The crystal structure of 3-(1H-benzo[d]imidazol-2-yl)-7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydroquinolin — dimethylsulfoxide (1/1), C21H19ClFN3O2S
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[1] Raed A. Al‐Qawasmeh,et al. Design, Synthesis and Qualitative Structure Activity Relationship Evaluations of Quinoline-Based Bisarylimidazoles as Antibacterial Motifs. , 2016, Medicinal chemistry (Shariqah (United Arab Emirates)).
[2] Richard J. Gildea,et al. The anatomy of a comprehensive constrained, restrained refinement program for the modern computing environment – Olex2 dissected , 2015, Acta crystallographica. Section A, Foundations and advances.
[3] G. Sheldrick. SHELXT – Integrated space-group and crystal-structure determination , 2015, Acta crystallographica. Section A, Foundations and advances.
[4] Jalal A. Zahra,et al. Design synthesis and antibacterial activity studies of new thiadiazoloquinolone compounds , 2014, Journal of enzyme inhibition and medicinal chemistry.
[5] Raed A. Al‐Qawasmeh,et al. Design, synthesis and in vitro antimicrobial evaluation of novel Imidazo[1,2-a]pyridine and imidazo[2,1-b][1,3]benzothiazole motifs. , 2011, European journal of medicinal chemistry.
[6] Jalal A. Zahra,et al. Synthesis and antibacterial activity of 9-cyclopropyl-4-fluoro-6-oxo- 6,9-dihydro-(1,2,5)thiadiazolo(3,4-h)quinoline-7-carboxylic acid and its ethyl ester , 2009 .
[7] Richard J. Gildea,et al. OLEX2: a complete structure solution, refinement and analysis program , 2009 .
[8] L. Mitscher. Bacterial topoisomerase inhibitors: quinolone and pyridone antibacterial agents. , 2005, Chemical reviews.
[9] Raed A. Al‐Qawasmeh,et al. Synthesis and properties of some 2,3‐disubstituted 6‐fluoro‐7‐(4‐methyl‐1‐piperazinyl)quinoxalines , 2000 .
[10] L. Mitscher,et al. The 2‐pyridone antibacterial agents: bacterial topoisomerase inhibitors , 2000, Medicinal research reviews.