Evidence map›Paper›PMID 34830055›Full record

ArticleInternational journal of molecular sciences2021

Design, Synthesis and Evaluation of Novel Derivatives of Curcuminoids with Cytotoxicity.

Chen-Yin Chen, Jin-Cherng Lien, Chien-Yu Chen, Chin-Chuan Hung, Hui-Chang Lin

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Chen-Yin ChenSchool of Pharmacy, China Medical University, No. 100, Sec. 1, Jingmao Road, Beitun Dist., Taichung 406040, Taiwan.ORCID 0000-0001-9844-3843
Jin-Cherng LienSchool of Pharmacy, China Medical University, No. 100, Sec. 1, Jingmao Road, Beitun Dist., Taichung 406040, Taiwan.ORCID 0000-0002-1211-0245
Chien-Yu ChenSchool of Pharmacy, China Medical University, No. 100, Sec. 1, Jingmao Road, Beitun Dist., Taichung 406040, Taiwan.
Chin-Chuan HungSchool of Pharmacy, China Medical University, No. 100, Sec. 1, Jingmao Road, Beitun Dist., Taichung 406040, Taiwan.ORCID 0000-0003-1395-4834
Hui-Chang LinSchool of Pharmacy, China Medical University, No. 100, Sec. 1, Jingmao Road, Beitun Dist., Taichung 406040, Taiwan.
China Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Curcumin and curcuminoids have been discussed frequently due to their promising functional groups (such as scaffolds of α,β-unsaturated β-diketone, α,β-unsaturated ketone and β'-hydroxy-α,β-unsaturated ketone connected with aromatic rings on both sides) that play an important role in various bioactivities, including antioxidant, anti-inflammatory, anti-proliferation and anticancer activity. A series of novel curcuminoid derivatives (a total of 55 new compounds) and three reference compounds were synthesized with good yields using three-step organic synthesis. The anti-proliferative activities of curcumin derivatives were examined for six human cancer cell lines: HeLaS3, KBvin, MCF-7, HepG2, NCI-H460 and NCI-H460/MX20. Compared to the IC

Indexed as

Drug DesignAntigens, DifferentiationAntineoplastic AgentsApoptosisCell CycleCell Line, TumorCell ProliferationDiarylheptanoidsDrug Screening Assays, AntitumorGADD45 ProteinsGene ExpressionGene Expression RegulationGenes, p53HumansKetonesMolecular Docking SimulationAntigens, DifferentiationAntineoplastic AgentsDiarylheptanoidsGADD45B protein, humanGADD45 ProteinsKetonesAlnusanticancer activityapoptosiscell cyclecurcumincurcuminoidsdiarylheptanoidsflow cytometryGADD45Bgene expressionmolecular dockingp53 pathwayα,β-unsaturated β-diketone

Identifiers

PMID34830055
PMCPMC8624111
OpenAlexW3212688768

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.