| Weight | 225.16 g/mol |
|---|---|
| Formula | C8H7N3O5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
UNII-5J9CPU3RE0 (67-45-8)
Furazolidone · Furoxone · Furazolidine
Score:
#449 in Microbiology
,
#3612 in Biology
,
#4534 in Chemistry
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- Prevalence of Helicobacter pylori Resistance to Metronidazole, Clarithromycin, Amoxicillin, Tetracycline, and Furazolidone in Brazil (Helicobacter, 2000)
- Determination of furazolidone in porcine tissue using thermospray liquid chromatographymass spectrometry and a study of the pharmacokinetics and stability of its residues (Analyst, 1995)
- Resistance to oxytetracycline, oxolinic acid and furazolidone in bacteria from marine sediments (Aquaculture, 1992)
- Rifabutin- and furazolidone-based Helicobacter pylori eradication therapies after failure of standard first- and second-line eradication attempts in dyspepsia patients (Alimentary Pharmacology & Therapeutics, 2005)
- Depletion of proteinbound furazolidone metabolites containing the 3amino2oxazolidinone sidechain from liver, kidney and muscle tissues from pigs (Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment, 1992)
- Clarithromycin vs. furazolidone in quadruple therapy regimens for the treatment of Helicobacter pylori in a population with a high metronidazole resistance rate (Alimentary Pharmacology & Therapeutics, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Furazolidone
- Furoxone
- Furazolidine
- Furazol
- Nifurazolidone
-
SMILESC1COC(=O)N1N=CC2=CC=C(O2)[N+](=O)[O-]
-
InChIKeyPLHJDBGFXBMTGZ-UHFFFAOYSA-N
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