Cefozopran

Cefozopran
Clinical data
AHFS/Drugs.com	International Drug Names
ATC code	J01DE03 (WHO) ;
Identifiers
	IUPAC name (6R,7R)-7-(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)- 2-methoxyiminoacetylamino-3-(imidazo2,3-fpyridazin- 4-ium-1-ylmethyl)-8-oxo-5-thia-1-azabicyclo4.2.0 oct-2-ene-2-carboxylate;
CAS Number	113359-04-9 ;
PubChem CID	9571080;
ChemSpider	7845546 ;
UNII	1LG87K28LW;
KEGG	D01052 ;
ChEMBL	ChEMBL1276663 ;
CompTox Dashboard (EPA)	DTXSID701025943 ;
ECHA InfoCard	100.107.680
Chemical and physical data
Formula	C19H17N9O5S2
Molar mass	515.52 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O=C2N1/C(=C(\CSC@@H1C@@H2NC(=O)C(=N\OC)/c3nc(sn3)N)Cn5c4cccnn+4cc5)C(O-)=O;
	InChI InChI=1S/C19H17N9O5S2/c1-33-24-11(14-23-19(20)35-25-14)15(29)22-12-16(30)28-13(18(31)32)9(8-34-17(12)28)7-26-5-6-27-10(26)3-2-4-21-27/h2-6,12,17H,7-8H2,1H3,(H3-,20,22,23,25,29,31,32)/b24-11-/t12-,17-/m1/s1 ; Key:QDUIJCOKQCCXQY-WHJQOFBOSA-N ;
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Cefozopran (INN) is a fourth-generation cephalosporin.^[1]

Spectrum of bacterial susceptibility and resistanceedit

Most of the strains of Stenotrophomonas maltophilia have developed resistance toward cefozopran.^[2]

Referencesedit

^ Chang XM (December 1996). "Chapter 34: Market to Market". In Bristol JA (ed.). Annual Reports in Medicinal Chemistry. Vol. 31. San Diego, Calif.: Academic Press. p. 339. ISBN 978-0-08-058375-4.
^ "Cefozopran Susceptibility and Resistance Data" (PDF). Retrieved 23 July 2013.

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[1] Chang XM (December 1996). "Chapter 34: Market to Market". In Bristol JA (ed.). Annual Reports in Medicinal Chemistry. Vol. 31. San Diego, Calif.: Academic Press. p. 339. ISBN 978-0-08-058375-4.

[2] "Cefozopran Susceptibility and Resistance Data" (PDF). Retrieved 23 July 2013.

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