Cefalonium

Synonym(s): cephalonium

Class: Beta-lactam (cephalosporin)

Spectrum of activity:	Gram-positive
Details of activity:	Active against Staphylococcus epidermidis and Staphylococcus caprae
Description:	Semi-synthetic compound
Year first mentioned:	1977
Development status:	Experimental

Chemical structure(s):
Canonical SMILES:	C1=CSC(=C1)CC(=O)N[C@@H]2C(=O)N3C(=C(C[N+]4=CC=C(C=C4)C(=O)N)CS[C@H]23)C(=O)[O-]
Isomeric SMILES:	C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)[O-])C[N+]4=CC=C(C=C4)C(=O)N
InChI:	InChI=1S/C20H18N4O5S2/c21-17(26)11-3-5-23(6-4-11)9-12-10-31-19-15(18(27)24(19)16(12)20(28)29)22-14(25)8-13-2-1-7-30-13/h1-7,15,19H,8-10H2,(H3-,21,22,25,26,28,29)/t15-,19-/m1/s1
InChI Key:	FMZXNVLFJHCSAF-DNVCBOLYSA-N
Structure link:	https://pubchem.ncbi.nlm.nih.gov/compound/21743

External links:
Guide to Pharmacology:	cefalonium
Main Source:	https://www.tandfonline.com/doi/full/10.1080/00480169.2010.65060#d1e287