Compound ID | 3253

Cefovecin

Class: Beta-lactam (cephalosporin)

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Active against Staphylococcus aureus, coagulase-negative staphylococci, streptococci, Pasteurella multocida, Escherichia coli, Proteus sp., Klebsiella sp., Enterobacter sp.
Description: Semi-synthetic compound; formulated for veterinary use
Year first mentioned: 2006
Development status: Experimental
Chemical structure(s):
Canonical SMILES: CO/N=C(/C1=CSC(=N1)N)\C(=O)N[C@@H]2C(=O)N3C(=C(CS[C@H]23)[C@@H]4CCCO4)C(=O)O
Isomeric SMILES: CO/N=C(/C1=CSC(=N1)N)\C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)[C@@H]4CCCO4)C(=O)O
InChI: InChI=1S/C17H19N5O6S2/c1-27-21-10(8-6-30-17(18)19-8)13(23)20-11-14(24)22-12(16(25)26)7(5-29-15(11)22)9-3-2-4-28-9/h6,9,11,15H,2-5H2,1H3,(H2,18,19)(H,20,23)(H,25,26)/b21-10-/t9-,11+,15+/m0/s1
InChI Key: ZJGQFXVQDVCVOK-QFKLAVHZSA-N
Structure link: https://pubchem.ncbi.nlm.nih.gov/compound/6336480
External links:
Main Source: https://journals.asm.org/doi/10.1128/aac.00077-06?url_ver=Z39.88-2003&rfr_id=ori%3Arid%3Acrossref.org&rfr_dat=cr_pub++0pubmed
Citation: https://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-2885.2006.00801.x

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