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7-(Alpha-(1-methyl-4-pyridinothio)-acetamido) cephalosporanic acid.7 -(α-(1-甲基-4-吡啶硫基)-乙酰胺基)头孢烷酸
Antimicrob Agents Chemother. 1972 Jan;1(1):67-72. doi: 10.1128/AAC.1.1.67.
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Microbiological properties of a new cephalosporin, BL-S 339: 7-(phenylacetimidoyl-aminoacetamido)-3-(2-methyl-1,3,4-thiadiazol-5-ylthiomethyl)ceph-3-em-4-carboxylic acid.一种新型头孢菌素BL-S 339的微生物学特性:7-(苯乙酰亚胺基氨基乙酰氨基)-3-(2-甲基-1,3,4-噻二唑-5-基硫代甲基)头孢-3-烯-4-羧酸
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Structure-activity relationships among a group of 7-(alpha-(N,N'-substituted-amidinothio)-acetamido) cephalosphoranic acids.一组7 -(α-(N,N'-取代脒硫基)-乙酰胺基)头孢菌素酸的构效关系
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A comparison of the in vitro activity of a new cephalosporin, cefuroxime, and cephalothin against 810 clinical isolates.一种新型头孢菌素头孢呋辛与头孢噻吩对810株临床分离菌的体外活性比较。
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引用本文的文献

1
New in vitro model to study the effect of antibiotic concentration and rate of elimination on antibacterial activity.用于研究抗生素浓度和消除速率对抗菌活性影响的新型体外模型。
Antimicrob Agents Chemother. 1978 Apr;13(4):570-6. doi: 10.1128/AAC.13.4.570.

本文引用的文献

1
Preliminary microbiological and pharmacological evaluation of 6-(R-alpha-amino-3-thienylacetamido) penicillanic acid (BL-P 875).
J Antibiot (Tokyo). 1969 Jan;22(1):1-11. doi: 10.7164/antibiotics.22.1.

7 -(α-(1-甲基-4-吡啶硫基)-乙酰胺基)头孢烷酸

7-(Alpha-(1-methyl-4-pyridinothio)-acetamido) cephalosporanic acid.

作者信息

Buck R E, Leitner F, Price K E

出版信息

Antimicrob Agents Chemother. 1972 Jan;1(1):67-72. doi: 10.1128/AAC.1.1.67.

DOI:10.1128/AAC.1.1.67
PMID:4670430
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC444167/
Abstract

7-[alpha-(1-Methyl-4-pyridiniothio)-acetamido] cephalosporanic acid, referred to herein as BL-S 217, is a new broad-spectrum semisynthetic cephalosporin that offers several advantages over cephalothin. A comparison of the activity in vitro of these antibiotics indicates that BL-S 217 is about eightfold more effective against Streptococcus pyogenes and Diplococcus pneumoniae. Against gram-negative bacteria, BL-S 217 possesses a broader antibacterial spectrum than cephalothin, particularly against members of the Enterobacteriaceae family; e.g., BL-S 217 inhibited over 20% more strains of both Escherichia coli and Klebsiella than cephalothin and also showed some advantage in tests against Salmonella and Enterobacter. Overall, of 208 strains of Enterobacteriaceae tested, 172 were susceptible to BL-S 217 compared to 149 for cephalothin. BL-S 217 was less bound to human serum proteins than cephalothin and gave higher peak blood levels in mice after intramuscular administration. The LD(50) of BL-S 217 in mice after subcutaneous administration was in excess of 4,000 mg/kg. When administered by the same route to mice experimentally infected with cephalothin-sensitive bacterial strains, this new cephalosporin was 20 times more effective than cephalothin in S. pyogenes and D. pneumoniae infections and 3 to 4 times more efficacious in an E. coli infection. Its therapeutic efficacy was comparable to that of cephalothin in infections produced by strains of Staphylococcus aureus, Klebsiella pneumoniae, and Proteus mirabilis.

摘要

7-[α-(1-甲基-4-吡啶硫基)-乙酰胺基]头孢烷酸,本文中称为BL-S 217,是一种新型广谱半合成头孢菌素,与头孢噻吩相比具有多个优势。这些抗生素的体外活性比较表明,BL-S 217对化脓性链球菌和肺炎双球菌的效力约为头孢噻吩的八倍。针对革兰氏阴性菌,BL-S 217比头孢噻吩具有更广泛的抗菌谱,特别是对肠杆菌科成员;例如,BL-S 217对大肠杆菌和克雷伯菌的抑制菌株比头孢噻吩多20%以上,并且在针对沙门氏菌和肠杆菌的测试中也显示出一些优势。总体而言,在测试的208株肠杆菌科菌株中,172株对BL-S 217敏感,而头孢噻吩为149株。与头孢噻吩相比,BL-S 217与人类血清蛋白的结合较少,肌肉注射后在小鼠体内产生的血药峰值较高。皮下给药后,BL-S 217在小鼠中的半数致死量超过4000 mg/kg。当以相同途径给实验感染头孢噻吩敏感菌株的小鼠给药时,这种新型头孢菌素在化脓性链球菌和肺炎双球菌感染中比头孢噻吩有效20倍,在大肠杆菌感染中效力高3至4倍。在由金黄色葡萄球菌、肺炎克雷伯菌和奇异变形杆菌菌株引起的感染中,其治疗效果与头孢噻吩相当。