scholarly journals Two rare meroterpenoidal rotamers from Ganoderma applanatum

RSC Advances ◽  
2017 ◽  
Vol 7 (6) ◽  
pp. 3413-3418 ◽  
Author(s):  
Qi Luo ◽  
Zheng-Chao Tu ◽  
Yong-Xian Cheng

Applanatumols Z3 (1) and Z4 (2), two novel natural product hybrids consisting of a meroterpenoid and a glycerol and three known compounds (3–5) were isolated from the fruiting bodies of the fungus Ganoderma applanatum.

2017 ◽  
Vol 12 (3) ◽  
pp. 1934578X1701200
Author(s):  
Qi Luo ◽  
Yan-Jiao Zhang ◽  
Zhi-Qiang Shen ◽  
Peng Chen ◽  
Yong-Xian Cheng

Ganoderma applanatum is a fungus used for the prevention and treatment of a variety of disorders in China. In the present study, four new compounds, named shushe acids A-D (1-4), were isolated from the fruiting bodies of this species. Their structures were identified on the basis of spectroscopic methods. Compounds 1-4 are all natural product hybrids composed of derivatives of gallic acid, glycerol and succinic acid. None of the four compounds showed activity against the MCF-7 cell line.


Molecules ◽  
2020 ◽  
Vol 25 (12) ◽  
pp. 2895
Author(s):  
Hitomi Sasaki ◽  
Yuzuru Kubohara ◽  
Hirotaka Ishigaki ◽  
Katsunori Takahashi ◽  
Hiromi Eguchi ◽  
...  

We report a protoilludane-type sesquiterpene, mucoroidiol, and a geranylated bicyclogermacranol, firmibasiol, isolated from Dictyostelium cellular slime molds. The methanol extracts of the fruiting bodies of cellular slime molds were separated by chromatographic methods to give these compounds. Their structures have been established by several spectral means. Mucoroidiol and firmibasiol are the first examples of more modified and oxidized terpenoids isolated from cellular slime molds. Mucoroidiol showed moderate osteoclast-differentiation inhibitory activity despite demonstrating very weak cell-proliferation inhibitory activity. Therefore, cellular slime molds produce considerably diverse secondary metabolites, and they are promising sources of new natural product chemistry.


1999 ◽  
Vol 52 (8) ◽  
pp. 749 ◽  
Author(s):  
Malcolm S. Buchanan ◽  
Melvyn Gill ◽  
Alberto Gimenez ◽  
Somphone Phonh-Axa ◽  
Evelin Raudies ◽  
...  

Flavomannin 6,6′,8-tri-O-methyl ether occurs in the fruiting bodies of the Australian toadstool Dermocybe sp. WAT 24274 as an anisochiral mixture of the (3S,3′S,P)- and (3R,3′R,M)-enantiomers (5) and (7), respectively, in which the former predominates to the extent of 50% e.e. The structure of the natural product is determined by spectroscopic methods and the absolute configuration and enantiomeric purity are deduced from the c.d. spectrum and by chemical degradation of the natural product to a mixture of stereoisomeric dihydroanthracenones that has been analysed by chiral h.p.l.c.


2005 ◽  
Vol 28 (6) ◽  
pp. 1103-1105 ◽  
Author(s):  
Sanghyun Lee ◽  
Sang Hee Shim ◽  
Ju Sun Kim ◽  
Kuk Hyun Shin ◽  
Sam Sik Kang

Author(s):  
Jing-Xia Shi ◽  
Guo-Yu Chen ◽  
Qian Sun ◽  
Shi-Yang Meng ◽  
Wei-Qun Chi

2007 ◽  
Vol 62 (10) ◽  
pp. 1329-1332 ◽  
Author(s):  
Fei Wang ◽  
Ze-Jun Dong ◽  
Ji-Kai Liu

Two new benzopyran-4-one derivatives, applanatins A (1) and B (2), were isolated from the fruiting bodies of the fungus Ganoderma applanatum (Ganodermataceae), along with one known analogue, ganoderma aldehyde (3), as well as four known ganoderenic acids. The structures of the new compounds were elucidated on the basis of extensive spectroscopic analysis. The partial assignments of the NMR spectra of 3 were also revised.


RSC Advances ◽  
2017 ◽  
Vol 7 (60) ◽  
pp. 38037-38043 ◽  
Author(s):  
Qi Luo ◽  
Zhen Wang ◽  
Jin-Feng Luo ◽  
Zheng-Chao Tu ◽  
Yong-Xian Cheng

Applanatumines B–D (1–3), three pairs of dimeric meroterpenoid enantiomers featuring the presence of a 6-oxo-4,4a,5,5a,6,8,8a,8b-octahydrofuro[3′,4′:4,5]cyclopenta[1,2-b]pyran-3-carbaldehyde structure core, were isolated from the fruiting bodies of Ganoderma applanatum.


2017 ◽  
Vol 4 (01) ◽  
pp. e1-e7 ◽  
Author(s):  
Simon Merdivan ◽  
Kristina Jenett-Siems ◽  
Karsten Siems ◽  
Timo Niedermeyer ◽  
Michael Solis ◽  
...  

Abstract Armillaria ostoyae (Romagn.) Herink is an edible honey mushroom from the family Physalacriaceae (Agaricales, Basidiomycota). Dichloromethane extracts of mushroom mycelium and fruiting bodies exhibited a significant degranulation inhibiting effect on RBL-2H3 cells using noncytotoxic concentrations. Bioactivity-guided fractionation of the mycelial dichloromethane extract led to the isolation of sesquiterpen aryl esters. Methyl linoleate could also be isolated. These substances were obtained from A. ostoyae for the first time, with one compound representing an undescribed natural product. Purified compounds melleolide H and J inhibited degranulation significantly. A. ostoyae could be a candidate for support of allergy treatments.


2019 ◽  
Vol 157 ◽  
pp. 103-110 ◽  
Author(s):  
XingRong Peng ◽  
Lei Li ◽  
JinRun Dong ◽  
ShuangYang Lu ◽  
Jing Lu ◽  
...  

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