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
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
| 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 |
DescriptionCurator's Comment: description was created based on several sources, including:
http://www.rxlist.com/cefobid-drug.htm
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.
CNS Activity
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2354204 Sources: https://www.ncbi.nlm.nih.gov/pubmed/6448021 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Curative | CEFOBID Approved UseRespiratory 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 Date1982 |
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| Curative | CEFOBID Approved UsePeritonitis and Other Intra-abdominal Infections caused by E. coli, P. aeruginosa,* and anaerobic gram-negative bacilli (including Bacteroides fragilis). Launch Date1982 |
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| Curative | CEFOBID Approved UseBacterial 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 Date1982 |
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| Curative | CEFOBID Approved UseInfections of the Skin and Skin Structures caused by S. aureus (penicillinase and non-penicillinase producing strains), S. pyogenes,* and P. aeruginosa. Launch Date1982 |
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| Curative | CEFOBID Approved UsePelvic 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 Date1982 |
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| Curative | CEFOBID Approved UseUrinary Tract Infections caused by Escherichia coli and Pseudomonas aeruginosa. Launch Date1982 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
154.9 mg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3619425 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3619425 |
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
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
211.62 mg × h/L per 1.73 m² EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3619425 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3619425 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6644441 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6644441 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6644441 |
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
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.649 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3619425 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3619425 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6644441 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6644441 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6644441 |
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
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| yes [IC50 1330 uM] | ||||
| yes [Ki 1890 uM] | ||||
| yes [Ki 210 uM] | ||||
| yes [Ki 2800 uM] |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Page: 5.0 |
yes | |||
| yes | ||||
| yes |
PubMed
| Title | Date | PubMed |
|---|---|---|
| [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 |
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
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19382669
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
Edited
Mon Mar 31 18:31:35 GMT 2025
by
admin
on
Mon Mar 31 18:31:35 GMT 2025
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| Record UNII |
7U75I1278D
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| Record Status |
Validated (UNII)
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NDF-RT |
N0000011161
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NDF-RT |
N0000011161
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WHO-VATC |
QJ01DD62
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NDF-RT |
N0000011161
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WHO-ATC |
J01DD62
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LIVERTOX |
NBK547862
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NDF-RT |
N0000011161
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NDF-RT |
N0000011161
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NDF-RT |
N0000011161
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NDF-RT |
N0000011161
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NDF-RT |
N0000011161
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LIVERTOX |
NBK548666
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NDF-RT |
N0000011161
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WHO-VATC |
QJ51DD12
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NCI_THESAURUS |
C357
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WHO-ATC |
J01DD12
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WHO-VATC |
QJ01DD12
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NDF-RT |
N0000175488
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NDF-RT |
N0000011161
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NDF-RT |
N0000011161
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NDF-RT |
N0000011161
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7U75I1278D
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263-749-4
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3493
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543
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44187
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SUB07402MIG
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CEFOPERAZONE
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CHEMBL507674
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C61663
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m3201
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62893-19-0
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100000081804
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Cefoperazone
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D002438
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2184
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DTXSID2022759
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DB01329
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4742
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SOLVATE->ANHYDROUS |
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SALT/SOLVATE -> PARENT |
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TRANSPORTER -> INHIBITOR | |||
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TRANSPORTER -> INHIBITOR | |||
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TRANSPORTER -> INHIBITOR | |||
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SALT/SOLVATE -> PARENT |
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METABOLITE TOXIC -> PARENT |
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| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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| Biological Half-life | PHARMACOKINETIC |
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