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dc.creatorUšjak, Ljuboš
dc.creatorMilutinović, Violeta
dc.creatorĐorđić Crnogorac, Marija J.
dc.creatorStanojković, Tatjana P.
dc.creatorNiketić, Marjan S.
dc.creatorKukić-Marković, Jelena
dc.creatorPetrović, Silvana
dc.date.accessioned2021-09-15T10:51:51Z
dc.date.available2021-09-15T10:51:51Z
dc.date.issued2021
dc.identifier.issn1612-1872
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/3957
dc.description.abstractDry MeOH extracts of the twig barks of Pyrus communis subsp. pyraster, P. spinosa and their hybrid P.×jordanovii nothosubsp. velenovskyi, collected in wild in Serbia, were analyzed. By LC/MS, the contents of arbutin (99.9–131.0 mg/g), chlorogenic acid (2.2–6.3 mg/g), catechin (1.0–5.3 mg/g) and total dimeric and trimeric procyanidins (42.2–61.3 mg/g), including procyanidin B2 (8.9–17.2 mg/g), were determined. Colorimetri- cally, high contents of total phenolics (436.2–533.4 mg GAE/g) and tannins (339.4–425.7 mg GAE/g), as well as strong total antioxidant activities (FRAP values 4.5–5.9 mmol Fe2+ /g), and DPPH (SC50 = 6.6–7.1 μg/ml) and hydroxyl radical (SC50 = 447.1–727.7 μg/ml) scavenging abilities were revealed. In vitro, all extracts exhibited notable inhibition of α-amylase (IC50 = 310.8–617.7 μg/ml) and particularly strong inhibition of α-glucosidase (IC50 = 2.1–3.7 μg/ml). Molecular docking predicted that among identified compounds procyanidin B2 is the best inhibitor of these carbohydrate-digesting enzymes. Obtained results showed that the barks of investigated Pyrus hybrid and its parent taxa have similar composition and bioactivity.
dc.publisherJohn Wiley and Sons Inc
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200161/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200043/RS//
dc.rightsrestrictedAccess
dc.sourceChemistry & Biodiversity
dc.subjectThree wild Pyrus taxa
dc.subjectbark dry extracts
dc.subjectliquid chromatography
dc.subjectbiological activity
dc.subjectmolecular docking
dc.titleBarks of Three Wild Pyrus Taxa: Phenolic Constituents, Antioxidant Activity, and in Vitro and in Silico Investigations of α-Amylase and α-Glucosidase Inhibition
dc.typearticle
dc.rights.licenseARR
dcterms.abstractУшјак, Љубош; Милутиновић, Виолета; Петровић, Силвана; Ђорђић Црногорац, Марија Ј.; Станојковић, Татјана П.; Никетић, Марјан С.; Кукић‐Марковић, Јелена;
dc.citation.volume18
dc.citation.issue10
dc.citation.rankM22
dc.identifier.wos000695725700001
dc.identifier.doi10.1002/cbdv.202100446
dc.identifier.scopus2-s2.0-85114306328
dc.type.versionpublishedVersion


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