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セフトロザン

2-[(Z)-[2-[[(6R,7R)-3-[[5-amino-4-(2-aminoethylcarbamoylamino)-1-methylpyrazol-2-ium-2-yl]methyl]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-7-yl]amino]-1-(5-amino-1,2,4-thiadiazol-3-yl)-2-oxoethylidene]amino]oxy-2-methylpropanoate

HCID 71457955
ノートを作成反応を作成見積依頼を出す印刷プレビュー
基本情報概要名称と識別子物性化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
689293-68-3
標準SMILES
Cn1c(N)c(NC(=O)NCCN)c[n+]1CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)/C(=N\OC(C)(C)C(=O)[O-])c3nsc(N)n3)[C@H]2SC1
InChIKey
JHFNIHVVXRKLEF-DCZLAGFPSA-N
分子式
C23H30N12O8S2
平均分子量
666.7 g/mol
単同位体質量
666.17509831

概要

Ceftolozane is a semi-synthetic broad-spectrum fifth generation cephalosporin. It was approved by the FDA in 2014 for use in combination with [Tazobactam] for the treatment of serious infections, such as intra-abdominal infections and complicated urinary tract infections. The manufacturer of this drug is Cubist Pharmaceuticals. Most recently, in June 2019, ceftolozane-tazobactam was approved for the treatment of hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia. Hospital-acquired pneumonia and ventilator-associated pneumonia are major causes of morbidity and mortality in hospitalized patients and the use of ceftolozane-tazobactam offers effective activity against various organisms causing these infections, such as Pseudomonas aeruginosa.

名称と識別子

優先名称
2-[(Z)-[2-[[(6R,7R)-3-[[5-amino-4-(2-aminoethylcarbamoylamino)-1-methylpyrazol-2-ium-2-yl]methyl]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-7-yl]amino]-1-(5-amino-1,2,4-thiadiazol-3-yl)-2-oxoethylidene]amino]oxy-2-methylpropanoate
IUPAC
2-[(Z)-[2-[[(6R,7R)-3-[[5-amino-4-(2-aminoethylcarbamoylamino)-1-methylpyrazol-2-ium-2-yl]methyl]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-7-yl]amino]-1-(5-amino-1,2,4-thiadiazol-3-yl)-2-oxoethylidene]amino]oxy-2-methylpropanoate
現地名
セフトロザン
英語名
Ceftolozane Sulfate
分子式
C23H30N12O8S2
分子量
666.69

名称と別名

CXA-101CHEMBL2103872SCHEMBL29359487セフトロザンCeftolozaneCeftolozane (CXA-101) TFA saltJNYY93683CeftalozaneCeftolozare[2H6]-CeftolozaneCeftolozane SulfateCeftolozaneQ: What is Ceftolozane Q: What is the CAS Number of Ceftolozane

データベース識別子

CAS
689293-68-3
PubChem CID
71457955
ChEMBL
CHEMBL2103872

物性

構造計算による物性

XLogP
-3.2
極性表面積
356 Ų
水素結合供与体数
7
水素結合受容体数
16
回転可能結合数
11
重原子数
45
形式電荷
0
複雑度
1,280

物理化学的性質

外見
Solid
色
White to off-white

化学と産業

薬理情報

Protein Binding16% to 21% bound to plasma proteins.
Pharmacodynamics · 1 件

Ceftolozane exerts bactericidal activities against susceptible gram-negative and gram-positive infections by interfering with bacterial cell wall synthesis. When it is combined with tazobactam, it exerts further activity against beta-lactamase enzyme producing bacteria, which are normally resistant to beta-lactam antibiotics and interfere with infection treatment. The addition of tazobactam strengthens the therapeutic response to ceftolozane, giving it the ability to treat a broader range of bacterial infections and resistant organisms.

Mechanism of Action · 1 件

Ceftolozane belongs to the cephalosporin class of antibacterial drugs. Ceftolozane exerts antibacterial effects, preventing the formation of cell walls that protect bacteria from injury and confer resistance to some antibiotics. Its antibacterial activity is also mediated through ceftolozane binding to penicillin-binding proteins (PBPs), which are required for peptidoglycan cross-linking for bacterial cell wall synthesis. As a result of cell wall synthesis inhibition, bacterial cells are killed, treating various infections. Ceftolozane has a particularly high affinity to the penicillin-binding proteins for Pseudomonas aeruginosa and Escherichia coli as well as Klebsiella pneumoniae and other enteric bacteria. In particular, a high affinity has been seen in vitro for penicillin-binding proteins 1b, 1c, 2, and 3 when compared to other antibiotics, ceftazidime and imipenem.

Biological Half-Life2.77 hours on day 1 of treatment on a dose of 1 g/0.5 g every 8 hours. 3.12 hours on day 10 of treatment on a dose of 1 g/0.5 g every 8 hours.
Metabolism/MetabolitesCertolozane is not metabolized to any significant extent. The beta-lactam ring of tazobactam, when administered as ceftolozane-tazobactam, is hydrolyzed to form an inactive metabolite.
Absorption, Distribution and Excretion · 4 件

The area under the curve (AUC) of ceftolozane-tazobactam after an injected dose of 1 g/0.5 g every 8 hours for 1 day was 172 mcg•h/mL. The Cmax (peak concentration) and AUC are dose-dependent. The Cmax on day one of the above dose of ceftolozane-tazobactam was 69.1 mcg/mL.

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関連反応

6 件
反応記録を作成
HRID 868757 の反応式
HRID 868757生成物としてuspto-grants-2015_03
HRID 1399504 の反応式
HRID 1399504反応物としてuspto-grants-2014_12
HRID 1399505 の反応式
HRID 1399505反応物としてuspto-grants-2014_12
HRID 1399506 の反応式
HRID 1399506生成物としてuspto-grants-2014_12
HRID 2167044 の反応式
HRID 2167044生成物としてuspto-grants-2015_06
HRID 2167045 の反応式
HRID 2167045生成物としてuspto-grants-2015_06

化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性化学と産業関連反応化合物ノート

Ceftolozane is mainly excreted in the urine.

13.5 L. Tissue distribution of ceftalozone-tazobactam is rapid and shows good penetration into the lung, rendering it an ideal treatment for bacterial pneumonia.

The renal clearance of was measured to be 3.41 – 6.69 L/h after a single dose of ceftolozane-tazobactam. Dose adjustments of this drug are required in patients with impaired renal function with a creatinine clearance of 50 mL/min or below. Consult official labeling for dosing adjustment guidelines.