| Weight | 294.31 g/mol |
|---|---|
| Formula | C17H14N2O3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
ROSOXACIN (40034-42-2)
Eracine · acrosoxacin · Eradacin
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- In vitro antimicrobial activity of rosoxacin against Neisseria gonorrhoeae, Chlamydia trachomatis, and Ureaplasma urealyticum. (Antimicrobial Agents and Chemotherapy, 1980)
- A selective spectrophotometric method for determination of rosoxacin antibiotic using sodium nitroprusside as a chromogenic reagent (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2008)
- Clinical evaluation of rosoxacin for the treatment of chancroid. (Antimicrobial Agents and Chemotherapy, 1986)
- Intraocular Penetration of Rosoxacin in Rabbits (Archives of Ophthalmology, 1982)
- Treatment of uncomplicated gonorrhea with rosoxacin. (Antimicrobial Agents and Chemotherapy, 1981)
- In vitro Activities of Ciprofloxacin, Ofloxacin, Norfloxacin and Rosoxacin Compared with Cinoxacin and Trimethoprim (Chemotherapy, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Eracine
- acrosoxacin
- Eradacin
- Win 35,213
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SMILESCCN1C=C(C(=O)C2=C1C=C(C=C2)C3=CC=NC=C3)C(=O)O
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InChIKeyXBPZXDSZHPDXQU-UHFFFAOYSA-N
- Pubchem - ROSOXACIN
- Wikipedia - rosoxacin
Rosoxacin (also known as acrosoxacin, tradename Eradacil) is a quinolone antibiotic indicated for the treatment of urinary tract infections and certain sexually transmitted diseases. Rosoxacin is not available in the United States. It was developed by Sanofi-Synthelabo (now part of sanofi-aventis).
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ROSOXACIN
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