Morusacerane: A new gammacerane triterpenoid from the trunk of Morus Alba linn. with α-glucosidase inhibitory activity

被引:2
|
作者
Phan, Hoang-Vinh-Truong [1 ,2 ]
Nguyen, Duy Vu [3 ]
Le, Thi-Kim-Dung [4 ,5 ]
Nguyen, Thi-Anh-Minh [6 ,7 ]
Dong, Phan-Si-Nguyen [1 ,2 ]
Tran, Thanh-Nha [8 ]
Dao, Ngoc-Van-Trang [6 ,7 ]
Nguyen, Hieu Cuong [9 ,10 ]
Luu, Hong Truong [9 ,10 ]
Chavasiri, Warinthorn [3 ]
Hoang, Le-Thuy-Thuy-Trang [11 ,12 ]
Nguyen, Van-Kieu [1 ,2 ]
机构
[1] Duy Tan Univ, Inst Fundamental & Appl Sci, Ho Chi Minh City, Vietnam
[2] Duy Tan Univ, Fac Nat Sci, Da Nang, Vietnam
[3] Chulalongkorn Univ, Fac Sci, Ctr Excellence Nat Prod Chem, Dept Chem, Bangkok, Thailand
[4] Ton Duc Thang Univ, Inst Adv Study Technol, Lab Biophys, Ho Chi Minh City, Vietnam
[5] Ton Duc Thang Univ, Fac Pharm, Ho Chi Minh City, Vietnam
[6] Duy Tan Univ, Inst Res & Dev, Da Nang, Vietnam
[7] Duy Tan Univ, Sch Engn & Technol, Da Nang, Vietnam
[8] Thu Dau Mot Univ, Dept Environm Engn, Binh Duong, Vietnam
[9] Vietnam Acad Sci & Technol, Southern Inst Ecol, Inst Appl Mat Sci, Ho Chi Minh City, Vietnam
[10] Vietnam Acad Sci & Technol, Grad Univ Sci & Technol, Ho Chi Minh City, Vietnam
[11] Ton Duc Thang Univ, Inst Adv Study Technol, Lab Adv Mat Chem, Ho Chi Minh City, Vietnam
[12] Ton Duc Thang Univ, Fac Appl Sci, Ho Chi Minh City, Vietnam
关键词
Morus Alba L; trunk; gammacerane; triterpenoid; alpha-glucosidase inhibitory; CULTIVATED MULBERRY TREE; ROOT BARK; LEAVES; CONSTITUENTS; FLAVONOIDS; STILBENE; ACID; L; PREDICTION; GLYCOSIDES;
D O I
10.1080/14786419.2024.2340043
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This phytochemistry investigation on the trunk of Morus alba L. resulted in the isolation of three triterpenoids, including a new gammacerane triterpenoid - morusacerane (1); along with two known compounds of betulinic acid (2) and ursolic acid (3). The structure elucidation was thoroughly conducted based on 1D, 2D-NMR and HRESIMS spectra, followed by a comparison with existing literatures. The evaluation on alpha-glucosidase inhibitory exhibited the great potential of the application of these isolated compounds in diabetes treatments. The results show that morusacerane (1), betulinic acid (2), and ursolic acid (3) demonstrate the strong inhibitory with the IC50 values of 106.1, 11.12, and 7.20 mu M, respectively. All of these compounds interacted well with the allosteric site enzyme alpha-glucosidase MAL32 through H-bonds and hydrophobic interaction.
引用
收藏
页数:10
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