5-Hydroxymethylmellein: An isocoumarin derivative from an endophytic fungus from red alga Asparagopsis taxiformis

Planta Medica ◽  
2014 ◽  
Vol 80 (16) ◽  
Author(s):  
R Medina ◽  
C Biasetto ◽  
A Somensi ◽  
N Yokoya ◽  
M Lopes ◽  
...  
2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Rebeca P. Medina ◽  
Angela R. Araujo ◽  
João M. Batista ◽  
Carmen L. Cardoso ◽  
Cláudia Seidl ◽  
...  

2000 ◽  
Vol 45 (2) ◽  
pp. 516-519 ◽  
Author(s):  
Rhoda A. Marshall ◽  
John T. G. Hamilton ◽  
Matthew J. Dring ◽  
David B. Harper

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.


1990 ◽  
Vol 31 (48) ◽  
pp. 7015-7016 ◽  
Author(s):  
Michihiro Sugano ◽  
Aiya Sato ◽  
Hidemi Nagak ◽  
Shinji Yoshiok ◽  
Tomoko Shiraki ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 23 (9) ◽  
pp. no-no
Author(s):  
M. SUGANO ◽  
A. SATO ◽  
H. NAGAKI ◽  
S. YOSHIOKA ◽  
T. SHIRAKI ◽  
...  

Marine Drugs ◽  
2019 ◽  
Vol 17 (11) ◽  
pp. 605 ◽  
Author(s):  
Li ◽  
Li ◽  
Yang ◽  
Meng ◽  
Li ◽  
...  

Three new prenylated phenol derivatives, terreprenphenols A–C (1–3), along with four known related compounds (4–7), were isolated from Aspergillus terreus EN-539, an endophytic fungus obtained from the marine red alga Laurencia okamurai. The structures of these compounds were established by extensive analysis of 1D/2D NMR data, mass spectrometric data, and optical rotation (OR). The corresponding relationship between absolute configuration and optical rotation for known compounds anodendroic acid (4) and asperterreusine C (5) was ambiguous in literature, and their absolute configurations were therefore discussed and confirmed for the first time by time-dependent density functional (TDDFT) ECD and OR calculations. Compounds 1–7 inhibited some common aquatic bacteria with MIC values ranging from 2 to 64 μg/mL.


Marine Drugs ◽  
2016 ◽  
Vol 14 (12) ◽  
pp. 223 ◽  
Author(s):  
Hong-Lei Li ◽  
Xiao-Ming Li ◽  
Hui Liu ◽  
Ling-Hong Meng ◽  
Bin-Gui Wang

2018 ◽  
Vol 33 (3) ◽  
pp. 443-446 ◽  
Author(s):  
Rebeca P. Medina ◽  
Angela R. Araujo ◽  
Raymond J. Andersen ◽  
Marcos A. Soares ◽  
Fabio de A. Silva ◽  
...  

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