ArticleCurrent health sciences journal
Plant Growth Regulating Activity of Some N-Substituted Chloroacetylanilines.
Article in Current health sciences journal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed, 1 citations in OpenAlex.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeThe synthesis and physico-chemical characterization of six N-substituted chloroacetylanilines and testing their plant growth regulating activity. MATERIAL/
methodsThe synthesis of the six N-substituted chloroacetylanilines was accomplished by condensation of N-substituted anilines, in an acidic medium, with chloroacetylchloride. Purified compounds obtained were physico-chemical characterized by elemental analysis and spectral analysis. Five different concentrations (0.1%, 0.5%, 0.75%, 1% and 5%) of the compounds solubilized in chloroform were used to analzyed their effects on the germination and mainly on the radicular elongation of wheat caryopses, Triticum aestivum subsp. aestivum (Poaceae), Dropia variety.
resultsThe N-substituted chloroacetylanilines were solid, differently colored, with high melting temperatures and high yields. Their structure was confirmed both by elemental analysis and by the spectral methods (UV-Vis, FTIR, 1H-NMR, 13C-NMR, GC-MS).
conclusionsFor the six analyzed compounds, at five different concentrations (0.1%, 0.5%, 0.75%, 1% and 5%), the experimental data obtained by the method of linear measurement, in the Triticum assay, showed the inhibition of mean radicular elongation compared with the reference.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.