Evidence map›Paper›PMID 25182645›Full record

ArticleAntimicrobial agents and chemotherapy2014

Nitrotriazole- and imidazole-based amides and sulfonamides as antitubercular agents.

Maria V Papadopoulou, William D Bloomer, Howard S Rosenzweig, Alexander Arena, Francisco Arrieta, Joseph C J Rebolledo, Diane K Smith

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  6. Article
  7. An insight on medicinal attributes of 1,2,4-triazoles.European journal of medicinal chemistry · 2020
    Review
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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

7 authors at 3 institutions in 1 country.

Maria V PapadopoulouNorthShore University HealthSystem, Department of Radiation Medicine, Evanston, Illinois, USA mpapadopoulou@northshore.org.
William D BloomerNorthShore University HealthSystem, Department of Radiation Medicine, Evanston, Illinois, USA.
Howard S RosenzweigOakton Community College, Des Plaines, Illinois, USA.
Alexander ArenaSan Diego State University, Department of Chemistry, San Diego, California, USA.
Francisco ArrietaSan Diego State University, Department of Chemistry, San Diego, California, USA.
Joseph C J RebolledoSan Diego State University, Department of Chemistry, San Diego, California, USA.
Diane K SmithSan Diego State University, Department of Chemistry, San Diego, California, USA.
San Diego State University · USNorthShore University HealthSystem · USOakton Community College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Twenty-three 3-nitrotriazole-based and 2-nitroimidazole-based amides and sulfonamides were screened for antitubercular (anti-TB) activity in aerobic Mycobacterium tuberculosis H37Rv by using the BacTiter-Glo (BTG) microbial cell viability assay. In general, 3-nitrotriazole-based sulfonamides demonstrated anti-TB activity, whereas 3-nitrotriazole-based amides and 2-nitroimidazole-based amides and sulfonamides were inactive. Three 3-nitrotriazole-based sulfonamides (compounds 4, 2, and 7) demonstrated 50% inhibitory concentration (IC50), IC90, and MIC values of 0.38, 0.43, and 1.56 μM (compound 4), 0.57, 0.98, and 3.13 μM (compound 2), and 0.79, 0.87, and 3.13 μM (compound 7), respectively. For 3-nitrotriazole-based sulfonamides, anti-TB activity increased with lipophilicity, whereas the one-electron reduction potential (E1/2) did not play a role. 2-Nitroimidazole-based analogs, which were inactive in the BTG assay, were significantly more active in the low-oxygen assay and more active than the 3-nitrotriazoles. All active nitrotriazoles in the BTG assay were similarly active or more potent (lower MIC values) against resistant strains, with the exception of compounds 2, 3, 4, and 8, which demonstrated greater MIC values against isoniazid-resistant strains. Five 3-nitrotriazole-based sulfonamides demonstrated activity in infected murine J774 macrophages, causing log reductions similar to those seen with rifampin. However, some compounds caused toxicity in uninfected macrophages. In conclusion, the classes of 3-nitrotriazole-based amides and sulfonamides merit further investigation as potential antitubercular agents.

Indexed as

AmidesAnimalsAntitubercular AgentsCell LineDrug Evaluation, PreclinicalDrug Resistance, BacterialImidazolesIsoniazidMacrophagesMiceMicrobial Sensitivity TestsMicrobial ViabilityMycobacterium tuberculosisNitroimidazolesSulfonamidesTuberculosis, PulmonaryAmidesAntitubercular AgentsimidazoleImidazolesIsoniazidNitroimidazolesSulfonamides

Identifiers

PMID25182645
PMCPMC4249394
OpenAlexW2079631518

What OpenQuestion holds

Textmetadata
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.