Asperolides A–C, Tetranorlabdane Diterpenoids from the Marine Alga-Derived Endophytic Fungus Aspergillus wentii EN-48

2012 ◽  
Vol 75 (2) ◽  
pp. 148-152 ◽  
Author(s):  
Hao-Fen Sun ◽  
Xiao-Ming Li ◽  
Li Meng ◽  
Chuan-Ming Cui ◽  
Shu-Shan Gao ◽  
...  
2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Vipul Swarup Bhatnagar ◽  
Prasun Bandyopadhyay ◽  
Girish H. Rajacharya ◽  
Sharanya Sarkar ◽  
Krishna Mohan Poluri ◽  
...  

2020 ◽  
Vol 73 (8) ◽  
pp. 585-588
Author(s):  
Jianjiao Wang ◽  
Qingyun Peng ◽  
Xingang Yao ◽  
Yonghong Liu ◽  
Xuefeng Zhou

Marine Drugs ◽  
2017 ◽  
Vol 15 (2) ◽  
pp. 24 ◽  
Author(s):  
Feng-Yu Du ◽  
Xin Li ◽  
Xiao-Ming Li ◽  
Li-Wei Zhu ◽  
Bin-Gui Wang

2018 ◽  
Vol 152 ◽  
pp. 45-52 ◽  
Author(s):  
Yin-Ping Song ◽  
Xiang-Hong Liu ◽  
Zhen-Zhen Shi ◽  
Feng-Ping Miao ◽  
Sheng-Tao Fang ◽  
...  

2016 ◽  
Vol 12 ◽  
pp. 2012-2018 ◽  
Author(s):  
Peng Zhang ◽  
Xiao-Ming Li ◽  
Xin-Xin Mao ◽  
Attila Mándi ◽  
Tibor Kurtán ◽  
...  

A new indolyl-6,10b-dihydro-5aH-[1]benzofuro[2,3-b]indole derivative, varioloid A (1), was isolated from the marine alga-derived endophytic fungus Paecilomyces variotii EN-291. Its structure was elucidated on the basis of extensive analysis of 1D and 2D NMR data and the absolute configuration was determined by time-dependent density functional theory-electronic circular dichroism (TDDFT-ECD) calculations. A similar compound, whose planar structure was previously described but the relative and absolute configurations and 13C NMR data were not reported, was also identified and was tentatively named as varioloid B (2). Both compounds 1 and 2 exhibited cytotoxicity against A549, HCT116, and HepG2 cell lines, with IC50 values ranging from 2.6 to 8.2 µg/mL.


Molecules ◽  
2018 ◽  
Vol 23 (11) ◽  
pp. 2995 ◽  
Author(s):  
Dan Chen ◽  
Peng Zhang ◽  
Tong Liu ◽  
Xiu-Fang Wang ◽  
Zhao-Xia Li ◽  
...  

A great deal of attention has been focused on the secondary metabolites produced by marine endophytic fungi, which can be better alternatives to chemicals, such as biopesticides, for control of polyphagous pests. On the basis of its novel biocontrol attributes, chemical investigation of a marine alga-derived endophytic fungus, Acremonium vitellinum, resulted in the isolation of three chloramphenicol derivatives (compounds 1–3). Their chemical structures were elucidated by detailed analysis of their nuclear magnetic resonance spectra, high-resolution electrospray ionization mass spectrometry, and by comparison with the data available in the literature. In this paper, compound 2 was firstly reported as the natural origin of these fungal secondary metabolites. The insecticidal activities of compounds 1–3 against the cotton bollworm, Helicoverpa armigera, were evaluated. The natural compound 2 presented considerable activity against H. armigera, with an LC50 value of 0.56 ± 0.03 mg/mL (compared to matrine with an LC50 value of 0.24 ± 0.01 mg/mL). Transcriptome sequencing was used to evaluate the molecular mechanism of the insecticidal activities. The results presented in this study should be useful for developing compound 2 as a novel, ecofriendly and safe biopesticide.


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