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NEISSERIA GONORRHOEAE IDENTIFICATION IN DIRECT SMEARS BY A FLUORESCENT ANTIBODY-COUNTERSTAIN METHOD.采用荧光抗体复染法对直接涂片进行淋病奈瑟菌鉴定。
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ABORTIVE INTESTINAL INFECTION WITH AN ESCHERICHIA COLI-SHIGELLA FLEXNERI HYBRID STRAIN.由大肠埃希菌-福氏志贺菌杂交菌株引起的顿挫型肠道感染
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[Studies on the tuberculostatic activity on new benzaledhyde and thiophene-aldehyde thiosemicarbazones in vitro and in vivo].新型苯甲醛及噻吩醛缩氨基硫脲体外及体内抗结核活性的研究
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2-Acetylpyridine thiosemicarbazones. 2. N4,N4-Disubstituted derivatives as potential antimalarial agents.2-乙酰基吡啶硫代半卡巴腙。2. N4,N4-二取代衍生物作为潜在的抗疟药。
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2-Acetylpyridine thiosemicarbazones. 1. A new class of potential antimalarial agents.2-乙酰吡啶硫代半卡巴腙。1. 一类新型潜在抗疟药。
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2-乙酰吡啶缩氨基硫脲对临床上重要细菌菌株的体外抑制作用。

Inhibition of clinically significant bacterial organisms in vitro by 2-acetylpyridine thiosemicarbazones.

作者信息

Dobek A S, Klayman D L, Dickson E T, Scovill J P, Tramont E C

出版信息

Antimicrob Agents Chemother. 1980 Jul;18(1):27-36. doi: 10.1128/AAC.18.1.27.

DOI:10.1128/AAC.18.1.27
PMID:7416748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC283934/
Abstract

Antibacterial activity of 65 2-acetylpyridine thiosemicarbazones and related compounds was determined by using clinical isolates of nine bacterial genera. Minimal inhibitory concentrations (MICs) of 0.002 to 0.062 micrograms/ml were obtained with 23% of the compounds for Neisseria gonorrhoeae and 0.016 to 0.062 micrograms/ml with 17% of the compounds for N. meningitidis. Staphylococcus aureus was inhibited in the MIC range of 0.125 to 0.5 micrograms/ml by 18% of the thiosemicarbazones, whereas 26% inhibited group D enterococcus with an MIC of 0.25 to 2.0 micrograms/ml. Poor antibacterial activity was shown toward the gram-negative bacilli, i.e., Pseudomonas, Klebsiella-Enterobacter, Shigella, Escherichia coli, and Proteus.

摘要

利用9个细菌属的临床分离菌株测定了65种2-乙酰基吡啶硫代半卡巴腙及相关化合物的抗菌活性。23%的化合物对淋病奈瑟菌的最低抑菌浓度(MIC)为0.002至0.062微克/毫升,17%的化合物对脑膜炎奈瑟菌的MIC为0.016至0.062微克/毫升。18%的硫代半卡巴腙对金黄色葡萄球菌的MIC范围为0.125至0.5微克/毫升,而26%的硫代半卡巴腙对D组肠球菌的MIC为0.25至2.0微克/毫升。对革兰氏阴性杆菌,即假单胞菌、克雷伯菌-肠杆菌、志贺菌、大肠杆菌和变形杆菌,显示出较弱的抗菌活性。