Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Jin-Tang Cheng"'
Autor:
Shu-Hui Wang, Cong Guo, Wen-Jin Cui, Qing-Xia Xu, Jun Zhang, Jin-Zhu Jiang, Yan Liu, Sha Chen, Chang Chen, Jin-Tang Cheng, An Liu
Publikováno v:
Natural Products and Bioprospecting, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract An undescribed pyrrole acid, 1-(4′-methoxy-4′-oxobutyl)-1 H-pyrrole-2,5-dicarboxylic acid (1) and one known pyrrole acid (2) were isolated from the fruits of Phyllanthus emblica. The structures of these compounds were elucidated via the
Externí odkaz:
https://doaj.org/article/e34ca3f3920b45989fae6bff074c3f8f
Autor:
Dan-Li Hao, Ya-Jie Wang, Jia-Ying Yang, Ran Xie, Ling-Yu Jia, Jin-Tang Cheng, Hai Ma, Ji-Xiang Tian, Shan-Shan Guo, Ting Liu, Feng Sui, Yu Zhao, Yan-Jun Chen, Qing-He Zhao
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Acute lung injury (ALI) or its aggravated stage acute respiratory distress syndrome (ARDS) is a common severe clinical syndrome in intensive care unit, may lead to a life-threatening form of respiratory failure, resulting in high mortality up to 30
Externí odkaz:
https://doaj.org/article/02d80b05a3df44808be202096bbb7b3e
Publikováno v:
World Journal of Traditional Chinese Medicine, Vol 4, Iss 1, Pp 21-27 (2018)
Objective: Anthraquinone (AQ), a major bioactive component of the traditional Chinese medicine HeShouWu, has widespread applications in industry and medicine. The objective of the current study is to explore the differences in the bioavailability of
Externí odkaz:
https://doaj.org/article/1e8ca372dfe34a52a498897fe4599386
Autor:
Jin-Tang Cheng, Shi-Tao Chen, Cong Guo, Meng-Jiao Jiao, Wen-Jin Cui, Shu-Hui Wang, Zhe Deng, Chang Chen, Sha Chen, Jun Zhang, An Liu
Publikováno v:
Natural Products and Bioprospecting, Vol 8, Iss 1, Pp 47-56 (2017)
Abstract Six new triterpenoid saponins, aesculusosides A–F (1–6), together with 19 known ones, were isolated from the seeds of Aesculus chinensis. The new structures were elucidated through extensive spectroscopic analyses and by comparison with
Externí odkaz:
https://doaj.org/article/94f8873359c449a991910e5702e23ec7
Publikováno v:
Organic Chemistry Frontiers. 9:973-978
Here we report that 2,4,6-triarylpyrylium salts could perform both energy transfer and electron transfer photocatalysis modes for E → Z isomerization of activated alkenes and cyclization of cinnamic or biaryl carboxylic acids.
Autor:
Zhe Zhuang, Shuang Liu, Jin‐Tang Cheng, Kap‐Sun Yeung, Jennifer X. Qiao, Nicholas A. Meanwell, Jin‐Quan Yu
Publikováno v:
Angewandte Chemie International Edition. 61
Publikováno v:
Angew Chem Int Ed Engl
We report the first example of selective Pd(II)-catalyzed tertiary C−H activation of cyclobutylmethyl ketones using a transient directing group. An electron-deficient 2-pyridone ligand was identified as the optimal external ligand to enable tertiar
Autor:
Han Gao, Shilin Chen, Qinggang Yin, Jin-Tang Cheng, Lianbao Ma, Jing Zhang, Shu-Hui Wang, An Liu, Cong Guo, Han Xiaoyan, Limin Sun
Publikováno v:
Horticulture Research. 8
As auxins are among the most important phytohormones, the regulation of auxin homeostasis is complex. Generally, auxin conjugates, especially IAA glucosides, are predominant at high auxin levels. Previous research on terminal glucosylation focused ma
Publikováno v:
Organic letters. 23(21)
Enamides are versatile precursors for synthesizing bioactive compounds. As their alkylations often require perstoichiometric amounts of oxidants, transition metals, or photocatalysts, we herein report a simple alternative for their alkylations by jus
Autor:
Jin-Tang Cheng, Shilin Chen, Lianbao Ma, An Liu, Cong Guo, Jing Zhang, Han Gao, Shu-Hui Wang, Limin Sun, Qinggang Yin
As a group of the most important phytohormone, auxin homeostasis is regulated in a complex manner. Generally, auxin conjugations especially IAA glucosides are dominant on high auxin level conditions. Former terminal glucosylation researches mainly fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6efdbb9da429e4286911ff6c788325b3
https://doi.org/10.1101/2020.08.30.249292
https://doi.org/10.1101/2020.08.30.249292