| Weight | 667.662 g/mol |
|---|---|
| Formula | C25H26N9NaO8S2 |
| Hydrogen Acceptors | 14 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 9 |
CEFOPERAZONE SODIUM (62893-20-3)
Cefoperazone · Cefobid · T 1551
Score:
#479 in Microbiology
,
#3797 in Biology
,
#4779 in Chemistry
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- Beta-lactam antibiotic therapy in febrile granulocytopenic patients: A randomized trial comparing cefoperazone plus piperacillin, ceftazidime plus piperacillin, and imipenem alone (Annals of Internal Medicine, 1991)
- Pharmacokinetics and Bacteriologic Efficacy of Moxalactam, Cefotaxime, Cefoperazone, and Rocephin in Experimental Bacterial Meningitis (The Journal of Infectious Diseases, 1981)
- Treatment of Typhoid Fever and Other Systemic Salmonelloses with Cefotaxime, Ceftriaxone, Cefoperazone, and Other Newer Cephalosporins (Clinical Infectious Diseases, 1987)
- Antibiotic management of surgically treated gangrenous or perforated appendicitis: Comparison of gentamicin and clindamycin versus cefamandole versus cefoperazone (American Journal of Surgery, 1982)
- Sulbactamcefoperazone polyhydroxybutyrateco hydroxyvalerate (PHBV) local antibiotic delivery system: In vivo effectiveness and biocompatibility in the treatment of implantrelated experimental osteomyelitis (Journal of Biomedical Materials Research, 1999)
- Reversal by Cefoperazone of Resistance to Etoposide, Doxorubicin, and Vinblastine in Multidrug Resistant Human Sarcoma Cells (Cancer Research, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Cefoperazone
- Cefobid
- T 1551
- Farmasierra Brand of Cefoperazone Sodium
- Cefoperazone Sodium Salt
- Cefoperazon
- Pfizer Brand of Cefoperazone Sodium
- T-1551
- Cfobis
- T1551
-
SMILESCCN1CCN(C(=O)C1=O)C(=O)NC(C2=CC=C(C=C2)O)C(=O)NC3C4N(C3=O)C(=C(CS4)CSC5=NN=NN5C)C(=O)[O-].[Na+]
-
InChIKeyNCFTXMQPRQZFMZ-UHFFFAOYSA-M
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