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两种研究用甘氨酰环素,即DMG-DMDOT和DMG-MINO。针对革兰氏阳性菌的抗菌活性研究。

Two investigational glycylcyclines, DMG-DMDOT and DMG-MINO. Antimicrobial activity studies against gram-positive species.

作者信息

Johnson D M, Jones R N

机构信息

Department of Pathology, University of Iowa College of Medicine, Iowa City 52242, USA.

出版信息

Diagn Microbiol Infect Dis. 1996 Jan;24(1):53-7. doi: 10.1016/0732-8893(95)00250-2.

Abstract

DMG-DMDOT (CL-331,002 OR CL-331,928) and DMG-MINO (CL-329,998 or CL-344,677) are two new semisynthetic tetracyclines called glycylcyclines, with a broad spectrum of activity and includes Enterobacteriaceae, Gram-positive cocci, JK diphtheroids, and Bacillus cereus. Potent activity was demonstrated against all Streptococcus spp. strains [minimum inhibitory concentrations] (MIC90S) 0.06-0.25 micrograms/ml) and staphylococci (oxacillin susceptible ans resistant; MIC90S 0.12-2 micrograms/ml). Both glycylcyclines (MIC90, 0.06 micrograms/ml) were more potent than minocycline (MIC90 8 micrograms/ml) against Enterococcus faecium, many of which were vancomycin resistant (116 strains). Organisms with minocycline MICs at > or = 8 micrograms/ml (Staphylococcus aureus, enterococci, beta-hemolytic streptococci, and pneumococci) had glycylcycline MIC results ranging from 0.06 to 0.5 micrograms/ml (e.g., apparent use against existing tetracycline-resistance phenotypes). Drugs in this class appear promising for therapy of infections caused by Gram-positive species now testing resistant to contemporary antimicrobial agents, and further development of compounds in this class is encouraged.

摘要

DMG - DMDOT(CL - 331,002或CL - 331,928)和DMG - MINO(CL - 329,998或CL - 344,677)是两种新的半合成四环素类药物,称为甘氨酰环素,具有广泛的活性,包括肠杆菌科、革兰氏阳性球菌、JK类白喉杆菌和蜡样芽孢杆菌。对所有链球菌属菌株均显示出强效活性[最低抑菌浓度](MIC90S为0.06 - 0.25微克/毫升)和葡萄球菌(对苯唑西林敏感和耐药;MIC90S为0.12 - 2微克/毫升)。两种甘氨酰环素(MIC90为0.06微克/毫升)对粪肠球菌的活性均强于米诺环素(MIC90为8微克/毫升),其中许多菌株对万古霉素耐药(116株)。米诺环素MICs≥8微克/毫升的微生物(金黄色葡萄球菌、肠球菌、β溶血性链球菌和肺炎球菌)的甘氨酰环素MIC结果为0.06至0.5微克/毫升(例如,对现有的四环素耐药表型有明显作用)。这类药物对于治疗目前对当代抗菌药物耐药的革兰氏阳性菌引起的感染似乎很有前景,因此鼓励对这类化合物进行进一步研发。

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