Inhibition of protein tyrosine phosphatase (PTP1B) and alpha-glucosidase by geranylated flavonoids from Paulownia tomentosaopen access
- Authors
- Song, Yeong Hun; Uddin, Zia; Jin, Young Min; Li, Zuopeng; Curtis-Long, Marcus John; Kim, Kwang Dong; Cho, Jung Keun; Park, Ki Hun
- Issue Date
- 2017
- Publisher
- TAYLOR & FRANCIS LTD
- Keywords
- PTP1B; alpha-glucosidase; Paulowinia tomentosa; enzyme inhibition; kinetic analysis
- Citation
- JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, v.32, no.1, pp 1195 - 1202
- Pages
- 8
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY
- Volume
- 32
- Number
- 1
- Start Page
- 1195
- End Page
- 1202
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/15033
- DOI
- 10.1080/14756366.2017.1368502
- ISSN
- 1475-6366
1475-6374
- Abstract
- Protein tyrosine phosphatase 1B (PTP1B) and alpha-glucosidase are important targets to treat obesity and diabetes, due to their deep correlation with insulin and leptin signalling, and glucose regulation. The methanol extract of Paulownia tomentosa fruits showed potent inhibition against both enzymes. Purification of this extract led to eight geranylated flavonoids (1-8) displaying dual inhibition of PTP1B and alpha-glucosidase. The isolated compounds were identified as flavanones (1-5) and dihydroflavonols (6-8). Inhibitory potencies of these compounds varied accordingly, but most of the compounds were highly effective against PTP1B (IC50 = 1.9-8.2 mu M) than alpha-glucosidase (IC50 = 2.2-78.9 mu M). Mimulone (1) was the most effective against PTP1B with IC50 = 1.9 mu M, whereas 6-geranyl-3,30,5,50,7-pentahydroxy-40-methoxyflavane (8) displayed potent inhibition against mu-glucosidase (IC50 = 2.2 mu M). All inhibitors showed mixed type I inhibition toward PTP1B, and were noncompetitive inhibitors of alpha-glucosidase. This mixed type behavior against PTP1B was fully demonstrated by showing a decrease in V-max, an increase of K-m, and K-ik/K-iv ratio ranging between 2.66 and 3.69.
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