and their biological properties.

Vanessa Asoh Shu, Donatus Bekindaka Eni, Fidele Ntie-Kang

Abstract readReview
In one paragraph

Review in Molecular diversity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
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.

Vanessa Asoh ShuCenter for Drug Discovery, Faculty of Science, University of Buea, Buea, Cameroon.
Donatus Bekindaka EniCenter for Drug Discovery, Faculty of Science, University of Buea, Buea, Cameroon. donatus.bekindaka@ubuea.cm.
Fidele Ntie-KangCenter for Drug Discovery, Faculty of Science, University of Buea, Buea, Cameroon. fidele.ntie-kang@ubuea.cm.

Funding

Gates Foundation INV-036848LifeArc 10646
6 · The paper itself

Abstract

The emergence of diverse infections worldwide, which is a serious global threat to human existence, necessitates the urgent development of novel therapeutic candidates that can combat these diseases with efficacy. Molecular hybridization has been established as an efficient technique in designing bioactive molecules capable of fighting infections. Isatin, a core nucleus of an array of compounds with diverse biological properties can be modified at different positions leading to the creation of novel drug targets, is an active area of medicinal chemistry. This review containing published articles from 2005 to 2022 highlights isatin hybrids which have been synthesized and reported in the literature alongside a discussion on their biological properties. The enriched structure-activity relationship studies discussed provides insights for the rational design of novel isatin hybrids with tailored biological properties as effective therapeutic candidates inspired by nature.

Indexed as

IsatinAnimalsHumansStructure-Activity RelationshipIsatinBiological propertiesIsatin hybridsMolecular hybridizationPharmacophoreStructure–activity relationship

Identifiers

PMID38833124
PMCPMC11909063

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.