AZLOCILLIN SODIUM

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 Search

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

Description
Sources: http://www.antimicrobe.org/new/drugpopup/Azlocillin.pdf | https://www.ncbi.nlm.nih.gov/pubmed/984809

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.

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Bacterial penicillin-binding protein 233 Target ID: CHEMBL2354204 Sources: http://www.antimicrobe.org/new/drugpopup/Azlocillin.pdf	Inhibitor 8297

Conditions

Condition	Modality	Targets	Highest Phase	Product
Bacterial infections 234 Sources: http://www.antimicrobe.org/new/drugpopup/Azlocillin.pdf	Curative		Approved 8429	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

C_max

Value	Dose	Co-administered	Analyte	Population
414 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3780161	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

Value	Dose	Analyte	Population
374 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3729353	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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2751284	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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2751284	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

T_1/2

Value	Dose	Analyte	Population
1.26 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3729353	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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2751284	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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2751284	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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3780161	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

Dose	Population	Adverse 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: https://pubmed.ncbi.nlm.nih.gov/6619026	unhealthy n = 21 Health Status: unhealthy Population Size: 21 Sources: https://pubmed.ncbi.nlm.nih.gov/6619026	Disc. AE: Macular rash, Pruritic rash... AEs leading to discontinuation/dose reduction: Macular rash (4 patients) Pruritic rash (4 patients) Sources: https://pubmed.ncbi.nlm.nih.gov/6619026

AEs

AE	Significance	Dose	Population
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: https://pubmed.ncbi.nlm.nih.gov/6619026	unhealthy n = 21 Health Status: unhealthy Population Size: 21 Sources: https://pubmed.ncbi.nlm.nih.gov/6619026
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: https://pubmed.ncbi.nlm.nih.gov/6619026	unhealthy n = 21 Health Status: unhealthy Population Size: 21 Sources: https://pubmed.ncbi.nlm.nih.gov/6619026

Sourcing

Vendor/Aggregator	ID	URL
ChEBI	CHEBI:2956	https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:2956
ChemicalBook	CB6511850	https://www.chemicalbook.com/ChemicalProductProperty_EN_CB6511850
MolPort	MolPort-023-314-370	https://www.molport.com/shop/molecule-link/MolPort-023-314-370
ZINC	ZINC000003830261	http://zinc15.docking.org/substances/ZINC000003830261

PubMed

Title	Date	PubMed
Sensitization to aztreonam and cross-reactivity with other beta-lactam antibiotics in high-risk patients with cystic fibrosis.	1991 Jan	1991925
The penicillins.	1999 Mar	10090000
[Hoigne syndrome as an acute non-allergic reaction to different drugs: case reports].	2001 Jun	11503262
Natural antibiotic susceptibility of Ewingella americana strains.	2003 Oct	14598935
The Malaysian Orthopaedic Association humanitarian mission to Indonesia and Sri Lanka.	2005 Jul	16381273
Placental transfer of antibiotics administered to the mother: a review.	2006 Feb	16502764
Searching for new antimalarial therapeutics amongst known drugs.	2006 Jun	16882315
Effects of treatment with antimicrobial agents on the human colonic microflora.	2008 Dec	19337440
Dynamic root exudation of sorgoleone and its in planta mechanism of action.	2009	19357432
A critical role for CD8 T cells in a nonhuman primate model of tuberculosis.	2009 Apr	19381260
Clinical and ultrasonographic features of abdominal tuberculosis in HIV positive adults in Zambia.	2009 Apr 17	19374757
Detection of Extended Spectrum β-lactamase Production Among Uropathogens.	2009 Jan	21938241
Molecular taxonomy, phylogeny and evolution in the family Stichopodidae (Aspidochirotida: Holothuroidea) based on COI and 16S mitochondrial DNA.	2010 Sep	20399872

Patents

Sample Use Guides

In Vivo Use Guide

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

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

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

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