Cefpirome

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Chemical compound

Cefpirome

Clinical data
AHFS/Drugs.com	International Drug Names
ATC code	J01DE02 (WHO)
Identifiers
IUPAC name 1-{[(6R,7R)-7-[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetamido]-2-carboxylato-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-5H,6H,7H-cyclopenta[b]pyridin-1-ium
CAS Number	84957-29-9 Y
PubChem CID	6917674
ChemSpider	23089536 N
UNII	S72Q2F09HY
KEGG	D07649 Y
ChEMBL	ChEMBL2106076 N
CompTox Dashboard (EPA)	DTXSID2048244
Chemical and physical data
Formula	C22H22N6O5S2
Molar mass	514.58 g·mol−1
3D model (JSmol)	Interactive image
SMILES CON=C(c1csc(n1)N)C(=O)NC2C3N(C2=O)C(=C(CS3)C[n+]4cccc5c4CCC5)C(=O)[O-]
InChI InChI=1S/C22H22N6O5S2/c1-33-26-15(13-10-35-22(23)24-13)18(29)25-16-19(30)28-17(21(31)32)12(9-34-20(16)28)8-27-7-3-5-11-4-2-6-14(11)27/h3,5,7,10,16,20H,2,4,6,8-9H2,1H3,(H3-,23,24,25,29,31,32)/b26-15-/t16-,20+/m1/s1 N Key:DKOQGJHPHLTOJR-XECLGWKCSA-N N
NY (what is this?)  (verify)

Cefpirome is a fourth-generation cephalosporin. Trade names include Cefrom, Keiten, Broact, and Cefir. Cefpirome is considered highly active against Gram-negative bacteria, including Pseudomonas aeruginosa, and Gram-positive bacteria.^{[citation needed]}

Spectrum of bacterial susceptibility and resistance[edit]

Bacteroides fragilis, enterococci, Pseudomonas spp. and staphylococci are resistant to cefpirome sulfate, and some Haemophilus spp. and pneumococci have developed resistance to it to varying degrees.^[1]

References[edit]

1. ^ "Cefpirome Sulfate spectrum of bacterial susceptibility and Resistance" (PDF). Archived from the original (PDF) on 3 March 2016. Retrieved 10 April 2012.

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