Quan-Xiang Wu

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Name: 武全香; Wu, QuanXiang
Organization: Lanzhou University , China
Department: College of Chemistry and Chemical Engineering
Title: Associate Professor(PhD)

TOPICS

Co-reporter:Ming-Ming Zhai, Feng-Ming Qi, Jie Li, Chun-Xiao Jiang, Yue Hou, Yan-Ping Shi, Duo-Long Di, Ji-Wen Zhang, and Quan-Xiang Wu
Journal of Agricultural and Food Chemistry 2016 Volume 64(Issue 11) pp:2298-2306
Publication Date(Web):March 14, 2016
DOI:10.1021/acs.jafc.6b00556
The fungus Clonostachys rosea is widely distributed all over the world. The destructive force of this fungus, as a biological control agent, is very strong to lots of plant pathogenic fungi. As part of the ongoing search for antibiotics from fungi obtained from soil samples, the secondary metabolites of C. rosea YRS-06 were investigated. Through efficient bioassay-guided isolation, three new bisorbicillinoids possessing open-ended cage structures, tetrahydrotrichodimer ether (1) and dihydrotrichodimer ether A and B (2 and 3), and 12 known compounds were obtained. Their structures were determined via extensive NMR, HR-ESI-MS, and CD spectroscopic analyses and X-ray diffraction data. Compounds 1–3 are rare bisorbicillinoids with a γ-pyrone moiety. The biological properties of 1–15 were evaluated against six different Gram-positive and Gram-negative bacteria. Bisorbicillinoids, 2–5, and TMC-151 C and E, 14 and 15, showed potent antibacterial activity.
Co-reporter:Ming-Ming Zhai;Jie Li;Chun-Xiao Jiang
Natural Products and Bioprospecting 2016 Volume 6( Issue 1) pp:1-24
Publication Date(Web):2016 February
DOI:10.1007/s13659-015-0081-3
The focus of this review is placed on the chemical structures from the species of the genus Talaromyces reported with reference to their biological activities. 221 secondary metabolites, including 43 alkaloids and peptides, 88 esters, 31 polyketides, 19 quinones, 15 steroid and terpenoids, and 25 other structure type compounds, have been included, and 66 references are cited.
Co-reporter:Ming-Ming Zhai, Hai-Tao Niu, Jie Li, Hui Xiao, Yan-Ping Shi, Duo-Long Di, Phillip Crews, and Quan-Xiang Wu
Journal of Agricultural and Food Chemistry 2015 Volume 63(Issue 43) pp:9558-9564
Publication Date(Web):October 15, 2015
DOI:10.1021/acs.jafc.5b04296
The green Chinese onion (Allium fistulosum L.), which is widely cultivated and has been naturalized in many places, is an important spice and vegetable in East and Southeast Asia. It is used to treat the common cold in China. In the ongoing search for antibacterial activity in fungi derived from natural, pungently scented vegetables, the secondary metabolites of Talaromyces pinophilus AF-02, which was isolated from the stem of the green Chinese onion, were investigated. The genus Talaromyces (Trichocomaceae) is an important fungal genus because of its ubiquity and the role of many of its species in food and agriculture production. Three new phthalide derivatives, talaromycolides A–C, 1–3; a new long-chain dicarboxylic acid, 11; and 12 known compounds were isolated from methanolic extracts of this fungus. Their structures were determined via extensive NMR, HR-ESI-MS, and CD spectroscopic analyses. Compounds 1–3 are rare phthalide derivatives with a novel linkage position between the phenyl and phthalide moieties. The biological properties of 1–16 were evaluated using six different bacteria, and 1–3, 5, and 11 exhibited significant antibacterial activity in response to some of the tested strains.
Co-reporter:Hai-Long Jiang, Xiao-Zheng Wang, Jie Xiao, Xiao-Hong Luo, Xiao-Jun Yao, Yuan-Yuan Zhao, Yong-Jia Chen, Phillip Crews, Quan-Xiang Wu
Tetrahedron 2013 69(32) pp: 6687-6692
Publication Date(Web):
DOI:10.1016/j.tet.2013.05.115
Co-reporter:Hai-Long Jiang, Jia Chen, Xiao-Jie Jin, Jun-Li Yang, Ya Li, Xiao-Jun Yao, Quan-Xiang Wu
Tetrahedron 2011 67(47) pp: 9193-9198
Publication Date(Web):
DOI:10.1016/j.tet.2011.09.070
2-Propenamide, N-(4-bromophenyl)-N,2-dimethyl-
2-Propenamide, N-(4-fluorophenyl)-N,2-dimethyl-
2-Propenamide, N-(4-methoxyphenyl)-N,2-dimethyl-
2-Propenamide, N,2-dimethyl-N-(4-methylphenyl)-
TRICHODIMEROL
N-(2-bromophenyl)-n,2-dimethylprop-2-enamide
4-[(2-hydroxyethyl)amino]-6-[(1R,2S,4aR,8aR)-2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-oxo-2H-pyran-3-carbaldehyde
2-Propenamide, N-(4-chlorophenyl)-N,2-dimethyl-
2H-1,4-Benzoxazin-2-one,3,4-dihydro-3-methyl-