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Comparative metabolic study of the chloroform fraction of three Cystoseira species based on UPLC/ESI/MS analysis and biological activities.
Aly, Shaza H; Elissawy, Ahmed M; El Hassab, Mahmoud A; Majrashi, Taghreed A; Hassan, Fatma E; Elkaeed, Eslam B; Eldehna, Wagdy M; Singab, Abdel Nasser B.
Afiliação
  • Aly SH; Department of Pharmacognosy, Badr University in Cairo (BUC), Badr City, Egypt.
  • Elissawy AM; Department of Pharmacognosy, Ain-Shams University, Cairo, Egypt.
  • El Hassab MA; Centre of Drug Discovery Research and Development, Ain Shams University, Cairo, Egypt.
  • Majrashi TA; Department of Medicinal Chemistry, King Salman International University (KSIU), South Sinai, Egypt.
  • Hassan FE; Department of Pharmacognosy, College of Pharmacy, King Khalid University, Asir, Saudi Arabia.
  • Elkaeed EB; Department of Physiology, General Medicine Practice Program, Batterjee Medical College, Jeddah, Saudi Arabia.
  • Eldehna WM; Medical Physiology Department, Kasr Alainy, Cairo University, Giza, Egypt.
  • Singab ANB; Department of Pharmaceutical Sciences, College of Pharmacy, AlMaarefa University, Riyadh, Saudi Arabia.
J Enzyme Inhib Med Chem ; 39(1): 2292482, 2024 Dec.
Article em En | MEDLINE | ID: mdl-38086785
ABSTRACT
This study aims to investigate the phytoconstituents of the chloroform fraction of three Cystoseira spp. namely C. myrica, C. trinodis, and C. tamariscifolia using UPLC/ESI/MS technique. The results revealed the identification of 19, 20 and 11 metabolites in C. myrica, C. trinodis, and C. tamariscifolia, respectively mainly terpenoids, flavonoids, phenolic acids and fatty acids. Also, an in vitro antioxidant study using FRAP and DPPH assays was conducted where the chloroform fraction of C. trinodis displayed the highest antioxidant activity in both assays, which would be attributed to its highest total phenolics and total flavonoids. Besides, the investigation of COX-1, α-glucosidase and α-amylase inhibitory activities were performed. Regarding C. trinodis, it showed the strongest inhibitory activity towards COX-1. Moreover, it showed potent inhibitory activity towards α-glucosidase and α-amylase enzymes. According to the molecular docking studies, the major compounds characterised showed efficient binding to the active sites of the target enzymes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Clorofórmio / Alfa-Glucosidases Idioma: En Revista: J Enzyme Inhib Med Chem / J. enzyme inhib. med. chem / Journal of enzyme inhibition & medicinal chemistry Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Clorofórmio / Alfa-Glucosidases Idioma: En Revista: J Enzyme Inhib Med Chem / J. enzyme inhib. med. chem / Journal of enzyme inhibition & medicinal chemistry Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito