U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C16H16ClN3O4.H2O
Molecular Weight 367.784
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LORACARBEF

SMILES

O.[H][C@]12CCC(Cl)=C(N1C(=O)[C@H]2NC(=O)[C@H](N)C3=CC=CC=C3)C(O)=O

InChI

InChIKey=GPYKKBAAPVOCIW-HSASPSRMSA-N
InChI=1S/C16H16ClN3O4.H2O/c17-9-6-7-10-12(15(22)20(10)13(9)16(23)24)19-14(21)11(18)8-4-2-1-3-5-8;/h1-5,10-12H,6-7,18H2,(H,19,21)(H,23,24);1H2/t10-,11-,12+;/m1./s1

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/7686466 | http://www.rxlist.com/lorabid-drug.htm

Loracarbef (KT3777) is carbacephem antibiotic structurally identical to cefaclor, except that the sulfur atom of position 1 of the cephem nucleus has been replaced by carbon. It showed good affinity for penicillin-binding proteins. At low concentrations (< 2 mg/L) in vitro, it inhibits Streptococcus pneumoniae, S. pyogenes, beta-haemolytic streptococci groups B, C and G. Proteus mirabilis and Moraxella catarrhalis, including beta-lactamase-producing strains. At therapeutic plasma concentrations it is also active in vitro against most strains of Staphylococcus aureus, S. saprophyticus, Escherichia coli and beta-lactamase-positive and -negative strains of Haemophilus influenzae. Loracarbef has been indicated in the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
LORABID

Approved Use

Loracarbef is indicated in the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms in the conditions listed below. (As recommended dosages, durations of therapy, and applicable patient populations vary among these infections, please see DOSAGE AND ADMINISTRATION for specific recommendations.) Lower Respiratory Tract: Secondary Bacterial Infection of Acute Bronchitis caused by S. pneumoniae, H. influenzae(including b-lactamase-producing strains), or M. catarrhalis (including b-lactamase-producing strains). Acute Bacterial Exacerbations of Chronic Bronchitis: caused by S. pneumoniae, H. influenzae (including b-lactamase-producing strains), or M. catarrhalis (including b-lactamase-producing strains). Pneumonia: caused by S. pneumoniae or H. influenzae (non-b-lactamase-producing strains only). Data are insufficient at this time to establish efficacy in patients with pneumonia caused by b-lactamase-producing strains of H. influenzae. Upper Respiratory Tract: Otitis Media† caused by S. pneumoniae, H. influenzae (including b-lactamase-producing strains), M. catarrhalis (including b-lactamase-producing strains), or S. pyogenes. Acute Maxillary Sinusitis:† caused by S. pneumoniae, H. influenzae (non-b-lactamase-producing strains only), or M. catarrhalis (including b-lactamase-producing strains). Data are insufficient at this time to establish efficacy in patients with acute maxillary sinusitis caused by b-lactamase-producing strains of H. influenzae. † NOTE: In a patient population with significant numbers of b-lactamase-producing organisms, loracarbef's clinical cure and bacteriological eradication rates were somewhat less than those observed with a product containing a b-lactamase inhibitor. Loracarbef's decreased potential for toxicity compared to products containing b-lactamase inhibitors along with the susceptibility patterns of the common microbes in a given geographic area should be taken into account when considering the use of an antimicrobial (see CLINICAL STUDIES.) Pharyngitis and Tonsillitis: caused by S. pyogenes. (The usual drug of choice in the treatment and prevention of streptococcal infections, including the prophylaxis of rheumatic fever, is penicillin administered by the intramuscular route. Loracarbef is generally effective in the eradication of S. pyogenes from the nasopharynx; however, data establishing the efficacy of loracarbef in the subsequent prevention of rheumatic fever are not available at present.) For information on use in pediatric patients, see PRECAUTIONS, Pediatric Use. Skin and Skin Structure: Uncomplicated Skin and Skin Structure Infections caused by S. aureus (including penicillinase-producing strains) or S. pyogenes. Abscesses should be surgically drained as clinically indicated. Urinary Tract: Uncomplicated Urinary Tract Infections (cystitis) caused by E. coli or S. saprophyticus*. NOTE: In considering the use of loracarbef in the treatment of cystitis, loracarbef's lower bacterial eradication rates and lower potential for toxicity should be weighed against the increased eradication rates and increased potential for toxicity demonstrated by some other classes of approved agents (see CLINICAL STUDIES.) Uncomplicated Pyelonephritis: caused by E. coli. *Although treatment of infections due to this organism in this organ system demonstrated a clinically acceptable overall outcome, efficacy was studied in fewer than 10 infections. Culture and susceptibility testing should be performed when appropriate to determine the causative organism and its susceptibility to loracarbef. Therapy may be started while awaiting the results of these studies. Once these results become available, antimicrobial therapy should be adjusted accordingly.

