Synthesis of Best-Seller Drugs 2016
DOI: 10.1016/b978-0-12-411492-0.00031-6
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Antibacterial Drugs

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Cited by 10 publications
(6 citation statements)
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“…(−)-Levofloxacin was found being twice as more active than ofloxacin. 422 The synthetic pathway including resolution of racemic mixture to obtain (−)-levofloxacin 384 was designed and performed as depicted in Scheme 52 . Based on this approach, the synthesis began from the reaction of 2,3-difluoro-6-nitrophenol 375 with chloroacetone 376 in the presence of K 2 CO 3 and potassium iodide to provide 1-(2,3-difluoro-6-nitrophenoxy)propan-2-one 377.…”
Section: Synthesis Of Nitrogen Prescribed Drugs Havingmentioning
confidence: 99%
“…(−)-Levofloxacin was found being twice as more active than ofloxacin. 422 The synthetic pathway including resolution of racemic mixture to obtain (−)-levofloxacin 384 was designed and performed as depicted in Scheme 52 . Based on this approach, the synthesis began from the reaction of 2,3-difluoro-6-nitrophenol 375 with chloroacetone 376 in the presence of K 2 CO 3 and potassium iodide to provide 1-(2,3-difluoro-6-nitrophenoxy)propan-2-one 377.…”
Section: Synthesis Of Nitrogen Prescribed Drugs Havingmentioning
confidence: 99%
“…Broad bimodal or multimodal profiles were observed for NIT. The basic action mechanism of nitrofuran ABs such as NIT is unclear (Vardanyan and Hruby, 2016). Multiple mechanisms like the inhibition of many microbial enzyme systems or damage to DNA, RNA and proteins are described (Blass, 2015;Vardanyan and Hruby, 2016).…”
Section: Discussionmentioning
confidence: 99%
“…The basic action mechanism of nitrofuran ABs such as NIT is unclear (Vardanyan and Hruby, 2016). Multiple mechanisms like the inhibition of many microbial enzyme systems or damage to DNA, RNA and proteins are described (Blass, 2015;Vardanyan and Hruby, 2016). These diverse mechanisms could explain the obtained profiles, since accumulations of different numbers of adequate resistance mechanisms could lead to a broad MIC distribution (Phillips, 1998).…”
Section: Discussionmentioning
confidence: 99%
“…Pradofloxacin is more active against Gram-positive bacteria comparative to previous generations. Also, pradofloxacin exhibits good activity against anaerobic bacteria, similar to moxifloxacin, and an equal or lower activity against Gram-negative bacteria [ 36 , 156 , 157 ]. The C8 cyano group appears to play an essential role in activity against Gram-positive when comparing finafloxacin with pradofloxacin ( Figure 7 ).…”
Section: Compounds In Therapy Since 2000mentioning
confidence: 99%