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

Details

Stereochemistry ABSOLUTE
Molecular Formula C25H27N9O8S2
Molecular Weight 645.667
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CEFOPERAZONE

SMILES

CCN1CCN(C(=O)N[C@@H](C(=O)N[C@H]2[C@H]3SCC(CSC4=NN=NN4C)=C(N3C2=O)C(O)=O)C5=CC=C(O)C=C5)C(=O)C1=O

InChI

InChIKey=GCFBRXLSHGKWDP-XCGNWRKASA-N
InChI=1S/C25H27N9O8S2/c1-3-32-8-9-33(21(39)20(32)38)24(42)27-15(12-4-6-14(35)7-5-12)18(36)26-16-19(37)34-17(23(40)41)13(10-43-22(16)34)11-44-25-28-29-30-31(25)2/h4-7,15-16,22,35H,3,8-11H2,1-2H3,(H,26,36)(H,27,42)(H,40,41)/t15-,16-,22-/m1/s1

HIDE SMILES / InChI

Molecular Formula C25H27N9O8S2
Molecular Weight 645.667
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including: http://www.rxlist.com/cefobid-drug.htm

Cefoperazone (marketed under the name Cefobid) is a third-generation cephalosporin antibiotic. Cefoperazone has a broad spectrum of activity: Respiratory Tract Infections caused by S. pneumoniae, H. influenzae, S. aureus (penicillinase and non-penicillinase producing strains), S. pyogenes (Group A beta-hemolytic streptococci), P. aeruginosa, Klebsiella pneumoniae, E. coli, Proteus mirabilis, and Enterobacter species. Peritonitis and Other Intra-abdominal Infections caused by E. coli, P. aeruginosa, and anaerobic gram-negative bacilli (including Bacteroides fragilis). Bacterial Septicemia caused by S. pneumoniae, S. agalactiae, S. aureus, Pseudomonas aeruginosa, E. coli, Klebsiella spp., Klebsiella pneumoniae, Proteus species (indole-positive and indole-negative), Clostridium spp. and anaerobic gram-positive cocci. Infections of the Skin and Skin Structures caused by S. aureus (penicillinase and non-penicillinase producing strains), S. pyogenes, and P. aeruginosa. Pelvic Inflammatory Disease, Endometritis, and Other Infections of the Female Genital Tract caused by N. gonorrhoeae, S. epidermidis, S. agalactiae, E. coli, Clostridium spp., Bacteroides species (including Bacteroides fragilis), and anaerobic gram-positive cocci. Cefobid has no activity against Chlamydia trachomatis. Therefore, when Cefobid is used in the treatment of patients with pelvic inflammatory disease and C. trachomatis is one of the suspected pathogens, appropriate anti-chlamydial coverage should be added. Urinary Tract Infections caused by Escherichia coli and Pseudomonas aeruginosa. Cefoperazone, a third-generation cephalosporin, interferes with cell wall synthesis by binding to the penicillin-binding proteins (PBPs), thus preventing cross-linking of nascent peptidoglycan. Cefoperazone is stable to penicillinases and has a high degree of stability to many beta-lactamases produced by gram-negative bacteria. When tested in vitro, cefoperazone has demonstrated synergistic interactions with aminoglycosides against gram-negative bacilli. As with all cephalosporins, hypersensitivity manifested by skin reactions or drug fever. Reversible neutropenia may occur with prolonged administration. Diarrhea or loose stools has been reported also.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
CEFOBID

Approved Use

Respiratory Tract Infections caused by S. pneumoniae, H. influenzae, S. aureus (penicillinase and non-penicillinase producing strains), S. pyogenes* (Group A beta-hemolytic streptococci), P. aeruginosa, Klebsiella pneumoniae, E. coli, Proteus mirabilis, and Enterobacter species.

Launch Date

1982
Curative
CEFOBID

Approved Use

Peritonitis and Other Intra-abdominal Infections caused by E. coli, P. aeruginosa,* and anaerobic gram-negative bacilli (including Bacteroides fragilis).

