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Morusacerane: A new gammacerane triterpenoid from the trunk of Morus Alba linn. with α-glucosidase inhibitory activity.
Phan, Hoang-Vinh-Truong; Nguyen, Duy Vu; Le, Thi-Kim-Dung; Nguyen, Thi-Anh-Minh; Dong, Phan-Si-Nguyen; Tran, Thanh-Nha; Dao, Ngoc-Van-Trang; Nguyen, Hieu Cuong; Luu, Hong Truong; Chavasiri, Warinthorn; Hoang, Le-Thuy-Thuy-Trang; Nguyen, Van-Kieu.
Afiliación
  • Phan HV; Institute of Fundamental and Applied Sciences, Duy Tan University, Ho Chi Minh City, Vietnam.
  • Nguyen DV; Faculty of Natural Sciences, Duy Tan University, Da Nang, Vietnam.
  • Le TK; Center of Excellence in Natural Products Chemistry, Department of Chemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok, Thailand.
  • Nguyen TA; Laboratory of Biophysics, Institute for Advanced Study in Technology, Ton Duc Thang University, Ho Chi Minh City, Vietnam.
  • Dong PS; Faculty of Pharmacy, Ton Duc Thang University, Ho Chi Minh City, Vietnam.
  • Tran TN; Institute of Research and Development, Duy Tan University, Da Nang, Vietnam.
  • Dao NV; School of Engineering & Technology, Duy Tan University, Da Nang, Vietnam.
  • Nguyen HC; Institute of Fundamental and Applied Sciences, Duy Tan University, Ho Chi Minh City, Vietnam.
  • Luu HT; Faculty of Natural Sciences, Duy Tan University, Da Nang, Vietnam.
  • Chavasiri W; Department of Environmental Engineering, Thu Dau Mot University, Binh Duong, Vietnam.
  • Hoang LT; Institute of Research and Development, Duy Tan University, Da Nang, Vietnam.
  • Nguyen VK; School of Engineering & Technology, Duy Tan University, Da Nang, Vietnam.
Nat Prod Res ; : 1-10, 2024 Apr 11.
Article en En | MEDLINE | ID: mdl-38600840
ABSTRACT
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 α-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 µM, respectively. All of these compounds interacted well with the allosteric site enzyme α-glucosidase MAL32 through H-bonds and hydrophobic interaction.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Nat Prod Res Año: 2024 Tipo del documento: Article País de afiliación: Vietnam

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Nat Prod Res Año: 2024 Tipo del documento: Article País de afiliación: Vietnam