Ten new thiocarbamyl ciprofloxacin derivatives and six their pivaloyloxymethyl esters were synthesized and evaluated for their antibacterial activity in vitro. Compound[11],N-methylthiocarbamyl ciprofloxacin exhibited the growth inhibitory activi...
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https://www.riss.kr/link?id=A30057145
1994
Korean
518
학술저널
133-143(11쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
Ten new thiocarbamyl ciprofloxacin derivatives and six their pivaloyloxymethyl esters were synthesized and evaluated for their antibacterial activity in vitro. Compound[11],N-methylthiocarbamyl ciprofloxacin exhibited the growth inhibitory activi...
Ten new thiocarbamyl ciprofloxacin derivatives and six their pivaloyloxymethyl esters were synthesized and evaluated for their antibacterial activity in vitro.
Compound[11],N-methylthiocarbamyl ciprofloxacin exhibited the growth inhibitory activity at a concentration of 0.5㎍/ml against S. aureus SG 511, 0.12㎍/ml against Ps. aeruginosa 1771M and 0.06㎍/ml against Ps. aeruginosa 1592E.
In general, aliphatic substituted thiocarbamyl ciprofloxacin showed more potent antibacterial activity than aromatic substituted thiocarbamyl ciprofloxacins.
4,5-Dihydro-6-[3-nitro-4-methoxyphenyl]-5-methyl-3-[2H]-pyridazinone과 Rolipram의 혈소판응집 억제작용
Mice에서 GPC phospocholine phosphodiesterase의 활성을 이용한 실험적 알러지성 뇌척수염의 약물 검색법에 관한 연구