| Weight | 394.403 g/mol |
|---|---|
| Formula | C18H23FN4O5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
Eperezolid (165800-04-4)
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- Mechanism of action of oxazolidinones: effects of linezolid and eperezolid on translation reactions. (Antimicrobial Agents and Chemotherapy, 1997)
- The oxazolidinone eperezolid binds to the 50S ribosomal subunit and competes with binding of chloramphenicol and lincomycin. (Antimicrobial Agents and Chemotherapy, 1997)
- Comparative In Vitro Activities and Postantibiotic Effects of the Oxazolidinone Compounds Eperezolid (PNU-100592) and Linezolid (PNU-100766) versus Vancomycin against Staphylococcus aureus, Coagulase-Negative Staphylococci, Enterococcus faecalis, and Enterococcus faecium (Antimicrobial Agents and Chemotherapy, 1998)
- Linezolid Compared with Eperezolid, Vancomycin, and Gentamicin in an In Vitro Model of Antimicrobial Lock Therapy for Staphylococcus epidermidis Central Venous Catheter-Related Biofilm Infections (Antimicrobial Agents and Chemotherapy, 2003)
- A short synthesis of oxazolidinone derivatives linezolid and eperezolid: a new class of antibacterials (Tetrahedron Letters, 1999)
- Oxazolidinone antibacterial agents: development of the clinical candidates eperezolid and linezolid (Expert Opinion on Investigational Drugs, 1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)NCC1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCN(CC3)C(=O)CO)F
-
InChIKeySIMWTRCFFSTNMG-UHFFFAOYSA-N
- Pubchem - Eperezolid
- Wikipedia - eperezolid
Eperezolid is an oxazolidinone antibiotic.
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