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Merck
CN

SML1631

Cefodizime Sodium

≥96% (HPLC)

Synonym(s):

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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About This Item

Empirical Formula (Hill Notation):
C20H18N6O7S4 · 2Na
CAS Number:
86329-79-5
Molecular Weight:
628.63
PubChem Substance ID:
329825515
UNSPSC Code:
12352200

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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.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

13 - Non Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
027M4860V

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