4.7 Article

BACE1 Inhibitory Meroterpenoids from Aspergillus terreus

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 81, Issue 9, Pages 1937-1945

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.7b01050

Keywords

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Funding

  1. National Natural Science Foundation of China [81502943, 31600266, 81573316, 21602068, 31670354, 31370372, 21702067]
  2. Program for Changjiang Scholars [T2016088]
  3. China Postdoctoral Science Foundation [2018M632879, 2017M610479]
  4. National Science Fund for Distinguished Young Scholars [81725021]
  5. Academic Frontier Youth Team of HUST
  6. Integrated Innovative Team for Major Human Diseases Program of Tongji Medical College (HUST)
  7. Innovative Research Groups of the National Natural Science Foundation of China [81721005]

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Sixteen 3,5-dimethylorsellinic acid-based (DMOA-based) meroterpenoids, including 10 new compounds, asperterpenes D-M (1-10), were obtained from Aspergillus terreus. The structures and absolute configurations of the new compounds were confirmed by extensive spectroscopy, single-crystal X-ray diffraction analysis, and experimental electronic circular dichroism (ECD) measurements. Compounds 2, 3, and 7 are the first 3,5-dimethylorsellinic acid-based meroterpenoids possessing a unique cis-fused A/B ring system. These new compounds were evaluated for their inhibitory activity against beta-site amyloid precursor protein-cleaving enzyme 1 (BACE1). Compounds 2, 3, and 7, the first 3,5-dimethylorsellinic acid based meroterpenoids possessing cis-fused A/B rings, exhibited significant inhibitory activities against BACE1 with IC50 values of 3.3, 5.9, and 31.7 mu M, respectively.

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