摘要
A new oxygenated tricyclic cyclopiazonic acid(CPA)alkaloid,asperorydine Q(1),along with seven known compounds,namely,asperorydines O(2)and J(3),speradine H(4),cyclopiamides A(5)and H(6),saadamysin(7),and pyrazinemethanol(8),were isolated from the coral-associated Aspergillus flavus GXIMD 02503.The structures were elucidated by physicochemical properties and comprehensive spectroscopic data analysis.Compounds 1−5 and 7−8 exhibited potent inhibition of lipopolysaccharide(LPS)-induced nuclear factor-κB(NF-κB)with the IC50 values ranging from 6.5 to 21.8μmol L^(−1).In addition,the most potent one,pyrazinemethanol(8),dose-dependently suppressed receptor activator of NF-κB ligand(RANKL)-induced osteoclast differentiation without obvious cytotoxicity in bone marrow macrophages cells(BMMCs),suggesting it is a promising lead compound for the treatment of osteolytic diseases.
基金
supported by the Natural Science Foundation of Guangxi(No.2020GXNSFGA297002)
the Specific Research Project of Guangxi for Research Bases and Talents(No.AD20297003)
the Special Fund for Bagui Scholars of Guangxi(Y.Liu)
the National Natural Science Foundation of China(Nos.U20A20101,22007019)
the Key State Laboratory Talent Project of Guangxi Normal University(No.CMEMR 2019-A05)
the Open Project of CAS Key Laboratory of Tropical Marine Bioresources and Ecology(No.LMB20211005).