Faropenem sodium hemipentahydrate

Bezeichnung:Faropenem sodium hemipentahydrate

CAS-Nr106560-14-9

Englisch Name:Faropenem sodium hemipentahydrate

CBNumberCB1300660

SummenformelC12H15NO5S

Molgewicht285.32

MOL-Datei106560-14-9.mol

Faropenem sodium hemipentahydrate physikalisch-chemischer Eigenschaften

Siedepunkt	570.2±50.0 °C(Predicted)
Dichte	1.56±0.1 g/cm3(Predicted)
pka	4.00±0.40(Predicted)
CAS Datenbank	106560-14-9

Gefahreninformationscode (GHS)

Faropenem sodium hemipentahydrate Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
Farom was launched in Japan for use as an antibiotic against common respiratory tract pathogens. It can be prepared by several related routes of about seven steps starting with tetrahydrofuran-2-thiocarboxylic acid and a silylated azetidinone. It is a broad spectrum oral penem antibiotic that is β-lactamase stable. Farom is the most active β-lactam against anaerobes (more than cefaclor, cefixime and amoxicillin) but also has activity against Gram-positive, Gram-negative and enterobacteriaceae. It is equally active against strains carrying plasmid and chromosome mediated β-lactamases. The short plasma elimination half-life is the result of hydrolysis by renal dehydropeptidase. It is more stable to hydrolysis by extended spectrum β-lactamases than some second and third generation cephalosporins.
Originator
Suntory (Japan)
Verwenden
Treatmentof bacterial infections.
Verwenden
Faropenem (cas# 106560-14-9) is a compound useful in organic synthesis.
Definition
ChEBI: 6alpha-[(R)-1-hydroxyethyl]-2-[(R)-tetrahydrofuran-2-yl]pen-2-em-3-carboxylic acid is a faropenem. It is a conjugate acid of a 6alpha-[(R)-1-hydroxyethyl]-2-[(R)-tetrahydrofuran-2-yl]pen-2-em-3-carboxylate.
Trademarks
Farom
Antimicrobial activity
An orally active penem with a broad spectrum of antibacterial activity, including activity against selected anaerobic pathogens. Although it is active against most enterobacteria, it has reduced activity against Ser. marcescens, Enterobacter spp. and some Providencia spp. It generally retains activity against many Gram-positive organisms, but has no useful activity against Ps. aeruginosa. It has reduced activity against E. faecium, methicillin-resistant Staph. aureus (MRSA) and some strains of coagulase-negative staphylococci. It is stable to hydrolysis by extended spectrum β-lactamases, but is hydrolyzed by carbapenemases. Esterified prodrugs with increased bioavailability have been studied in clinical trials but have not received regulatory approval.

Faropenem sodium hemipentahydrate Upstream-Materialien And Downstream Produkte

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