About: Fosfomycin     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/drugbank/Drug, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
http://linked.open...gbank/description
  • An antibiotic produced by Streptomyces fradiae. [PubChem] (en)
http://linked.open...y/drugbank/dosage
http://linked.open...gy/drugbank/group
  • approved (en)
http://linked.open...drugbank/halfLife
  • 5.7 (± 2.8) hours. The elimination half-life is 40 hours in anuric patients undergoing hemodialysis. (en)
http://linked.open...ugbank/indication
  • For the treatment of uncomplicated urinary tract infections (acute cystitis) in women due to susceptible strains of <i>Escherichia coli</i> and <i>Enterococcus faecalis</i>. (en)
http://linked.open...bank/manufacturer
sameAs
Title
  • Fosfomycin (en)
adms:identifier
http://linked.open...mechanismOfAction
  • Fosfomycin is a phosphoenolpyruvate analogue produced by Streptomyces that irreversibly inhibits enolpyruvate transferase (MurA), which prevents the formation of N-acetylmuramic acid, an essential element of the peptidoglycan cell wall. (en)
http://linked.open...drugbank/packager
http://linked.open...outeOfElimination
  • Fosfomycin is excreted unchanged in both urine and feces. (en)
http://linked.open.../drugbank/synonym
  • Fosfocina (en)
  • Phosphomycin (en)
  • Phosphonomycin (en)
  • FOSFOMYCIN (en)
  • (-)-(1R,2S)-(1,2-Epoxypropyl)phosphonic acid (en)
  • (1R,2S)-Epoxypropylphosphonic acid (en)
  • (2R-cis)-(3-Methyloxiranyl)phosphonic acid (en)
  • 1R-cis-(1,2-Epoxypropyl)phosphonic acid (en)
  • FCM (en)
  • Fosfomicina (en)
  • Fosfomycine (en)
  • Fosfomycinum (en)
  • L-cis-1,2-Epoxypropylphosphonic acid (en)
  • Phosphonemycin (en)
  • cis-(1R,2S)-Epoxypropylphosphonic acid (en)
http://linked.open...drugbank/toxicity
  • LD<sub>50</sub>>5 g/kg (rats). Side effects may include diarrhea (en)
http://linked.open...umeOfDistribution
  • * 136.1 ±44.1 L (en)
http://linked.open.../drug/hasAHFSCode
http://linked.open...k/foodInteraction
  • Food decreases Cmax slightly. (en)
  • Take without regard to meals. (en)
http://linked.open...nk/proteinBinding
  • 0% (not bound to plasma proteins) (en)
http://linked.open...ogy/drugbank/salt
  • (en)
http://linked.open...ynthesisReference
  • Graziano Castaldi, Claudio Giordano, "Process for the preparation of intermediates for the synthesis of fosfomycin." U.S. Patent US4937367, issued March, 1972. (en)
http://linked.open...y/mesh/hasConcept
foaf:page
http://linked.open...ugbank/IUPAC-Name
http://linked.open...gy/drugbank/InChI
http://linked.open...Molecular-Formula
http://linked.open.../Molecular-Weight
http://linked.open...noisotopic-Weight
http://linked.open...y/drugbank/SMILES
http://linked.open.../Water-Solubility
http://linked.open...ogy/drugbank/logP
http://linked.open...ogy/drugbank/logS
http://linked.open...l/drug/hasATCCode
http://linked.open...nd-Acceptor-Count
http://linked.open...-Bond-Donor-Count
http://linked.open...drugbank/InChIKey
http://linked.open...urface-Area--PSA-
http://linked.open...nk/Polarizability
http://linked.open...bank/Refractivity
http://linked.open...atable-Bond-Count
http://linked.open...ugbank/absorption
  • Fosfomycin tromethamine is rapidly absorbed following oral administration and converted to fosfomycin. Oral bioavailability under fasting conditions is 37%. When given with food, oral bioavailability is reduced to 30% (en)
http://linked.open.../affectedOrganism
  • Enteric bacteria and other eubacteria (en)
http://linked.open...casRegistryNumber
  • 23155-02-4 (en)
http://linked.open...drugbank/category
  • (en)
http://linked.open...rugbank/clearance
  • * 16.9 +/- 3.5 L/hr (en)
http://linked.open...gbank/containedIn
http://linked.open...k/Bioavailability
http://linked.open...bank/Ghose-Filter
http://linked.open...nk/MDDR-Like-Rule
http://linked.open...ank/Melting-Point
http://linked.open...k/Number-of-Rings
http://linked.open...siological-Charge
http://linked.open...bank/Rule-of-Five
http://linked.open...tional-IUPAC-Name
http://linked.open...strongest-acidic-
http://linked.open...-strongest-basic-
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