Launch Date

1982
Curative
CEFOBID

Approved Use

Bacterial Septicemia caused by S. pneumoniae, S. agalactiae, S. aureus, Pseudomonas aeruginosa, E. coli, Klebsiella spp., Klebsiella pneumoniae, Proteus species (indole-positive and indole-negative), Clostridium spp. and anaerobic gram-positive cocci.

Launch Date

1982
Curative
CEFOBID

Approved Use

Infections of the Skin and Skin Structures caused by S. aureus (penicillinase and non-penicillinase producing strains), S. pyogenes,* and P. aeruginosa.

Launch Date

1982
Curative
CEFOBID

Approved Use

Pelvic Inflammatory Disease, Endometritis, and Other Infections of the Female Genital Tract caused by N. gonorrhoeae, S. epidermidis, S. agalactiae, E. coli, Clostridium spp., Bacteroides species (including Bacteroides fragilis), and anaerobic gram-positive cocci.

Launch Date

1982
Curative
CEFOBID

Approved Use

Urinary Tract Infections caused by Escherichia coli and Pseudomonas aeruginosa.

Launch Date

1982
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
154.9 mg/mL
1 g single, intravenous
dose: 1 g
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
221.8 mg/mL
2 g single, intravenous
dose: 2 g
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
211.62 mg × h/L per 1.73 m²
1 g single, intravenous
dose: 1 g
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
421.63 mg × h/L per 1.73 m²
2 g single, intravenous
dose: 2 g
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
541.2 mg × h/L
50 mg/kg 3 times / day multiple, intravenous
dose: 50 mg/kg
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: NEWBORN
sex: UNKNOWN
food status: UNKNOWN
1147.5 mg × h/L
100 mg/kg 3 times / day multiple, intravenous
dose: 100 mg/kg
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: NEWBORN
sex: UNKNOWN
food status: UNKNOWN
761.7 mg × h/L
100 mg/kg single, intravenous
dose: 100 mg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: NEWBORN
sex: UNKNOWN
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.649 h
1 g single, intravenous
dose: 1 g
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
2.044 h
2 g single, intravenous
dose: 2 g
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
0.185 h
50 mg/kg 3 times / day multiple, intravenous
dose: 50 mg/kg
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: NEWBORN
sex: UNKNOWN
food status: UNKNOWN
0.063 h
100 mg/kg 3 times / day multiple, intravenous
dose: 100 mg/kg
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: NEWBORN
sex: UNKNOWN
food status: UNKNOWN
0.063 h
100 mg/kg single, intravenous
dose: 100 mg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CEFOPERAZONE serum
Homo sapiens
population: UNHEALTHY
age: NEWBORN
sex: UNKNOWN
food status: UNKNOWN
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer







Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
yes [IC50 1330 uM]
yes [Ki 1890 uM]
yes [Ki 210 uM]
yes [Ki 2800 uM]
Drug as victim
PubMed

