In this work, we evaluated the antidermatophytic activities of three resorcinol derivatives that have a history of use in dermo-cosmetic applications to discover molecules with multiple dermatological activities (i.e., multi-target drugs), thereby reducing the cost and time necessary for new drug development. The antidermatophytic activities of the three skin lighteners were evaluated relative to the known antifungal drug fluconazole on nine dermatophytes responsible for the most common dermatomycoses: , , , , , , , and . Among the three tested resorcinols, only two showed promising properties, with the ability to inhibit the growth of all tested dermatophytes; additionally, the IC values of these two resorcinols against the nine dermatophytes confirmed their good antifungal activity, particularly for phenylethyl resorcinol against . Ultrastructural alterations exhibited by the fungus were observed using scanning electron microscopy and transmission electron microscopy and reflected a dose-dependent response to treatment with the activation of defence and self-preservation strategies.
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http://dx.doi.org/10.3390/molecules21101306 | DOI Listing |
Sci Rep
December 2024
Department of Chemistry, Faculty of Science, K. N. Toosi University of Technology, P.O. Box 15875-4416, Tehran, Iran.
This research presents an innovative approach for synthesizing 2-amino-4H-chromene derivatives, utilizing 30 mg of NS-doped graphene oxide quantum dots (GOQDs) as a catalyst in a one-pot, three-component reaction conducted in ethanol. The NS-doped GOQDs were synthesized using a cost-effective bottom-up method through the condensation of citric acid (CA) with thiourea and the reaction was carried out at 185 C, resulting in the elimination of water. The catalytic performance of the synthesized NS-doped GOQDs resulted in high product yields, achieving up to 98% for the 2-amino-4H-chromene derivatives from aromatic aldehydes, malononitrile, resorcinol, -naphthol, and dimedone.
View Article and Find Full Text PDFOrg Lett
December 2024
Department of Chemistry, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Republic of Korea.
A novel protocol for the synthesis of monoprotected resorcinol -methyliminodiacetate (MIDA) boronates was developed via the chemoselective deprotection of diprotected resorcinol MIDA derivatives with identical protecting groups, utilizing the MIDA boronate moiety as a blocking group for deprotection. This protocol exhibited a broad substrate scope, and the resulting MIDA boronates were readily isolated by simple filtration from the reaction mixture. Furthermore, the utility of this protocol was demonstrated by converting the resulting MIDA boronates into value-added chemicals containing resorcinol scaffolds.
View Article and Find Full Text PDFGels
November 2024
Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100 Siena, Italy.
Environ Health
November 2024
Environmental and Occupational Health Sciences Institute, Rutgers University, 170 Frelinghuysen Road Piscataway, 08854, Piscataway, NJ, USA.
J Nat Prod
December 2024
CIIMAR - Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Matosinhos 4450-208, Portugal.
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