Hucheng Zhu

Prof. Hucheng Zhu


Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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5 April 2017 in Angewandte Chemie International Edition
Verified
Journal Article
Closed access
PDF file
HZHucheng Zhu
Hucheng Zhu
CCChunmei Chen
Chunmei Chen
QTQingyi Tong
Qingyi Tong
JYJing Yang
Jing Yang
GWGuangzheng Wei
Guangzheng Wei
YZYonghui Zhang
Yonghui Zhang

17 July 2018 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
HLHuaqiang Li
Huaqiang Li
WSWeiguang Sun
Weiguang Sun
MDMengyi Deng
Mengyi Deng
QZQun Zhou
Qun Zhou
JWJianping Wang
Jianping Wang
YZYonghui Zhang
Yonghui Zhang

7 August 2017 in Organic Letters
Verified
Journal Article
Closed access
GWGuangzheng Wei
Guangzheng Wei
CCChunmei Chen
Chunmei Chen
QTQingyi Tong
Qingyi Tong
JHJinfeng Huang
Jinfeng Huang
WWWenjing Wang
Wenjing Wang
YZYonghui Zhang
Yonghui Zhang

13 March 2019 in Organic Letters
Verified
Journal Article
Closed access
QLQin Li
Qin Li
CCChunmei Chen
Chunmei Chen
MWMengsha Wei
Mengsha Wei
CDChong Dai
Chong Dai
LCLi Cheng
Li Cheng
YZYonghui Zhang
Yonghui Zhang

16 October 2018 in Organic Letters
Verified
Journal Article
Closed access
WWWenjing Wang
Wenjing Wang
FZFanrong Zeng
Fanrong Zeng
QBQiong Bie
Qiong Bie
CDChong Dai
Chong Dai
CCChunmei Chen
Chunmei Chen
YZYonghui Zhang
Yonghui Zhang

2 May 2018 in Marine Drugs
Verified
Journal Article
Open access
PDF file
WWWen-Jing Wang
Wen-Jing Wang
XWXiao Wan
Xiao Wan
JLJunjun Liu
Junjun Liu
JWJianping Wang
Jianping Wang
HZHucheng Zhu
Hucheng Zhu
YZYonghui Zhang
Yonghui Zhang
A new sesquiterpenoid 9,10-diolhinokiic acid (1) and a new diterpenoid roussoellol C (2), together with 4 known compounds, were isolated from the extracts of laboratory cultures of marine-derived fungus Talaromyces purpurogenus. 9,10-diolhinokiic acid is the first thujopsene-type sesquiterpenoid containing a 9,10-diol moiety, and roussoellol C possesses a novel tetracyclic fusicoccane framework with an unexpected hydroxyl at C-4. These new structures were confirmed by spectroscopic data, chemical method, NMR data calculations and electronic circular dichroism (ECD) calculations. The selected compounds were evaluated for cytotoxicities against five human cancer cell lines, including SW480, HL-60, A549, MCF-7, and SMMC-7721 and the IC50 values of compound 2 against MCF-7 and 3 against HL-60 cells were 6.5 and 7.9 μM, respectively.