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Antidiabetic and antimicrobial flavonoids from the twigs and roots of Erythrina subumbrans (Hassk.) Merr.
Phukhatmuen, Piyaporn; Meesakul, Pornphimol; Suthiphasilp, Virayu; Charoensup, Rawiwan; Maneerat, Tharakorn; Cheenpracha, Sarot; Limtharakul, Thunwadee; Pyne, Stephen G; Laphookhieo, Surat.
Afiliação
  • Phukhatmuen P; Center of Chemical Innovation for Sustainability (CIS) and School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand.
  • Meesakul P; Center of Chemical Innovation for Sustainability (CIS) and School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand.
  • Suthiphasilp V; Center of Chemical Innovation for Sustainability (CIS) and School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand.
  • Charoensup R; School of Integrative Medicine, Mae Fah Luang University, Chiang Rai, 57100, Thailand.
  • Maneerat T; Medicinal Plant Innovation Center of Mae Fah Luang University, Chiang Rai, 57100, Thailand.
  • Cheenpracha S; Center of Chemical Innovation for Sustainability (CIS) and School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand.
  • Limtharakul T; Medicinal Plant Innovation Center of Mae Fah Luang University, Chiang Rai, 57100, Thailand.
  • Pyne SG; School of Science, University of Phayao, Phayao, 56000, Thailand.
  • Laphookhieo S; Department of Chemistry, Faculty of Science and Research Center on Chemistry for Development of Health Promoting Products from Northern Resources, Chiang Mai University, Chiang Mai, 50200, Thailand.
Heliyon ; 7(4): e06904, 2021 Apr.
Article em En | MEDLINE | ID: mdl-33997418
ABSTRACT
The phytochemical investigation of the twig and root extracts of Erythrina subumbrans (Hassk.) Merr. (Fabaceae) resulted in the isolation and identification of a new pterocarpan, erythrinocarpan (1), along with 27 known compounds (2-28). All isolated compounds were evaluated for their antidiabetic, antimicrobial, and anti-inflammatory properties. Compounds 3, 8, 9, and 22 had α-glucosidase inhibitory activity with IC50 values of 13.4 ± 0.05, 24.5 ± 0.13, 29.0 ± 0.05, and 12.8 ± 0.14 µM, respectively, while compound 2 inhibited α-amylase activity with an IC50 value of 67.6 ± 1.12 µM. Compounds 22 and 24 inhibited glycation activity with the IC50 values of 36.9 ± 0.62 and 40.5 ± 0.37 µM, respectively. From cell-based assays, compound 27 showed the highest ability to induce glucose consumption (IC50 29.1 ± 0.86 µM) and glucose uptake (2.8-fold), and to inhibit nitric oxide (NO) production (IC50 52.5 ± 0.56 µM) without cell toxicity. Furthermore, compound 9 showed antimicrobial activities against Gram-positive bacteria and fungi with MIC values ranging from 2-4 µg/mL.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article