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Details

Stereochemistry RACEMIC
Molecular Formula C8H7O3.H4N
Molecular Weight 169.1778
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMMONIUM MANDELATE

SMILES

[NH4+].OC(C([O-])=O)C1=CC=CC=C1

InChI

InChIKey=BDEXTKUJIZCFST-UHFFFAOYSA-N
InChI=1S/C8H8O3.H3N/c9-7(8(10)11)6-4-2-1-3-5-6;/h1-5,7,9H,(H,10,11);1H3

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including, http://dermage.com.br/dermage/paginas/article.pdf

Mandelic acid is an aromatic alpha hydroxy acid that is used for the treatment of urinary tract infections. The drug is marketed in Canada under the name Mandelamine (as a complex with methenamine). Mandelic acid exerts its antibacterial effect mainly by increasing urine acidity. Moreover, mandelic acid is used as a serum for the treatment of wrinkles.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Mandelamine

Approved Use

For the suppression or elimination of bacteriuria associated with pyelonephritis, cystitis and other urinary tract infections.
Doses

Doses

DosePopulationAdverse events​
45 % 1 times / 2 weeks multiple, topical
Dose: 45 %, 1 times / 2 weeks
Route: topical
Route: multiple
Dose: 45 %, 1 times / 2 weeks
Sources:
unhealthy, 19.4
n = 25
Health Status: unhealthy
Condition: acne vulgaris
Age Group: 19.4
Sex: M+F
Population Size: 25
Sources:
Other AEs: Burning sensation, Erythema...
Other AEs:
Burning sensation (1 patient)
Erythema (2 patients)
Sources:
1 % 2 times / day multiple, topical
Dose: 1 %, 2 times / day
Route: topical
Route: multiple
Dose: 1 %, 2 times / day
Co-administed with::
benzoylperoxide(4%; 2/day)
lactobionic acid(1%; 2/day)
sulfate zinc(1%; 2/day)
Sources:
unhealthy
n = 20
Health Status: unhealthy
Condition: facial acne
Sex: M+F
Population Size: 20
Sources:
Other AEs: Skin erythema desquamative...
Other AEs:
Skin erythema desquamative (5%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Burning sensation 1 patient
45 % 1 times / 2 weeks multiple, topical
Dose: 45 %, 1 times / 2 weeks
Route: topical
Route: multiple
Dose: 45 %, 1 times / 2 weeks
Sources:
unhealthy, 19.4
n = 25
Health Status: unhealthy
Condition: acne vulgaris
Age Group: 19.4
Sex: M+F
Population Size: 25
Sources:
Erythema 2 patients
45 % 1 times / 2 weeks multiple, topical
Dose: 45 %, 1 times / 2 weeks
Route: topical
Route: multiple
Dose: 45 %, 1 times / 2 weeks
Sources:
unhealthy, 19.4
n = 25
Health Status: unhealthy
Condition: acne vulgaris
Age Group: 19.4
Sex: M+F
Population Size: 25
Sources:
Skin erythema desquamative 5%
1 % 2 times / day multiple, topical
Dose: 1 %, 2 times / day
Route: topical
Route: multiple
Dose: 1 %, 2 times / day
Co-administed with::
benzoylperoxide(4%; 2/day)
lactobionic acid(1%; 2/day)
sulfate zinc(1%; 2/day)
Sources:
unhealthy
n = 20
Health Status: unhealthy
Condition: facial acne
Sex: M+F
Population Size: 20
Sources:
PubMed

