Evidence map›Paper›PMID 38998962›Full record

ArticleMolecules (Basel, Switzerland)2024

Synthesis, Anticancer Activity, and Molecular Docking of New 1,2,3-Triazole Linked Tetrahydrocurcumin Derivatives.

Meitao Duan, Ahmed Mahal, Anas Alkouri, Chen Wang, Zhiqiang Zhang, Jungang Ren, Ahmad J Obaidullah

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

7 authors.

Meitao DuanSchool of Pharmacy, Xiamen Medical College, Xiamen 361023, China.
Ahmed MahalDepartment of Medical Biochemical Analysis, College of Health Technology, Cihan University-Erbil, Erbil 44001, Kurdisan Region, Iraq.ORCID 0000-0002-6977-3752
Anas AlkouriCollege of Pharmacy, Cihan University-Erbil, Erbil 44001, Kurdisan Region, Iraq.
Chen WangSchool of Pharmacy, Xiamen Medical College, Xiamen 361023, China.
Zhiqiang ZhangSchool of Pharmacy, Xiamen Medical College, Xiamen 361023, China.
Jungang RenSchool of Pharmacy, Xiamen Medical College, Xiamen 361023, China.
Ahmad J ObaidullahDepartment of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-7532-6318

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is one of the deadliest diseases to humanity. There is significant progress in treating this disease, but developing some drugs that can fight this disease remains a challenge in the field of medical research. Thirteen new 1,2,3-triazole linked tetrahydrocurcumin derivatives were synthesized by click reaction, including a 1,3-dipolar cycloaddition reaction of tetrahydrocurcumin baring mono-alkyne with azides in good yields, and their in vitro anticancer activity against four cancer cell lines, including human cervical carcinoma (HeLa), human lung adenocarcinoma (A549), human hepatoma carcinoma (HepG2), and human colon carcinoma (HCT-116) were investigated using MTT(3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyltetraz-olium bromide) assay. The newly synthesized compounds had their structures identified using NMR HRMS and IR techniques. Some of prepared compounds, including compounds

Indexed as

Antineoplastic AgentsCurcuminMolecular Docking SimulationTriazolesA549 CellsCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorHCT116 CellsHep G2 CellsHumansMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsCurcumintetrahydrocurcuminTriazolesanticancerclick reactiondrug discoverytetrahydrocurcumintriazole

Identifiers

PMID38998962
PMCPMC11243220

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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.