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R42/43:Sensibilisierung durch Einatmen und Hautkontakt m?glich.
S-S?tze Betriebsanweisung:
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Beschreibung
Cephalexin was first synthesized in 1967 by Glaxo Research Laboratories and first produced on an industrial scale by Eli Lilly & Co. in the same year. It is a deacetoxylated derivative of cephaloglycin that is not metabolized in vivo. When administered orally, it shows a much higher serum concentration and much lower tendency to induce diarrhea than cephaloglycin. Cephalexin has been used widely and is the most popular orally active antibiotic in the world for treatment of respiratory tract, urinary tract, surgical, ear and nose, and other infections caused by Staphylococcus, Streptococcus, Escherichia coli, Klebsiella, Enterobacter, and Proteus.
Chemische Eigenschaften
White to Off-White Solid
Verwenden
Cephalosporin antibacterial.
Definition
ChEBI: The hydrate of cephalexin.
CEPHALEXIN MONOHYDRATE Upstream-Materialien And Downstream Produkte
Cephalexin MonohydrateQ: What is
Cephalexin Monohydrate Q: What is the CAS Number of
Cephalexin Monohydrate Q: What is the storage condition of
Cephalexin Monohydrate
Cephalexin (1099008)
CEPHALEXIN 1-HYDRATE
cephalexin monohydrfate
Cephalexin hydrate in 0.1 M HCl
23325-78-2
C16H17N3O4SH2O
KEFLEX
Antibiotics for Research and Experimental Use
beta-Lactams (Antibiotics for Research and Experimental Use)
Biochemistry
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