This study evaluates the antioxidant, anti-inflammatory, and anticancer activities of camphor, menthol, and their equimolar combination. In silico toxicity analysis confirmed the absence of toxic effects for both compounds. Antioxidant activity, assessed by 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays, revealed a synergistic effect of the equimolar combination with half-maximal inhibitory concentration (IC) values of 10.3 µg/mL (DPPH) and 8.9 µg/mL (ABTS), surpassing the efficacy of ascorbic acid (IC = 12.4 µg/mL). Evaluation of anti-inflammatory activity showed that the combination more effectively inhibited 5-lipoxygenase (72.5% vs. 48.3% for camphor and 52.9% for menthol) and COX-1 and COX-2 cyclooxygenases (78.1% and 79.4% respectively, vs. 60.4% and 62.7% for camphor, 64.2% and 66.3% for menthol). Anticancer activity, tested on MCF-7, MDA-MB-231, and MDA-MB-436 breast cancer lines, revealed that the equimolar combination exhibited IC of 27.6, 31.2, and 36.5 µg/mL, respectively, with an IC of 52.3 µg/mL on normal cells, demonstrating remarkable selectivity for cancer cells. These results suggest that the camphor-menthol combination represents a promising therapeutic approach against pathologies associated with oxidative stress, inflammation, and carcinogenesis.
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http://dx.doi.org/10.1002/cbdv.202403098 | DOI Listing |
J Phys Chem B
March 2025
Department of Chemistry, University of Rome Sapienza, Rome 00185, Italy.
We present a structural characterization of a low-transition-temperature mixture (LTTM), consisting of thymol and carvacrol, at an equimolar ratio. Carvacrol and thymol are natural regioisomers of terpenes. When combined at an equimolar ratio, they form a liquid mixture at room temperature, with supercooling capability and glass transition at ca.
View Article and Find Full Text PDFBiophys J
February 2025
Department of Chemistry, University of Texas at Austin, 105 E 24(th) St. A5300, Austin, TX 78712, USA. Electronic address:
Interfacial hydrogen bonding partly determines membrane structure, heterogeneity, and dynamics. Given the chemical diversity of lipids, it is important to understand how composition determines lipid-lipid interactions and how those are translated to H-bond populations and dynamics. Here we investigate the role of palmitoyl sphingomyelin (PSM) in modulating lipid H-bond networks in combination with dipalmitoyl phosphatidylcholine (DPPC) using of ultrafast two-dimensional infrared (2D IR) spectroscopy and molecular dynamics (MD) simulations.
View Article and Find Full Text PDFBiochemistry
March 2025
Department of Chemistry, University of Miami, Coral Gables, Florida 33146, United States.
Huntington's disease (HD) is a fatal neurodegenerative disease characterized by the expression of huntingtin protein (htt) that has a polyglutamine (CAG; polyQ) repeat domain consisting of 36 or more glutamines (mhtt). Historically, mhtt is more broadly associated with HD severity, as are elevated metal levels observed in HD patients. The depletion of wild-type (WT) htt (fewer than 36Qs) is also recognized as a contributing factor to HD progression; however, many questions remain about the interactions of biorelevant metals with WT htt and the impact of the interactions on protein aggregation.
View Article and Find Full Text PDFTalanta
June 2025
Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, Universitätsstraße 31, Regensburg, 93053, Germany. Electronic address:
Background: Electrochemistry offers a range of powerful techniques for solving analytical problems, each with its own advantages and limitations that can significantly affect the information obtained. These variations lead to diverse requirements for newly developed methods. Applying multiple electrochemical techniques simultaneously can optimize information extraction from a sample, aiding in the selection of the best analytical approach.
View Article and Find Full Text PDFChemistryOpen
February 2025
Department of Chemistry, Supramolecular Organic and Organometallic Chemistry Centre, Faculty of Chemistry and Chemical Engineering, Babeş-Bolyai University, Cluj-Napoca, RO-400028, Romania.
A series of C,O-chelated organotin(IV) alkoxides, LPhSnOBu (4), LPhSnOMe (6), LSn(OBu) (11), and siloxides LPhSnOSiPh (3), LSn(OSiPh) (10) (L=[2-(CHO)CH]CH), was prepared by salt elimination reactions. They were obtained from the organotin(IV) iodides LPhSnI (1) or LSnI (2) upon reactions with BuOK, MeONa or PhSiONa, respectively, in dry THF or methanol. Under non-inert conditions, compounds 4 and 6 undergo combined hydrolysis and condensation to give the hexaorganodistannoxane (LPhSn)O (5).
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