A new cineol derivative, polyphenols and norterpenoids from Saharan myrtle tea (Myrtus nivellei) Isolation, structure determination, quantitative determination and antioxidant activity /

Abstract The phytochemical profile of decoction and infusion, obtained from the dried leaves of M. nivellei, consumed as tea in Saharan region, was characterized by UHPLC-PDA-HRMS. Fourteen compounds were characterized and, to confirm the proposed structures a preparative procedure followed by NMR s...

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Elmentve itt :
Bibliográfiai részletek
Szerzők: Mansour Amira
Celano Rita
Mencherini Teresa
Picerno Patrizia
Piccinelli Anna Lisa
Foudil-Cherif Yazid
Csupor Dezső
Rahili Ghania
Yahi Nassima
Nabavi Seyed Mohammad
Aquino Rita Patrizia
Rastrelli Luca
Dokumentumtípus: Cikk
Megjelent: 2017
Sorozat:FITOTERAPIA 119
doi:10.1016/j.fitote.2017.03.013

mtmt:3207173
Online Access:http://publicatio.bibl.u-szeged.hu/12400
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245 1 2 |a A new cineol derivative, polyphenols and norterpenoids from Saharan myrtle tea (Myrtus nivellei)  |h [elektronikus dokumentum] :  |b Isolation, structure determination, quantitative determination and antioxidant activity /  |c  Mansour Amira 
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490 0 |a FITOTERAPIA  |v 119 
520 3 |a Abstract The phytochemical profile of decoction and infusion, obtained from the dried leaves of M. nivellei, consumed as tea in Saharan region, was characterized by UHPLC-PDA-HRMS. Fourteen compounds were characterized and, to confirm the proposed structures a preparative procedure followed by NMR spectroscopy was applied. Compound 3 (2-hydroxy-1,8-cineole disaccharide) was a never reported whereas a bycyclic monoterpenoid glucoside (2), two ionol glucosides (1 and 12), a tri-galloylquinic acid (4), two flavonol glycosides (5 and 9), and a tetra-galloylglucose (7), were reported in Myrtus spp. for the first time. Five flavonol O-glycosides (6, 8, 10–11, and 14) togheter a flavonol (13) were also identified. Quantitative determination of phenolic constituents from decoction and infusion has been performed by HPLC-UV-PDA. The phenolic content was found to be 150.5 and 102.6 mg/g in decoction and infusion corresponding to 73.8 and 23.6 mg/100 mL of a single tea cup, respectively. Myricetin 3-O-β-d-(6″-galloyl)glucopyranoside (5), isomyricitrin (6) and myricitrin (8) were the compounds present in the highest concentration. The free-radical scavenging activities of teas and isolated compounds was measured by the DPPH assay and compared with the values of other commonly used herbal teas (green and black teas). Decoction displayed higher potency in scavenging free-radicals than the infusion and green and black teas. 
700 0 1 |a Celano Rita  |e aut 
700 0 1 |a Mencherini Teresa  |e aut 
700 0 1 |a Picerno Patrizia  |e aut 
700 0 1 |a Piccinelli Anna Lisa  |e aut 
700 0 2 |a Foudil-Cherif Yazid  |e aut 
700 0 2 |a Csupor Dezső  |e aut 
700 0 2 |a Rahili Ghania  |e aut 
700 0 2 |a Yahi Nassima  |e aut 
700 0 2 |a Nabavi Seyed Mohammad  |e aut 
700 0 2 |a Aquino Rita Patrizia  |e aut 
700 0 2 |a Rastrelli Luca  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/12400/1/Proof_de_lArticle_u.pdf  |z Dokumentum-elérés  
856 4 0 |u http://publicatio.bibl.u-szeged.hu/12400/7/Fitoterapia_2017_119_tartj.pdf  |z Dokumentum-elérés