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Tinctoric acid A-B, two new hopan-type triterpenoids from the Vietnamese lichen, Parmotrema tinctorum (Despr. ex Nyl.) hale with α-glucosidase inhibitory activity.
Hoang, Le-Thuy-Thuy-Trang; Phan, Hoang-Vinh-Truong; Nguyen-Si, Hoai-Vu; Tran, Thanh-Nha; Vo, Thi-Phi-Giao; Le, Huong Thi Thu; Dao, Ngoc-Van-Trang; Huynh, Thi-Minh-Suong; Mai, Dinh-Tri; Dong, Phan-Si-Nguyen; Nguyen, Van-Kieu.
Afiliação
  • Hoang LT; Laboratory of Advanced Materials Chemistry, Institute for Advanced Study in Technology, Ton Duc Thang University, Ho Chi Minh City, Vietnam.
  • Phan HV; Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City, Vietnam.
  • Nguyen-Si HV; Institute of Fundamental and Applied Sciences, Duy Tan University, Ho Chi Minh City, Vietnam.
  • Tran TN; Faculty of Natural Sciences, Duy Tan University, Da Nang, Vietnam.
  • Vo TP; Institute of Fundamental and Applied Sciences, Duy Tan University, Ho Chi Minh City, Vietnam.
  • Le HTT; Faculty of Natural Sciences, Duy Tan University, Da Nang, Vietnam.
  • Dao NV; Department of Environmental Engineering, Thu Dau Mot University, Binh Duong, Vietnam.
  • Huynh TM; Department of Ecology-Evolutionary Biology, University of Science, Ho Chi Minh City, Vietnam.
  • Mai DT; Vietnam National University Ho Chi Minh City, Thu Duc City, Vietnam.
  • Dong PS; Department of Chemistry, Ho Chi Minh City University of Education, Ho Chi Minh City, Vietnam.
  • Nguyen VK; Institute of Fundamental and Applied Sciences, Duy Tan University, Ho Chi Minh City, Vietnam.
Nat Prod Res ; : 1-8, 2024 Jan 23.
Article em En | MEDLINE | ID: mdl-38258412
ABSTRACT
Two new hopan-type triterpenoids, namely tinctoric acid A-B (1-2), were isolated from the lichen Parmotrema tinctorum (Despr. ex Nyl.) Hale. Their structures were elucidated by extensive spectroscopic analyses (1D and 2D NMR). The absolute configuration at C-22 of 1 was established through DP4 probability. Compounds 1-2 were evaluated for their inhibitory activity against α-glucosidase and found to be more potent than those of positive control (acarbose, IC50 168 µM) with values IC50 74.7 and 98.2 µM, respectively. Both of these compounds interacted well with enzyme α-glucosidase MAL32 through H-bonds and hydrophobic interaction.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Prod Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Vietnã País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Prod Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Vietnã País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM