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| | Cefteram pivoxil Basic information |
| | Cefteram pivoxil Chemical Properties |
| Melting point | >175°C (dec.) | | density | 1.95±0.1 g/cm3(Predicted) | | storage temp. | -20°C Freezer | | solubility | DMF (Slightly), DMSO (Slightly), Methanol (Slightly) | | pka | 2.62±0.50(Predicted) | | form | Solid | | color | White to Pale Yellow | | InChIKey | XSPUSVIQHBDITA-RKYNPMAHSA-N | | SMILES | N12[C@@]([H])([C@H](NC(/C(/C3=CSC(N)=N3)=N\OC)=O)C1=O)SCC(CN1N=NC(C)=N1)=C2C(O)=O | | CAS DataBase Reference | 82547-58-8(CAS DataBase Reference) |
| | Cefteram pivoxil Usage And Synthesis |
| Description | Cefteram pivoxil is an orally-active cephalosponn antibiotic with a broad spectrum of
activity. It is reportedly effective against Cirrobacrer, indole-positive Proreus and
Enrerobacrer species resistant to cefaclor, cephalexin and amoxicillin. Cefteram pivoxil is
indicated primarily for urinary tract infections. | | Chemical Properties | Pale Yellow Solid | | Originator | Toyama (Japan) | | Uses | Orally active cephalosporin antibiotic, antibacterial. | | Definition | ChEBI: Cefteram is a cephalosporin compound having (5-methyl-2H-tetrazol-2-yl)methyl and [(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino side-groups; a third-generation cephalosporin antibiotic. | | Brand name | Tomiron | | Antimicrobial activity | A semisynthetic cephalosporin formulated for oral administration
as the prodrug ester, cefteram pivoxil. Activity is similar
to that of cefixime, but with slightly better activity against
staphylococci and some Gram-negative rods.
Available in Japan. |
| | Cefteram pivoxil Preparation Products And Raw materials |
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