PubMed

TitleDatePubMed
[Efficacy of mandelic acid in treating acute toxoplasmosis in mice].
2001
Liquid chromatography/electrospray tandem mass spectrometry characterization of styrene metabolism in man and in rat.
2002
Relation between colour vision loss and occupational styrene exposure level.
2002 Dec
Interest of genotyping and phenotyping of drug-metabolizing enzymes for the interpretation of biological monitoring of exposure to styrene.
2002 Dec
High-throughput screening of enantioselective catalysts by immunoassay.
2002 Jan 4
Use of mandelic acid condensation polymer (SAMMA), a new antimicrobial contraceptive agent, for vaginal prophylaxis.
2002 Nov
Assessment of sperm DNA integrity in workers exposed to styrene.
2002 Nov
Fluorescent sensors for the enantioselective recognition of mandelic acid: signal amplification by dendritic branching.
2002 Nov 27
[A study on the adduct characteristics of styrene and DNA].
2002 Oct
The role of various biomarkers in the evaluation of styrene genotoxicity.
2003
Exposure assessment of monoterpenes and styrene: a comparison of air sampling and biomonitoring.
2003 Aug
Synthesis of optically active atropisomeric anilide derivatives through diastereoselective N-allylation with a chiral Pd-pi-allyl catalyst.
2003 Dec 12
Structural and kinetic analysis of catalysis by a thiamin diphosphate-dependent enzyme, benzoylformate decarboxylase.
2003 Feb 25
Chloride present in biological samples as a tool for enhancement of sensitivity in capillary zone electrophoretic analysis of anionic trace analytes.
2003 Jan
Nonlinear amplification of circular dichroism activity upon cyclodimerization of a chiral saddle-shaped porphyrin.
2003 Jan 7
The mandelamide keto-enol system in aqueous solution. Generation of the enol by hydration of phenylcarbamoylcarbene.
2003 Jan 8
Solvent ototoxicity in the rat and guinea pig.
2003 Jan-Feb
Comparison of isotopic fractionation in lactic acid and ethanol fermentations.
2003 Jun
Inhibition of mandelate racemase by alpha-fluorobenzylphosphonates.
2003 Jun 16
Sperm-FISH analysis and human monitoring: a study on workers occupationally exposed to styrene.
2003 Jun 6
A glycopeptide antibiotic chiral stationary phase for the enantiomer resolution of hydroxy acid derivatives by capillary electrochromatography.
2003 Mar
Use of short-end injection capillary packed with a glycopeptide antibiotic stationary phase in electrochromatography and capillary liquid chromatography for the enantiomeric separation of hydroxy acids.
2003 Mar 21
Use of ionic liquids in a lipase-facilitated supported liquid membrane.
2003 May
Effects of clay minerals on Cr(VI) reduction by organic compounds.
2003 May
Asymmetric environments in encapsulation complexes.
2003 May 21
A transient intermediate in the reaction catalyzed by (S)-mandelate dehydrogenase from Pseudomonas putida.
2003 Nov 11
A high-throughput amenable colorimetric assay for enantioselective screening of nitrilase-producing microorganisms using pH sensitive indicators.
2003 Oct
C4'-spiroalkylated nucleosides having sulfur incorporated at the apex position.
2003 Oct 31
[Experimental study on the in vitro resistance to Toxoplasma gondii by murine lymphocyte].
2003 Sep
Nitration of endogenous para-hydroxyphenylacetic acid and the metabolism of nitrotyrosine.
2003 Sep 1
Exceptional chiral recognition of racemic carboxylic acids by calix[4]arenes bearing optically pure alpha,beta-amino alcohol groups.
2004 Apr 15
Heptakis(6-amino-6-deoxy)-beta-cyclodextrin as a chiral selector for the separation of anionic analyte enantiomers by capillary electrophoresis.
2004 Aug
Influence of (hydroxy)alkylamino substituents on enantioseparation ability of single-isomer amino-beta-cyclodextrin derivatives in chiral capillary electrophoresis.
2004 Aug
Determination of urinary styrene metabolites in the general Italian population by liquid chromatography-tandem mass spectrometry.
2004 Aug
Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase activity.
2004 Aug 24
Quininium (R)-mandelate, a structure with large Z' described as an incommensurately modulated structure in (3+1)-dimensional superspace.
2004 Feb
Esters of mandelic acid as substrates for (S)-mandelate dehydrogenase from Pseudomonas putida: implications for the reaction mechanism.
2004 Feb 24
Synthesis and antibiotic activity of the tricyclic furo[3,2-c] isochromen-2-trione unit of the pyranonaphthoquinones.
2004 Feb 9
Construction of an electro-enzymatic bioreactor for the production of (R)-mandelate from benzoylformate.
2004 Jan
A rapid HPLC method for the determination of carboxylic acids in human urine using a monolithic column.
2004 Jan
High resolution structures of an oxidized and reduced flavoprotein. The water switch in a soluble form of (S)-mandelate dehydrogenase.
2004 Jan 30
Altered substrate specificity in flavocytochrome b2: structural insights into the mechanism of L-lactate dehydrogenation.
2004 Jul 27
Cytogenetic markers, DNA single-strand breaks, urinary metabolites, and DNA repair rates in styrene-exposed lamination workers.
2004 Jun
Mandelamide hydrolase from Pseudomonas putida: characterization of a new member of the amidase signature family.
2004 Jun 22
Evaluation of the efficiency of respiratory protective equipment based on the biological monitoring of styrene in fibreglass reinforced plastics industries.
2004 Mar
Chiral synthesis of (2S,3S)-2-(2-morpholin-2-yl-2-phenylmethoxy)phenol.
2004 Mar
Human urine certified reference material CZ 6009: creatinine, styrene metabolites (mandelic acid and phenylglyoxylic acid).
2004 Mar
Hydrophobic nature of the active site of mandelate racemase.
2004 Mar 9
Current trends in quantitative structure activity relationships on FXa inhibitors: evaluation and comparative analysis.
2004 Nov
Prevalence of varicose veins and venous anatomy in patients without truncal saphenous reflux.
2004 Oct
Patents

