Evidence map›Paper›PMID 35974029›Full record

ArticleScientific reports2022

Development of spiro-3-indolin-2-one containing compounds of antiproliferative and anti-SARS-CoV-2 properties.

Nehmedo G Fawazy, Siva S Panda, Ahmed Mostafa, Benson M Kariuki, Mohamed S Bekheit, Yassmin Moatasim, Omnia Kutkat, Walid Fayad, May A El-Manawaty, Ahmed A F Soliman and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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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

14 authors.

Nehmedo G FawazyDepartment of Pesticide Chemistry, National Research Centre, Dokki, Giza, 12622, Egypt.
Siva S PandaDepartment of Chemistry and Physics, Augusta University, Augusta, GA, 30912, USA.
Ahmed MostafaCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, 12622, Egypt.
Benson M KariukiSchool of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3AT, UK.
Mohamed S BekheitDepartment of Pesticide Chemistry, National Research Centre, Dokki, Giza, 12622, Egypt.
Yassmin MoatasimCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, 12622, Egypt.
Omnia KutkatCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, 12622, Egypt.
Walid FayadDrug Bioassay-Cell Culture Laboratory, Pharmacognosy Department, National Research Centre, Dokki, Giza, 12622, Egypt.
May A El-ManawatyDrug Bioassay-Cell Culture Laboratory, Pharmacognosy Department, National Research Centre, Dokki, Giza, 12622, Egypt.
Ahmed A F SolimanDrug Bioassay-Cell Culture Laboratory, Pharmacognosy Department, National Research Centre, Dokki, Giza, 12622, Egypt.
Riham A El-ShiekhDepartment of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt.
Aladdin M SrourDepartment of Therapeutic Chemistry, National Research Centre, Dokki, Giza, 12622, Egypt.
Reham F BarghashDepartment of Pesticide Chemistry, National Research Centre, Dokki, Giza, 12622, Egypt.
Adel S GirgisDepartment of Pesticide Chemistry, National Research Centre, Dokki, Giza, 12622, Egypt. girgisas10@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of 1″-(alkylsulfonyl)-dispiro[indoline-3,2'-pyrrolidine-3',3″-piperidine]-2,4″-diones 6a‒o has been synthesized through regioselective multi-component azomethine dipolar cycloaddition reaction of 1-(alkylsulfonyl)-3,5-bis(ylidene)-piperidin-4-ones 3a‒h. X-ray diffraction studies (6b‒d,h) confirmed the structures. The majority of the synthesized analogs reveal promising antiproliferation properties against a variety of human cancer cell lines (MCF7, HCT116, A431 and PaCa2) with good selectivity index towards normal cell (RPE1). Some of the synthesized agents exhibit potent inhibitory properties against the tested cell lines with higher efficacies than the standard references (sunitinib and 5-fluorouracil). Compound 6m is the most potent. Multi-targeted inhibitory properties against EGFR and VEGFR-2 have been observed for the synthesized agents. Flow cytometry supports the antiproliferation properties and shows the tested agents as apoptosis and necrosis forming. Vero cell viral infection model demonstrates the anti-SARS-CoV-2 properties of the synthesized agents. Compound 6f is the most promising (about 3.3 and 4.8 times the potency of the standard references, chloroquine and hydroxychloroquine). QSAR models explain and support the observed biological properties.

Indexed as

Antineoplastic AgentsCOVID-19 Drug TreatmentSpiro CompoundsCell Line, TumorHumansIndolesMolecular StructureSARS-CoV-2Antineoplastic AgentsIndolesindolin-2-oneSpiro Compounds

Identifiers

PMID35974029
PMCPMC9380671

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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.