Evidence map›Paper›PMID 38082105›Full record

ArticleMolecular diversity2024

A novel strategy to bind pyrimidine sulfonamide derivatives with odd even chains: exploration of their design, synthesis and biological activity evaluation.

Meng Zhou, Ying Liu, Shuo Wang, Jiankang Feng, Huiyan Ni, Chichong Lu, Guofan Jin

Abstract read
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Article in Molecular diversity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Meng ZhouSchool of Pharmacy, Jiangsu University, Zhenjiang, 212013, China.
Ying LiuSchool of Pharmacy, Jiangsu University, Zhenjiang, 212013, China.
Shuo WangSchool of Pharmacy, Jiangsu University, Zhenjiang, 212013, China.
Jiankang FengSchool of Pharmacy, Jiangsu University, Zhenjiang, 212013, China.
Huiyan NiDepartment of Pharmacy, The Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, 212013, China. jszhp20@163.com.
Chichong LuCollege of Chemistry and Materials Engineering, Beijing Technology and Business University, Beijing, 100048, China. luchichong@btbu.edu.cn.
Guofan JinSchool of Pharmacy, Jiangsu University, Zhenjiang, 212013, China. 1000004770@ujs.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Based on the hybridization strategy of dominant fragments, a series of pyrimidine sulfonamide (PS) derivatives were obtained by combining the pharmacophore fragments (sulfonamide group and pyrimidine group) with different biological activities, and evaluated as a new type of anticancer drug. The compounds were evaluated for in vitro cytotoxicity against four human cancer cell lines (HeLa, HCT-116, A-549 and HepG2) and the normal human cell line L02. Compared with the anti-cancer drug 5-fluorouracil (5-FU), the antiproliferative activity of compound PS14 was close to 5-FU and it has good antitumor activity. The IC

Indexed as

Antineoplastic AgentsDrug DesignPyrimidinesSulfonamidesApoptosisCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorHumansMolecular Docking SimulationStructure-Activity RelationshipAntineoplastic AgentsPyrimidinesSulfonamidesCytotoxicityHybridization strategyMolecular dockingPyrimidineSulfonamide

Identifiers

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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.