CAS 23155-02-4|Fosfomycin

Introduction:Basic information about CAS 23155-02-4|Fosfomycin, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameFosfomycin
CAS Number23155-02-4Molecular Weight138.05900
Density1.561g/cm3Boiling Point342.651ºC at 760 mmHg
Molecular FormulaC3H7O4PMelting Point94ºC
MSDS/Flash Point161.03ºC

Names

Namefosfomycin
SynonymMore Synonyms

Fosfomycin BiologicalActivity

DescriptionFosfomycin (MK-0955) is a broad-spectrum antibiotic. Fosfomycin can cross blood-brain barrier penetrating, and irreversibly inhibits an early stage in cell wall synthesis. Fosfomycin shows anti-bacteria activity for a range of bacteria, including multidrug-resistant (MDR), extensively drug-resistant (XDR), and pan-drug-resistant (PDR) bacteria[1][2].
Related CatalogResearch Areas >>InfectionSignaling Pathways >>Anti-infection >>Bacterial
In VivoFosfomycin (80 mg/kg; i.v. or p.o.) displays the protective effect on the nephrotoxicity of double beckacin, and is not affected by different administration routes in rats[3]. Pharmacokinetic of Fosfomycin in Rats[4] Dibekacin Dose (mg) Vdss (l/kg) β (min-1) T1/2 (min) Urinary recovery (%) 30 0.261 0.0244 28.4 85 Animal Model: Fischer 344 rats[3] Dosage: 320 mg/kg Administration: Intramuscular injection, 5 schedules: 1 h, 0.5 h earlier than dibekacin, concomitantly, 0.5 h later and 1 h later; 11 days Result: Reduced polyuria, proteinuria, enzymes and cytosine caused by dibecacin (40 mg/kg), followed by the previous treatment. Animal Model: Dehydrated Wistar rat with acute renal failure (8-week-old)[4] Dosage: 120 mg/kg Administration: Intravenous injection; once Result: Recovered the exclusion rate of rats basically to normal, and improved the nephrotoxicity parameters. Protects proximal tubular lysosomes from aminoglycosides by inhibiting myeloid formation and protecting the integrity of lysosomal membrane of rats treated with double bekacin.
References

[1]. Falagas ME, et al. Fosfomycin. Clin Microbiol Rev. 2016 Apr. 29(2):321-47.

[2]. Dijkmans AC, et al. Fosfomycin: Pharmacological, Clinical and Future Perspectives. Antibiotics (Basel). 2017 Oct 31. 6(4):24.

[3]. Inouye S, et al. Mode of protective action of fosfomycin against dibekacin-induced nephrotoxicity in the dehydrated rats. J Pharmacobiodyn. 1982 Dec. 5(12):941-50.

Chemical & Physical Properties

Density1.561g/cm3
Boiling Point342.651ºC at 760 mmHg
Melting Point94ºC
Molecular FormulaC3H7O4P
Molecular Weight138.05900
Flash Point161.03ºC
Exact Mass138.00800
PSA79.87000
Vapour Pressure0mmHg at 25°C
Index of Refraction1.486
InChIKeyYMDXZJFXQJVXBF-STHAYSLISA-N
SMILESCC1OC1P(=O)(O)O

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
SZ7890000
CHEMICAL NAME :
Phosphonic acid, (1,2-epoxypropyl)-, (1R,2S)-(-)-
CAS REGISTRY NUMBER :
23155-02-4
BEILSTEIN REFERENCE NO. :
1680831
LAST UPDATED :
199612
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C3-H7-O4-P
MOLECULAR WEIGHT :
138.07
WISWESSER LINE NOTATION :
T3OTJ BPQQO C1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
4 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value

MUTATION DATA

TYPE OF TEST :
Mutation in microorganisms
TEST SYSTEM :
Microorganism - not otherwise specified
DOSE/DURATION :
10 gm/L
REFERENCE :
MILEDM Microbios Letters. (Faculty Press, 88 Regent St., Cambridge, UK) V.1- 1976- Volume(issue)/page/year: 8,27,1978

Safety Information

HS Code2931900090

Customs

HS Code2931900090
Summary2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

Synonyms

Veramina
MFCD00242804
Fosfocina
[(2R,3S)-3-methyloxiran-2-yl]phosphonic acid
phosphomycin
Fosfomycinum
FOSFOMYCIN
Fosfomicina
EINECS 245-463-1
Phosphonomycin
Fosfomycine
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