Evidence map›Paper›PMID 35611357›Full record

ArticleDrug design, development and therapy2022

Design, Synthesis and Biological Evaluation of New 3,4-Dihydro-2(1

Jie Guo, Airen Xu, Maojun Cheng, Yang Wan, Rikang Wang, Yuanying Fang, Yi Jin, Sai-Sai Xie, Jing Liu

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. One-pot four-component sequential synthesis ofBeilstein journal of organic chemistry · 2026
    Article
  3. Article
  4. 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

9 authors at 2 institutions in 1 country.

Jie Guo *National Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, People's Republic of China.
Airen Xu *Clinical Pharmacology Research Center, The Second Hospital of Yinzhou, Ningbo, Zhejiang, People's Republic of China.
Maojun ChengNational Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, People's Republic of China.
Yang WanNational Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, People's Republic of China.
Rikang WangNational Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, People's Republic of China.
Yuanying FangNational Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, People's Republic of China.
Yi JinNational Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, People's Republic of China.
Sai-Sai XieNational Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, People's Republic of China.
Jing LiuSchool of Pharmacy, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, People's Republic of China.
Jiangxi University of Traditional Chinese Medicine · CNNingbo No. 2 Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Alzheimer's disease (AD) belongs to neurodegenerative disease, and the increasing number of AD patients has placed a heavy burden on society, which needs to be addressed urgently. ChEs/MAOs dual-target inhibitor has potential to treat AD according to reports. Purpose: To obtain effective multi-targeted agents for the treatment of AD, a novel series of hybrid compounds were designed and synthesized by fusing the pharmacophoric features of 3,4-dihydro-2 (1 Methods: All compounds were evaluated for their inhibitory abilities of ChEs and MAOs. Then, further biological activities of the most promising candidate Results: Most compounds showed potent and clear inhibition to AChE and MAOs. Among them, compound Conclusion: This work indicated that compound

Indexed as

Alzheimer DiseaseNeurodegenerative DiseasesQuinolonesAcetylcholinesteraseAmyloid beta-PeptidesAnimalsCholinesterase InhibitorsDrug DesignHumansHydroquinonesKineticsMiceMonoamine OxidaseMonoamine Oxidase InhibitorsRatsStructure-Activity Relationship3,4-dihydro-2(1H)-quinolinoneAcetylcholinesteraseAmyloid beta-PeptidesCholinesterase InhibitorsHydroquinonesMonoamine OxidaseMonoamine Oxidase InhibitorsQuinolones3,4-dihydro-2(1H)-quinolinoneAlzheimer’s diseasecholinesterasedithiocarbamatemonoamine oxidase

Identifiers

PMID35611357
PMCPMC9124477
OpenAlexW4280586080

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.