Cefapirin

Clinical data
AHFS/ Drugs.com	International Drug Names
MedlinePlus	a601206
Routes of administration	Intravenous, intramuscular
ATC code	J01DB08 ( WHO) QG51AA05 ( WHO) QJ51DB08 ( WHO)
Legal status
Legal status	US: ℞-only
Identifiers
CAS Number	21593-23-7 Y
PubChem CID	30699
DrugBank	DB01139 Y
ChemSpider	28486 Y
UNII	89B59H32VN
KEGG	D07636 Y
ChEBI	CHEBI:554446 Y
ChEMBL	ChEMBL1599 Y
CompTox Dashboard ( EPA)	DTXSID9022784
ECHA InfoCard	100.040.409
Chemical and physical data
Formula	C17H17N3O6S2
Molar mass	423.46 g·mol−1
3D model ( JSmol)	Interactive image
SMILES O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)CSc3ccncc3)COC(=O)C)C(=O)O
InChI InChI=1S/C17H17N3O6S2/c1-9(21)26-6-10-7-28-16-13(15(23)20(16)14(10)17(24)25)19-12(22)8-27-11-2-4-18-5-3-11/h2-5,13,16H,6-8H2,1H3,(H,19,22)(H,24,25)/t13-,16-/m1/s1 Y Key:UQLLWWBDSUHNEB-CZUORRHYSA-N Y
(verify)

Cefapirin ( INN, also spelled cephapirin) is an injectable, first-generation cephalosporin antibiotic. It is marketed under the trade name Cefadyl. Production for use in humans has been discontinued in the United States. ^[1]

It also has a role in veterinary medicine as Metricure, an intrauterine preparation, and combined with prednisolone in Mastiplan, an intramammary preparation. Both are licensed in cattle.^{[ citation needed]}

Synthesis

In one of the syntheses, 7-aminocephalosporanic acid ( 7-ACA) is reacted with bromoacetyl chloride to give the amide. The halo group is then displaced by 4-thiopyridine. ^[2]

References

This systemic antibiotic-related article is a stub. You can help Wikipedia by expanding it.

• v
• t
• e