Results 151 to 160 of about 4,187 (207)

Rapid determination of caine-based anesthetics and their metabolite residues in fish using a modified QuEChERS method coupled with UPLC-MS/MS. [PDF]

Food Chem X
Lin S, Qiu W, Hua Y, Yang Y.
europepmc   +1 more source

Optimizing Odorants for Olfactory Training Based on Olfactory Receptor-Ligand Pair Analysis. [PDF]

Laryngoscope
Nishijima H, Holbrook EH, Schwob JE, Mori E, Kagoya R, Ogawa K, Horikiri K, Kondo K.   +7 more
europepmc   +1 more source

Direct synthesis of mycophenolic acid aryl esters with antioxidant and antiproliferative properties. [PDF]

Sci Rep
Walczak J, Iwaszkiewicz-Grześ D, Śliwka-Kaszyńska M, Kurdyn A, Augustin E, Viapiana A, Plenis A, Cholewiński G.   +7 more
europepmc   +1 more source

Engineering a coenzyme-independent dioxygenase for one-step production of vanillin from ferulic acid. [PDF]

Appl Environ Microbiol
Fujimaki S, Sakamoto S, Shimada S, Kino K, Furuya T.   +4 more
europepmc   +1 more source

Synthesis of Alcoxymethyl Ethers of Isochavibetol and Isoeugenol

NIPPON KAGAKU KAISHI, 1933
openaire   +2 more sources

Unlocking the Aromatic Profile of Wild-Grown Croatian Fennel: A Comparative Study of Essential Oils and Hydrolates. [PDF]

Molecules
Vučak A, Generalić Mekinić I, Brzović P, Skroza D, Frleta Matas R, Burčul F.   +5 more
europepmc   +1 more source

Molecular Docking Studies of Ortho-Substituted Phenols to Tyrosinase Helps Discern If a Molecule Can Be an Enzyme Substrate. [PDF]

Int J Mol Sci
Montenegro MF, Teruel JA, García-Molina P, Tudela J, Rodríguez-López JN, García-Cánovas F, García-Molina F.   +6 more
europepmc   +1 more source

A one-pot organocatalytic process for the synthesis of cyclic carbonates from CO₂ and alkenes using cumene hydroperoxide as a green oxidant.

Green Chem
Scopano A, Potenza N, Berluti G, Havenith RWA, Kleij AW, Pescarmona PP.   +5 more
europepmc   +1 more source

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Metabolism of isoeugenol via isoeugenol-diol by a newly isolated strain of Bacillussubtilis HS8

Applied Microbiology and Biotechnology, 2006
A bacterium designated as HS8 was newly isolated from soil based on its ability to degrade isoeugenol. The strain was identified as Bacillus subtilis according to its 16S rDNA sequence analysis and biochemical characteristics. The metabolic pathway for the degradation of isoeugenol was examined.
Ping Xu, Shuai Han, Cuiqing Ma
exaly   +3 more sources

Chemistry of Isoeugenol and Its Oxidation Products: Mechanism and Kinetics of Isoeugenol as a Skin Sensitizer

Chemical Research in Toxicology, 2023
Structurally similar phytochemical compounds may elicit markedly different skin sensitization responses. Eugenol and isoeugenol are natural phenylpropanoids found in various essential oils are frequently used as fragrance ingredients in consumer products due to their pleasing aromatic properties. Both compounds are also skin sensitizers with isoeugenol
Jongmin Ahn, Cristina Avonto, Pankaj Pandey, Shabana I. Khan, Ikhlas A. Khan, David W. Roberts, Amar G. Chittiboyina   +6 more
openaire   +2 more sources