Evidence map›Paper›PMID 38362078›Full record

ArticleRSC advances2024

Synthesis, computational chemical study, antiproliferative activity screening, and molecular docking of some thiophene-based oxadiazole, triazole, and thiazolidinone derivatives.

Amna S Elgubbi, Eman A E El-Helw, Abdullah Y A Alzahrani, Sayed K Ramadan

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

14 citing papers in PubMed, 39 citations in OpenAlex.

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  2. Synthesis andRSC advances · 2026
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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

4 authors at 3 institutions in 3 countries.

Amna S ElgubbiChemistry Department, Faculty of Science, Misurata University 2478 Misurata Libya.ORCID https://orcid.org/0009-0009-0450-1447
Eman A E El-HelwChemistry Department, Faculty of Science, Ain Shams University Cairo 11566 Egypt eman.abdelrahman@sci.asu.edu.eg.ORCID https://orcid.org/0000-0001-5104-6170
Abdullah Y A AlzahraniChemistry Department, Faculty of Science and Arts, King Khalid University Mohail Assir Abha Saudi Arabia.
Sayed K RamadanChemistry Department, Faculty of Science, Ain Shams University Cairo 11566 Egypt eman.abdelrahman@sci.asu.edu.eg.ORCID https://orcid.org/0000-0003-2743-6544
Ain Shams University · EGKing Khalid University · SAMisurata University · LY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thiophene-2-carbohydrazide was used in this study to produce some thiophene-containing oxadiazole, triazole, and thiazolidinone derivatives through reactions with various carbon-centered electrophiles. Besides, the hydrazone obtained was allowed to react with mercaptoacetic acid and acetic anhydride to construct thiazolidinone and oxadiazole derivatives. The results of computational chemical study and outcomes of the experiments were in good agreement. The

Identifiers

PMID38362078
PMCPMC10867554
OpenAlexW4391852209

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.