Weight | 405.432 g/mol |
---|---|
Formula | C18H19N3O6S |
Hydrogen Acceptors | 7 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 6 |
Cefaloglycin (3577-01-3)
Cephaloglycin · Cephaloglycine · Cephaloglycin Dihydrate
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- Mechanisms of cephalosporin nephrotoxicity: A comparison of cephaloridine and cephaloglycin (Kidney International, 1980)
- Synthesis of antibiotics (cephaloglycin) catalyzed by penicillin G acylase: Evaluation and optimization of different synthetic approaches (Enzyme and Microbial Technology, 1996)
- Crystal Pseudopolymorphism of Cephaloglycin and Cephalexin (Journal of Pharmaceutical Sciences, 1970)
- In Vitro and In Vivo Laboratory Evaluation of Cephaloglycin and Cephaloridine (Applied and Environmental Microbiology, 1965)
- Oxidative and mitochondrial toxic effects of cephalosporin antibiotics in the kidney: A comparative study of cephaloridine and cephaloglycin (Biochemical Pharmacology, 1989)
- Chemistry of cephalosporin antibiotics. VII. Synthesis of cephaloglycin and some homologs. (Journal of Medicinal Chemistry, 1966)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Cephaloglycin
- Cephaloglycine
- Cephaloglycin Dihydrate
-
SMILESCC(=O)OCC1=C(N2C(C(C2=O)NC(=O)C(C3=CC=CC=C3)N)SC1)C(=O)O
-
InChIKeyFUBBGQLTSCSAON-UHFFFAOYSA-N
- Pubchem - Cefaloglycin
- Wikipedia - cephaloglycin anhydrous
Cefaloglycin INN (also spelled cephaloglycin) is a first-generation cephalosporin antibiotic.
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