Evidence map›Paper›PMID 25561913›Full record

ArticleIranian journal of pharmaceutical research : IJPR2015

Synthesis, Characterization and Antibacterial Activity of some Novel Thiosemicarbazides, 1,2,4-Triazol-3-thiols and their S-substituted Derivatives.

Mehdi Kalhor, Mahboobeh Shabani, Iraj Nikokar, Seyedeh Reyhaneh Banisaeed

Abstract read
In one paragraph

Article in Iranian journal of pharmaceutical research : IJPR, 2015. 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

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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.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Mehdi KalhorDepartment of Chemistry, Payame Noor University, Tehran , Iran .
Mahboobeh ShabaniDepartment of Chemistry, Payame Noor University, Tehran , Iran .
Iraj NikokarLaboratory of Microbiology and Immunology of Infectious Diseases, Guilan University of Medical Sciences, Guilan, Iran.
Seyedeh Reyhaneh BanisaeedLaboratory of Microbiology and Immunology of Infectious Diseases, Guilan University of Medical Sciences, Guilan, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The thiosemicarbazides 3a-c were appeared by reaction of the corresponding substituted hydrazides 1a-c with allylisothiocyanate 2. Synthesis of some novel 1,2,4-triazole-thiols 4a-c bearing a pyridyl unit using 1-(x-picolinoyl)-4-allyl-thiosemicarbazides (x = 2,3,4) in an alkaline solution, is reported. Also, the S-alkylation of triazole derivatives 5-7a-c is described. The structure of the synthesized compounds resulted from the IR, (1)H and -(13)C NMR spectroscopy and elemental analysis data. The antibacterial studies to all of the synthesized compounds against B. cereus, E. coli, P. aeroginosa, S. aureus and E. faecalis as MIC values are reported. Some of these compounds such as 7a, 4a and 3a exhibited a good to significant antibacterial activity.

Indexed as

124-Triazole-3-thiolAntibacterial activityMicroorganismsS-alkylationThiosemicarbazide

Identifiers

PMID25561913
PMCPMC4277620

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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.