所有图片(1)
About This Item
经验公式（希尔记法）:
C16H16N5NaO7S2
CAS号:
分子量:
477.45
Beilstein:
5711411
EC號碼:
MDL號碼:
分類程式碼代碼:
51101500
推荐产品
化驗
≥98.0% (TLC)
雜質
≤5% water
溶解度
H2O: 50 mg/mL, clear, light yellow
作用方式
cell wall synthesis | interferes
儲存溫度
2-8°C
SMILES 字串
[Na+].[H][C@]12SCC(COC(C)=O)=C(N1C(=O)[C@H]2NC(=O)C(=N/OC)\c3csc(N)n3)C([O-])=O
InChI
1S/C16H17N5O7S2.Na/c1-6(22)28-3-7-4-29-14-10(13(24)21(14)11(7)15(25)26)19-12(23)9(20-27-2)8-5-30-16(17)18-8;/h5,10,14H,3-4H2,1-2H3,(H2,17,18)(H,19,23)(H,25,26);/q;+1/p-1/b20-9-;/t10-,14-;/m1./s1
InChI 密鑰
AZZMGZXNTDTSME-JUZDKLSSSA-M
正在寻找类似产品? 访问 产品对比指南
一般說明
Chemical structure: ß-lactam
生化／生理作用
Cefotaxim inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) which inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls. As a result, bacteria lyse due to cell wall autolytic enzymes.
其他說明
Broad spectrum third generation cephalosporin antibiotic.
This product has been replaced by C7912-SIGMA | Cefotaxime sodium salt potency: 916-964 μg per mg
其他客户在看
Laetitia Betelli et al.
Talanta, 184, 210-218 (2018-04-21)
The accurate identification of β-lactamases produced by Enterobacteriaceae is a major challenge in clinical laboratories in order to optimize antimicrobial treatment and patient care. We describe here a rapid voltammetric-based method to detect and to discriminate β-lactamase activity in Enterobacteriaceae
Carola E H Rosenkilde et al.
Nature communications, 10(1), 618-618 (2019-02-08)
Antibiotic resistance is a major challenge to global public health. Discovery of new antibiotics is slow and to ensure proper treatment of bacterial infections new strategies are needed. One way to curb the development of antibiotic resistance is to design
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门