Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jing-Mei Yuan"'
Autor:
Mao-Lin Li, Jing-Mei Yuan, Hao Yuan, Bi-Han Wu, Shi-Liang Huang, Qing-Jiang Li, Tian-Miao Ou, Hong-Gen Wang, Jia-Heng Tan, Ding Li, Shuo-Bin Chen, Zhi-Shu Huang
Publikováno v:
Journal of Medicinal Chemistry. 65:12675-12700
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5266df396b14895123914afea378ad4
https://doi.org/10.1021/acs.jmedchem.2c00467
https://doi.org/10.1021/acs.jmedchem.2c00467
Autor:
Xin-Chen Jiang, Fang-Hai Tu, Li-Yuan Wei, Bo-Zheng Wang, Hao Yuan, Jing-Mei Yuan, Yong Rao, Shi-Liang Huang, Qing-Jiang Li, Tian-Miao Ou, Hong-Gen Wang, Jia-Heng Tan, Shuo-Bin Chen, Zhi-Shu Huang
Publikováno v:
Journal of Medicinal Chemistry. 65:12346-12366
The development of triple-negative breast cancer (TNBC) is highly associated with G-quadruplex (G4); thus, targeting G4 is a potential strategy for TNBC therapy. Because concomitant histone deacetylases (HDAC) inhibition could amplify the impact of G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69ee936cf4c88cd1bc4652ea3f6093fb
https://doi.org/10.1021/acs.jmedchem.2c01058
https://doi.org/10.1021/acs.jmedchem.2c01058
Autor:
Fengting Zhu, Jinnan Li, Jiali Xu, Jing-Mei Yuan, Zhiping Liu, Qiuli Liang, Guo-Bao Huang, Heyang Zhou, Jun Huang
Publikováno v:
New Journal of Chemistry. 44:3189-3193
A visible-light promoted radical cascade reaction of N-propargylanilines with sodium sulfinates as sulfonyl radical precursors was developed under metal-free conditions. This mild protocol represents a speedy and efficient method for synthesizing 3-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16bcb6fe2732753d7d0fb0799522a371
https://doi.org/10.1039/c9nj05248h
https://doi.org/10.1039/c9nj05248h
Autor:
Cheng-Xue Pan, Nan-Ying Chen, Gui-Fa Su, Hao-Ran Liao, Dong-Liang Mo, Xiao-Juan Li, Guo-Hai Zhang, Jing-Mei Yuan, Zi-Yu Gu
Publikováno v:
New Journal of Chemistry. 44:11203-11214
Twenty-seven 3-(benzo[d]thiazol-2-yl)-4-aminoquinoline derivatives have been designed and synthesized as topoisomerase I inhibitors. The in vitro anti-proliferation evaluation against four human cancer cell lines (MGC-803, HepG-2, T24, and NCI-H460)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd14e1c5c7c5f2b6b04c19b9754905f0
https://doi.org/10.1039/c9nj05846j
https://doi.org/10.1039/c9nj05846j
Autor:
Jun Huang, Wen-Qiang Chen, Congyu Li, Jiarong Sheng, Jing-Mei Yuan, Qi Xiao, Yimiao He, Yan-Min Huang, Chusheng Huang
Publikováno v:
Chemistry – An Asian Journal. 14:2584-2587
Defluorinative C(sp3 )-P bond formation of α-trifluoromethyl alkenes with phosphine oxides or phosphonates have been achieved under catalyst- and oxidant-free conditions, giving phosphorylation gem-difluoroalkenes as products. α-Trifluoromethyl alk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28a2cdc7d36feb17c90383268fd115f0
https://doi.org/10.1002/asia.201900533
https://doi.org/10.1002/asia.201900533
Autor:
Nan-Ying Chen, Xin-Wei Wei, Guo-Hai Zhang, Dong-Liang Mo, Jing-Mei Yuan, Gui-Fa Su, Kai Wei, Cheng-Xue Pan
Publikováno v:
European Journal of Medicinal Chemistry. 169:144-158
Thirty Cryptolepine and Aromathecin based mimics were designed and synthesized. Their cytotoxicity was evaluated in four human cancer cell lines (HepG-2, T24, NCI-H460 and MGC-803) and one normal human cell line (HL-7702). Most compounds exhibited po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30af4877bc8c85e3db3358d0d8684661
https://doi.org/10.1016/j.ejmech.2019.02.072
https://doi.org/10.1016/j.ejmech.2019.02.072
Autor:
Yun-Qiong Gu, Xiao-Min Zhu, Yan Mi, Feilong Hu, Yan-Fang Jing, Peng Yu, Wen-Ying Shen, Jing-Mei Yuan
Publikováno v:
RSC Advances. 9:35671-35676
Herein, a dual-response fluorescent sensor, L, based on pyrazolopyrimidine was designed and developed for the simultaneous detection of Ni2+ and Cu2+ ions in the presence of other metal ions; the structural characterization of L was carried out by FT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::017fbe2837431e46bdef196328a46744
https://doi.org/10.1039/c9ra06227k
https://doi.org/10.1039/c9ra06227k
Autor:
Jing-Mei Yuan, Wen-Jun Lv, Xiao-Xiao Wang, Huang Haolian, Zhang Yanhong, Tian-Ting Yang, Fang Yuanyuan, Gao Ying, Qian Ruilian, Qing-Qing Wang
Publikováno v:
Journal of Nursing Management
Aims To explore the association between cognitive emotion regulation strategies and anxiety and depression among nurses during the COVID-19 outbreak. Background Nurses play a vital role in responding to the COVID-19 outbreak, but many of them suffer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd3bc4b31b1cd0b3fcabc9c177e9b278
Autor:
Nan-Ying Chen, Ke Lu, Gui-Fa Su, Jing-Mei Yuan, Zi-Yu Gu, Cheng-Xue Pan, Dong-Liang Mo, Xiao-Juan Li
Publikováno v:
Bioorganic Chemistry. 114:105101
Thirty-eight new 3-arylaminoquinoxaline-2-carboxamide derivatives were in silico designed, synthesized and their cytotoxicity against five human cancer cell lines and one normal cells WI-38 were evaluated. Molecular mechanism studies indicated that N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9ea3dcc34ac5e740bef3b1d8e55b96b
https://doi.org/10.1016/j.bioorg.2021.105101
https://doi.org/10.1016/j.bioorg.2021.105101
Autor:
Guo-Xue He, Shi-Lin Kong, Gui-Fa Su, Jing-Mei Yuan, Cheng-Xue Pan, Ling-Yun Wang, Kai Wei, Dong-Liang Mo, Hai-Miao Zhu
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 27:1660-1664
2,2-Dihydroxyarylethanones, readily prepared from the commercially available aromatic ethyl ketones, were reacted with resorcinol, 3-methoxyphenol or 2-methoxyphenol in multi steps one-pot manner promoted by trifluoroacetic acid to furnish the 2,3-di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2518265a213c4ee24b99406a20114701
https://doi.org/10.1016/j.bmcl.2017.03.010
https://doi.org/10.1016/j.bmcl.2017.03.010