Evidence map›Paper›PMID 28025555›Full record

ArticleMolecules (Basel, Switzerland)2016

Synthesis, Biological Evaluation, and Docking Studies of a Novel Sulfonamido-Based Gallate as Pro-Chondrogenic Agent for the Treatment of Cartilage.

Xiao Lin, Ling Chai, Buming Liu, Hailan Chen, Li Zheng, Qin Liu, Cuiwu Lin

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Special Issue: Sulfonamides.Molecules (Basel, Switzerland) · 2017
    Article
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 at 3 institutions in 1 country.

Xiao LinSchool of Chemistry and Chemical Engineering, Guangxi University, Nanning 530005, China. linxiaolegend@163.com.
Ling ChaiGuangxi Key Laboratory of Traditional Chinese Medicine Quality Standards, Guangxi Institute of Traditional Medical and Pharmaceutical Sciences, Nanning 530022, China. cicichai001@163.com.
Buming LiuGuangxi Key Laboratory of Traditional Chinese Medicine Quality Standards, Guangxi Institute of Traditional Medical and Pharmaceutical Sciences, Nanning 530022, China. liu_buming@163.com.
Hailan ChenGuangxi Key Laboratory of Traditional Chinese Medicine Quality Standards, Guangxi Institute of Traditional Medical and Pharmaceutical Sciences, Nanning 530022, China. hlchen319@163.com.
Li ZhengThe Medical and Scientific Research Center, Guangxi Medical University, Nanning 530021, China. zhengli224@163.com.
Qin LiuThe Medical and Scientific Research Center, Guangxi Medical University, Nanning 530021, China. liuqin_2001@163.com.
Cuiwu LinSchool of Chemistry and Chemical Engineering, Guangxi University, Nanning 530005, China. cuiwulin@163.com.
Guangxi University of Chinese Medicine · CNGuangxi Medical University · CNGuangxi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gallic acid (GA) and its derivatives are anti-inflammatory agents and are reported to have potent effects on Osteoarthritis (OA) treatment. Nonetheless, it is generally accepted that the therapeutic effect and biocompatibility of GA is much weaker than its esters due to the high hydrophilicity. The therapeutic effect of GA on OA could be improved if certain structural modifications were made to increase its hydrophobicity. In this study, a novel sulfonamido-based gallate was synthesized by bonding sulfonamide with GA, and its biological evaluations on OA were investigated. Results show that 5-[4-(Pyrimidin-2-ylsulfamoylphenyl)]-carbamoyl-benzene-1,2,3-triyl triacetate (HAMDC) was able to reverse the effects induced by Interleukin-1 (IL-1) stimulation, and it also had a great effect on chondro-protection via promoting cell proliferation and maintaining the phenotype of articular chondrocytes, as well as enhancing synthesis of cartilage specific markers such as aggrecan, collagen II and Sox9. Furthermore, a docking study showed that HAMDC fits into the core of the active site of a disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5), which provides an explanation for its activity and selectivity.

Indexed as

ADAMTS5 ProteinAggrecansAnimalsAnti-Inflammatory AgentsCartilage, ArticularCell ProliferationCell SurvivalChondrocytesChondrogenesisCollagen Type IIGallic AcidGene Expression RegulationGlycosaminoglycansHydrophobic and Hydrophilic InteractionsInterleukin-1betaMatrix Metalloproteinase 15-(4-(pyrimidin-2-ylsulfamoylphenyl)carbamoylbenzene-1,2,3-triyl triacetateADAMTS5 ProteinAggrecansAnti-Inflammatory AgentsCollagen Type IIGallic AcidGlycosaminoglycansInterleukin-1betaMatrix Metalloproteinase 1Matrix Metalloproteinase 3SOX9 Transcription FactorSulfonamidesTissue Inhibitor of Metalloproteinase-1gallic acidmolecular dockingpro-chondrogenic agentsulfadiazine sodium

Identifiers

PMID28025555
PMCPMC6155774
OpenAlexW2565556299

What OpenQuestion holds

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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.