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

Details

Stereochemistry ABSOLUTE
Molecular Formula C20H22N5O6S.Na
Molecular Weight 483.473
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AZLOCILLIN SODIUM

SMILES

[Na+].[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](NC(=O)N3CCNC3=O)C4=CC=CC=C4)C([O-])=O

InChI

InChIKey=UVOCNBWUHNCKJM-XFAPPKAWSA-M
InChI=1S/C20H23N5O6S.Na/c1-20(2)13(17(28)29)25-15(27)12(16(25)32-20)22-14(26)11(10-6-4-3-5-7-10)23-19(31)24-9-8-21-18(24)30;/h3-7,11-13,16H,8-9H2,1-2H3,(H,21,30)(H,22,26)(H,23,31)(H,28,29);/q;+1/p-1/t11-,12-,13+,16-;/m1./s1

HIDE SMILES / InChI
Azlocillin is a semisynthetic penicillin with broad spectrum of anti-bacterial action. The drug is effective against gram-negative and gram-positive infections and acts by inhibition of penicillin-binding protein (PBP)-dependent bacterial cell wall synthesis. Azlocillin was marketed in the USA under the name Azlin (sodium salt), however, its approval was discontinued.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
AZLIN

Approved Use

Treatment of Gram-positive (Streptococcus spp., Enterococcus, Listeria monocytogenes) and Gram-negative (H. influenzae, E. coli, Proteus mirabilis, Salmonella spp., Shigella spp.) infections.

Launch Date

1982
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
414 μg/mL
4 g 4 times / day multiple, intravenous
dose: 4 g
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
AZLOCILLIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
374 μg × h/mL
4 g single, intravenous
dose: 4 g
route of administration: Intravenous
experiment type: SINGLE
co-administered:
AZLOCILLIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
592 μg × h/mL
4 g 4 times / day multiple, intravenous
dose: 4 g
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
AZLOCILLIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
772 μg × h/mL
5 g 3 times / day multiple, intravenous
dose: 5 g
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
AZLOCILLIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.26 h
4 g single, intravenous
dose: 4 g
route of administration: Intravenous
experiment type: SINGLE
co-administered:
AZLOCILLIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
1.29 h
4 g 4 times / day multiple, intravenous
dose: 4 g
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
AZLOCILLIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
1.46 h
5 g 3 times / day multiple, intravenous
dose: 5 g
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
AZLOCILLIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
1.1 h
4 g 4 times / day multiple, intravenous
dose: 4 g
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
AZLOCILLIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
17 g 1 times / day multiple, intravenous|intramuscular
Dose: 17 g, 1 times / day
Route: intravenous|intramuscular
Route: multiple
Dose: 17 g, 1 times / day
Sources:
unhealthy
n = 21
Health Status: unhealthy
Population Size: 21
Sources:
Disc. AE: Macular rash, Pruritic rash...
AEs leading to
discontinuation/dose reduction:
Macular rash (4 patients)
Pruritic rash (4 patients)
Sources:
AEs

AEs

AESignificanceDosePopulation
Macular rash 4 patients
Disc. AE
17 g 1 times / day multiple, intravenous|intramuscular
Dose: 17 g, 1 times / day
Route: intravenous|intramuscular
Route: multiple
Dose: 17 g, 1 times / day
Sources:
unhealthy
n = 21
Health Status: unhealthy
Population Size: 21
Sources:
Pruritic rash 4 patients
Disc. AE
17 g 1 times / day multiple, intravenous|intramuscular
Dose: 17 g, 1 times / day
Route: intravenous|intramuscular
Route: multiple
Dose: 17 g, 1 times / day
Sources:
unhealthy
n = 21
Health Status: unhealthy
Population Size: 21
Sources:
PubMed

