Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jing-ru Song"'
Publikováno v:
Molecules, Vol 24, Iss 3, p 437 (2019)
A series of novel structurally simple analogues based on nitidine was designed and synthesized in search of potent anticancer agents. The antitumor activity against human cancer cell lines (HepG2, A549, NCI-H460, and CNE1) was performed by 3-(4,5-dim
Externí odkaz:
https://doaj.org/article/20b39bf28137473386a96020071c95f9
Publikováno v:
Molecules, Vol 23, Iss 7, p 1732 (2018)
Microporous organic polymers (MOPs) are promising materials for gas sorption because of their intrinsic and permanent porosity, designable framework, and low density. The introduction of nitrogen-rich building block in MOPs will greatly enhance the g
Externí odkaz:
https://doaj.org/article/9b7afcc17acf4813a110c8f0468fc5ac
Autor:
Xue‐Rong Yang, Jing‐Ru Song, Xiao‐Hua Jiang, Fei Dong, Xiao‐Jie Yan, Jian‐Xing Li, Xue‐Ying Zhao, Dian‐Peng Li, Feng‐Lai Lu
Publikováno v:
Chemistry & Biodiversity. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fd6d68d889de0415c10de612e1c9566
https://doi.org/10.1002/cbdv.202300025
https://doi.org/10.1002/cbdv.202300025
Rhodomollosides A and B, glycosides of methyl everninate from the aerial parts of Rhododendron molle
Autor:
Xue-Rong Yang, Naonobu Tanaka, Jing-Ru Song, Feng-Lai Lu, Xiao-Jie Yan, Jian-Xing Li, Xue-Ying Zhao, Yoshiki Kashiwada, Dian-Peng Li
Publikováno v:
Journal of Asian Natural Products Research. 24:1025-1032
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::036434f453d4540655e7372103429d0a
https://doi.org/10.1080/10286020.2021.2011241
https://doi.org/10.1080/10286020.2021.2011241
Publikováno v:
Food Bioscience. 52:102379
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e09ec11e34d53708761e521ebf39a25
https://doi.org/10.1016/j.fbio.2023.102379
https://doi.org/10.1016/j.fbio.2023.102379
Publikováno v:
Bioorganicmedicinal chemistry letters. 74
A class of novel mogrol derivatives modified on A ring were synthesized. The screening result showed that indole-fused derivatives exhibited lower toxicity and better anti-inflammatory activity in LPS-induced RAW 264.7 cells model than mogrol and oth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44098f0f03d76fe5a858e84753e4b9ff
https://pubmed.ncbi.nlm.nih.gov/35944853
https://pubmed.ncbi.nlm.nih.gov/35944853
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 42:128090
A series of novel derivatives based on mogrol were designed and synthesized in attempt to improve anti-lung cancer activity. The cytotoxicity against human lung cancer cells including A549 and NCI-H460 were performed by Cell Counting Kit-8 (CCK8) ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1430b26d605adde515af142fd8b81da8
https://doi.org/10.1016/j.bmcl.2021.128090
https://doi.org/10.1016/j.bmcl.2021.128090
Publikováno v:
Chinese Journal of Chemistry. 33:765-770
Five organic complexes are prepared by cocrystallization of tri-[(N-methyl-2-imidazoly)methoxy]cyclotriguiacylene (TMIM-CTG) with corresponding acids. While hydrogen bonds are the basic interactions in the five complexes, the homo-included motifs wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d85f49a3b3037363cbff37b734825033
https://doi.org/10.1002/cjoc.201500199
https://doi.org/10.1002/cjoc.201500199
Publikováno v:
Chem. Commun.. 50:788-791
Two new 2D COFs were synthesized from triformylcyclotrianisylene, which show not only thermal stability but also hydrolytic stability. CTV-COF-1 with smaller pore size stored a high hydrogen level of 1.3 wt% at low pressure, while CTV-COF-2 with larg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::961d514c0fef475480dd9f8dcfa30648
https://doi.org/10.1039/c3cc47652a
https://doi.org/10.1039/c3cc47652a
Publikováno v:
Tetrahedron. 69:7308-7313
C1-symmetric cyclotriveratrylene analogues 2–8 with various functional groups at one benzene moiety were prepared starting from the selectively demethylated compound 1. Through the chemical resolution, a pair of enantiomers of C1-symmeric compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92e1160c0d89beb5cf4b6f8be86b078b
https://doi.org/10.1016/j.tet.2013.06.077
https://doi.org/10.1016/j.tet.2013.06.077