DC Field | Value | Language |
---|---|---|
dc.contributor.author | S Shrestha | - |
dc.contributor.author | J H Park | - |
dc.contributor.author | J G Cho | - |
dc.contributor.author | D Y Lee | - |
dc.contributor.author | Ji Hyun Kang | - |
dc.contributor.author | Hua Li | - |
dc.contributor.author | Tae Sook Jeong | - |
dc.contributor.author | S K Cho | - |
dc.contributor.author | D S Lee | - |
dc.contributor.author | N I Baek | - |
dc.date.accessioned | 2017-04-19T10:06:08Z | - |
dc.date.available | 2017-04-19T10:06:08Z | - |
dc.date.issued | 2015 | - |
dc.identifier.issn | 1229-2737 | - |
dc.identifier.uri | 10.3839/jabc.2015.019 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/12649 | - |
dc.description.abstract | Fruits of Rhus parviflora were extracted with 80% aqueous methanol (MeOH), and the concentrated extract was partitioned using ethyl acetate (EtOAc), n-butanol (n-BuOH), and H2O, successively. Purification of EtOAc fraction led to isolation of fifteen polyphenols of which structures were identified by spectroscopic methods including 2D-NMR. Most compounds apart from compound 10 inhibited low density lipoproteinoxidation within IC50 value of 10 μM. Among compounds, taxifolin (2), quercetin 3-O-α-L-rhamnopyranoside (13), agathisflavone (5) sulfuretin (4), and aureusidin (3) showed IC50 values 0.9, 0.8, 5.8, 2.9, and 2.4 μM which were of highly significant in comparison positive control butylated hydroxytoluene with IC50 value of 2.1 μM. The results indicate fruits of R. parviflora as a source of antihypercholesterolemic compounds. | - |
dc.publisher | Springer | - |
dc.title | Low density lipoprotein-oxidation inhibitory phytochemicals from the fruits of rhus parviflora | - |
dc.title.alternative | Low density lipoprotein-oxidation inhibitory phytochemicals from the fruits of rhus parviflora | - |
dc.type | Article | - |
dc.citation.title | Journal of Applied Biological Chemistry | - |
dc.citation.number | 2 | - |
dc.citation.endPage | 112 | - |
dc.citation.startPage | 109 | - |
dc.citation.volume | 58 | - |
dc.contributor.affiliatedAuthor | Ji Hyun Kang | - |
dc.contributor.affiliatedAuthor | Hua Li | - |
dc.contributor.affiliatedAuthor | Tae Sook Jeong | - |
dc.contributor.alternativeName | Shrestha | - |
dc.contributor.alternativeName | 박지해 | - |
dc.contributor.alternativeName | 조진경 | - |
dc.contributor.alternativeName | 이대영 | - |
dc.contributor.alternativeName | 강지현 | - |
dc.contributor.alternativeName | 이화 | - |
dc.contributor.alternativeName | 정태숙 | - |
dc.contributor.alternativeName | 조소미 | - |
dc.contributor.alternativeName | 이동선 | - |
dc.contributor.alternativeName | 백남인 | - |
dc.identifier.bibliographicCitation | Journal of Applied Biological Chemistry, vol. 58, no. 2, pp. 109-112 | - |
dc.identifier.doi | 10.3839/jabc.2015.019 | - |
dc.subject.keyword | Anacardiaceae | - |
dc.subject.keyword | Anti-hypercholesterolemic | - |
dc.subject.keyword | Aurone | - |
dc.subject.keyword | Biflavonoid | - |
dc.subject.keyword | Low density lipoprotein-oxidation | - |
dc.subject.keyword | Rhus parviflora | - |
dc.subject.local | Anacardiaceae | - |
dc.subject.local | Anti-hypercholesterolemic | - |
dc.subject.local | Aurone | - |
dc.subject.local | Biflavonoids | - |
dc.subject.local | Biflavonoid | - |
dc.subject.local | low-density lipoprotein oxidation | - |
dc.subject.local | Low-density lipoprotein-oxidation | - |
dc.subject.local | Low density lipoprotein-oxidation | - |
dc.subject.local | Low density lipoptotein (LDL) oxidation | - |
dc.subject.local | Low-density lipoprotein oxidation | - |
dc.subject.local | Low density lipoprotein oxidation | - |
dc.subject.local | Rhus parviflora | - |
dc.description.journalClass | Y | - |
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