PubMed

TitleDatePubMed
Broth microdilution testing of susceptibilities to 30 antimicrobial agents of Mycobacterium avium strains from patients with acquired immune deficiency syndrome.
1987 Oct
Evaluation of the immunologic cross-reactivity of aztreonam in patients with cystic fibrosis who are allergic to penicillin and/or cephalosporin antibiotics.
1991 May-Jun
The penicillins.
1999 Mar
Natural antibiotic susceptibility of Ewingella americana strains.
2003 Oct
Placental transfer of antibiotics administered to the mother: a review.
2006 Feb
Searching for new antimalarial therapeutics amongst known drugs.
2006 Jun
Problematic clinical isolates of Pseudomonas aeruginosa from the university hospitals in Sofia, Bulgaria: current status of antimicrobial resistance and prevailing resistance mechanisms.
2007 Jul
Human oral drugs absorption is correlated to their in vitro uptake by brush border membrane vesicles.
2007 May 4
Phylogeography and recolonization of the Swiss Alps by the Valais shrew (Sorex antinorii), inferred with autosomal and sex-specific markers.
2008 Sep
Detection of Extended Spectrum β-lactamase Production Among Uropathogens.
2009 Jan
Data correction pre-processing for electronically stored blood culture results: implications on microbial spectrum and empiric antibiotic therapy.
2009 Jun 7
Role of the BACTEC radiometric method in the evaluation of patients with clinically probable tuberculous meningitis.
2010 Apr
Laboratory diagnosis of tuberculous meningitis - is there a scope for further improvement?
2010 Jan
Pleistocene climatic cycling drives intra-specific diversification in the intermediate horseshoe bat (Rhinolophus affinis) in Southern China.
2010 Jul
Contrasting patterns of phylogeographic relationships in sympatric sister species of ironclad beetles (Zopheridae: Phloeodes spp.) in California's Transverse Ranges.
2010 Jun 24
Patents

Sample Use Guides

Gram-negative infections: 2 to 5 grams every 8 hours IV. Serious infections: 225 to 300 mg/kg/day IV in 4 to 6 divided doses (usual IV doses 3g q4h or 4g q6h) (up to 18 g/day).
Route of Administration: Intravenous
In Vitro Use Guide
Sources: www.ncbi.nlm.nih.gov/pubmed/111616
In vitro activity of Azlocillin against different bacterial strains was determined. MIC50 values were 2 ugml (Enterococcus), 8 ug/ml (E. coli), 16 ug/ml (Enterobacter spp.), 64 ug/ml (Klebsiella spp.), 4 ug/ml (P. mirabilis), 16 ug/ml (P. aeruginosa, gentamicin susceptible)).
Name Type Language
AZLOCILLIN SODIUM
MART.   ORANGE BOOK   VANDF   WHO-DD  
Common Name English
AZLOCILLIN SODIUM [MART.]
Common Name English
BAY-E 6905
Code English
BAY-E-6905
Code English
Sodium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(R)-2-(2-oxo-1-imidazolidinecarboxamido)-2-phenylacetamido]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
Systematic Name English
AZLOCILLIN SODIUM SALT
MI  
Common Name English
Azlocillin sodium [WHO-DD]
Common Name English
AZLOCILLIN SODIUM [VANDF]
Common Name English
AZLIN
Brand Name English
SODIUM (2S,5R,6R)-3,3-DIMETHYL-7-OXO-6-(((2R)-2-(((2-OXOIMIDAZOLIDIN-1-YL)CARBONYL)AMINO)-2-PHENYLACETYL)AMINO)-4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLATE
Systematic Name English
AZLOCILLIN SODIUM SALT [MI]
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID, 3,3-DIMETHYL-7-OXO-6-(((((2-OXO-1-IMIDAZOLIDINYL)CARBONYL)AMINO)PHENYLACETYL)AMINO)-, MONOSODIUM SALT, (2S-(2.ALPHA.,5.ALPHA.,6.BETA.(S*)))-
Common Name English
AZLOCILLIN SODIUM [ORANGE BOOK]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1500
Created by admin on Fri Dec 15 15:18:48 GMT 2023 , Edited by admin on Fri Dec 15 15:18:48 GMT 2023
Code System Code Type Description
DRUG BANK
DBSALT000431
Created by admin on Fri Dec 15 15:18:48 GMT 2023 , Edited by admin on Fri Dec 15 15:18:48 GMT 2023
PRIMARY
NCI_THESAURUS
C65243
Created by admin on Fri Dec 15 15:18:48 GMT 2023 , Edited by admin on Fri Dec 15 15:18:48 GMT 2023
PRIMARY
ChEMBL
CHEMBL1537
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PRIMARY
EVMPD
SUB00645MIG
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PRIMARY
RXCUI
203836
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PRIMARY RxNorm
FDA UNII
DWV1EFW947
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PRIMARY
CAS
37091-65-9
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PRIMARY
EPA CompTox
DTXSID6045581
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PRIMARY
ECHA (EC/EINECS)
253-347-7
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PRIMARY
PUBCHEM
23685176
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PRIMARY
MERCK INDEX
m2178
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PRIMARY Merck Index
SMS_ID
100000084969
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PRIMARY
CHEBI
51864
Created by admin on Fri Dec 15 15:18:48 GMT 2023 , Edited by admin on Fri Dec 15 15:18:48 GMT 2023
PRIMARY