Evidence map›Paper›PMID 39613919›Full record

ArticleScientific reports2024

Cellular internalization, cytotoxicity and DNA binding property of 2,3-diaminophenazine, synthesized using Jeanbandyite, a heterogeneous catalyst.

Subhadeep Sen, Subhankar Basak, Samit Pandit, Pappu Sarkar, Tae Wan Kim, Nandan Ghosh, Hye Jeong Kong, Jae Sung Ryu, Bhagat Singh, Rosni Roy and 6 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Subhadeep SenDepartment of Chemistry, Coochbehar Panchanan Barma University, Panchanan Nagar, Coochbehar, 736101, India.
Subhankar BasakDepartment of Chemistry, Coochbehar Panchanan Barma University, Panchanan Nagar, Coochbehar, 736101, India.
Samit PanditDepartment of Chemistry, Coochbehar Panchanan Barma University, Panchanan Nagar, Coochbehar, 736101, India.
Pappu SarkarDepartment of Chemistry, Coochbehar Panchanan Barma University, Panchanan Nagar, Coochbehar, 736101, India.
Tae Wan KimDepartment of Medical Life Science, Soonchunhyang University, Asan, 31538, Republic of Korea.
Nandan GhoshDepartment of Electronic Materials, Devices, and Equipment Engineering, Soonchunhyang University, Asan, 31538, Republic of Korea.
Hye Jeong KongDepartment of Medical Life Science, Soonchunhyang University, Asan, 31538, Republic of Korea.
Jae Sung RyuDepartment of Medical Life Science, Soonchunhyang University, Asan, 31538, Republic of Korea.
Bhagat SinghDepartment of Chemistry and Biochemistry, University of North Carolina, Greensboro, NC, USA.
Rosni RoyUGC-DAE Consortium for Scientific Research, Kolkata Centre, III-LB/8 Bidhannagar, Kolkata, 700106, India.
Rajib MondalUGC-DAE Consortium for Scientific Research, Kolkata Centre, III-LB/8 Bidhannagar, Kolkata, 700106, India.
Abhijit SahaUGC-DAE Consortium for Scientific Research, Kolkata Centre, III-LB/8 Bidhannagar, Kolkata, 700106, India.
Seob JeonDepartment of Obstetrics and Gynecology, College of Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, 31151, Republic of Korea.
Sumantra BhattacharyaDepartment of Chemistry, National Institute of Technology Sikkim, Barfung Block, Ravangla Sub-Division, Dist. Namchi, Sikkim, 737139, India. sumantrabhattacharya1@gmail.com.
Jungkyun ImDepartment of Chemical Engineering, Soonchunhyang University, Asan, 31538, Republic of Korea. jkim5279@sch.ac.kr.
Goutam BiswasDepartment of Chemistry, Coochbehar Panchanan Barma University, Panchanan Nagar, Coochbehar, 736101, India. goutam@cbpbu.ac.in.

Funding

National Research Foundation of Korea 2021R1F1A1062951
6 · The paper itself

Abstract

In recent years, the development of novel chemistry routes for the synthesis of organic compounds has attracted special attention. 2,3-Diaminophenazine (DAP), a derivative of Phenazine, is a large group of nitrogen-containing heterocyclic compound with diverse chemical structure and various biological activities, such as antibacterial, antimicrobial, anti-inflammatory, and anticancer activities. Phenazine is a fluorescent molecule with wide range of biological properties. Therefore, a novel chemical methodology is required for effective synthesis of this product. Numerous oxidants can easily oxidize ortho-phenylenediamine (OPD) to create luminous DAP. This article discusses a simple, sustainable, and safe way to synthesize DAP using water as a green solvent and Jeanbandyite as a catalyst. Mass spectrometry,

Indexed as

DNAMolecular Docking SimulationPhenazinesCatalysisCell Line, TumorHumansDNAPhenazinesCatalysisCellular internalizationGreen chemistryJeanbandyitePhenazine

Identifiers

PMID39613919
PMCPMC11607075

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.