Deverra tortuosa and Deverra triradiata are desert perennial shrubs growing extensively in Egypt. We aimed to assess the antioxidant, antiaging, and skin-whitening activities of the aqueous MeOH extract of their roots and flowers, as well as their phenolic content, using HPLC-MS-MS. D. triradiata contained higher phenolic content than D. tortuosa . Phenolic acids and flavonoids account for a significant portion of their extracts. All extracts demonstrated antioxidant activity and inhibited the enzymes elastase, collagenase, and tyrosinase. Compounds 3 , 13 , 14 , and 19 exhibited promising binding to the three enzymes. They displayed the highest affinity to collagenase with binding energies of − 9.1, − 9.0, − 8.4, and − 9.2 kcal mol− 1 , respectively. In conclusion, the two Deverra species are rich in polyphenols and can be used for controlling free radicals and skin aging-related disorders.

HPLC-MS/MS Phenolic Profiling, Antioxidant, Antiaging Activities, and Molecular Docking Studies for Deverra tortuosa and Deverra triradiata Roots and Flowers

Doaa, Abouelenein;Giovanni, Caprioli;Ahmed M. , Mustafa;
2026-01-01

Abstract

Deverra tortuosa and Deverra triradiata are desert perennial shrubs growing extensively in Egypt. We aimed to assess the antioxidant, antiaging, and skin-whitening activities of the aqueous MeOH extract of their roots and flowers, as well as their phenolic content, using HPLC-MS-MS. D. triradiata contained higher phenolic content than D. tortuosa . Phenolic acids and flavonoids account for a significant portion of their extracts. All extracts demonstrated antioxidant activity and inhibited the enzymes elastase, collagenase, and tyrosinase. Compounds 3 , 13 , 14 , and 19 exhibited promising binding to the three enzymes. They displayed the highest affinity to collagenase with binding energies of − 9.1, − 9.0, − 8.4, and − 9.2 kcal mol− 1 , respectively. In conclusion, the two Deverra species are rich in polyphenols and can be used for controlling free radicals and skin aging-related disorders.
2026
antioxidant activity; Deverra; HPLC; molecular docking; skin aging
262
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/499164
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