Talaroacids A-D and Talaromarane A, Diterpenoids with Anti-Inflammatory Activities from Mangrove Endophytic Fungus Talaromyces sp. JNQQJ-4.
Guisheng WangJianying WuZhaokun LiTao ChenYufeng LiuBo WangYan ChenZhi-Gang ShePublished in: International journal of molecular sciences (2024)
Five new diterpenes including four diterpenes with 1,2,3,4,4a,5,6,8a-octalin skeleton talaroacids A-D ( 1 - 4 ) and an isopimarane diterpenoid talaromarane A ( 5 ) were isolated from the mangrove endophytic fungus Talaromyces sp. JNQQJ-4. Their structures and absolute configurations were determined by analysis of high-resolution electrospray ionization mass spectroscopy (HRESIMS), 1D/2D Nuclear Magnetic Resonance (NMR) spectra, single-crystal X-ray diffraction, quantum chemical calculation, and electronic circular dichroism (ECD). Talaromarane A ( 5 ) contains a rare 2-oxabicyclo [3.2.1] octan moiety in isopimarane diterpenoids. In bioassays, compounds 1 , 2 , 4 , and 5 displayed significant anti-inflammatory activities with the IC 50 value from 4.59 to 21.60 μM.