Evidence map›Paper›PMID 35608808›Full record

ArticleMolecular diversity2023

Aryl-n-hexanamide linked enaminones of usnic acid as promising antimicrobial agents.

Pavan Kumar Bangalore, Ravi Kumar Pedapati, Abburi Naga Pranathi, Uma Rajeswari Batchu, Sunil Misra, Madhurekha Estharala, Dharmarajan Sriram, Srinivas Kantevari

Abstract read
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In one paragraph

Article in Molecular diversity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Unassuming Lichens: Nature's Hidden Antimicrobial Warriors.International journal of molecular sciences · 2025
    Review
  4. Review
  5. 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

8 authors.

Pavan Kumar BangaloreFluoro and Agrochemicals Division, CSIR- Indian Institute of Chemical Technology, Hyderabad, Telangana, 500007, India. pavanb.1488@gmail.com.ORCID http://orcid.org/0000-0001-9637-8216
Ravi Kumar Pedapati *Fluoro and Agrochemicals Division, CSIR- Indian Institute of Chemical Technology, Hyderabad, Telangana, 500007, India.
Abburi Naga Pranathi *Fluoro and Agrochemicals Division, CSIR- Indian Institute of Chemical Technology, Hyderabad, Telangana, 500007, India.
Uma Rajeswari BatchuApplied Biology Division, CSIR- Indian Institute of Chemical Technology, Hyderabad, Telangana, 500007, India.
Sunil MisraApplied Biology Division, CSIR- Indian Institute of Chemical Technology, Hyderabad, Telangana, 500007, India.
Madhurekha EstharalaMedicinal Chemistry and Antimycobacterial Research Laboratory, Pharmacy Group, Birla Institute of Technology and Science-Pilani, Hyderabad Campus, Jawahar Nagar, Hyderabad, Telangana, 500078, India.
Dharmarajan SriramMedicinal Chemistry and Antimycobacterial Research Laboratory, Pharmacy Group, Birla Institute of Technology and Science-Pilani, Hyderabad Campus, Jawahar Nagar, Hyderabad, Telangana, 500078, India.
Srinivas KantevariFluoro and Agrochemicals Division, CSIR- Indian Institute of Chemical Technology, Hyderabad, Telangana, 500007, India. kantevari@yahoo.com.

Funding

Science and Engineering Research Board EMR/2017/002946
6 · The paper itself

Abstract

Lichen secondary metabolites are well explored medicinal agents with diverse pharmacological properties. One of the important antibiotic lichen secondary metabolites is usnic acid. Its diverse medicinal profiles prompted us to explore it as a potential antitubercular molecule. Towards this direction, continuing our efforts on the discovery and development of new analogs with potent antitubercular properties we designed, synthesized, and evaluated a set of 37 usnic acid enaminone-coupled aryl-n-hexanamides (3-39). The study yielded a 3,4-dimethoxyphenyl compound (13, 5.3 µM) as the most active anti-TB molecule. The docking studies were performed on 7 different enzymes to better understand the binding modes, where it was observed that compound 13 bound strongly with glucose dehydrogenase (Gscore: - 9.03). Further antibacterial investigations revealed compound 2 with potent inhibition on Salmonella typhi and Bacillus subtilis (MIC 3 µM) and MIC values of 7 and 14 µM on Streptococcus mutans and Escherichia coli respectively. Compound 19 (3-F-5-CF

Indexed as

Anti-Infective AgentsEscherichia coliAmidesAnti-Bacterial AgentsAntitubercular AgentsBenzofuransMicrobial Sensitivity TestsMolecular Docking SimulationAmidesAnti-Bacterial AgentsAnti-Infective AgentsAntitubercular AgentsBenzofuranscaproamideusnic acidAntimicrobialAntitubercularMolecular dockingSecondary metaboliteUsnic acid

Identifiers

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Registered trials

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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.