76470-66-1
76470-66-1
Chemical Structure
Loracarbef
- CAS No.: 76470-66-1
- Formula:C16H16ClN3O4
- Molecular Weight:349.77
IUPAC Name: (6R,7S)-7-((R)-2-amino-2-phenylacetamido)-3-chloro-8-oxo-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
InChIKey: JAPHQRWPEGVNBT-UTUOFQBUSA-N
SMILES: O=C(C(N12)=C(Cl)CC[C@]2([H])[C@H](NC([C@H](N)C3=CC=CC=C3)=O)C1=O)O
Biological Activity: Loracarbef, a cephalosporin antibiotic, is an orally active second-generation synthetic beta-lactam antibiotic of the carbacephem class[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Loracarbef | Loracarbef, a cephalosporin antibiotic, is an orally active second-generation synthetic beta-lactam antibiotic of the carbacephem class. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. M Hu, et al. Mechanisms of Transport of Quinapril in Caco-2 Cell Monolayers: Comparison With Cephalexin. Pharm Res. 1995 Aug;12(8):1120-5. [Content Brief]
- [2]. J W Dyke, et al. Antimicrobial Activity of New Antibiotics Against Bacterial Isolates From a Community Hospital. Chemotherapy. Sep-Oct 1993;39(5):315-21. [Content Brief]
