Evidence map›Paper›PMID 24300121›Full record

ArticleMolecules (Basel, Switzerland)2013

Design, synthesis, biological activities and 3D-QSAR of new N,N'-diacylhydrazines containing 2,4-dichlorophenoxy moieties.

Guo-Xiang Sun, Zhao-Hui Sun, Ming-Yan Yang, Xing-Hai Liu, Yi Ma, Yun-Yang Wei

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2013. 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
–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

4 citing papers in PubMed.

  1. Synthesis of 2-Amino-Molecules (Basel, Switzerland) · 2024
    Article
  2. Article
  3. Article
  4. 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

6 authors.

Guo-Xiang SunSchool of Chemical and Biological Engineering, Yancheng Institute of Technology, Yancheng 224051, Jiangsu, China. xhliu@zjut.edu.cn.
Zhao-Hui Sun
Ming-Yan Yang
Xing-Hai Liu
Yi Ma
Yun-Yang Wei

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of new N,N'-diacylhydrazine derivatives were designed and synthesized. Their structures were verified by 1H-NMR, MS and elemental analysis. The herbicidal activities and plant growth regulating activity of these N,N'-diacylhydrazines were evaluated. The herbicidal activity results showed that most of these N,N'-diacyl-hydrazines showed excellent in vivo activities against Echinochloa crus-galli, Digitaria sanguinalis, Brassica napus, Amaranthus retroflerus. Most of them exhibited higher herbicidal activities against dicotyledonous weeds than monocotyledonous weeds. To further investigate the structure-activity relationship, comparative molecular field analysis (CoMFA) was performed on the basis of herbicidal activity data. Both the steric and electronic field distributions of CoMFA are in good agreement in this work.

Indexed as

Quantitative Structure-Activity RelationshipCombinatorial Chemistry TechniquesHerbicidesHydrazinesInhibitory Concentration 50Mass SpectrometryModels, MolecularMolecular ConformationMolecular StructureNuclear Magnetic Resonance, BiomolecularHerbicidesHydrazines

Identifiers

PMID24300121
PMCPMC6270310

What OpenQuestion holds

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LicenceCC BY
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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.