Evidence map›Paper›PMID 40192831›Full record

ArticleBiotechnology letters2025

Optimization of esterification reactions of perillyl alcohol with different fatty acids catalyzed by Novozym® 435 lipase.

Gustavo Dos Santos Martins, Daniel Luiz Reis Simas, Patrick Gabry Soares, Maíra Barcellos Marini, Michelle Frazão Muzitano, Ivana Correa Ramos Leal

Abstract read
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In one paragraph

Article in Biotechnology letters, 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

6 authors.

Gustavo Dos Santos MartinsLaboratory of Natural Products and Biological Assays, Department of Natural Products and Food, Pharmacy School, Health Science Center, Federal University of Rio de Janeiro (UFRJ), University City, Rio de Janeiro, RJ, 21941-902, Brazil.
Daniel Luiz Reis SimasLaboratory of Natural Products and Biological Assays, Department of Natural Products and Food, Pharmacy School, Health Science Center, Federal University of Rio de Janeiro (UFRJ), University City, Rio de Janeiro, RJ, 21941-902, Brazil.
Patrick Gabry SoaresLaboratory of Natural Products and Biological Assays, Department of Natural Products and Food, Pharmacy School, Health Science Center, Federal University of Rio de Janeiro (UFRJ), University City, Rio de Janeiro, RJ, 21941-902, Brazil.
Maíra Barcellos MariniLaboratory of Natural Products and Biological Assays, Department of Natural Products and Food, Pharmacy School, Health Science Center, Federal University of Rio de Janeiro (UFRJ), University City, Rio de Janeiro, RJ, 21941-902, Brazil.
Michelle Frazão MuzitanoLaboratory of Bioactive Products, Institute of Pharmaceutical Sciences, Federal University of Rio de Janeiro (UFRJ), Av. Aluizio da Silva Gomes, N.° 50, Granja dos Cavaleiros, Macaé, RJ, 27930-560, Brazil.
Ivana Correa Ramos LealLaboratory of Natural Products and Biological Assays, Department of Natural Products and Food, Pharmacy School, Health Science Center, Federal University of Rio de Janeiro (UFRJ), University City, Rio de Janeiro, RJ, 21941-902, Brazil. ivanafarma@yahoo.com.br.ORCID http://orcid.org/0000-0002-6917-9323

Funding

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/201.168/2022Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26.210.097/2023Instituto Nacional de Ciência e Tecnologia da Criosfera 316542/2021-0
6 · The paper itself

Abstract

Perillyl alcohol is a monoterpene known for its potent antitumor activity. In this study, we focused on esterification reactions of perillyl alcohol catalyzed by the immobilized enzyme Novozym 435 from Pseudozyma antarctica. Initially, the reaction conditions using a molar ratio of 1:4 (2:5 mmol of monoterpene: 10 mmol of octanoic acid), 40 mg of Novozym 435, 30 °C, and 150 rpm, 10 mL of cyclohexane, resulted in conversions up to 90% by 24 h. To explore the impact of different fatty acid carbon chain lengths on conversion, we conducted reactions with fatty acids containing chain lengths with 3, 6, 8, 12, and 18 carbons, evaluating the impact of the molar ratio of monoterpene:fatty acid. The observed impacts on conversion led to the categorization of fatty acids into two groups: the first group (C

Indexed as

Fatty AcidsFungal ProteinsLipaseMonoterpenesCaprylatesEnzymes, ImmobilizedEsterificationCaprylatesEnzymes, ImmobilizedFatty AcidsFungal ProteinsLipaseMonoterpenesNovozyme 435octanoic acidBiocatalysisCCRDEsterificationMonoterpenePseudozyma antarcticaRecycle

Identifiers

PMID40192831

What OpenQuestion holds

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Registered trials

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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.