TY - JOUR
T1 - Dysiscalarones A-E, scalarane sesterterpenoids with nitric oxide production inhibitory activity from marine sponge Dysidea granulosa
AU - Sun, Jia-Bao
AU - Hong, Li-Li
AU - Shang, Ru-Yi
AU - Liu, Hong-Yan
AU - Zhang, Lu
AU - Liu, Li-Yun
AU - Zhao, Lu
AU - Zhang, Wei
AU - Sun, Fan
AU - Jiao, Wei-Hua
AU - Lin, Hou-Wen
PY - 2021/6
Y1 - 2021/6
N2 - Dysiscalarones A-E (1–5), five new scalarane-type bishomoscalarane sesterterpenoids, were isolated from marine sponge Dysidea granulosa collected from the South China Sea, together with two known ones, honulactone A (6) and phyllofolactone I (7). The new structures were determined by extensive spectroscopic analysis including HR-ESI-MS and 1D and 2D NMR data, and their absolute configurations were assigned by single crystal X-ray diffraction analyses. The inhibitory activity of all the seven isolates on the production of nitric oxide (NO) stimulated by lipopolysaccharide (LPS) in mouse RAW 264.7 macrophages was evaluated. Of these metabolites, dysiscalarones A-B (1–2), honulactone A (6), and phyllofolactone I (7) showed inhibitory activities with respective IC50 values of 16.4, 18.5, 2.6, and 3.7 μM, which suggested that the γ-methylated α,β-unsaturated γ-lactone might be the functional group. In addition, all the seven metabolites showed no significant cytotoxicity against lung cancer PC9 cell line at the concentration of 20 μM.
AB - Dysiscalarones A-E (1–5), five new scalarane-type bishomoscalarane sesterterpenoids, were isolated from marine sponge Dysidea granulosa collected from the South China Sea, together with two known ones, honulactone A (6) and phyllofolactone I (7). The new structures were determined by extensive spectroscopic analysis including HR-ESI-MS and 1D and 2D NMR data, and their absolute configurations were assigned by single crystal X-ray diffraction analyses. The inhibitory activity of all the seven isolates on the production of nitric oxide (NO) stimulated by lipopolysaccharide (LPS) in mouse RAW 264.7 macrophages was evaluated. Of these metabolites, dysiscalarones A-B (1–2), honulactone A (6), and phyllofolactone I (7) showed inhibitory activities with respective IC50 values of 16.4, 18.5, 2.6, and 3.7 μM, which suggested that the γ-methylated α,β-unsaturated γ-lactone might be the functional group. In addition, all the seven metabolites showed no significant cytotoxicity against lung cancer PC9 cell line at the concentration of 20 μM.
KW - Dysidea granulosa
KW - Production of nitric oxide (NO)
KW - Scalarane-type
KW - Sesterterpenoids
UR - http://www.scopus.com/inward/record.url?scp=85103958262&partnerID=8YFLogxK
U2 - 10.1016/j.bioorg.2021.104791
DO - 10.1016/j.bioorg.2021.104791
M3 - Article
C2 - 33848723
AN - SCOPUS:85103958262
VL - 111
JO - Bioorganic Chemistry
JF - Bioorganic Chemistry
SN - 0045-2068
M1 - 104791
ER -