Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Hui-Yuan Guo"'
Publikováno v:
Molecules, Vol 16, Iss 3, Pp 2626-2635 (2011)
A series of novel 7-(3-amino-6,7-dihydro-2-methyl-2H-pyrazolo[4,3-c]pyridin- 5(4H)-yl)fluoroquinolone derivatives were designed, synthesized and characterized by 1H-NMR, MS and HRMS. These fluoroquinolones were evaluated for their in vitro antibacter
Externí odkaz:
https://doaj.org/article/c84557b6a8e0411483f70e8e3f50b503
Autor:
Yunhe Geng, Hui-Yuan Guo, Zengquan Wei, Lu-Xin Na, Zhi Xu, Shu Zhang, Xue-Fu You, Lianshun Feng, Ming-Liang Liu
Publikováno v:
Revue Roumaine de Chimie. 64:101-107
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93cb9799204cd27f199e85886932ea6b
https://doi.org/10.33224/rrch.2019.64.1.10
https://doi.org/10.33224/rrch.2019.64.1.10
Autor:
Zhi Xu, Shu Zhang, Lian-Shun Feng, Xiao-Ning Li, Guo-Cheng Huang, Yun Chai, Zao-Sheng Lv, Hui-Yuan Guo, Ming-Liang Liu
Publikováno v:
Molecules, Vol 22, Iss 7, p 1171 (2017)
A series of novel 8-OMe ciprofloxacin (CPFX)-hydrazone/azole hybrids were designed, synthesized, and evaluated for their in vitro biological activities. Our results reveal that all of the hydrozone-containing hybrids (except for 7) show potency again
Externí odkaz:
https://doaj.org/article/ce025dc21574453cbab34f7410f34424
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 2, Pp o282-o282 (2009)
In the title compound, C13H23N3O4, the piperidine ring adopts a chair conformation. An intramolecular N—H...O hydrogen bond is observed between the carbamoyl and carboxylate groups. In the crystal structure, molecules form inversion dimers linked b
Externí odkaz:
https://doaj.org/article/6d70cab00a3e4db191734ace0d77af0a
Autor:
Xuefu You, Hui-Yuan Guo, Wei-Xin Zhang, Congran Li, Xuan-Wang You, Min Yuan, Shan Cen, Ren-Hui Lou, Guoqing Li, Jiang Jiandong, Xinyi Yang, Xinxin Hu
Publikováno v:
Chemotherapy. 58:175-184
Background: Chinfloxacin is a novel synthetic fluoroquinolone with a structure similar to moxifloxacin. The in vitro activity of chinfloxacin was evaluated in the current study. Method: Chinfloxacin was tested against a total of 1,739 clinical isolat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b208515c06ca146a60c154fcccf87f0d
https://doi.org/10.1159/000337084
https://doi.org/10.1159/000337084
Publikováno v:
Journal of Food Biochemistry. 36:706-717
This article investigates the impact of sesame protein isolate (SPI) and increased calcium in milk on the biochemistry, rheology and micro-structure of cheese. The characteristics of two sets of cheeses made from raw milk and milk of 8% protein subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1b730a090656abb8cc5527a1d65bc54
https://doi.org/10.1111/j.1745-4514.2011.00593.x
https://doi.org/10.1111/j.1745-4514.2011.00593.x
Publikováno v:
Chinese Chemical Letters. 21:1141-1144
A series of novel 7-(3-aminopyrrolo[3,4-c]pyrazol-5(2H,4H,6H)-yl)quinolone derivatives were designed, synthesized and evaluated for in vitro antibacterial activities. Compounds 6g, 7g and 7h with the potencies similar to those of gemifloxacin, moxifl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e4830a5832a98677abfc067177d2bbe
https://doi.org/10.1016/j.cclet.2010.06.011
https://doi.org/10.1016/j.cclet.2010.06.011
Publikováno v:
Chinese Chemical Letters. 21:55-58
A series of novel 7-(4-alkoxyimino-3-hydroxypiperidin-1-yl)quinolone derivatives were designed, synthesized and evaluated for in vitro antibacterial activities. Compounds 8f, 8g, 8i and 8j with the potencies similar to or better than those of levoflo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ca08ef2d04bfa4aba70e5186068309
https://doi.org/10.1016/j.cclet.2009.07.011
https://doi.org/10.1016/j.cclet.2009.07.011
Autor:
Hui Yuan Guo, Yun Xu Yang
Publikováno v:
Chinese Chemical Letters. 18:1479-1482
Several 6,8-dichloroquinolone analogues were synthesized from the key intermediate compound of 2,3,4,5-tetrachlorobenzene carbonyl chloride, which was obtained from the starting material of tetrachlorophthalic anhydride. Their in vitro antibacterial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e03c2112dcc5fa2cedc98a0cd8a3dc4d
https://doi.org/10.1016/j.cclet.2007.10.012
https://doi.org/10.1016/j.cclet.2007.10.012
Publikováno v:
Chinese Chemical Letters. 18:1169-1172
7-[4-(Aminomethyl)-3-(methoxyimino) pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-8-difluoromethoxy-1, 4-dihydro-4-oxoquinoline-3-carboxylic acid and its analogues have been prepared and evaluated for antibacterial activity in vitro.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d58d2da355d5cfb835ec0c858c07d1ff
https://doi.org/10.1016/j.cclet.2007.07.030
https://doi.org/10.1016/j.cclet.2007.07.030