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某些环异羟肟酸及相关内酰胺的体外抗菌活性。

In vitro antimicrobial activity of some cyclic hydroxamic acids and related lactams.

作者信息

Davis A L, Hulme K L, Wilson G T, McCord T J

出版信息

Antimicrob Agents Chemother. 1978 Mar;13(3):542-4. doi: 10.1128/AAC.13.3.542.

DOI:10.1128/AAC.13.3.542
PMID:400828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC352279/
Abstract

Against Enterobacter aerogenes 13048, Serratia marcescens 13880, Klebsiella pneumoniae 10031, Pseudomonas aeruginosa 10145, Escherichia coli 9723, Lactobacillus casei 7469, Lactobacillus plantarum 8014, Leuconostoc dextranicum 8086, and Streptococcus faecalis 8043, the mean minimal inhibitory concentrations of three cyclic hydroxamic acids, 3-amino-3,4-dihydro-1-hydroxycarbostyril, the 6-chloro analog, and the 7-chloro analog, were 0.6, 0.6, and 0.2 micrograms/ml, and those of the corresponding lactams, 3-amino-3,4-dihydrocarbostyril, the 6-chloro analog, and the 7-chloro analog, were 60, 60, and 6 micrograms/ml, respectively. Under the same assay conditions the mean minimal inhibitory concentrations of chloramphenicol and kanamycin were both 2 micrograms/ml. In addition, the cyclic hydroxamic acids but not the lactams inhibited the growth of Candida albicans at minimal inhibitory concentrations ranging from 20 to 200 micrograms/ml, at pH 7, as compared with that of amphotericin B, at 2 micrograms/ml.

摘要

针对产气肠杆菌13048、粘质沙雷氏菌13880、肺炎克雷伯菌10031、铜绿假单胞菌10145、大肠杆菌9723、干酪乳杆菌7469、植物乳杆菌8014、右旋糖酐明串珠菌8086和粪肠球菌8043,三种环异羟肟酸(3-氨基-3,4-二氢-1-羟基咔唑、6-氯类似物和7-氯类似物)的平均最低抑菌浓度分别为0.6、0.6和0.2微克/毫升,相应内酰胺(3-氨基-3,4-二氢咔唑、6-氯类似物和7-氯类似物)的平均最低抑菌浓度分别为60、60和6微克/毫升。在相同的检测条件下,氯霉素和卡那霉素的平均最低抑菌浓度均为2微克/毫升。此外,在pH值为7时,与两性霉素B(2微克/毫升)相比,环异羟肟酸而非内酰胺在20至200微克/毫升的最低抑菌浓度下抑制白色念珠菌的生长。

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本文引用的文献

1
Growth Requirements of Virus-Resistant Mutants of Escherichia Coli Strain "B".大肠杆菌菌株“B”的抗病毒突变体的生长需求
Proc Natl Acad Sci U S A. 1946 May;32(5):120-8. doi: 10.1073/pnas.32.5.120.
2
SYNTHESIS AND MICROBIOLOGICAL PROPERTIES OF 3-AMINO-3,4-DIHYDRO-1-HYDROXYCARBOSTYRIL.3-氨基-3,4-二氢-1-羟基咔唑的合成及其微生物学性质
J Med Chem. 1964 Sep;7:632-4. doi: 10.1021/jm00335a014.
3
Inhibition studies with peptides of thienylalanine and phenylalanine.用噻吩丙氨酸和苯丙氨酸肽进行的抑制研究。
J Biol Chem. 1956 Apr;219(2):809-22.
4
Some interrelationships of aspartic acid, threonine, and lysine.
J Biol Chem. 1954 Jan;206(1):391-400.
5
Synthesis and microbiological properties of some substituted derivatives of 3-amino-3,4-dihydrocarbostyril.
J Med Chem. 1970 May;13(3):549-50. doi: 10.1021/jm00297a050.
6
Synthesis and microbiological properties of 3-amino-1-hydroxy-2-indolinone and related compounds.
J Med Chem. 1973 Sep;16(9):1043-5. doi: 10.1021/jm00267a020.
7
Preparation and antimicrobial properties of the D and L forms of 3-amino-3,4-dihydro-1-hydroxycarbostyril.
J Med Chem. 1972 Mar;15(3):325-7. doi: 10.1021/jm00273a028.
8
Hydroxamic acids in nature.自然界中的异羟肟酸。
Science. 1967 Jun 16;156(3781):1443-7. doi: 10.1126/science.156.3781.1443.
9
Synthesis and antibacterial activities of some chloro analogs of 3 amino-3,4-dihydro-1-hydroxycarbostyril.
J Med Chem. 1975 Jul;18(7):752-5. doi: 10.1021/jm00241a022.