14:00 - 16:00
Room: Singapore
Lecture Session
Chair/s:
Dayar Arbain
Triple high-resolution α-glucosidase/α-amylase/PTP1B inhibition profiling combined with HPLC-HRMS-SPE-NMR for identification of anti-diabetic constituents from Morus alba L.
Zhao Yong, Kongstad Kenneth t., Jäger Anna K., Staerk Dan
Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen,, Copenhagen, Denmark

Morus alba L. is one of the most well-known and widely distributed trees of the family Moraceae, and many parts of this plant are used for anti-diabetic purposes [1]. In the present study, the crude EtOAc extract of M. alba root bark was found to possess potent inhibition of α-glucosidase, α-amylase and protein-tyrosine phosphatase 1B (PTP1B) with IC50 values of 1.70 ± 0.72, 5.16 ± 0.69 and 5.07 ± 0.68 µg/mL. The extract was subsequently investigated by triple high-resolution α-glucosidase/α-amylase/PTP1B inhibition profiling combined with HPLC-HRMS-SPE-NMR [2]. This lead to the identification of six natural Diels-Alder adducts and seven isoprenylated flavonoids as potent α-glucosidase and α-amylase inhibitors with IC50 values in the range of 0.60 ± 0.09 to 27.15 ± 7.10 µM (for α-glucosidase) and 1.22 ± 0.34 to 69.38 ± 8.58 µM (for α-amylase) respectively. These compounds were together with two 2-arylbenzofurans found to exhibit potent PTP1B inhibition with IC50 values ranging from 4.04 ± 0.38 to 21.67 ± 3.38 µM as well. This is the first report of all these compounds as α-glucosidase, α-amylase and/or PTP1B inhibitors. These findings provide the scientific rationale for developing M. alba into a polypharmacological herbal remedy.

Acknowledgements: Yong Zhao acknowledges the Chinese Scholarship Council for a scholarship. Arife Önder is thanked for technical assistance.

Keywords: α-glucosidase, α-amylase, PTP1B, HR-bioassay/ HPLC-HRMS-SPE-NMR, Morus alba L.

References:

[1] Grajek K, Wawro A, Kokocha D. Bioactivity of Morus alba L. extracts - an overview. Int J Pharm Sci Res 2015; 6: 3110-3122.

[2] Wubshet SG, Tahtah Y, Heskes AM, Kongstad KT, Pateraki I, Hamberger B, Møller BM, Staerk D. Identification of PTP1B and α-glucosidase inhibitory serrulatanes from Eremophila spp. by combined use of dual high-resolution PTP1B and α-glucosidase inhibition profiling and HPLC-HRMS-SPE-NMR. J Nat Prod 2016; 79: 1063-1072.


Reference:
Tu-Analytical Studies & Natural Products Chemistry II-SL-03:
Session:
Analytical Studies & Natural Products Chemistry II
Presenter/s:
Yong Zhao
Presentation type:
Short lecture (oral presentation)
Room:
Singapore
Chair/s:
Dayar Arbain
Date:
Tuesday, 5th September, 2017
Time:
14:30 - 14:45
Session times:
14:00 - 16:00