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关于此项目
经验公式(希尔记法):
C22H22N6O7S2 · xH2O
化学文摘社编号:
分子量:
546.58 (anhydrous basis)
NACRES:
NA.85
PubChem Substance ID:
UNSPSC Code:
51284108
MDL number:
Quality Level
assay
90.0-105.0%
form
powder or crystals
contains
~10% sodium carbonate as stabilizer
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria
mode of action
cell wall synthesis | interferes
storage temp.
2-8°C
SMILES string
[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].CC(C)(O\N=C(/C(=O)N[C@H]1[C@H]2SCC(C[n+]3ccccc3)=C(N2C1=O)C([O-])=O)c4csc(N)n4)C(O)=O
InChI
1S/C22H22N6O7S2.5H2O/c1-22(2,20(33)34)35-26-13(12-10-37-21(23)24-12)16(29)25-14-17(30)28-15(19(31)32)11(9-36-18(14)28)8-27-6-4-3-5-7-27;;;;;/h3-7,10,14,18H,8-9H2,1-2H3,(H4-,23,24,25,29,31,32,33,34);5*1H2/b26-13-;;;;;/t14-,18-;;;;;/m1...../s1
InChI key
NMVPEQXCMGEDNH-TZVUEUGBSA-N
General description
广谱抗生素;第三代头孢菌素
化学结构式:β-内酰胺
Application
用于研究青霉素结合蛋白特别是 PBP3 的表达、结合和抑制对细菌细胞壁粘肽合成的影响。
用头孢他啶水合物研究青霉素结合蛋白特别是 PBP3 的表达、结合和抑制对细菌细胞壁粘肽合成的影响。也用于细菌敏感性研究 和选择相关突变菌落。
Biochem/physiol Actions
头孢类抗生素如头孢他啶可破坏细菌细胞壁肽聚糖层的合成。
Other Notes
将容器密闭保存在干燥和通风良好的地方。置干燥处保存
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signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Resp. Sens. 1 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
涉药品监管产品
此项目有
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Colistin is an 'old' drug, which is being increasingly utilized due to limited therapeutic options. However, resistance emergence during monotherapy is concerning. Here, our objective was to optimize colistin combinations against Pseudomonas aeruginosa by profiling the time course of synergistic
Kristopher R Genschmer et al.
Cell, 176(1-2), 113-126 (2019-01-12)
Here, we describe a novel pathogenic entity, the activated PMN (polymorphonuclear leukocyte, i.e., neutrophil)-derived exosome. These CD63+/CD66b+ nanovesicles acquire surface-bound neutrophil elastase (NE) during PMN degranulation, NE being oriented in a configuration resistant to α1-antitrypsin (α1AT). These exosomes bind and
Melissa D Barnes et al.
mBio, 9(6) (2018-12-13)
Pseudomonas aeruginosa produces a class C β-lactamase (e.g., PDC-3) that robustly hydrolyzes early generation cephalosporins often at the diffusion limit; therefore, bacteria possessing these β-lactamases are resistant to many β-lactam antibiotics. In response to this significant clinical threat, ceftolozane, a
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| C3809-1G | 04061833486436 |
| C3809-5G | 04061833486443 |