Launch Date

1991
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
19.21 mg/L
400 mg single, oral
dose: 400 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LORACARBEF serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
13.64 mg/L
400 mg single, oral
dose: 400 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LORACARBEF serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
14 μg/mL
400 mg single, oral
dose: 400 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LORACARBEF plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
8 μg/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LORACARBEF plasma
Homo sapiens
population: UNHEALTHY
age: CHILD
sex: UNKNOWN
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
33.04 mg × h/L
400 mg single, oral
dose: 400 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LORACARBEF serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
35.38 mg × h/L
400 mg single, oral
dose: 400 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LORACARBEF serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
70.31 min
400 mg single, oral
dose: 400 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LORACARBEF serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
102.33 min
400 mg single, oral
dose: 400 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LORACARBEF serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
Doses

Doses

DosePopulationAdverse events​
400 mg 2 times / day steady, oral
Recommended
Dose: 400 mg, 2 times / day
Route: oral
Route: steady
Dose: 400 mg, 2 times / day
Sources:
unhealthy, adult
n = 235
Health Status: unhealthy
Condition: bacterial infections
Age Group: adult
Sex: unknown
Population Size: 235
Sources:
Disc. AE: Diarrhea, Allergic exanthema...
AEs leading to
discontinuation/dose reduction:
Diarrhea (1 patient)
Allergic exanthema (1 patient)
Abdominal pain (1 patient)
Sources:
30 mg/kg 1 times / day steady, oral (max)
Highest studied dose
Dose: 30 mg/kg, 1 times / day
Route: oral
Route: steady
Dose: 30 mg/kg, 1 times / day
Sources:
unhealthy, children and adults
n = 4506
Health Status: unhealthy
Condition: bacterial infections
Age Group: children and adults
Sex: M+F
Population Size: 4506
Sources:
Disc. AE: Hypersensitivity, Diarrhea...
AEs leading to
discontinuation/dose reduction:
Hypersensitivity (16 patients)
Diarrhea (12 patients)
Nausea and vomiting (16 patients)
Abdominal pain (9 patients)
Headache (5 patients)
Neurologic disorder NOS (2 patients)
Sources:
AEs

AEs

AESignificanceDosePopulation
Abdominal pain 1 patient
Disc. AE
400 mg 2 times / day steady, oral
Recommended
Dose: 400 mg, 2 times / day
Route: oral
Route: steady
Dose: 400 mg, 2 times / day
Sources:
unhealthy, adult
n = 235
Health Status: unhealthy
Condition: bacterial infections
Age Group: adult
Sex: unknown
Population Size: 235
Sources:
Allergic exanthema 1 patient
Disc. AE
400 mg 2 times / day steady, oral
Recommended
Dose: 400 mg, 2 times / day
Route: oral
Route: steady
Dose: 400 mg, 2 times / day
Sources:
unhealthy, adult
n = 235
Health Status: unhealthy
Condition: bacterial infections
Age Group: adult
Sex: unknown
Population Size: 235
Sources:
Diarrhea 1 patient
Disc. AE
400 mg 2 times / day steady, oral
Recommended
Dose: 400 mg, 2 times / day
Route: oral
Route: steady
Dose: 400 mg, 2 times / day
Sources:
unhealthy, adult
n = 235
Health Status: unhealthy
Condition: bacterial infections
Age Group: adult
Sex: unknown
Population Size: 235
Sources:
Diarrhea 12 patients
Disc. AE
30 mg/kg 1 times / day steady, oral (max)
Highest studied dose
Dose: 30 mg/kg, 1 times / day
Route: oral
Route: steady
Dose: 30 mg/kg, 1 times / day
Sources:
unhealthy, children and adults
n = 4506
Health Status: unhealthy
Condition: bacterial infections
Age Group: children and adults
Sex: M+F
Population Size: 4506
Sources:
Hypersensitivity 16 patients
Disc. AE
30 mg/kg 1 times / day steady, oral (max)
Highest studied dose
Dose: 30 mg/kg, 1 times / day
Route: oral
Route: steady
Dose: 30 mg/kg, 1 times / day
Sources:
unhealthy, children and adults
n = 4506
Health Status: unhealthy
Condition: bacterial infections
Age Group: children and adults
Sex: M+F
Population Size: 4506
Sources:
Nausea and vomiting 16 patients
Disc. AE
30 mg/kg 1 times / day steady, oral (max)
Highest studied dose
Dose: 30 mg/kg, 1 times / day
Route: oral
Route: steady
Dose: 30 mg/kg, 1 times / day
Sources:
unhealthy, children and adults
n = 4506
Health Status: unhealthy
Condition: bacterial infections
Age Group: children and adults
Sex: M+F
Population Size: 4506
Sources:
Neurologic disorder NOS 2 patients
Disc. AE
30 mg/kg 1 times / day steady, oral (max)
Highest studied dose
Dose: 30 mg/kg, 1 times / day
Route: oral
Route: steady
Dose: 30 mg/kg, 1 times / day
Sources:
unhealthy, children and adults
n = 4506
Health Status: unhealthy
Condition: bacterial infections
Age Group: children and adults
Sex: M+F
Population Size: 4506
Sources:
Headache 5 patients
Disc. AE
30 mg/kg 1 times / day steady, oral (max)
Highest studied dose
Dose: 30 mg/kg, 1 times / day
Route: oral
Route: steady
Dose: 30 mg/kg, 1 times / day
Sources:
unhealthy, children and adults
n = 4506
Health Status: unhealthy
Condition: bacterial infections
Age Group: children and adults
Sex: M+F
Population Size: 4506
Sources:
Abdominal pain 9 patients
Disc. AE
30 mg/kg 1 times / day steady, oral (max)
Highest studied dose
Dose: 30 mg/kg, 1 times / day
Route: oral
Route: steady
Dose: 30 mg/kg, 1 times / day
Sources:
unhealthy, children and adults
n = 4506
Health Status: unhealthy
Condition: bacterial infections
Age Group: children and adults
Sex: M+F
Population Size: 4506
Sources:
PubMed

