scholarly journals Bisabolane, cyclonerane, and harziane derivatives from the marine-alga-endophytic fungus Trichoderma asperellum cf44-2

2018 ◽  
Vol 152 ◽  
pp. 45-52 ◽  
Author(s):  
Yin-Ping Song ◽  
Xiang-Hong Liu ◽  
Zhen-Zhen Shi ◽  
Feng-Ping Miao ◽  
Sheng-Tao Fang ◽  
...  
Fitoterapia ◽  
2019 ◽  
Vol 135 ◽  
pp. 107-113
Author(s):  
Yin-Ping Song ◽  
Feng-Ping Miao ◽  
Xiang-Hong Liu ◽  
Xiu-Li Yin ◽  
Nai-Yun Ji

2012 ◽  
Vol 75 (2) ◽  
pp. 148-152 ◽  
Author(s):  
Hao-Fen Sun ◽  
Xiao-Ming Li ◽  
Li Meng ◽  
Chuan-Ming Cui ◽  
Shu-Shan Gao ◽  
...  

Marine Drugs ◽  
2019 ◽  
Vol 17 (5) ◽  
pp. 252 ◽  
Author(s):  
Yin-Ping Song ◽  
Feng-Ping Miao ◽  
Xiang-Hong Liu ◽  
Xiu-Li Yin ◽  
Nai-Yun Ji

Seven previously unreported cyclonerane derivatives, namely, 3,7,11-trihydroxycycloneran-10-one, cycloneran-3,7,10,11-tetraol, cycloneran-3,7,11-triol, 11,12,15-trinorcycloneran-3,7,10-triol, 7,10S-epoxycycloneran-3,15-diol, 7,10R-epoxycycloneran-3,15-diol, and (10Z)-15-acetoxy-10-cycloneren-3,7-diol, were isolated in addition to the known (10Z)-cyclonerotriol, (10E)-cyclonerotriol, catenioblin C, and chokol E from the culture of Trichoderma asperellum A-YMD-9-2, an endophytic fungus obtained from the marine red alga Gracilaria verrucosa. The structures of previously unreported compounds were established by spectroscopic techniques, including 1D/2D NMR, MS, and IR. The isolation of these new cyclonerane derivatives greatly adds to the structural diversity of unusual cyclonerane sesquiterpenes, and several isolates exhibit potent inhibition against some marine phytoplankton species.


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

2019 ◽  
Vol 32 ◽  
pp. 38-41 ◽  
Author(s):  
Yin-Ping Song ◽  
Feng-Ping Miao ◽  
Xiao-Rui Liang ◽  
Xiu-Li Yin ◽  
Nai-Yun Ji

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.


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