Abstract
The conditions for determining the antioxidant properties of cyclitols (D-pinitol, L-quebrachitol, myo-, L-chiro-, and D-chiro-inositol), selected flavanones (hesperetin, naringenin, eriodictyol, and liquiriti-genin) and glutathione by spectrophotometric methods—CUPRAC and with DPPH radical, and by a chromatographic method DPPH-UHPLC-UV, have been identified. Interactions of the tested compounds and their impact on the ox-red properties were investigated. The RSA (%) of the compounds tested was determined. Very low antioxidative properties of cyclitols, compared with flavanones and glutathione alone, were revealed. However, a significant increase in the determined antioxidative properties of glutathione by methyl-ether derivatives of cyclitols (D-pinitol and L-quebrachitol) was demonstrated for the first time. Thus, cyclitols seem to be a good candidate for creating drugs for the treatment of many diseases associated with reactive oxygen species (ROS) generation.
| Original language | English |
|---|---|
| Article number | 158 |
| Journal | Molecules |
| Volume | 27 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 1 Jan 2022 |
Keywords
- Antioxidant activity
- Cyclitols
- Flavonoids
- Glutathione
- Liquid chromatography
- Radical-scavenging activity
ASJC Scopus subject areas
- Analytical Chemistry
- Chemistry (miscellaneous)
- Molecular Medicine
- Pharmaceutical Science
- Drug Discovery
- Physical and Theoretical Chemistry
- Organic Chemistry
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