Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Qiu-ye Wu"'
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 7, Pp o1743-o1744 (2011)
The title compound, C15H23N2S+·Cl−·0.5H2O, was prepared from (6aS,11aR,11cS)-2,3,5,6,6a,7,11,11a,11b,11c-decahydro-3a,7a-diaza-1H,4H-benzo[de]anthracene-8-one (sophocarpine) and Lawesson's reagent. The thione-substituted ring is in an envelope co
Externí odkaz:
https://doaj.org/article/21e0625e6503494cb0959af46a80bd23
Autor:
Xiang, Li, Ralph, Krafczyk, Jakub, Macošek, Yu-Lei, Li, Yan, Zou, Bernd, Simon, Xing, Pan, Qiu-Ye, Wu, Fang, Yan, Shan, Li, Janosch, Hennig, Kirsten, Jung, Jürgen, Lassak, Hong-Gang, Hu
Publikováno v:
Chemical Science
Here we describe a potent tool to investigate arginine rhamnosylation and develop novel antibiotics.
A previously discovered posttranslational modification strategy – arginine rhamnosylation – is essential for elongation factor P (EF-P) depe
A previously discovered posttranslational modification strategy – arginine rhamnosylation – is essential for elongation factor P (EF-P) depe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d90660bb21d978303e79fe7dbe770440
https://pubmed.ncbi.nlm.nih.gov/28451135
https://pubmed.ncbi.nlm.nih.gov/28451135
Publikováno v:
Academic Journal of Second Military Medical University. 31:754-758
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cbe68974858c801e022043a3fca3b14
https://doi.org/10.3724/sp.j.1008.2011.00754
https://doi.org/10.3724/sp.j.1008.2011.00754
Publikováno v:
Chinese Chemical Letters. 22:631-634
The first synthesis of the naturally occurring cyclic peptide euryjanicin B has been achieved. A general method was described to synthesize the cyclic peptide by a two-step solid-phase/solution synthesis strategy. All the amino acids in this study ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4c093f6c21e2d000f6b109a30a00b67
https://doi.org/10.1016/j.cclet.2010.12.039
https://doi.org/10.1016/j.cclet.2010.12.039
Publikováno v:
Chinese Chemical Letters. 22:519-522
Based on the active site of lanosterol 14α-demethylase of azole antifungal agents, sixteen 1-(1H-1,2,4-triazole-1-yl)- 2-(2,4-difluorophenyl)-3-(N-n-butyl-N-1-substitutedbenzyl-4-methylene-1H-1,2,3-triazole)-2-propanols have been designed, synthesiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dab19884c302877cda3f17bd90279aeb
https://doi.org/10.1016/j.cclet.2010.11.029
https://doi.org/10.1016/j.cclet.2010.11.029
Autor:
Zhong-jun Guan, Qiu-ye Wu, Zhi-gang Dan, Shi-chong Yu, Ning Wei, Xiao-yun Chai, Xiao-zhong Zhao
Publikováno v:
Academic Journal of Second Military Medical University. 29:1052-1057
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54348724ec19ae470f00176b7965dadb
https://doi.org/10.3724/sp.j.1008.2009.01052
https://doi.org/10.3724/sp.j.1008.2009.01052
Publikováno v:
Chinese Chemical Letters. 20:935-938
A series of 1-(1H-1,2,4-triazole-1-yl)-2-(2,4-difluorophenyl)-3-(N-isoproyl-N-substituted-amino)-2-propanols have been designed and synthesized on the basis of the active site of lanosterol 14a-demethylase (CYP51). Their structures were confirmed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b4d7a512f3f5b95b09e684bdf4fb1cb
https://doi.org/10.1016/j.cclet.2009.03.027
https://doi.org/10.1016/j.cclet.2009.03.027
Publikováno v:
Chinese Medical Journal. 120:1678-1684
Multiple myeloma (MM) is a B lineage plasma cell malignancy which is essentially incurable.1 For the exploration of effective MM cures, immunotherapy, including dendritic cell (DC) based immunotherapy, has attracted significant interest recently due
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c8797dc622b3ce0744e3c62dcbab678
https://doi.org/10.1097/00029330-200710010-00007
https://doi.org/10.1097/00029330-200710010-00007
Publikováno v:
Chinese Chemical Letters. 20:52-54
[1,2,4]-Triazole-[4,3-a]-quinoxaline is an important component of many drugs. The yield of the reported methods for triazole cyclization step was usually as low as 20%. In this article, the triazole cyclization step was successfully done by using mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab62ea1f2be19ae1cb9e1fb77d1215c1
https://doi.org/10.1016/j.cclet.2008.10.019
https://doi.org/10.1016/j.cclet.2008.10.019
Publikováno v:
Chinese Chemical Letters. 18:670-672
Twenty-three 1-(1H-1, 2, 4-thazole-1-yl)-2-(2, 4-difluorophenyl)-3-(N-cycloproyl-N-substituted-amino)-2-propanols were designed and synthesized on the basis of the active site of lanosterol 14α-demethylase. In vitro antifungal activities showed that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a0c078e95fd86341b377e6dfa2939ff
https://doi.org/10.1016/j.cclet.2007.04.019
https://doi.org/10.1016/j.cclet.2007.04.019