Evidence map›Paper›PMID 29166796›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2018

Structure-activity relationship investigation of benzamide and picolinamide derivatives containing dimethylamine side chain as acetylcholinesterase inhibitors.

Xiao-Hui Gao, Lin-Bo Liu, Hao-Ran Liu, Jing-Jing Tang, Lu Kang, Hongnian Wu, Peiwu Cui, Jianye Yan

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2018. 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
1.9field-weighted citation impact, top 15% of its field
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, 27 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Xiao-Hui Gaoa Key Laboratory Breeding Base of Hu'nan Oriented Fundamental and Applied Research of Innovative Pharmaceutics, College of Pharmacy , Changsha Medical University , Changsha , China.
Lin-Bo Liub College of Chemistry and Chemical Engineering , Hu'nan University , Changsha , China.
Hao-Ran Liub College of Chemistry and Chemical Engineering , Hu'nan University , Changsha , China.
Jing-Jing Tangb College of Chemistry and Chemical Engineering , Hu'nan University , Changsha , China.
Lu Kangb College of Chemistry and Chemical Engineering , Hu'nan University , Changsha , China.
Hongnian Wuc College of Pharmacy , Hu'nan University of Chinese Medicine , Changsha , China.
Peiwu Cuic College of Pharmacy , Hu'nan University of Chinese Medicine , Changsha , China.
Jianye Yanc College of Pharmacy , Hu'nan University of Chinese Medicine , Changsha , China.
Hunan University · CNHunan University of Traditional Chinese Medicine · CNChangsha Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of benzamide and picolinamide derivatives containing dimethylamine side chain (4a-4c and 7a-7i) were synthesised and evaluated for acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activity in vitro. Structure-activity relationship investigation revealed that the substituted position of dimethylamine side chain markedly influenced the inhibitory activity and selectivity against AChE and BChE. In addition, it seemed that the bioactivity of picolinamide amide derivatives was stronger than that of benzamide derivatives. Among them, compound 7a revealed the most potent AChE inhibitory activity (IC

Indexed as

AcetylcholinesteraseAmidesAnimalsBenzamidesButyrylcholinesteraseCholinesterase InhibitorsDimethylaminesDose-Response Relationship, DrugEelsHumansModels, MolecularMolecular StructurePicolinic AcidsStructure-Activity RelationshipAcetylcholinesteraseAmidesbenzamideBenzamidesButyrylcholinesteraseCholinesterase InhibitorsdimethylamineDimethylaminespicolinamidePicolinic AcidsAlzheimer's diseasebenzamideCholinesterase inhibitorspicolinamidestructure–activity relationship

Identifiers

PMID29166796
PMCPMC6009985
OpenAlexW2769925604

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.