Evidence map›Paper›PMID 36629423›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2023

Discovery of potent tubulin inhibitors targeting the colchicine binding site via structure-based lead optimization and antitumor evaluation.

Wei Liu, Youyou He, Zhongjie Guo, Miaomiao Wang, Xiaodong Han, Hairui Jia, Jin He, Shanshan Miao, Shengzheng Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2023. 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
1.8field-weighted citation impact, top 17% 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

9 authors at 2 institutions in 1 country.

Wei LiuFaculty of Pharmacy, School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an, China.
Youyou HeFaculty of Pharmacy, School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an, China.
Zhongjie GuoDepartment of Medicinal Chemistry and Pharmaceutical Analysis, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
Miaomiao WangFaculty of Pharmacy, School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an, China.
Xiaodong HanDepartment of Medicinal Chemistry and Pharmaceutical Analysis, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
Hairui JiaFaculty of Pharmacy, School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an, China.
Jin HeDepartment of Medicinal Chemistry and Pharmaceutical Analysis, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
Shanshan MiaoDepartment of Medicinal Chemistry and Pharmaceutical Analysis, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
Shengzheng WangDepartment of Medicinal Chemistry and Pharmaceutical Analysis, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
Air Force Medical University · CNShaanxi University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The colchicine binding site of tubulin is a promising target for discovering novel antitumour agents. Previously, we identified 2-aryl-4-amide-quinoline derivatives displayed moderate tubulin polymerisation inhibitory activity and broad-spectrum

Indexed as

Antineoplastic AgentsTubulin ModulatorsAnimalsBinding SitesCell Line, TumorCell ProliferationColchicineDrug Screening Assays, AntitumorHumansMolecular StructureStructure-Activity RelationshipTubulinAntineoplastic AgentsColchicineTubulinTubulin Modulatorsantitumour activitycolchicine binding sitestructural optimisationTubulin inhibitors

Identifiers

PMID36629423
PMCPMC9848350
OpenAlexW4315619469

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.