セファロチンナトリウム 化学特性,用途語,生産方法
外観
白色～うすい黄色, 結晶～粉末
溶解性
水に溶けやすく、メタノールに溶けにくく、エタノール(95)に極めて溶けにくく，アセトニトリルにほとんど溶けない。
用途
第 1 世代セフェム系抗生物質
です。ペニシリン結合タンパク質に結合し、
細胞壁の合成阻害作用を示します。抗菌スペ
クトルは狭いが、ブドウ球菌などに抗菌作用
を示します。
用途
第 1 世代のセファロスポリン
系抗生物質です。ペニシリン結合タンパクに
結合し、細胞壁の合成阻害作用を示します。
抗菌スペクトルは狭いが、ブドウ球菌等に抗
菌作用を示します。
効能
抗生物質, 細胞壁合成阻害薬
説明
Cefalothin is a β-lactam cephalosporin antibiotic. It inhibits the growth of various Gram-positive and Gram-negative bacteria, including several strains of
S. pyogenes,
S. aureus,
C. tetani,
N. gonorrhoeae,
Salmonella, and
Shigella (MICs = 0.1-0.2, 0.312-0.625, 0.078, 1.25, 1.56-6.25, and 3.12-12.5 μg/ml, respectively). Cefalothin binds to
E. coli penicillin-binding proteins (PBPs; IC
50s = <0.25, 16, 37, and 1 μg/ml for PBP1a, 1bs, 2, and 3, respectively, in a radioligand binding assay), which interferes with bacterial morphogenesis. It exhibits antibacterial activity in mouse models of infection with
S. pyogenes,
D. pneumoniae, and
S. aureus. Formulations containing cefalothin were previously used in the prophylaxis and treatment of bacterial infections.
化学的特性
Crystalline
使用
Cephalothin sodium salt is used to study the mechanism of liposome encapsulated antibiotics1, strategies for co-opting β-lactamases of Gram-negative bacteria for treatment of antibiotics2, and for immunology studies in relation to antibiotics.3 It is used to study the effect of expression, binding and inhibition of penicillin-binding proteins especially PBP6 on bacterial cell wall mucopeptide synthesis.
一般的な説明
Cephalothin, along with cephaloridine, was the first of the synthetic cephalosporin C class antibiotics to be introduced clinically. It was synthesized from 7-amino-cephalosporanic acid by Lilly Research Laboratories in 1962. Cephalothin shows strong activity against gram-positive and gram-negative bacteria and Leptospira, including benzylpenicillin-resistant strains. It has been used intravenously and intramuscularly to treat a variety of infections caused by Staphylococcus, Streptococcus, Escherichia coli, and Neisseria. The drug is metabolized in vivo, and the metabolite, deacetylcephalothin, is almost inactive.
臨床応用
Cephalothin sodium (Keflin) occurs as a white to off-white,crystalline powder that is practically odorless. It is freelysoluble in water and insoluble in most organic solvents.Although it has been described as a broad-spectrum antibacterialcompound, it is not in the same class as the tetracyclines.Its spectrum of activity is broader than that ofpenicillin G and more similar to that of ampicillin. Unlikeampicillin, cephalothin is resistant to penicillinase producedby S. aureus and provides an alternative to the use ofpenicillinase-resistant penicillins for the treatment of infectionscaused by such strains.
Cephalothin is absorbed poorly from the GI tract andmust be administered parenterally for systemic infections. It is relatively nontoxic and acid stable. It is excreted rapidlythrough the kidneys; about 60% is lost within 6 hours of administration.Pain at the site of intramuscular injection andthrombophlebitis following intravenous injection have beenreported. Hypersensitivity reactions have been observed,and there is some evidence of cross-sensitivity in patientsnoted previously to be penicillin sensitive.
セファロチンナトリウム 上流と下流の製品情報
原材料
準備製品