| 词条 | Cefteram |
| 释义 |
| IUPAC_name = (6R,7R)-7-([(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino)-3-[(5-methyltetrazol-2-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | image = Cefteram.png | tradename = | Drugs.com = {{drugs.com|international|cefteram}} | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = | legal_UK = | legal_US = | legal_status = Rx-only | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number = 82547-58-8 | ATC_prefix = J01 | ATC_suffix = DD18 | ATC_supplemental = | PubChem = 6537431 | DrugBank = | ChEMBL = 2105953 | ChemSpiderID = 4576594 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 74CQ4Q3N63 | KEGG = D07655 | chemical_formula = | C=16 | H=17 | N=9 | O=5 | S=2 | molecular_weight = 479.49 g/mol | smiles = O=C2N1/C(=C(\\CS[C@@H]1[C@@H]2NC(=O)C(=N\\OC)\\c3nc(sc3)N)Cn4nc(nn4)C)C(=O)O }}Cefteram (INN) is a third-generation cephalosporin antibiotic.[1] References1. ^{{cite journal|title=In vitro antibacterial activities of cefteram and other beta-lactam agents against recent clinical isolates|journal=The Japanese Journal of Antibiotics|volume=51|issue=1|pages=11–25|pmid=9557273|year=1998|last1=Yamaguchi|first1=K.|last2=Ohno|first2=A.|last3=Takahashi|first3=S.|last4=Hayashi|first4=M.|last5=Yamanaka|first5=K.|last6=Hirakata|first6=Y.|last7=Mitsuyama|first7=J.}} {{CephalosporinAntiBiotics}}{{antibiotic-stub}} 4 : Cephalosporin antibiotics|Thiazoles|Tetrazoles|Ketoximes |
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