Evidence map›Paper›PMID 40895728›Full record

ArticleRSC advances2025

Design, synthesis, and

A Niranjana Kumar, G Soumya, V Kanchana, Kavita Singh, Nidhi Maurya, Sourabh Kumar, Akanksha Singh, J Kotesh Kumar, K V N S Srinivas, Debabrata Chanda and 4 more

Abstract read
In one paragraph

Article in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

14 authors.

A Niranjana KumarPhytochemistry Division, CSIR-Central Institute of Medicinal and Aromatic Plants, Research Centre Boduppal Hyderabad-500092 India koteshkumarj@cimap.res.in kvn.satyasrinivas@cimap.res.in +91-40-27202602.
G SoumyaCentre for Pharmaceutical Sciences, JNTU College of Engineering Science and Technology, Jawaharlal Nehru Technological University Hyderabad-500 085 India.
V KanchanaDepartment of Applied Biology, CSIR-Indian Institute of Chemical Technology Hyderabad-500 007 India.
Kavita SinghIn-vivo Testing Facility, Bio-Prospection and Product Development, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow-226 015 India.
Nidhi MauryaBio-Prospection and Product Development Division, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow-226 015 India.
Sourabh KumarIn-vivo Testing Facility, Bio-Prospection and Product Development, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow-226 015 India.
Akanksha SinghBio-Prospection and Product Development Division, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow-226 015 India.
J Kotesh KumarPhytochemistry Division, CSIR-Central Institute of Medicinal and Aromatic Plants, Research Centre Boduppal Hyderabad-500092 India koteshkumarj@cimap.res.in kvn.satyasrinivas@cimap.res.in +91-40-27202602.ORCID https://orcid.org/0000-0001-8294-2234
K V N S SrinivasPhytochemistry Division, CSIR-Central Institute of Medicinal and Aromatic Plants, Research Centre Boduppal Hyderabad-500092 India koteshkumarj@cimap.res.in kvn.satyasrinivas@cimap.res.in +91-40-27202602.
Debabrata ChandaIn-vivo Testing Facility, Bio-Prospection and Product Development, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow-226 015 India.
Suaib LuqmanBio-Prospection and Product Development Division, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow-226 015 India.
Sunil MisraDepartment of Applied Biology, CSIR-Indian Institute of Chemical Technology Hyderabad-500 007 India.
Abha MeenaBio-Prospection and Product Development Division, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow-226 015 India.
B BalakishanNMR Division, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow-226 015 India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cinnamaldehyde is a natural compound known for its antimicrobial and anticancer properties. Fourteen novel cinnamaldehyde-chalcone analogues (5a-5n) were synthesized and evaluated for anti-cancer, anti-bacterial, and anti-fungal activities. Among these, bromoethane chalcone 5n exhibited significant cytotoxicity against DU145 (IC50: 8.719 ± 1.8 μM), SKBR-3 (IC50: 7.689 μM), and HEPG2 (IC50: 9.380 ± 1.6 μM) cell lines, surpassing other derivatives. Compounds para methyl benzyl chalcone 5j and 2,3-dichloro benzyl chalcone 5b also demonstrated notable activity against SKBR-3 (IC50 7.871 μM) and HEPG2 (IC50 9.190 μM) cell lines. Erythrocyte osmotic fragility (EOF) analysis showed higher erythrocyte fragility for 5n (MEF

Identifiers

PMID40895728
PMCPMC12394810

What OpenQuestion holds

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LicenceCC BY-NC
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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.