PubMed

TitleDatePubMed
[Survey of the utilization and adverse effects of antibacterial drugs in patients admitted for respiratory diseases].
2005-02
[Distribution and drug-resistance of 3 500 gram-negative bacteria in Guangzhou].
2005-02
Effective antibiotic regime for postoperative acute cholangitis in biliary atresia--an evolving scene.
2004-12
Pharmacokinetics of quinacrine in the treatment of prion disease.
2004-11-29
[Comparison of efficacy between ceftriaxone and cefoperazone plus sulbactam in peri-operative treatment of acute suppurative cholangitis].
2004-11-17
In vitro activity of cefepime and cefpirome compared to other third-generation cephem antibiotics against gram-negative nosocomial pathogens.
2004-11
In vitro bactericidal activity of antimicrobial agents against enterohaemorrhagic Escherichia coli.
2004-11
Arcobacter species in humans.
2004-10
Acute interstitial nephritis due to cefoperazone.
2004-09
External decontamination of wild leeches with hypochloric acid.
2004-08-25
Flies and Campylobacter infection of broiler flocks.
2004-08
Vibrio vulnificus in Taiwan.
2004-08
Antibiotic susceptibility of coagulase-negative staphylococci isolated from goats' milk.
2004-06
In vitro activities of beta-lactam antibiotics alone and in combination with sulbactam against Gram-negative bacteria.
2004-06
[Changes in plasma levels of LPS, TNFalpha and IL-6 in burn patients with severe infection treated with Imipenem or Cefoperazone].
2004-04
Pacemaker lead endocarditis caused by Achromobacter xylosoxidans.
2004-04
Isolation and characterisation of Arcobacter butzleri from meat.
2004-02-15
[Activity of fourth generation cephalosporins against clinical isolates of Enterobacteriaceae].
2004-02-06
Amebic liver abscess, Mirizzi syndrome, and acute hepatic failure.
2004-02
Comparison in a rat thigh abscess model of imipenem, meropenem and cefoperazone-sulbactam against Acinetobacter baumannii strains in terms of bactericidal efficacy and resistance selection.
2004-01-08
[Study of resistance mechanism on cefotaxime resistant Proteus mirabilis isolated from clinical specimens and its clinical background].
2004-01
Derivatives of phosphate Schiff base transition metal complexes: synthesis, studies and biological activity.
2004-01
Separation of cefoperazone enantiomers using beta-cyclodextrin as chiral additive by capillary zone electrophoresis.
2004-01
[Clinical and bacteriological substantiation of the use of cefoperazone/sulbactam in complex therapy of patients with pyo-destructive forms of lower respiratory tract infection (LRTI)].
2004
Double-disk synergy test positivity in Stenotrophomonas maltophilia clinical strains.
2004
[Surveillance of susceptibility of clinical isolates to cefmetazole between 2000 and 2002].
2003-12
[Current data on antibiotic resistance of the most important bovine mastitis pathogens in Switzerland].
2003-12
Preoperative antimicrobial administration for prevention of postoperative infection in patients with laparoscopic cholecystectomy.
2003-10
The susceptibility of non-fermentative Gram-negative bacilli to cefperazone and sulbactam compared with other antibacterial agents.
2003-10
Pharmacodynamics and pharmacokinetics of cefoperazone and cefamandole in dogs following single dose intravenous and intramuscular administration.
2003-09
Square-wave voltammetric determination of cefoperazone in a bacterial culture, pharmaceutical drug, milk, and urine.
2003-09
[Yearly changes in antibacterial activities of cefozopran against various clinical isolates between 1996 and 2001--II. Gram-negative bacteria].
2003-08
Carbapenem-resistant Pseudomonas aeruginosa-carrying VIM-2 metallo-beta-lactamase determinants, Croatia.
2003-08
The status of drug resistance and ampC gene expression in Enterobacter cloacae.
2003-08
[Assay of Acinetobacter SPP drug-resistance by Kirby-Bauer and Etest method].
2003-05
Interaction of human and rat organic anion transporter 2 with various cephalosporin antibiotics.
2003-03-28
[Changes of antimicrobial resistance among nonfermenting gram-negative bacilli isolated from intensive care units from 1994 to 2001 in China].
2003-03-10
Retrospective analysis of antibiotic susceptibility patterns of respiratory isolates of Pseudomonas aeruginosa in a Turkish University Hospital.
2003-03-07
Emergence of ceftriaxone-resistant Salmonella isolates and rapid spread of plasmid-encoded CMY-2-like cephalosporinase, Taiwan.
2003-03
Detection limits of antimicrobials in ewe milk by delvotest photometric measurements.
2003-02
[Comparative analysis of the effectiveness and costs of azithromycin and cefoperazone treatment of patients during COPD exacerbation].
2003-01
Current status of drug resistance among gram-negative bacilli isolated from admitted cases in a tertiary care centre.
2003-01
[Efficacy and safety of cefoperazone/sulbactam in the treatment of children with mucoviscidosis during exacerbation of the bronchopulmonary process].
2003
[Comparative clinical and epidemiological evaluation of beta-lactam antibiotics in the treatment of intraabdominal infections].
2003
[Sulperazone in the treatment of severe infections in patients with cancer].
2003
[A control study on bacterial resistance and clinical features of lower respiratory tract infection with Pseudomonas aeruginosa in medical intensive care unit and general ward].
2002-12
[beta-lactamase-producing activity and antimicrobial susceptibility of major pathogenic bacteria isolated from clinical samples. Japan beta-lactamase Research Group].
2002-09
Rat renal organic anion transporter rOAT1 mediates transport of urinary-excreted cephalosporins, but not of biliary-excreted cefoperazone.
2002
[Complex detoxication therapy in obstructive jaundice of tumor genesis].
2002
[Characterization of cefoperazone resistance gene on plasmid pFC in E. coli HX88108].
2001-03
Patents

