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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H17N9O5S2
Molecular Weight 479.493
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFTERAM

SMILES

CO\N=C(/C(=O)N[C@H]1[C@H]2SCC(CN3N=NC(C)=N3)=C(N2C1=O)C(O)=O)C4=CSC(N)=N4

InChI

InChIKey=XSPUSVIQHBDITA-RKYNPMAHSA-N
InChI=1S/C16H17N9O5S2/c1-6-20-23-24(21-6)3-7-4-31-14-10(13(27)25(14)11(7)15(28)29)19-12(26)9(22-30-2)8-5-32-16(17)18-8/h5,10,14H,3-4H2,1-2H3,(H2,17,18)(H,19,26)(H,28,29)/b22-9-/t10-,14-/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H17N9O5S2
Molecular Weight 479.493
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 1
Optical Activity UNSPECIFIED

Cefteram is a semisynthetic cephalosporin formulated for oral administration as the prodrug ester, cefteram pivoxil. The mechanism of action of cefteram is inhibition of bacterial cell wall synthesis. Cefteram exerts its bactericidal activity by strongly binding to penicillin-binding protein (PBP) 3, 1A, and 1Bs. The drug is available in Japan and is used for the treatment of bacterial infections.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
TOMIRON

Approved Use

To treat pharyngitis/laryngitis, tonsillitis (including peritonsillitis and peritonsillar abscess), acute bronchitis, pneumonia, and secondary infections in chronic respiratory lesion; cystitis, pyelonephritis and urethritis; bartholinitis, intrauterine infection and uterine adnexitis; otitis media and sinusitis; periodontitis, pericoronitis and gnathitis
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
1.32 μg/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
1.22 μg/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
1.65 μg/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
1.73 μg/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
2.79 μg × h/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
2.7 μg × h/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
4.89 μg × h/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
4.76 μg × h/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.16 h
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
1.1 h
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
1.32 h
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
1.33 h
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CEFTERAM plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
200 mg 3 times / day multiple, oral
Studied dose
Dose: 200 mg, 3 times / day
Route: oral
Route: multiple
Dose: 200 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: FED
Sources:
PubMed

PubMed

TitleDatePubMed
Preliminary antimicrobial susceptibility interpretive criteria for cefetamet (Ro 15-8074) and cefteram (Ro 19-5247) disk tests.
1987-09
In vitro activity of Ro 19-5247 (T-2525) and interpretive criteria for disk diffusion susceptibility testing.
1987-07
In vitro activity of Ro 15-8074, Ro 19-5247, A-56268, and roxithromycin (RU 28965) against Neisseria gonorrhoeae and Chlamydia trachomatis.
1987-03
In vitro activity and beta-lactamase stability of two oral cephalosporins, ceftetrame (Ro 19-5247) and cefetamet (Ro 15-8074).
1986-09
In vitro activity of Ro 15-8074 and Ro 19-5247, two orally administered cephalosporin metabolites.
1986-06
Patents

Sample Use Guides

The usual adult dosage for oral use is 150 − 600 mg (potency) of cefteram pivoxil daily in 3 divided doses after meals.
Route of Administration: Oral
The activity of cefteram was compared with that of other P-lactams against a total of 491 bacterial strains. The drug was highly active (MIC for 90% of the strains tested [MIC90] < 2 ug/ml) against the majority of the members of the family Enterobacteriaceae, Haemophilus influenzae, Neisseria spp., and Streptococcuspneumoniae, being at least 16-fold more active than cephalexin and 8-fold more active than cefuroxime. There was no activity against Pseudomonas aeruginosa, Enterobacter sp., and Citrobacter sp. Staphylococcus aureus was moderately susceptible to cefteram (MIC90, 8 ug/ml).
Substance Class Chemical
Created
by admin
on Wed Apr 02 06:56:17 GMT 2025
Edited
by admin
on Wed Apr 02 06:56:17 GMT 2025
Record UNII
74CQ4Q3N63
Record Status Validated (UNII)
Record Version
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Name Type Language
RO 19-5247
Preferred Name English
CEFTERAM
INN   MI   WHO-DD  
INN  
Official Name English
(+)-(6R,7R)-7-(2-(2-AMINO-4-THIAZOLYL)GLYOXYLAMIDO)-3-((5-METHYL-2H-TETRAZOL-2-YL)METHYL)-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7(SUP 2)-(Z)-(O-METHYLOXIME)
Common Name English
CEFTERAM [MI]
Common Name English
CEFTERAM [JAN]
Common Name English
cefteram [INN]
Common Name English
Cefteram [WHO-DD]
Common Name English
CEFTERAM PIVOXIL [JAN]
Common Name English
Classification Tree Code System Code
WHO-ATC J01DD18
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
NCI_THESAURUS C357
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
Code System Code Type Description
PUBCHEM
6537431
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
EVMPD
SUB07423MIG
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
CAS
82547-58-8
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
SMS_ID
100000081833
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105953
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
CHEBI
135776
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
DRUG CENTRAL
3076
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
FDA UNII
74CQ4Q3N63
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
NCI_THESAURUS
C81035
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
MERCK INDEX
m3219
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY Merck Index
INN
5947
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID7048821
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
WIKIPEDIA
Cefteram
Created by admin on Wed Apr 02 06:56:17 GMT 2025 , Edited by admin on Wed Apr 02 06:56:17 GMT 2025
PRIMARY
Related Record Type Details
PRODRUG -> METABOLITE ACTIVE
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ACTIVE MOIETY