Hui Guo

Hui Guo


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2019 in Carbohydrate Polymers
Verified
Journal Article
Closed access
XYXinyi Yang
Xinyi Yang
YCYunfei Chen
Yunfei Chen
SYShen Yao
Shen Yao
JQJunqing Qian
Junqing Qian
HGHui Guo
Hui Guo
XCXiaohua Cai
Xiaohua Cai

1 May 2019 in Colloids and Surfaces A: Physicochemical and Engineering Aspects
Verified
Journal Article
Closed access
CPCunli Pan
Cunli Pan
JQJunqing Qian
Junqing Qian
JFJing Fan
Jing Fan
HGHui Guo
Hui Guo
LGLihong Gou
Lihong Gou
CLChanghai Liang
Changhai Liang

1 August 2021 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
HGHui Guo
Hui Guo
BLBingshuang Lei
Bingshuang Lei
JYJianwei Yu
Jianwei Yu
YCYunfei Chen
Yunfei Chen
JQJunqing Qian
Junqing Qian

1 June 2016 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
HGHui Guo
Hui Guo
YTYi Tang
Yi Tang
YYYang Yu
Yang Yu
LXLu Xue
Lu Xue
JQJun-Qing Qian
Jun-Qing Qian

5 December 2018 in Molecules
Verified
Journal Article
Open access
PDF file
JOJinkui Ouyang
Jinkui Ouyang
ZMZiling Mao
Ziling Mao
HGHui Guo
Hui Guo
YXYun-Ying Xie
Yun-Ying Xie
ZCZehua Cui
Zehua Cui
STShan Tijiang
Shan Tijiang
Four new depsidones, mollicellins O–R (compounds 1–4), along with three known compounds 5–7, were isolated from cultures of the fungus Chaetomium sp. Eef-10, an endophyte isolated from Eucalyptus exserta. The structures of the new compounds were elucidated by analysis of the 1D and 2D NMR and HR-ESI-MS spectra. The known compounds were identified by comparison of their spectral data with published values. Compounds 1–7 were evaluated for antibacterial activities against Staphylococcus aureus (sensitive and resistant strains), Escherichia coli, Agrobacterium tumefaciens, Salmonella typhimurium, Pseudomonas lachrymans, Ralstonia solanacearum, Xanthomonas vesicatoria and cytotoxic activities against two human cancer cell lines (HepG2 and Hela). Mollicellin H (6) displayed best antibacterial activity, with IC50 values of 5.14 µg/mL against S. aureus ATCC29213 and 6.21 µg/mL against S. aureus N50, MRSA, respectively. Mollicellin O (1) and mollicellin I (7) also exhibited antibacterial activities against S. aureus ATCC29213 and S. aureus N50. Mollicellin G (5) was active against both two human cancer cell lines, with IC50 values of 19.64 and 13.97 µg/mL while compounds 6 and 7 only showed cytotoxic activity against one cell line. In addition, mollicellin O (1) showed antioxidant activity based on DPPH radical scavenging, with an IC50 value of 71.92 µg/mL.

1 September 2019 in European Polymer Journal
Verified
Journal Article
Closed access
YCYan Chen
Yan Chen
JQJunQing Qian
JunQing Qian
CZChangYan Zhao
ChangYan Zhao
LYLieChao Yang
LieChao Yang
JDJing Ding
Jing Ding
HGHui Guo
Hui Guo