Evidence map›Paper›PMID 40741052›Full record

ArticleRSC medicinal chemistry2025

Microwave-assisted synthesis of tubulin assembly inhibitors as anticancer agents by aryl ring reversal and conjunctive approach.

Domiziana Masci, Michela Puxeddu, Claudia Colla, Antonio Coluccia, Martina Santelli, Pietro Sciò, Elena Mariotto, Giampietro Viola, Ernest Hamel, Rosa Lerose and 3 more

Abstract read
In one paragraph

Article in RSC medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Domiziana MasciDepartment of Basic Biotechnological Sciences, Intensivological and Perioperative Clinics, Catholic University of the Sacred Heart Largo Francesco Vito 1 00168 Rome Italy.ORCID https://orcid.org/0000-0002-5615-5111
Michela PuxedduLaboratory affiliated with the Institute Pasteur Italy - Cenci Bolognetti Foundation, Department of Drug Chemistry and Technologies, Sapienza University of Rome Piazzale Aldo Moro 5 00185 Rome Italy romano.silvestri@uniroma1.it.
Claudia CollaLaboratory affiliated with the Institute Pasteur Italy - Cenci Bolognetti Foundation, Department of Drug Chemistry and Technologies, Sapienza University of Rome Piazzale Aldo Moro 5 00185 Rome Italy romano.silvestri@uniroma1.it.
Antonio ColucciaLaboratory affiliated with the Institute Pasteur Italy - Cenci Bolognetti Foundation, Department of Drug Chemistry and Technologies, Sapienza University of Rome Piazzale Aldo Moro 5 00185 Rome Italy romano.silvestri@uniroma1.it.
Martina SantelliDepartment of Basic Biotechnological Sciences, Intensivological and Perioperative Clinics, Catholic University of the Sacred Heart Largo Francesco Vito 1 00168 Rome Italy.
Pietro SciòLaboratory affiliated with the Institute Pasteur Italy - Cenci Bolognetti Foundation, Department of Drug Chemistry and Technologies, Sapienza University of Rome Piazzale Aldo Moro 5 00185 Rome Italy romano.silvestri@uniroma1.it.
Elena MariottoDepartment of Woman's and Child's Health, University of Padua, Hemato-oncology Lab Via Giustiniani 3 35128 Padua Italy.
Giampietro ViolaDepartment of Woman's and Child's Health, University of Padua, Hemato-oncology Lab Via Giustiniani 3 35128 Padua Italy.ORCID https://orcid.org/0000-0001-9329-165X
Ernest HamelMolecular Pharmacology Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, Frederick National Laboratory for Cancer Research, National Cancer Institute, National Institutes of Health Frederick Maryland 21702 USA.ORCID https://orcid.org/0000-0003-3648-103X
Rosa LeroseHospital Pharmacy, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB) 85028 Rionero in Vulture Italy.
Carmela MazzoccoliHospital Pharmacy, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB) 85028 Rionero in Vulture Italy.
Romano SilvestriLaboratory affiliated with the Institute Pasteur Italy - Cenci Bolognetti Foundation, Department of Drug Chemistry and Technologies, Sapienza University of Rome Piazzale Aldo Moro 5 00185 Rome Italy romano.silvestri@uniroma1.it.ORCID https://orcid.org/0000-0003-2489-0178
Giuseppe La ReginaLaboratory affiliated with the Institute Pasteur Italy - Cenci Bolognetti Foundation, Department of Drug Chemistry and Technologies, Sapienza University of Rome Piazzale Aldo Moro 5 00185 Rome Italy romano.silvestri@uniroma1.it.ORCID https://orcid.org/0000-0003-3252-1161

Funding

CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

Microwave-assisted synthesis of new pyrrole and indole derivatives as tubulin assembly inhibitors was performed with remarkably improved yields and short reaction times. In designing the new inhibitors, aryl ring reversal and conjunctive approach notions were applied. (4-(4-Methoxyphenyl)-1-(pyridin-2-yl)-1

Identifiers

PMID40741052
PMCPMC12306498

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.