Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Qin-Hua Chen"'
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
A series of γ-lactone derivatives (E)-4-arylidene-5-oxotetrahydrofuran derivatives were synthesized via a tandem Passerini 3CC/SN cyclization microwave-assisted one-pot method efficiently starting from Baylis Hillman acids, aryl glyoxals and isocyan
Externí odkaz:
https://doaj.org/article/a2b14b38f3f0433aa9f7c822919761b2
Autor:
Li-Na Ke, Ling-Qi Kong, Xiu-Lian Zhu, Feng-Xu Wu, Qin-Hua Chen, Bin Li, Yun Dong, Hong-Mei Wang, Xiao-Hua Zeng
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
We have synthesized Rhopaladins’ analog (2E,4E)-4-chlorobenzylidene-2-(4-chlorostyryl)-N-cyclohexyl-1-(4-fluorophenyl)-5-oxopyrrolidine-2-carboxamide (RPDPRH) via a highly facile, inexpensive and green approach and verified the structural superiori
Externí odkaz:
https://doaj.org/article/4092eb5537d84574b2ac145bcd7d0de3
Autor:
Li-Na Ke, Ling-Qi Kong, Huan-Huan Xu, Qin-Hua Chen, Yun Dong, Bin Li, Xiao-Hua Zeng, Hong-Mei Wang
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
Gynecological malignancy seriously threatens the physical and mental health of women. Shikonin is a naphthoquinone compound with a variety of biological activities. Studies have shown that shikonin can inhibit cell proliferation, promote cell apoptos
Externí odkaz:
https://doaj.org/article/ca90a662e24c417d9a3b611075038f18
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
Heterocyclic compounds were widely used in many domains; pyrrolidone is a derivative of heterocycles that can be used to synthesize anticancer drugs. A new fluorine-containing rhopaladins’ analog(E)-2-(4-bromobenzoyl)-N-(tert-butyl)-4-(4-fluoro ben
Externí odkaz:
https://doaj.org/article/71420cfb444142d78ca5a271a41ecbbb
Autor:
Jun Zhu, Ling-Qi Kong, Qin-Hua Chen, Bin Li, Lun Wu, Feng-Ying Ran, Li-Na Ke, Xiao-Hua Zeng, Hong-Mei Wang
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
Marine alkaloids have novel structures and antitumor activities. Therefore, we synthesized rhopaladins’ analogs from marine alkaloids rhopaladins A-D and modified their structures to synthesize 4-benzylidene-5-pyrrolidone derivatives. Among the com
Externí odkaz:
https://doaj.org/article/6a4d8c957d174ec98ec83817762f9c24
Autor:
Long Chen, Qian Zhang, Qin-Hua Chen, Feng-Yin Ran, Li-Mei Yu, Xiu Liu, Qiang Fu, Gong-Yu Song, Jun-Ming Tang, Tao Zhang
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2019)
Mobilized peripheral blood-derived mesenchymal stem cells (PB-MSCs) mainly derived from bone marrow-derived MSCs (BM-MSCs) exert a similar anti-inflammatory effect. However, the mechanism of anti-inflammatory effect of mobilized PB-MSCs by a combinat
Externí odkaz:
https://doaj.org/article/e21438a258a842258cec48712adfcfcd
Autor:
Jing Zhu, Yang Yang, Ling‐Yi Xin, Shi‐Yu Wan, Na He, Hang‐Tian Wang, Xi‐Yu Chen, Quan‐Xi Mei, Guang‐Jun Feng, Qin‐Hua Chen, Guang‐Yi Yang
Publikováno v:
Journal of Separation Science. 46
Autor:
Yang Yang, Jing Zhu, Chang‐liang Yao, De‐an Guo, Na He, Quan‐xi Mei, Guang‐jun Feng, Qin‐hua Chen, Guang‐yi Yang
Publikováno v:
Biomedical Chromatography. 36
Mahuang Xuanfei Zhike (MXZ) syrup, a Chinese patent medicine, has been widely used in the clinical treatment of cough. However, there is no reported method for the quantitative analysis of the effective components of MXZ syrup in biological samples.
Autor:
Lin, Xiong1,2, Qin‐Hua, Chen2, Peng, Li2, Chun‐Lei, Li1,2, Guang‐De, Yang1 jmw52@mail.xjtu.edu.cn
Publikováno v:
Chemical Biology & Drug Design. Jan2018, Vol. 91 Issue 1, p105-115. 11p.
Autor:
Lun Wu(Former Corresponding Author), Wen-Bo Zhou, Jiao Zhou, Ying Wei, Hong-Mei Wang, Xian-de Liu, Xiao-Chun Chen, Wei Wang, Lin Ye, Li Chao Yao, Qin-Hua Chen, Zhi-Gang Tang(New Corresponding Author)
Background Circulating exosomal microRNAs are reflective of the characteristics of the tumor, are valuable biomarkers in different types of tumors, and play important roles in tumor progression and metastasis. The purpose of this study was to investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6419b806decb5ab5a23592137c5ca88
https://doi.org/10.21203/rs.2.22716/v1
https://doi.org/10.21203/rs.2.22716/v1