Evidence map›Paper›PMID 19462241›Full record

ArticlePlant foods for human nutrition (Dordrecht, Netherlands)2009

New synthetic glucosyl-curcuminoids, and their (1)H and (13)C NMR characterization, from Curcuma longa L.

Monica Saladini, Sandra Lazzari, Francesca Pignedoli, Roberto Rosa, Ferdinando Spagnolo, Erika Ferrari

Abstract read
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Article in Plant foods for human nutrition (Dordrecht, Netherlands), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

6 authors.

Monica SaladiniDepartment of Chemistry, University of Modena and Reggio Emilia, Modena, Italy.
Sandra Lazzari
Francesca Pignedoli
Roberto Rosa
Ferdinando Spagnolo
Erika Ferrari

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Turmeric extracts, among which curcumin and bis-demethoxycurcumin, are by far known for their therapeutic activities. In this study we propose easy and low cost synthetic pathways in order to obtain glucosyl-curcuminoids, safe and water soluble potential drugs and dyes, which may be implied in different fields ranging from pharmacology to food chemistry. The complete (1)H and (13)C NMR characterization of naturally occurring curcumin, bis-demethoxycurcumin and new synthetic glucosyl-curcuminoids is reported.

Indexed as

AntioxidantsCurcumaCurcuminDiarylheptanoidsMagnetic Resonance SpectroscopyPlant Extracts1,7-bis(4-hydroxyphenyl)-1,6-heptadiene-3,5-dioneAntioxidantsCurcuminDiarylheptanoidsPlant Extractsturmeric extract

Identifiers

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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.