Sample Use Guides

The usual adult daily dose is 2 to 4 grams per day administered in equally divided doses every 12 hours. In severe infections or infections caused by less sensitive organisms, the total daily dose and/or frequency may be increased. Patients have been successfully treated with a total daily dosage of 6–12 grams divided into 2, 3 or 4 administrations ranging from 1.5 to 4 grams per dose. When treating infections caused by Streptococcus pyogenes, therapy should be continued for at least 10 days.
Route of Administration: Other
MIC90 of cefoperazone against S. marcescens, E. cloacae, ESBL-K. pneumoniae and A. baumannii were >128 mg/L.
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:31:35 GMT 2025
Edited
by admin
on Mon Mar 31 18:31:35 GMT 2025
Record UNII
7U75I1278D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEFOPERAZONE
INN   MI   VANDF   WHO-DD  
INN  
Official Name English
PERACEF
Preferred Name English
CEFOPERAZONE [MI]
Common Name English
CEFOPERAZONE [VANDF]
Common Name English
cefoperazone [INN]
Common Name English
5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((((4-ETHYL-2,3-DIOXO-1-PIPERAZINYL)CARBONYL)AMINO)(4-HYDROXYPHENYL)ACETYL)AMINO)-3-(((1-METHYL-1H-TETRAZOL-5-YL)THIO)METHYL)-8-OXO, (6R-(6.ALPHA.,7.BETA.(R*)))-
Common Name English
Cefoperazone [WHO-DD]
Common Name English
(6R,7R)-7-((R)-2-(4-ETHYL-2,3-DIOXO-1-PIPERAZINECARBOXAMIDO)-2-(P-HYDROXYPHENYL)ACETAMIDO-3-(((1-METHYL-1H-TETRAZOL-5-YL)THIO)METHYL)-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID
Common Name English
Classification Tree Code System Code
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
WHO-VATC QJ01DD62
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
WHO-ATC J01DD62
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
LIVERTOX NBK547862
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
LIVERTOX NBK548666
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
WHO-VATC QJ51DD12
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NCI_THESAURUS C357
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
WHO-ATC J01DD12
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
WHO-VATC QJ01DD12
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000175488
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
NDF-RT N0000011161
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
Code System Code Type Description
FDA UNII
7U75I1278D
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
ECHA (EC/EINECS)
263-749-4
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
CHEBI
3493
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
DRUG CENTRAL
543
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
PUBCHEM
44187
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
EVMPD
SUB07402MIG
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
WIKIPEDIA
CEFOPERAZONE
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
ChEMBL
CHEMBL507674
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
NCI_THESAURUS
C61663
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
MERCK INDEX
m3201
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY Merck Index
CAS
62893-19-0
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
SMS_ID
100000081804
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
LACTMED
Cefoperazone
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
MESH
D002438
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
RXCUI
2184
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY RxNorm
EPA CompTox
DTXSID2022759
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
DRUG BANK
DB01329
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
INN
4742
Created by admin on Mon Mar 31 18:31:36 GMT 2025 , Edited by admin on Mon Mar 31 18:31:36 GMT 2025
PRIMARY
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Biological Half-life PHARMACOKINETIC