Evidence map›Paper›PMID 32676156›Full record

ArticleACS medicinal chemistry letters2020

Antiglioma Activity of Aryl and Amido-Aryl Acetamidine Derivatives Targeting iNOS: Synthesis and Biological Evaluation.

Cristina Maccallini, Fabio Arias, Marialucia Gallorini, Pasquale Amoia, Alessandra Ammazzalorso, Barbara De Filippis, Marialuigia Fantacuzzi, Letizia Giampietro, Amelia Cataldi, María Encarnación Camacho and 1 more

Open access · greenAbstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 17 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

11 authors at 2 institutions in 2 countries.

Cristina MaccalliniDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
Fabio AriasDepartamento de Química Farmacéutica y Orgánica, Facultad de Farmacia, Universidad de Granada, Campus de Cartuja s/n, 18071 Granada, Spain.
Marialucia GalloriniDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
Pasquale AmoiaDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
Alessandra AmmazzalorsoDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
Barbara De FilippisDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
Marialuigia FantacuzziDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
Letizia GiampietroDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
Amelia CataldiDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
María Encarnación CamachoDepartamento de Química Farmacéutica y Orgánica, Facultad de Farmacia, Universidad de Granada, Campus de Cartuja s/n, 18071 Granada, Spain.
Rosa AmorosoDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini, 31-66100 Chieti, Italy.
University of Chieti-Pescara · ITUniversidad de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nitric oxide is an important inflammation mediator with a recognized role in the development of different cancers. Gliomas are primary tumors of the central nervous system with poor prognosis, and the expression of the inducible nitric oxide synthase correlates with the degree of malignancy, changes in vascular reactivity, and neo-angiogenesis. Therefore, targeting the nitric oxide biosynthesis appears as a potential strategy to impair glioma progression. In the present work a set of aryl and amido-aryl acetamidine derivatives were synthesized to obtain new potent and selective inducible nitric oxide synthase inhibitors with improved physicochemical parameters with respect to the previously published molecules. Compound

Identifiers

PMID32676156
PMCPMC7357225
OpenAlexW3037705960

What OpenQuestion holds

Textmetadata
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.