| Weight | 367.814 g/mol |
|---|---|
| Formula | C15H14ClN3O4S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
cefaclor (53994-73-3)
Ceclor · S6472 · Lilly 99638
Score:
#263 in Microbiology
,
#2363 in Biology
,
#2928 in Chemistry
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- Treatment of acute maxillary sinusitis in childhood: A comparative study of amoxicillin and cefaclor (The Journal of Pediatrics, 1984)
- Bacteriologic efficacies of oral azithromycin and oral cefaclor in treatment of acute otitis media in infants and young children (Antimicrobial Agents and Chemotherapy, 2000)
- Effects of Amino Acid Alterations in Penicillin-Binding Proteins (PBPs) 1a, 2b, and 2x on PBP Affinities of Penicillin, Ampicillin, Amoxicillin, Cefditoren, Cefuroxime, Cefprozil, and Cefaclor in 18 Clinical Isolates of Penicillin-Susceptible, -Intermediate, and -Resistant Pneumococci (Antimicrobial Agents and Chemotherapy, 2002)
- Serum sicknesslike reactions to cefaclor: Role of hepatic metabolism and individual susceptibility (The Journal of Pediatrics, 1994)
- Serum sickness-like reactions to cefaclor (Journal of Clinical Epidemiology, 1992)
- Quantitative comparison of adverse reactions to cefaclor vs. amoxicillin in a surveillance study. (Pediatric Infectious Disease, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Ceclor
- S6472
- Lilly 99638
- S 6472
- Cefaclor Monohydrate
- Keclor
- S-6472
- Cefaclor Anhydrous
-
SMILESC1C(=C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)Cl
-
InChIKeyQYIYFLOTGYLRGG-UHFFFAOYSA-N
- Pubchem - cefaclor
- Wikipedia - cefaclor anhydrous
Cefaclor, developed by Eli Lilly under the trade name Ceclor, is a second-generation cephalosporin antibiotic used to treat some infections caused by bacteria such as pneumonia and infections of the ear, lung, skin, throat, and urinary tract. It is also available from other manufacturers as a generic.
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