Isocoumarindole A, a Chlorinated Isocounnarin and Indole Alkaloid Hybrid Metabolite from an Endolichenic Fungus Aspergillus sp.

被引:58
|
作者
Chen, Minghua [1 ,2 ,3 ]
Wang, Renzhong [1 ,2 ,4 ]
Zhao, Wuli [1 ,2 ]
Yu, Liyan [1 ,2 ]
Zhang, Conghui [1 ,2 ]
Chang, Shanshan [1 ,2 ]
Li, Yan [1 ,2 ]
Zhang, Tao [1 ,2 ]
Xing, Jianguo [3 ]
Gan, Maoluo [1 ,2 ]
Feng, Feng [4 ]
Si, Shuyi [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Med Biotechnol, NHC Key Lab Microbial Drug Bioengn, Beijing 100050, Peoples R China
[2] Peking Union Med Coll, Beijing 100050, Peoples R China
[3] Inst Mat Med Xinjiang Uygur Autonomous Reg, Key Lab Uighur Med, Urumqi 830004, Peoples R China
[4] China Pharmaceut Univ, Sch Tradit Chinese Pharm, Dept Nat Med Chem, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
DERIVATIVES; DIVERSITY; LICHEN; ACIDS;
D O I
10.1021/acs.orglett.9b00385
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Isocoumarindole A (1), a novel polyketide synthetase-nonribosomal peptide synthetase (PKS-NRPS) hybrid metabolite, was isolated from the endolichenic fungus Aspergillus sp. CPCC 400810. The structure of isocoumar-indole A (1) was featured by an unprecedented skeleton containing chlorinated isocoumarin and indole diketopiperazine alkaloid moieties linked by a carbon carbon bond, which was determined by a combination of spectroscopic analyses, Marfey's method, and calculations of NMR chemical shifts, ECD spectra, and optical rotation values. Isocoumarindole A showed significant cytotoxicity and mild antifungal activities.
引用
收藏
页码:1530 / 1533
页数:4
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