Evidence map›Paper›PMID 39459284›Full record

ArticleMolecules (Basel, Switzerland)2024

New Phytol Derivatives with Increased Cosmeceutical Potential.

Gonçalo P Rosa, Ana M L Seca, Diana C G A Pinto, M Carmo Barreto

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. GC-Ms, UHPLC-MS/MSChemistry & biodiversity · 2026
    Article
  3. Article
  4. 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

4 authors.

Gonçalo P RosaLAQV-REQUIMTE, Department of Chemistry, University of Aveiro, Campus de Santiago, 3810-193 Aveiro, Portugal.ORCID 0000-0002-0706-8505
Ana M L SecaLAQV-REQUIMTE, Department of Chemistry, University of Aveiro, Campus de Santiago, 3810-193 Aveiro, Portugal.ORCID 0000-0002-7709-2375
Diana C G A PintoLAQV-REQUIMTE, Department of Chemistry, University of Aveiro, Campus de Santiago, 3810-193 Aveiro, Portugal.ORCID 0000-0003-4249-7089
M Carmo BarretoUniversity of the Azores, Faculty of Sciences and Technology, cE3c- Centre for Ecology, Evolution and Environmental Changes, Azorean Biodiversity Group, CHANGE-Global Change and Sustainability Institute, 9500-321 Ponta Delgada, Portugal .ORCID 0000-0001-5797-8913

Funding

Fundação para a Ciência e Tecnologia FCT-UIDB/00329/2020-2024Fundação para a Ciência e Tecnologia SFRH/BD/144446/2019Fundação para a Ciência e Tecnologia UIDB/50006/2020 and UIDP/50006/2020Portuguese NMR Network Infrastructure Project No. 022161
6 · The paper itself

Abstract

Natural compounds are widely incorporated into cosmetic products for many purposes. Diterpenes often function as fragrances, enhancing the sensory experience of these formulations. However, current trends in cosmetic science aim to develop multifunctional products, where compounds traditionally used for texture or fragrance also possess biological activities that contribute to the product's efficacy. In this context, this study focuses on synthesizing derivatives of phytol-a compound already presents in cosmetic formulations-to enhance its anti-aging properties. The derivatives were synthesized through esterification with substituted benzoic and cinnamic acids, known for their antioxidant and enzyme inhibition properties. Reaction yields ranged from 91.0% to 5.2%, depending on the substituents in acid derivatives. The structures of the synthesized compounds were confirmed through NMR and MS techniques. Both the natural and newly synthesized derivatives were evaluated for their cosmeceutical potential using antioxidant assays and inhibition assays for tyrosinase, elastase, collagenase, and hyaluronidase. This work presents the first report of the synthesis and cosmetic evaluation of several of these derivatives. Comparing with phytol (

Indexed as

AntioxidantsCosmeceuticalsMolecular Docking SimulationMonophenol MonooxygenasePhytolCinnamatesCollagenasesCosmeticsEnzyme InhibitorsHumansHyaluronoglucosaminidaseMolecular StructurePancreatic ElastaseStructure-Activity RelationshipAntioxidantsCinnamatesCollagenasesCosmeceuticalsCosmeticsEnzyme InhibitorsHyaluronoglucosaminidaseMonophenol MonooxygenasePancreatic ElastasePhytolanti-aging activitycosmeceutical potentialphytol derivativesstructural modificationstyrosinase inhibition

Identifiers

PMID39459284
PMCPMC11510177

What OpenQuestion holds

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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.