Back to Search
Start Over
Phytochemical Profiling and Evaluation of Pharmacological Activities of Hypericum scabrum L.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2015 Jun 18; Vol. 20 (6), pp. 11257-71. Date of Electronic Publication: 2015 Jun 18. - Publication Year :
- 2015
-
Abstract
- Phytochemical investigations of ethyl acetate-soluble part of the aerial part of Hypericum scabrum L. delivered eight pure phenolic compounds 1-8. The pure compounds were identified through physico-chemical, NMR (1D, 2D) and mass spectrometric studies as: 3-8''-bisapigenin (1), quercetin (2), quercetin-3-O-α-l-arabinofuranoside (3), quercetin-3-O-α-l-rhamnoside (4), quercetin-3-O-β-d-glucopyranoside (5), quercetin-3-O-β-d-galactopyranoside (6), (-)-epicatechin (7), (+)-catechin (8). Total polyphenolic compounds and total flavonoids contents were determined in the extract as 0.107 mg∙mg-1 and 0.023 mg∙mg-1 of the dried extract, respectively. Antioxidant activity using DPPH free radical scavenging assay delivered very strong activity for compounds 2 and 5, 6 and crude extract 10. Protein tyrosine phosphatase 1B (PTP-1B) inhibition experiment of isolated compounds and crude extracts resulted in significant inhibition activity for samples 2, 7a, 8a, 11 and 12 with IC50 values ranging from 1.57 to 2.91 µM. Antimicrobial activity of the pure compounds and extracts produced average results against Staphylococcus aureus, Escherichia coli and Candida albicans strains. From our literature survey, it appears that all pure compounds except 2 were isolated and reported for the first time in H. scabrum.
- Subjects :
- Anti-Infective Agents chemistry
Anti-Infective Agents pharmacology
Antioxidants chemistry
Antioxidants pharmacology
Magnetic Resonance Spectroscopy
Mass Spectrometry
Protein Tyrosine Phosphatase, Non-Receptor Type 1 antagonists & inhibitors
Hypericum chemistry
Phytochemicals chemistry
Phytochemicals pharmacology
Plant Extracts chemistry
Plant Extracts pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 20
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 26096433
- Full Text :
- https://doi.org/10.3390/molecules200611257