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Bioinspired oxidation in cytochrome P450 of isomers orientin and isoorientin using Salen complexes.
Chagas, Mariane B; Pontes, Daniel O B; Albino, Allan V D; Ferreira, Emanuel J; Alves, Jovelina S F; Paiva, Anallicy S; Pontes, Daniel L; Langansser, Silvana M Z; Ferreira, Leandro S.
Afiliación
  • Chagas MB; Pharmacy Department, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59012-570, Brazil.
  • Pontes DOB; Pharmacy Department, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59012-570, Brazil.
  • Albino AVD; Pharmacy Department, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59012-570, Brazil.
  • Ferreira EJ; Pharmacy Department, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59012-570, Brazil.
  • Alves JSF; Pharmacy Department, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59012-570, Brazil.
  • Paiva AS; Institute of Chemistry, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59072-970, Brazil.
  • Pontes DL; Institute of Chemistry, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59072-970, Brazil.
  • Langansser SMZ; Pharmacy Department, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59012-570, Brazil.
  • Ferreira LS; Pharmacy Department, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, 59012-570, Brazil.
Rapid Commun Mass Spectrom ; 34 Suppl 3: e8757, 2020 Sep.
Article en En | MEDLINE | ID: mdl-32061191
ABSTRACT
RATIONALE Orientin and isoorientin are C-glycosidic flavonoids, considered as markers of some plant species such as Passiflora edulis var. flavicarpa Degener, and reported in the literature to have pharmacological properties. In order to evaluate and characterize the in vitro metabolism of these flavonoids, phase I biotransformation reactions were simulated using Salen complexes.

METHODS:

These flavonoids were oxidized separately in biomimetic reactions in different proportions, using one oxidant, m-chloroperbenzoic acid or iodosylbenzene, and one catalyst, the Jacobsen catalyst or [Mn(3-MeOSalen)Cl]. The [Mn(3-MeOSalen)Cl] catalyst was synthesized and characterized using spectrometric techniques. The oxidation potentials of the catalysts were compared. All reactions were monitored and analyzed using ultrahigh-performance liquid chromatography diode-array detection (UHPLC-DAD) and high-performance liquid chromatography/tandem mass spectrometry (HPLC/MS/MS).

RESULTS:

The analysis by UHPLC-DAD and HPLC/MS/MS showed that isoorientin produces more products than orientin and that [Mn(3-MeOSalen)Cl] produces more products than the Jacobsen catalyst. In addition, [Mn(3-MeOSalen)Cl], which has a higher oxidation potential, formed products with the addition of one or two atoms of oxygen, while the Jacobsen catalyst formed compounds with only one added oxygen atom. The products with the addition of one oxygen atom were mainly epoxides, while those with two added oxygens formed an epoxide in the C-ring and incorporated the other oxygen into the glycosidic moiety.

CONCLUSIONS:

The formation of epoxides is common in biomimetic reactions and they may represent a safety risk in medicinal products due to their high reactivity. This study may serve as a basis for subsequent pharmacological and toxicological studies that investigate the presence of these compounds as phase I metabolites, and ensure the safe use of plant products containing orientin as a chemical marker.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Flavonoides / Luteolina / Glucósidos Idioma: En Revista: Rapid Commun Mass Spectrom Año: 2020 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Flavonoides / Luteolina / Glucósidos Idioma: En Revista: Rapid Commun Mass Spectrom Año: 2020 Tipo del documento: Article País de afiliación: Brasil
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