Evidence map›Paper›PMID 28752040›Full record

ArticleActa pharmaceutica Sinica. B2017

The reaction of cinnamaldehyde and cinnam(o)yl derivatives with thiols.

Alessandro Autelitano, Alberto Minassi, Alberto Pagani, Orazio Taglialatela-Scafati, Giovanni Appendino

Abstract read
In one paragraph

Article in Acta pharmaceutica Sinica. B, 2017. 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
–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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. TRPA1 Modulating CMolecules (Basel, Switzerland) · 2018
    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

5 authors.

Alessandro AutelitanoDipartimento di Scienze del Farmaco, Università del Piemonte Orientale, Largo Donegani 2, Novara 28100, Italy.
Alberto MinassiDipartimento di Scienze del Farmaco, Università del Piemonte Orientale, Largo Donegani 2, Novara 28100, Italy.
Alberto PaganiDipartimento di Scienze del Farmaco, Università del Piemonte Orientale, Largo Donegani 2, Novara 28100, Italy.
Orazio Taglialatela-ScafatiDipartimento di Farmacia, Università di Napoli Federico II, Via Montesano 49, Napoli 80131, Italy.
Giovanni AppendinoDipartimento di Scienze del Farmaco, Università del Piemonte Orientale, Largo Donegani 2, Novara 28100, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spurred by the alleged relevance of the thia-Michael reaction in the bioactivity of various classes of cinnam(o)yl natural products and by the development of a quick NMR assay to study this reaction, we have carried out a systematic study of the "native" reactivity of these compounds with dodecanethiol and cysteamine as models, respectively, of simple thiols and reactive protein thiols that can benefit from iminium ion catalysis in Michael reactions. Cinnamoyl esters and amides, as well as cinnamyl ketones and oximes, did not show any reactivity with the two probe thiols, while cinnamaldehyde (

Indexed as

ChalconesCinnmaldeydeConjugationCysteamineElectrophilesMichael addition

Identifiers

PMID28752040
PMCPMC5518654

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.