Evidence map›Paper›PMID 35625210›Full record

ReviewAntibiotics (Basel, Switzerland)2022

Molecular Insights into Coumarin Analogues as Antimicrobial Agents: Recent Developments in Drug Discovery.

Rameshwar S Cheke, Harun M Patel, Vaishali M Patil, Iqrar Ahmad Ansari, Jaya P Ambhore, Sachin D Shinde, Adel Kadri, Mejdi Snoussi, Mohd Adnan, Prashant S Kharkar and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Antibiotics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.1field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
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  8. Dual-Ligand Strategy in Rh-Catalyzed Sequential Hydrofunctionalization of Valylene.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  12. Discovery ofFrontiers in chemistry · 2025
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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

12 authors at 6 institutions in 5 countries.

Rameshwar S ChekeDepartment of Pharmaceutical Chemistry, Dr. Rajendra Gode College of Pharmacy, Malkapur 443101, India.ORCID 0000-0002-3111-6896
Harun M PatelDepartment of Pharmaceutical Chemistry, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur 425405, India.
Vaishali M PatilDepartment of Pharmaceutical Chemistry, KIET School of Pharmacy, KIET Groups of Institutions, Delhi-NCR, Delhi 201206, India.
Iqrar Ahmad AnsariDepartment of Pharmaceutical Chemistry, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur 425405, India.ORCID 0000-0002-7697-9572
Jaya P AmbhoreDepartment of Pharmaceutical Chemistry, Dr. Rajendra Gode College of Pharmacy, Malkapur 443101, India.
Sachin D ShindeDepartment of Pharmacology, Shri. R. D. Bhakt College of Pharmacy, Jalna 431213, India.ORCID 0000-0002-9884-269X
Adel KadriFaculty of Science of Sfax, Department of Chemistry, University of Sfax, B.P. 1171, Sfax 3000, Tunisia.
Mejdi SnoussiDepartment of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.ORCID 0000-0002-2309-2601
Mohd AdnanDepartment of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.ORCID 0000-0002-7080-6822
Prashant S KharkarDepartment of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Matunga, Mumbai 400019, India.
Visweswara Rao PasupuletiDepartment of Biomedical Sciences and Therapeutics, Faculty of Medicine & Health Sciences, University Malaysia Sabah, Kota Kinabalu 44800, Malaysia.ORCID 0000-0002-4454-3408
Prashant K DeshmukhDepartment of Pharmaceutics, Dr. Rajendra Gode College of pharmacy, Malkapur 443101, India.
Shri Vile Parle Kelavani Mandal · INInstitute of Chemical Technology · INUniversiti of Malaysia Sabah · MYUniversity of Ha'il · SAUniversity of Monastir · TNUniversity of Sfax · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major global health risk has been witnessed with the development of drug-resistant bacteria and multidrug-resistant pathogens linked to significant mortality. Coumarins are heterocyclic compounds belonging to the benzophenone class enriched in different plants. Coumarins and their derivatives have a wide range of biological activity, including antibacterial, anticoagulant, antioxidant, anti-inflammatory, antiviral, antitumour, and enzyme inhibitory effects. In the past few years, attempts have been reported towards the optimization, synthesis, and evaluation of novel coumarin analogues as antimicrobial agents. Several coumarin-based antibiotic hybrids have been developed, and the majority of them were reported to exhibit potential antibacterial effects. In the present work, studies reported from 2016 to 2020 about antimicrobial coumarin analogues are the focus. The diverse biological spectrum of coumarins can be attributed to their free radical scavenging abilities. In addition to various synthetic strategies developed, some of the structural features include a heterocyclic ring with electron-withdrawing/donating groups conjugated with the coumarin nucleus. The suggested structure-activity relationship (SAR) can provide insight into how coumarin hybrids can be rationally improved against multidrug-resistant bacteria. The present work demonstrates molecular insights for coumarin derivatives having antimicrobial properties from the recent past. The detailed SAR outcomes will benefit towards leading optimization during the discovery and development of novel antimicrobial therapeutics.

Indexed as

antibacterialcoumarin hybridscoumarinsmicrobial resistanceSAR

Identifiers

PMID35625210
PMCPMC9137837
OpenAlexW4224308379

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.