Sample Use Guides

500 mg - 2 tablets 4 times a day (in the form of (Methenamine Mandelate Tablets U.S.P.).
Route of Administration: Oral
In Vitro Use Guide
Antimicrobal activity of mandelic acid was determined by disc diffusion method. S. aureus type strains (ATCC 700698 and ATCC 25923) and 19 isolates were incubated with 10 ul of 160, 80, 40, 30, 20 and 10 mg/ml of the acid. Concentrations required to inhibit 50 and 90% of the clinical isolates (MIC50 and MIC90) were 20 and 40 (mg/ml) respectively and those required to kill 50 and 90% of the strains (MBC50 and MBC90) were 20 and 80 (mg/ml) respectively.
Name Type Language
AMMONIUM MANDELATE
MI  
Common Name English
MANDELIC ACID AMMONIUM SALT
Common Name English
AMMONIUM MANDELATE [MI]
Common Name English
.ALPHA.-HYDROXYBENZENEACETIC ACID AMMONIUM SALT (1:1)
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID30967475
Created by admin on Fri Dec 15 18:45:00 GMT 2023 , Edited by admin on Fri Dec 15 18:45:00 GMT 2023
PRIMARY
MERCK INDEX
m1799
Created by admin on Fri Dec 15 18:45:00 GMT 2023 , Edited by admin on Fri Dec 15 18:45:00 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
208-475-8
Created by admin on Fri Dec 15 18:45:00 GMT 2023 , Edited by admin on Fri Dec 15 18:45:00 GMT 2023
PRIMARY
CAS
530-31-4
Created by admin on Fri Dec 15 18:45:00 GMT 2023 , Edited by admin on Fri Dec 15 18:45:00 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105969
Created by admin on Fri Dec 15 18:45:00 GMT 2023 , Edited by admin on Fri Dec 15 18:45:00 GMT 2023
PRIMARY
FDA UNII
6PGE18556E
Created by admin on Fri Dec 15 18:45:00 GMT 2023 , Edited by admin on Fri Dec 15 18:45:00 GMT 2023
PRIMARY
PUBCHEM
10732
Created by admin on Fri Dec 15 18:45:00 GMT 2023 , Edited by admin on Fri Dec 15 18:45:00 GMT 2023
PRIMARY