PubMed

TitleDatePubMed
Loracarbef versus penicillin VK in the treatment of streptococcal pharyngitis and tonsillitis in an adult population.
1992 Jun 22
Transport mechanisms responsible for the absorption of loracarbef, cefixime, and cefuroxime axetil into human intestinal Caco-2 cells.
1994 Apr 20
Natural antimicrobial susceptibilities of strains of 'unusual' Serratia species: S. ficaria, S. fonticola, S. odorifera, S. plymuthica and S. rubidaea.
2003 Apr
[Sensitivity of Haemophilus influenzae isolates in Spain to 17 oral antibiotics].
2003 Mar
Limited spread of penicillin-nonsusceptible pneumococci, Skåne County, Sweden.
2004 Jun
Penicillin V, loracarbef and clindamycin in tonsillar surface fluid during acute group A streptococcal pharyngotonsillitis.
2005
Staphylococcal skin infections in children: rational drug therapy recommendations.
2005
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Patents

Sample Use Guides

In the treatment of adults with pharyngitis, acute bronchitis, tonsillitis and uncomplicated infections of skin and skin structures, loracarbef was studied at a dosage of 200mg twice daily. Patients with acute pneumonia, sinusitis and uncomplicated pyelonephritis were treated with 400mg twice daily in clinical studies. Seven-day courses of 200 or 400mg twice daily were used to treat acute exacerbations of chronic bronchitis (acute superimposed on chronic). A once-daily dose of 200mg is used to treat acute cystitis. In infants and children, 30 mg/kg in divided doses 12-hourly is used to treat acute otitis media, while 15 mg/kg is recommended for the treatment of pharyngitis, tonsillitis and impetigo. Dosage should be adjusted in patients with renal impairment whose creatine clearance is below 2.9 L/h (49 ml/min).
Route of Administration: Oral
In Vitro Use Guide
The MIC50 of loracarbef (KT3777) ranged from 0.2 to 3.13 micrograms/ml for clinical isolates of Staphylococcus aureus, Streptococci, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Haemophilus influenzae, and Neisseria gonorrhoeae.
Name Type Language
LORACARBEF
ORANGE BOOK   USAN   USP   USP-RS   VANDF  
USAN  
Official Name English
LORACARBEF [USAN]
Common Name English
LORABID
Brand Name English
LY163892 MONOHYDRATE
Code English
(6R,7S)-7-[(R)-2-Amino-2-phenylacetamido]-3-chloro-8-oxo-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, monohydrate
Common Name English
LY-163892 MONOHYDRATE
Code English
1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-((AMINOPHENYLACETYL)AMINO)-3-CHLORO-8-OXO-, MONOHYDRATE, (6R-(6.ALPHA.,7.BETA.(R*)))-
Common Name English
LORACARBEF [VANDF]
Common Name English
LORACARBEF [JAN]
Common Name English
LORACARBEF [USP IMPURITY]
Common Name English
LORACARBEF MONOHYDRATE
MI  
Common Name English
LORACARBEF [ORANGE BOOK]
Common Name English
LORACARBEF MONOHYDRATE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C357
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NDF-RT N0000175488
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WHO-ATC J01DC08
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WHO-VATC QJ01DC08
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LIVERTOX 569
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Code System Code Type Description
ChEMBL
CHEMBL1013
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PRIMARY
SMS_ID
100000089072
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LACTMED
Loracarbef
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RXCUI
28981
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PRIMARY RxNorm
CHEBI
214480
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PRIMARY
DRUG BANK
DB00447
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DRUG CENTRAL
1603
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EVMPD
SUB23249
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MESH
C054920
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NCI_THESAURUS
C47588
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CHEBI
281056
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FDA UNII
3X11EVM5SU
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MERCK INDEX
m6903
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PRIMARY Merck Index
WIKIPEDIA
LORACARBEF
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PRIMARY
EPA CompTox
DTXSID5048718
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PUBCHEM
5284584
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PRIMARY
USAN
BB-95
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PRIMARY
CHEBI
47544
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PRIMARY
CAS
121961-22-6
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