Structure via PubChem · Public domain (PubChem)
fosfomisin
Sign in to saveAlso known as Phosphonemycin, Fosfomycinum, Phosphonomycin, 1R-cis-(1,2-Epoxypropyl)phosphonic acid, FCM, (1R,2S)-Epoxypropylphosphonic acid, (-)-(1R,2S)-(1,2-Epoxypropyl)phosphonic acid, (2R-cis)-(3-Methyloxiranyl)phosphonic acid
kimyasal bileşik
Key facts
- Drug.Watchedfields
- changed
- Drug.verifiedrevid
- 461113563
- Drug.image
- Fosfomycin.svg
- Drug.image_class
- skin-invert-image
- Drug.width
- 125
- Drug.alt
- Structural formula of fosfomycin
- Drug.image2
- Fosfomycin 3D ball.png
- Drug.image_class2
- bg-transparent
- Drug.width2
- 150
- Drug.alt2
- Ball-and-stick model of the fosfomycin molecule
- Drug.tradename
- Monuril, Monurol, Ivozfo, others
- Drug.synonyms
- Phosphomycin, phosphonomycin, fosfomycin tromethamine
- Drug.MedlinePlus
- a697008
- Drug.DailyMedID
- Fosfomycin
- Drug.routes_of_administration
- Intravenous, By mouth
- Drug.ATC_prefix
- J01
- Drug.ATC_suffix
- XX01
- Drug.legal_AU
- S4
via Wikipedia infobox
Chemical data
- Formula
- C3H7O4P
- Molecular weight
- 138.06 g/mol
- IUPAC name
- [(2R,3S)-3-methyloxiran-2-yl]phosphonic acid
- SMILES
- C[C@H]1[C@H](O1)P(=O)(O)O
- InChIKey
- YMDXZJFXQJVXBF-STHAYSLISA-N
- XLogP
- -1.4
- Polar surface area
- 70.1 Ų
- H-bond donors
- 2
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 1996
- Admin. routes
- oral
- Indications
- Pseudomonas infection, urinary tract infection, gonorrhea, osteomyelitis
via ChEMBL · EBI
Research
5,297 papers- Fosfomycin Tromethamine: A Urinary Antibiotic.The Journal of the Association of Physicians of India · 2025
- Fosfomycin: 50 Years of A Great Discovery (1969-2019).Archivos espanoles de urologia · 2022
- Fosfomycin for bacterial prostatitis: a review.International journal of antimicrobial agents · 2020
- [Fosfomycin].Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2003
- Mobile fosfomycin resistance genes in Enterobacteriaceae-An increasing threat.MicrobiologyOpen · 2020
via PubMed
Wikidata facts
- Mass
- 138.008
- Has use
- medication
Show 10 more facts
- route of administration
- intravenous infusion and defusion
- Commons category
- Fosfomycin
- subject has role
- antibiotic
- chemical formula
- C₃H₇O₄P
- medical condition treated
- cystitis
- canonical SMILES
- CC1C(O1)P(=O)(O)O
- isomeric SMILES
- C[C@H]1[C@H](O1)P(=O)(O)O
- World Health Organisation international non-proprietary name
- fosfomycin
- different from
- fosmidomycin
- found in taxon
- Streptomyces
Sources (6)
via Wikidata · CC0