In a previous study, we reported ten new polyoxygenated cyathane diterpenoids, neocyathins A–J, and their anti-neuroinflammatory effects from the liquid culture of the medicinal Basidiomycete Cyathus africanus. In the present study, eight new highly polyoxygenated cyathane diterpenoids, named neocyathins K–R (1–8), were isolated from the solid culture of C. africanus cultivated on cooked rice, together with three known congeners (9–11). The structures and the absolute configurations of the new compounds were elucidated through comprehensive NMR and HRESIMS spectroscopic data, electronic circular dichroism (ECD) data, and chemical conversion. Compounds 1 and 2 represent the first reported naturally occurring compounds with 4,9-seco-cyathane carbon skeleton incorporating an unprecedented medium-sized 9/7 fused ring system, while the 3,4-seco-cyathane derivative (3) was isolated from Cyathus species for the first time. All compounds were evaluated for their neurotrophic and anti-neuroinflammatory activity. All the isolates at 1–25 μM displayed differential nerve growth factor (NGF)-induced neurite outgrowth-promoting activity in PC-12 cells, while one of the compounds, allocyathin B2 (11), inhibited NO production in lipopolysaccharide (LPS)-stimulated microglia BV-2 cells. In addition, molecular docking studies showed that compound 11 generated interactions with the inducible nitric oxide synthase (iNOS) protein.
Six new cyathane diterpenoids, cyahookerins
A–F (1–6), as well as nine
known analogues (7–15), were isolated
from the liquid culture of
the basidiomycete Cyathus hookeri. Their structures
were elucidated on the basis of extensive spectroscopic analyses (1D
and 2D NMR, HRESIMS, and ECD), and the absolute configurations of
compounds 1 and 4 were determined by single-crystal
X-ray crystallography. Compounds 1 and 2 represent the first unusual cyathane acetals featuring a dioxolane
ring. Compounds 1–6 displayed differential
nerve growth factor-induced neurite outgrowth-promoting activity in
PC-12 cells at concentrations of 10 μM. In addition, cyahookerin
B (2), cyathin E (9), cyathin B2 (12), and cyathin Q (13) showed significant
nitric oxide production inhibition in Lipopolysaccharide (LPS)-activated
BV-2 microglial cells with IC50 values of 12.0, 6.9, 10.9,
and 9.1 μM, respectively. Similar binding modes of the four
compounds were indicated by molecular-docking studies, and structure–activity
relationships are discussed.
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