Penithoketone and Penithochromones A-L, Polyketides from the Deep-Sea-Derived Fungus Penicillium thomii YPGA3

被引:27
作者
Li, Qin [1 ]
Xu, Wei [2 ]
Fan, Runzhu [3 ]
Zhang, Jia [1 ]
Li, Yuanli [1 ]
Wang, Xiaowen [1 ]
Han, Shouye [1 ]
Liu, Wan [1 ]
Pan, Menghua [1 ]
Cheng, Zhongbin [1 ]
机构
[1] Henan Univ, Sch Pharm, Kaifeng 475004, Peoples R China
[2] Minist Nat Resources, Key Lab Marine Biogenet Resources, Inst Oceanog 3, Xiamen 361005, Peoples R China
[3] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2020年 / 83卷 / 09期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
MAIRE; METABOLITES; PREDICTION;
D O I
10.1021/acs.jnatprod.0c00571
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Twelve new polyketides, including a naphthoquinone derivative, penithoketone (1), and 11 chromone derivatives, penithochromones A-L (2-12), together with three known compounds (13-15) were isolated from the deep-sea-derived fungus Penicillium thomii YPGA3. The structures of the metabolites were elucidated based on extensive analyses of the spectroscopic data, and the configuration of 1 was resolved by quantum chemical calculations of NMR shifts and ECD spectra and comparisons to experimental data. Compound 1, containing a naphthoquinone-derived moiety substituted with a butenolide unit, represents a new modified naphthoquinone skeleton. Interestingly, the 5,7-dioxygenated chromone derivatives 2-13 possessed different alkyl acid or alkyl ester side chain lengths, and those with side chain lengths of seven carbon atoms were discovered from nature for the first time. The metabolites were evaluated for their cytotoxicity against four cancer cell lines; compounds 1 and 15 were found to be active, with IC50 values ranging from 4.9 to 9.1 mu M.
引用
收藏
页码:2679 / 2685
页数:7
相关论文
共 20 条
[11]   Beyond DP4: an Improved Probability for the Stereochemical Assignment of Isomeric Compounds using Quantum Chemical Calculations of NMR Shifts [J].
Grimblat, Nicolas ;
Zanardi, Maria M. ;
Sarotti, Ariel M. .
JOURNAL OF ORGANIC CHEMISTRY, 2015, 80 (24) :12526-12534
[12]   Chemical Constituents of Branches and Barks of Juglans mandshurica [J].
Jang, Hyeon Seok ;
Choi, Seong Yeon ;
Jeong, Birang ;
Min, Hee Jeong ;
Yang, Heejung ;
Bae, Young Soo .
CHEMISTRY OF NATURAL COMPOUNDS, 2018, 54 (02) :342-343
[13]  
Jiang Ting, 2002, Yaoxue Xuebao, V37, P271
[14]   Minimalist Relativistic Force Field: Prediction of Proton-Proton Coupling Constants in 1H NMR Spectra Is Perfected with NBO Hybridization Parameters [J].
Kutateladze, Andrei G. ;
Mukhina, Olga A. .
JOURNAL OF ORGANIC CHEMISTRY, 2015, 80 (10) :5218-5225
[15]   Computational Prediction of 1H and 13C Chemical Shifts: A Useful Tool for Natural Product, Mechanistic, and Synthetic Organic Chemistry [J].
Lodewyk, Michael W. ;
Siebert, Matthew R. ;
Tantillo, Dean J. .
CHEMICAL REVIEWS, 2012, 112 (03) :1839-1862
[16]   Pallidopenillines: Polyketides from the Alga-Derived Fungus Penicillium thomii Maire KMM 4675 [J].
Sobolevskaya, Maria P. ;
Leshchenko, Elena V. ;
Hoai, Trinh P. T. ;
Denisenko, Vladimir A. ;
Dyshlovoy, Sergey A. ;
Kirichuk, Natalya N. ;
Khudyakova, Yuliya V. ;
Kim, Natalya Yu. ;
Berdyshev, Dmitrii V. ;
Pislyagin, Evgeny A. ;
Kuzmich, Aleksandra S. ;
Gerasimenko, Andrey V. ;
Popov, Roman S. ;
von Amsberg, Gunhild ;
Antonov, Alexandr S. ;
Afiyatullov, Shamil Sh. .
JOURNAL OF NATURAL PRODUCTS, 2016, 79 (12) :3031-3038
[17]   New metabolites from the alga-derived fungi Penicillium thomii Maire and Penicillium lividum Westling [J].
Sobolevskaya, Maria P. ;
Zhuravleva, Olesya I. ;
Leshchenko, Elena V. ;
Zakharenko, Alexander M. ;
Denisenko, Vladimir A. ;
Kirichuk, Natalya N. ;
Popov, Roman S. ;
Berdyshev, Dmitrii V. ;
Pislyagin, Evgeny A. ;
Pivkin, Mikhael V. ;
Afiyatullov, Shamil Sh. .
PHYTOCHEMISTRY LETTERS, 2016, 15 :7-12
[18]   2-Methoxyjuglone Induces Apoptosis in HepG2 Human Hepatocellular Carcinoma Cells and Exhibits in Vivo Antitumor Activity in a H22 Mouse Hepatocellular Carcinoma Model [J].
Yu, Heng-Yi ;
Zhang, Xiao-Qiong ;
Xue-Li ;
Zeng, Fan-Bo ;
Ruan, Han-Li .
JOURNAL OF NATURAL PRODUCTS, 2013, 76 (05) :889-895
[19]   Sargassopenillines A-G, 6,6-Spiroketals from the Alga-Derived Fungi Penicillium thomii and Penicillium lividum [J].
Zhuravleva, Olesya I. ;
Sobolevskaya, Maria P. ;
Afiyatullov, Shamil Sh. ;
Kirichuk, Natalya N. ;
Denisenko, Vladimir A. ;
Dmitrenok, Pavel S. ;
Yurchenko, Ekaterina A. ;
Dyshlovoy, Sergey A. .
MARINE DRUGS, 2014, 12 (12) :5930-5943
[20]   Meroterpenoids from the Alga-Derived Fungi Penicillium thomii Maire and Penicillium lividum Westling [J].
Zhuravleva, Olesya I. ;
Sobolevskaya, Maria P. ;
Leshchenko, Elena V. ;
Kirichuk, Natalya N. ;
Denisenko, Vladimir A. ;
Dmitrenok, Pavel S. ;
Dyshlovoy, Sergey A. ;
Zakharenko, Alexander M. ;
Kim, Natalya Yu. ;
Afiyatullov, Shamil Sh. .
JOURNAL OF NATURAL PRODUCTS, 2014, 77 (06) :1390-1395