Hamamelitannin’s Antioxidant Effect and Its Inhibition Capability on α-Glycosidase, Carbonic Anhydrase, Acetylcholinesterase, and Butyrylcholinesterase Enzymes

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Hamamelitannin (2′,5-di-O-galloyl-hamamelose) bears two-gallate moieties in its structure, and is a natural phenolic product in the leaves and the bark of Hamamelis virginiana. The antioxidant capacity of hamamelitannin was evaluated by a range of methods, with the following findings: the ability to reduce potassium ferric cyanide; the scavenging of N,N-dimethyl-p-phenylenediamine dihydrochloride radical (DMPD•+); the scavenging of 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulphonate) radical (ABTS•+); the scavenging of 1,1-diphenyl-2-picrylhydrazyl radical (DPPH•); and the ability to reduce cupric ions (Cu2+). Additionally, reference antioxidants of α-Tocopherol, butylated hydroxyanisole (BHA), Trolox, and butylated hydroxytoluene (BHT) were used for comparison. For DPPH radical scavenging, hamamelitannin had an IC50 value of 19.31 μg/mL, while the IC50 values for BHA, BHT, Trolox, and α-Tocopherol were 10.10, 25.95, 7.05, and 11.31 μg/mL, respectively. The study found that hamamelitannin functioned similarly to BHA, α-tocopherol, and Trolox in terms of DPPH• scavenging, but better than BHT. Additionally, as a polyphenolic secondary metabolite, the hamamelitannin inhibition capability of several metabolic enzymes was demonstrated, including acetylcholinesterase (AChE), butyrylcholinesterase (BChE), carbonic anhydrase I (CA I), carbonic anhydrase II (CA II) and α-glycosidase. The Ki values of hamamelitannin exhibited 7.40, 1.99, 10.18, 18.26, and 25.79 nM toward AChE, BChE, hCA I, hCA II, and α-glycosidase, respectively. © 2024 by the authors.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11070Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.3390/pr12112341Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorDurmaz, Lokman
dc.contributor.authorKarageçili, Hasan
dc.contributor.authorErturk, Adem
dc.contributor.authorOzden, Eda Mehtap
dc.contributor.authorTaslimi, Parham
dc.contributor.authorAlwasel, Saleh
dc.contributor.authorGülçin, İlhami
dc.date.accessioned2026-10-18T20:26:10.228180040Z
dc.date.available2026-10-18T20:26:10.228180040Z
dc.date.issued2024
dc.description.abstractHamamelitannin (2′,5-di-O-galloyl-hamamelose) bears two-gallate moieties in its structure, and is a natural phenolic product in the leaves and the bark of Hamamelis virginiana. The antioxidant capacity of hamamelitannin was evaluated by a range of methods, with the following findings: the ability to reduce potassium ferric cyanide; the scavenging of N,N-dimethyl-p-phenylenediamine dihydrochloride radical (DMPD•+); the scavenging of 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulphonate) radical (ABTS•+); the scavenging of 1,1-diphenyl-2-picrylhydrazyl radical (DPPH•); and the ability to reduce cupric ions (Cu2+). Additionally, reference antioxidants of α-Tocopherol, butylated hydroxyanisole (BHA), Trolox, and butylated hydroxytoluene (BHT) were used for comparison. For DPPH radical scavenging, hamamelitannin had an IC50 value of 19.31 μg/mL, while the IC50 values for BHA, BHT, Trolox, and α-Tocopherol were 10.10, 25.95, 7.05, and 11.31 μg/mL, respectively. The study found that hamamelitannin functioned similarly to BHA, α-tocopherol, and Trolox in terms of DPPH• scavenging, but better than BHT. Additionally, as a polyphenolic secondary metabolite, the hamamelitannin inhibition capability of several metabolic enzymes was demonstrated, including acetylcholinesterase (AChE), butyrylcholinesterase (BChE), carbonic anhydrase I (CA I), carbonic anhydrase II (CA II) and α-glycosidase. The Ki values of hamamelitannin exhibited 7.40, 1.99, 10.18, 18.26, and 25.79 nM toward AChE, BChE, hCA I, hCA II, and α-glycosidase, respectively. © 2024 by the authors.
dc.description.sponsorshiplhami Gulcin is a member Turkish Academy of Sciences (TUBA). He would liketo extend his sincere appreciation to the TUBA for their financial support. Saleh Alwasel would liketo extend his sincere appreciation to the Researchers Supporting Project (RSP-2024/59), King SaudUniversity, Saudi Arabia.
dc.identifier.doi10.3390/pr12112341
dc.identifier.eissn2227-9717
dc.identifier.issn2227-9717
dc.identifier.issue11
dc.identifier.scopus2-s2.0-85210299542
dc.identifier.startpage2341
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11070
dc.identifier.volume12
dc.identifier.wosWOS:001365898900001
dc.language.isoen
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.ispartofProcesses
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectacetylcholinesterase
dc.subjectantioxidant activity
dc.subjectbutyrylcholinesterase
dc.subjectcarbonic anhydrase
dc.subjecthamamelitannin
dc.subjectpolyphenolic compound
dc.subjectα-glycosidase
dc.subjectButylated hydroxyanisole
dc.subjectPolyphenolic compounds
dc.subjectAnhydrase
dc.subjectAntioxidant activities
dc.subjectButylated hydroxytoluene
dc.subjectGlycosidases
dc.subjectPolyphenolics
dc.subjectα-Tocopherol
dc.subjectMetabolites
dc.titleHamamelitannin’s Antioxidant Effect and Its Inhibition Capability on α-Glycosidase, Carbonic Anhydrase, Acetylcholinesterase, and Butyrylcholinesterase Enzymes
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus24
rdl.citation.wos23
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)