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Merck
CN

SML1631

Sigma-Aldrich

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
UNSPSC Code:
12352200
PubChem Substance ID:
329825515

Key Documents

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biological source

synthetic

Assay

≥96% (HPLC)

form

powder

solubility

H2O: soluble 270 mg/mL

storage temp.

2-8°C

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

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

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

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2

Storage Class Code

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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