4.7 Article

Brasilterpenes A-E, Bergamotane Sesquiterpenoid Derivatives with Hypoglycemic Activity from the Deep Sea-Derived Fungus Paraconiothyrium brasiliense HDN15-135

Journal

MARINE DRUGS
Volume 20, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/md20050338

Keywords

marine-derived fungus; ascomycete fungus Paraconiothyrium brasiliense; bergamotane sesquiterpenoids; hypoglycemic activity

Funding

  1. Major national science and technology projects of the Ministry of science and technology [81991522]
  2. Key Laboratory of Marine Biotechnology of Fujian Province [2021MB02]
  3. National Science and Technology Major Project for Significant New Drugs Development [2018ZX09735004]
  4. Major Basic Research Programs of Natural Science Foundation of Shandong Province [ZR2019ZD18, ZR2021ZD28]
  5. Taishan Scholar Youth Expert Program in Shandong Province [tsqn201812021]
  6. Pilot National Laboratory for Marine Science and Technology [LMDBKF201805]
  7. Fundamental Research Funds for the Central Universities [201941001, 2019KJM004, 202172002]

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Five bergamotane sesquiterpenoid derivatives were isolated from a deep sea-derived fungus, and their hypoglycemic activity was evaluated. Brasilterpene C showed promising potential for the treatment of diabetes, and other compounds also exhibited hypoglycemic activity.
Five bergamotane sesquiterpenoid derivatives, brasilterpenes A-E (1-5), bearing an unreported spiral 6/4/5 tricyclic ring system, were isolated from the deep sea-derived ascomycete fungus Paraconiothyrium brasiliense HDN15-135. Their structures, including absolute configurations, were established by extensive spectroscopic methods complemented by single-crystal X-ray diffraction analyses, electronic circular dichroism (ECD), and density-functional theory (DFT) calculations of nuclear magnetic resonance (NMR) data including DP4+ analysis. The hypoglycemic activity of these compounds was assessed using a diabetic zebrafish model. Brasilterpenes A (1) and C (3) significantly reduced free blood glucose in hyperglycemic zebrafish in vivo by improving insulin sensitivity and suppressing gluconeogenesis. Moreover, the hypoglycemic activity of compound 3 was comparable to the positive control, anti-diabetes drug rosiglitazone. These results suggested brasilterpene C (3) had promising anti-diabetes potential.

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