Review Article
Therapeutic Potential of Punica granatum and Isolated Compounds: Evidence-Based Advances to Treat Bacterial Infections
Table 2
Chemical characterization of P. granatum extracts.
| Identification techniques | Majority compounds identified | Molecular formula | Action of the active compounds | Reference |
| HPLC | Punicalagin | C48H28O30 | Antibacterial | [30] |
| HPLC LC-MS/MS | Valoneic acid dilactone Mono galloyl-hexoside Hexahydroxydiphenoyl-hexoside coumaric acid | C21H10 | Antibacterial | [11] | C13H16O10 | C20H18O14 | C9H8O3 |
| GC-MS | 5-Hydroxymethylfurfural | C6H6O3 | Antioxidant | [34] | 4-Fluorobenzyl alcohol | C7H7FO | Antimicrobial |
| UPLC LC-MS | Punicalin Rutin p-coumaric acid (+)-Catechin (−)-Epicatechin Hesperidin | C34H22O22 | Antioxidant, antibacterial antityrosinase | [36] | C27H30O16 | C9H8O3 | C15H14O6 | C15H14O6 | C28H34O15 |
| HPLC-ESI/MS LC-MS | Gallic acid | C7H6O5 | Antibacterial Antioxidant Tyrosinase inhibition | [45] | Catechin | C15H14O6 | Epicatechin | C15H14O6 | Ellagic acid | C14H6O8 | Rutin | C27H30O16 |
| HPLC | α-Punicalagin | C48H28O30 | Antibacterial | [56] | β-Punicalagin | C48H28O30 | Gallic acid | C7H6O5 | Ellagic acid | C14H6O8 |
| HPLC | α-Punicalagin | C48H28O30 | Antimicrobial | [51] | β-Punicalagin | C48H28O30 | α-Punicalin | C34H22O22 | β-Punicalin | C34H22O22 |
|
|
GAE, gallic acid; CE, catechin; HPLC, high-performance liquid chromatography; LC-MS/MS, liquid chromatography-tandem-mass spectrometry; GC-MS, gas chromatography-mass spectrometry; UPLC, ultraperformance liquid chromatography; LC-MS, liquid chromatography mass spectrometry.
|