Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Kui, Jing"'
Autor:
Sheng-Ge Li, Xu Hu, Qin Zhang, Yan-Hui Zan, Kai-Bo Wang, Chun-Yu Jiang, Jing-Jing Xue, Yong-Xiang Liu, Bin Lin, Yong-Kui Jing, Da-Hong Li, Hui-Ming Hua
Publikováno v:
Organic & Biomolecular Chemistry. 20:8528-8532
Two pairs of unprecedented β-carboline-phenylpropanoid alkaloids, (±)-pheharmines A–B (1–4), characterized by a morpholino[4,3,2-hi]β-carboline core with two chiral centers, were isolated from the roots of Peganum harmala.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb044aad6173b5e3e0614c2764649684
https://doi.org/10.1039/d2ob01608g
https://doi.org/10.1039/d2ob01608g
Autor:
Chun-Xue Zhao, Hui Liu, Xin Zhang, Meng-Yue Yang, Yue-Tong Wang, Yi-Jia Xing, Jun-Xin Hua, Qin Zhang, Da-Hong Li, Jiao Bai, Yong-Kui Jing, Hui-Ming Hua
Publikováno v:
Organic & Biomolecular Chemistry. 20:7076-7084
1 is the first nitrogen-oxidized homoerythrina-type alkaloid isolated from Cephalotaxus genus. 31 exhibited a significant antitumor effect in THP-1 and K562 cancer cell lines with GI50 values of 0.24 and 0.29 μM.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eb5d71cb9d70766044f5d40d34fe0a8
https://doi.org/10.1039/d2ob01242a
https://doi.org/10.1039/d2ob01242a
Publikováno v:
Journal of Global Optimization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9c7859883d27bfd4627feb961ea54bb
https://doi.org/10.1007/s10898-022-01259-4
https://doi.org/10.1007/s10898-022-01259-4
Publikováno v:
Advances in Applied Chemistry and Industrial Catalysis ISBN: 9781003308553
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cb5894c0208d0560e48f02af3b7eb10
https://doi.org/10.1201/9781003308553-58
https://doi.org/10.1201/9781003308553-58
Autor:
Meng-Yue Yang, Zhao-Xiang Shao, Yue-Tong Wang, Yong-Lian Hou, Ding-Kang Zhu, Sha Chen, Ya-Hui Zhang, Fei Cao, Yong-Kui Jing, Bin Lin, Zhan-Lin Li, Da-Hong Li, Hui-Ming Hua
Publikováno v:
Phytochemistry. 205
Stilbenes (based on the 1,2-diphenylethylene skeleton) are a class of plant polyphenols with rich structural and bioactive diversity. Twenty-six stilbenes, including five undescribed compounds (7,8-dioxy-4,3',5'-trihydroxystilbene, trans-13'-methoxyg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13228e213acceed7feb57cf82efd0551
https://pubmed.ncbi.nlm.nih.gov/36403670
https://pubmed.ncbi.nlm.nih.gov/36403670
Autor:
Hui-Ming Hua, Jingjing Xue, Yong-Kui Jing, Yue-Tong Wang, Qin Zhang, Dahong Li, Bin Lin, Kai-Bo Wang, Sheng-Ge Li
Publikováno v:
Organic Letters. 22:7522-7525
Two nonbiaryl axially chiral β-carboline-quinazoline dimers, pegaharmols A (1) and B (2), were isolated from the roots of Peganum harmala. Their planar structures were elucidated by the spectroscopic methods of high-resolution mass spectrometry and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa25912611b67194246c9c0c03238f58
https://doi.org/10.1021/acs.orglett.0c02709
https://doi.org/10.1021/acs.orglett.0c02709
Publikováno v:
International Transactions in Operational Research. 29:87-112
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f71c3fb59b474d810c282dbd1b6dc2f7
https://doi.org/10.1111/itor.12856
https://doi.org/10.1111/itor.12856
Publikováno v:
Molecules, Vol 14, Iss 10, Pp 4166-4179 (2009)
A series of novel 2-phenylaminopyrimidine (PAP) derivatives structurally related to STI-571 were designed and synthesized. The abilities of these compounds to inhibit proliferation were tested in human chronic myeloid leukemia K562 cells. (E)-3-(2-br
Externí odkaz:
https://doaj.org/article/61932666a7954473b901348f985eb047
Publikováno v:
Molecules, Vol 13, Iss 7, Pp 1487-1500 (2008)
Twenty-six 5-azacytidine analogues have been synthesized, including 4-amino- 6-alkyl-1-pyranosyl/ribofuranosyl-1,3,5-triazin-2(1H)-ones 1a-j, 6-amino-4-alkyl/aryl-1- pyranosyl/ribofuranosyl-1,3,5-triazin-2(1H)-ones 2a-f and 4-amino-6-alkyl-1,3,5-tria
Externí odkaz:
https://doaj.org/article/a3ce0f5beb494df89193278217355892