cas: 87239-81-4 — see every product listed under this CAS number, including other names
Cefpodoxime Proxetil (CAS 87239-81-4) is a chemical reagent available from Chemat. Available pack sizes: 100mg, 25mg, 10mM (in 1ml dmso), 50mg, 5g, 2g, 10g, 100g. Offered by: GLPBio, Biosynth, Fluorochem.
| brand | GLPBio |
|---|---|
| catalog number | GC11777-100 |
| cas | 87239-81-4 |
| size | 100mg |
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| brand | size | price | |
|---|---|---|---|
| GLPBio | 100mg | 774.90 Pln | |
| GLPBio | 25mg | 578.32 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 597.04 Pln | |
| GLPBio | 50mg | 662.57 Pln | |
| Biosynth | 5g | price on request | |
| Biosynth | 2g | price on request | |
| Biosynth | 10g | price on request | |
| Biosynth | 100g | price on request | |
| Biosynth | 50g | price on request | |
| Fluorochem | 10mg | 128.10 Pln | |
| Fluorochem | 250mg | 133.30 Pln | |
| Fluorochem | 1g | 190.58 Pln | |
| Fluorochem | 5g | 419.66 Pln | |
| Fluorochem | 25g | 1101.71 Pln |
| purity | No data |
|---|---|
| delivery time | To be confirmed by Chemat |
Cefpodoxime proxetil is the 1-[(isopropoxycarbonyl)oxy]ethyl (proxetil) ester prodrug of cefpodoxime. After swallowing, hydrolysis of the ester group occurs in the intestinal epithelium, to release active cefpodoxime in the bloodstream. It is used to treat acute otitis media, pharyngitis, and sinusitis. It has a role as an antibacterial drug and a prodrug. It is a cephalosporin, a carboxylic ester and a carboxylic acid. It is functionally related to a cefpodoxime and a 4-{((R)-2-Carboxy-3-methoxymethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-en-7-ylcarbamoyl)-[(Z)-methoxyimino]-methyl}-thiazol-2-yl-ammonium.
Source: ChEBI
| Molecular formula | C21H27N5O9S2 |
|---|---|
| Molecular weight | 557.6 g/mol |
| IUPAC name | 1-propan-2-yloxycarbonyloxyethyl (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate |
| InChIKey | LTINZAODLRIQIX-FBXRGJNPSA-N |
| SMILES | CC(C)OC(=O)OC(C)OC(=O)C1=C(CS[C@H]2N1C(=O)[C@H]2NC(=O)/C(=N\OC)/C3=CSC(=N3)N)COC |
Computed by PubChem (NCBI)