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DC Field | Value | Language |
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dc.contributor.author | Yang, Jun Li | - |
dc.contributor.author | Hà, Thị Kim Quy | - |
dc.contributor.author | Oh, Won Keun | - |
dc.contributor.author | Lee, Ba Wool | - |
dc.contributor.author | Kim, Jinwoong | - |
dc.date.accessioned | 2018-09-27T00:02:03Z | - |
dc.date.available | 2018-09-27T00:02:03Z | - |
dc.date.issued | 2017 | - |
dc.identifier.uri | http://dspace.ctu.edu.vn/jspui/handle/123456789/4496 | - |
dc.description.abstract | To find PTP1B inhibitors from natural products, two new compounds (1 and 2), along with nine known compounds (3–11), were isolated from a methanol-soluble extract of Iris sanguinea seeds. The structures of compounds 1 and 2 were determined based on extensive spectroscopic data analysis including UV, IR, NMR, and MS. The IC₅₀ value of compound 5 on protein tyrosine phosphatase 1B (PTP1B) inhibitory activity is 7.30 ± 0.88 mM with a little activity compared to the IC50 values of the tested positive compound. Compound 5 significantly enhanced glucose uptake and activation of pACC, pAMPK and partially Erk1/2 signaling. These results suggest that compound 5 from Iris sanguinea seeds are utilized as both PTP1B inhibitors and regulators of glucose uptake. These beneficial effects could be applied to treat metabolic diseases such as diabetes and obesity. | vi_VN |
dc.language.iso | en | vi_VN |
dc.relation.ispartofseries | Bioorganic & Medicinal Chemistry Letters;27 .- p. 5076-5081 | - |
dc.subject | Iris sanguinea | vi_VN |
dc.subject | Triterpene | vi_VN |
dc.subject | PTP1B | vi_VN |
dc.subject | AMPK | vi_VN |
dc.subject | Glucose uptake | vi_VN |
dc.title | PTP1B inhibitors from the seeds of Iris sanguinea and their insulin mimetic activities via AMPK and ACC phosphorylation | vi_VN |
dc.type | Article | vi_VN |
Appears in Collections: | Tạp chí quốc tế |
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