Evidence map›Paper›PMID 37880270›Full record

ArticleScientific reports2023

Synthesis of potent MDA-MB 231 breast cancer drug molecules from single step.

Senthilnathan Govindaraj, Kilivelu Ganesan, Mahendiran Dharmasivam, Lakshmisundaram Raman, Mohammed Mujahid Alam, Mohammed Amanullah

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Senthilnathan GovindarajPG& Research Department of Chemistry, Presidency College, Chennai, 600005, India.
Kilivelu GanesanPG& Research Department of Chemistry, Presidency College, Chennai, 600005, India. kiliveluganesan@yahoo.co.in.
Mahendiran DharmasivamCentre for Cancer Cell Biology and Drug Discovery, Griffith Institute for Drug Discovery, Griffith University, Nathan, Brisbane, QLD, 4111, Australia.
Lakshmisundaram RamanSri Ramachandra Faculty of Pharmacy, Sri Ramachandra Institute of Higher Educational and Research (DU), Porur, Chennai, 600116, India.
Mohammed Mujahid AlamDepartment of Chemistry, College of Science, King Khalid University, PO Box 9004, Abha, 61413, Kingdom of Saudi Arabia.
Mohammed AmanullahDepartment of Clinical Biochemistry, College of Medicine, King Khalid University, Abha, 61413, Kingdom of Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have prepared novel potent breast cancer drug molecules from non-toxic and inexpensive method. Column chromatography is not necessary for purification of target molecules. The value of overall atom economy, environmental factor, environmental catalyst and product mass intensity gives additional merits for this synthetic method. Synthesized flexible dimeric imidazolium bromides showed less toxicity and gives excellent anticancer response against normal mammary epithelial cells. Novel dimeric pyridinium bromides showed excellent anticancer response against tested cancer cell lines. In cell cycle, novel flexible dimeric pyridinium bromides showed significant arrest in the G2/M phase by nearly three folds, when compared with control drug. We have studied the targeting epidermal growth factor receptor for all the synthesized flexible amino substituted and methyl substituted dimeric pyridinium bromides.

Indexed as

Antineoplastic AgentsBreast NeoplasmsApoptosisBromidesCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorFemaleHumansAntineoplastic AgentsBromides

Identifiers

PMID37880270
PMCPMC10600176

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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.