Pheneticillin - Misplaced Pages

Chemical compound Pharmaceutical compound

Pheneticillin
Clinical data

AHFS/Drugs.com	International Drug Names
ATC code	J01CE05 (WHO)
Identifiers
IUPAC name (2S,5R,6R)-3,3-dimethyl-7-oxo-6--4-thia-1-azabicycloheptane-2-carboxylic acid
CAS Number	147-55-7
PubChem CID	272833
ChemSpider	240055
UNII	EFA30X554H
KEGG	D08350
ChEMBL	ChEMBL1614637
CompTox Dashboard (EPA)	DTXSID6023448
ECHA InfoCard	100.005.175
Chemical and physical data
Formula	C₁₇H₂₀N₂O₅S
Molar mass	364.42 g·mol
3D model (JSmol)	Interactive image
SMILES CC(C(=O)N12N(C1=O)(C(S2)(C)C)C(=O)O)OC3=CC=CC=C3
InChI InChI=1S/C17H20N2O5S/c1-9(24-10-7-5-4-6-8-10)13(20)18-11-14(21)19-12(16(22)23)17(2,3)25-15(11)19/h4-9,11-12,15H,1-3H3,(H,18,20)(H,22,23)/t9?,11-,12+,15-/m1/s1 Key:NONJJLVGHLVQQM-JHXYUMNGSA-N
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Pheneticillin (or phenethicillin) is a penicillin. It is not approved by the FDA for use in the United States.

References

Index Nominum: International Drug Directory. Swiss Pharmaceutical Society. Jan 2000. p. 816. ISBN 978-3887630751. Retrieved 20 April 2015.
Dougherty T, Pucci MJ (21 Dec 2011). Antibiotic Discovery and Development (2012 ed.). Springer. p. 86. ISBN 978-1461413998. Retrieved 20 April 2015.

β-lactams
(inhibit synthesis
of peptidoglycan
layer of bacterial
cell wall by binding
to and inhibiting
PBPs, a group of
D-alanyl-D-alanine
transpeptidases)

β-lactamase sensitive (1st generation)	Benzylpenicillin (G) Benzathine benzylpenicillin Procaine benzylpenicillin Phenoxymethylpenicillin (V) Propicillin Pheneticillin Azidocillin Clometocillin Penamecillin
β-lactamase resistant (2nd generation)	Cloxacillin (Dicloxacillin Flucloxacillin) Oxacillin Nafcillin Methicillin

Aminopenicillins (3rd generation)	Amoxicillin Ampicillin (Pivampicillin Hetacillin Bacampicillin Lenampicillin Metampicillin Talampicillin) Epicillin
Carboxypenicillins (4th generation)	Ticarcillin Carbenicillin / Carindacillin Temocillin
Ureidopenicillins (4th generation)	Piperacillin Azlocillin Mezlocillin
Other	Mecillinam (Pivmecillinam) Sulbenicillin

1st generation	Cefazolin Cefalexin Cefadroxil Cefapirin Cefazedone Cefazaflur Cefradine Cefroxadine Ceftezole Cefaloglycin Cefacetrile Cefalonium Cefaloridine Cefalotin Cefatrizine
2nd generation	Cefaclor Cefprozil Cefuroxime Cefuroxime axetil Cefamandole Cefonicid Ceforanide Cefuzonam Cephamycin (Cefoxitin Cefotetan Cefminox Cefbuperazone Cefmetazole) Carbacephem (Loracarbef)
3rd generation	Cefixime Ceftriaxone Cefotaxime Antipseudomonal (Ceftazidime Cefoperazone) Cefdinir Cefcapene Cefdaloxime Ceftizoxime Cefmenoxime Cefpiramide Cefpodoxime Ceftibuten Cefditoren Cefotiam Cefetamet Cefodizime Cefpimizole Cefsulodin Cefteram Ceftiolene Oxacephem (Flomoxef Latamoxef)
4th generation	Cefepime Cefozopran Cefpirome Cefquinome
5th generation	Ceftaroline fosamil Ceftolozane Ceftobiprole
Siderophore	Cefiderocol
Veterinary	Ceftiofur Cefquinome Cefovecin

Combinations

Lipopeptides	Insert into bacterial cell wall causing perforation and depolarization: Daptomycin Surfactin
Other	Inhibits PG elongation and crosslinking: Ramoplanin

Intracellular

Inhibit PG subunit synthesis and transport: NAM synthesis inhibition (Fosfomycin)
DADAL/AR inhibitors (Cycloserine)
bactoprenol inhibitors (Bacitracin)

Other

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