SML1631
Cefodizime Sodium
≥96% (HPLC)
别名:
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-(2-amino-4-thiazoly)(methoxyimino)acetyl}-3-[[[5-(carboxymethyl)-4-methyl-2-thiazilyl]-8-oxo-, sodium salt (1:2), (6R,7R)-
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关于此项目
经验公式（希尔记法）:
C20H18N6O7S4 · 2Na
化学文摘社编号:
分子量:
628.63
PubChem Substance ID:
UNSPSC Code:
12352200
InChI
1S/C20H20N6O7S4.2Na/c1-7-10(3-11(27)28)37-20(22-7)36-5-8-4-34-17-13(16(30)26(17)14(8)18(31)32)24-15(29)12(25-33-2)9-6-35-19(21)23-9;;/h6,13,17H,3-5H2,1-2H3,(H2,21,23)(H,24,29)(H,27,28)(H,31,32);;/q;2*+1/p-2/b25-12-;;/t13-,17-;;/m1../s1
InChI key
WBOBLQIRACJNPA-AEKYOGSZSA-L
SMILES string
O=C1[C@@H](NC(/C(C2=CSC(N)=N2)=N\OC)=O)[C@]3([H])N1C(C([O-])=O)=C(CSC4=NC(C)=C(CC([O-])=O)S4)CC3
biological source
synthetic
assay
≥96% (HPLC)
form
powder
solubility
H2O: soluble 270 mg/mL
storage temp.
2-8°C
Biochem/physiol Actions
Cefodizime is a third generation cephalosporin with a broad spectrum of antibacterial activity.
Cefodizime is a third generation cephalosporin with a broad spectrum of antibacterial activity. Cefodizime was demonstrated to be effective against upper and lower respiratory tract infections, urinary tract infections, and gonorrhea. Cefodizime regulates the cytokines expression of neutrophils through toll-like receptor 4 (TLR-4) stimulated by Klebsiella pneumonie.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
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