Yin-He Yang

Dr. Yin-He Yang

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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1 March 2017 in Fitoterapia
Verified
Journal Article
Closed access
FYFei-Xue Yu
Fei-Xue Yu
ZLZhe Li
Zhe Li
YCYao Chen
Yao Chen
YYYin-He Yang
Yin-He Yang
GLGuo-Hong Li
Guo-Hong Li
PZPei-Ji Zhao
Pei-Ji Zhao

12 June 2017 in Natural Product Research
Verified
Journal Article
Closed access
FYFei-Xue Yu
Fei-Xue Yu
YCYao Chen
Yao Chen
YYYin-He Yang
Yin-He Yang
GLGuo-Hong Li
Guo-Hong Li
PZPei-Ji Zhao
Pei-Ji Zhao
A new compound 6-formamide-chetomin (1) together with chetomin (2) was isolated from solid fermentation products of the endophytic fungus Chaetomium sp. M336, which were elucidated by extensive spectroscopic analyses, including 1D and 2D NMR, and HR-ESI-MS experiments. The bioassay result showed that compound 1 had strong antibacterial activity against Escherichia coli, Staphylococcus aureus, Salmonella typhimurium ATCC 6539 and Enterococcus faecalis with minimum inhibitory concentration (MIC) value of 0.78 μg/mL; meanwhile it exhibited strong cytotoxicity with IC50 values of 21.6–27.1 nM against cell lines HeLa, SGC-7901 and A549.

17 September 2015 in Molecules
Verified
Journal Article
Open access
PDF file
YCYan-Mei Chen
Yan-Mei Chen
YYYin-He Yang
Yin-He Yang
XLXiao-Nian Li
Xiao-Nian Li
CZCheng Zou
Cheng Zou
PZPei-Ji Zhao
Pei-Ji Zhao
Two new tetranorlabdane diterpenoids, named botryosphaerins G (1) and H (2), were isolated from the solid fermentation products of Botryosphaeria sp. P483 along with seven known tetranorlabdane diterpenes (3–9). Their structures were elucidated by extensive analysis, including 1D and 2D nuclear magnetic resonance (NMR) spectroscopy, and high-resolution electrospray ionization mass spectrometry (HR-ESI-MS). Their absolute configuration was confirmed by single-crystal X-ray diffraction analyses using the anomalous scattering of Cu Kα radiation. All of the isolated compounds were tested for activity against phytopathogenic fungi and nematodes. Compounds 2 and 3 showed antifungal activity and compound 2 showed weak nematicidal activity.

22 October 2014 in Phytochemistry Letters
Verified
Journal Article
Closed access
JXJin Xie
Jin Xie
JLJing Li
Jing Li
YYYin-He Yang
Yin-He Yang
YCYu-Hui Chen
Yu-Hui Chen
PZPei-Ji Zhao
Pei-Ji Zhao

28 June 2012 in Journal of Natural Products
Verified
Journal Article
Closed access
YYYin-He Yang
Yin-He Yang
XFXiao-Li Fu
Xiao-Li Fu
LLLiang-Qun Li
Liang-Qun Li
YZYing Zeng
Ying Zeng
CLCheng-Yun Li
Cheng-Yun Li
PZPei-Ji Zhao
Pei-Ji Zhao

1 March 2015 in Phytochemistry Letters
Verified
Journal Article
Closed access
BLBa-Yi Lang
Ba-Yi Lang
JLJing Li
Jing Li
XZXiao-Xue Zhou
Xiao-Xue Zhou
YCYu-Hui Chen
Yu-Hui Chen
YYYin-He Yang
Yin-He Yang
PZPei-Ji Zhao
Pei-Ji Zhao