Weight | 520.48 g/mol |
---|---|
Formula | C20H20N6O9S |
Hydrogen Acceptors | 12 |
Hydrogen Donors | 4 |
Aromatic Rings | 2 |
Rotatable Bonds | 9 |
Latamoxef (79120-38-0, 64952-97-2)
Moxalactam · Moxalactam Disodium · Disodium Moxalactam
Score:
#398 in Microbiology
,
#3113 in Biology
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- 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)
- Prolonged Bleeding Times and Bleeding Diathesis Associated With Moxalactam Administration (JAMA, 1983)
- Enterococcal superinfection and colonization after therapy with moxalactam, a new broad-spectrum antibiotic. (Annals of Internal Medicine, 1981)
- Pharmacokinetics and Bacteriologic Efficacy of Moxalactam, Cefotaxime, Cefoperazone, and Rocephin in Experimental Bacterial Meningitis (The Journal of Infectious Diseases, 1981)
- Effects of Moxalactam on Blood Coagulation and Platelet function (Clinical Infectious Diseases, 1982)
- Moxalactam plus Piperacillin versus Moxalactam plus Amikacin in Febrile Granulocytopenic Patients (The American Journal of Medicine, 1984)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Moxalactam
- Moxalactam Disodium
- Disodium Moxalactam
- S-6059
- 1-Oxacephalosporin
- 6059 S
- 6059S
- Ly127935
- Festamoxin
- Shiomarin
- 6059-S
- Lamoxactam
- Disodium Latamoxef
- Ly 127935
- S6059
- Lilly 127935
- 1 Oxacephalosporin
- Ly-127935
- S 6059
-
SMILESCN1C(=NN=N1)SCC2=C(N3C(C(C3=O)(NC(=O)C(C4=CC=C(C=C4)O)C(=O)O)OC)OC2)C(=O)O
-
InChIKeyJWCSIUVGFCSJCK-UHFFFAOYSA-N
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