| Weight | 427.46 g/mol |
|---|---|
| Formula | C16H17N3O7S2 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
cefoxitin (35607-66-0)
Mefoxin · Cefoxitin Sodium · MSD Brand of Cefoxitin Sodium
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- Transferable resistance to cefotaxime, cefoxitin, cefamandole and cefuroxime in clinical isolates of Klebsiella pneumoniae and Serratia marcescens (Infection, 1983)
- Evaluation of Three Techniques for Detection of Low-Level Methicillin-Resistant Staphylococcus aureus (MRSA): a Disk Diffusion Method with Cefoxitin and Moxalactam, the Vitek 2 System, and the MRSA-Screen Latex Agglutination Test (Journal of Clinical Microbiology, 2002)
- In vivo selection of porin-deficient mutants of Klebsiella pneumoniae with increased resistance to cefoxitin and expanded-spectrum-cephalosporins. (Antimicrobial Agents and Chemotherapy, 1996)
- .beta.-Lactamase proceeds via an acyl-enzyme intermediate. Interaction of the Escherichia coli RTEM enzyme with cefoxitin (Biochemistry, 1980)
- Beta-lactamase production and susceptibilities to amoxicillin, amoxicillin-clavulanate, ticarcillin, ticarcillin-clavulanate, cefoxitin, imipenem, and metronidazole of 320 non-Bacteroides fragilis Bacteroides isolates and 129 fusobacteria from 28 U.S. centers. (Antimicrobial Agents and Chemotherapy, 1990)
- Results of Disk Diffusion Testing with Cefoxitin Correlate with Presence of mecA in Staphylococcus spp. (Journal of Clinical Microbiology, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Mefoxin
- Cefoxitin Sodium
- MSD Brand of Cefoxitin Sodium
- Mefoxitin
- MK-306
- Merck Sharp and Dohme Brand of Cefoxitin Sodium
- Merck Frosst Brand of Cefoxitin Sodium
- MK306
- Mfoxin
- Merck Brand of Cefoxitin Sodium
- MK 306
-
SMILESCOC1(C2N(C1=O)C(=C(CS2)COC(=O)N)C(=O)O)NC(=O)CC3=CC=CS3
-
InChIKeyWZOZEZRFJCJXNZ-UHFFFAOYSA-N
- Pubchem - cefoxitin
- Wikipedia - cefoxitin
Cefoxitin is a second-generation cephamycin antibiotic developed by Merck & Co., Inc. from Cephamycin C in the year following its discovery, 1972. It was synthesized in order to create an antibiotic with a broader spectrum.
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