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Details

Stereochemistry ACHIRAL
Molecular Formula C6H12N4.2H3O4P
Molecular Weight 336.1766
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHENAMINE DIPHOSPHATE

SMILES

OP(O)(O)=O.OP(O)(O)=O.C1N2CN3CN1CN(C2)C3

InChI

InChIKey=BGAZSPYPJDSHIT-UHFFFAOYSA-N
InChI=1S/C6H12N4.2H3O4P/c1-7-2-9-4-8(1)5-10(3-7)6-9;2*1-5(2,3)4/h1-6H2;2*(H3,1,2,3,4)

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including, http://www.accessdata.fda.gov/drugsatfda_docs/label/2008/016151s025lbl.pdf

Methenamine is an antibacterial agent for preventing recurrent urinary tract infection. It can be used as methenamine hippurate or methenamine mandelate preparations and is United States Food and Drug Administration-approved. Methenamine exerts its activity because it is hydrolyzed to formaldehyde in acid urine.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
UREX

Approved Use

FOR URAMIT MB™: URAMIT MB™ is indicated for the treatment of symptoms of irritative voiding. Indicated for the relief of local symptoms, such as inflammation, hypermotility, and pain, which accompany lower urinary tract infections. Indicated for the relief of urinary tract symptoms caused by diagnostic procedures.

Launch Date

1967
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
34 μg/mL
1 g 2 times / day multiple, oral
dose: 1 g
route of administration: Oral
experiment type: MULTIPLE
co-administered:
METHENAMINE serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
177 μg × h/mL
1 g 2 times / day multiple, oral
dose: 1 g
route of administration: Oral
experiment type: MULTIPLE
co-administered:
METHENAMINE serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
4.8 h
1 g 2 times / day multiple, oral
dose: 1 g
route of administration: Oral
experiment type: MULTIPLE
co-administered:
METHENAMINE serum
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
1 g 2 times / day multiple, oral
Recommended
Dose: 1 g, 2 times / day
Route: oral
Route: multiple
Dose: 1 g, 2 times / day
Sources:
healthy, 24-65
n = 10
Health Status: healthy
Age Group: 24-65
Sex: M+F
Population Size: 10
Sources:
1 g single, oral
Recommended
Dose: 1 g
Route: oral
Route: single
Dose: 1 g
Sources:
healthy, 24-65
n = 10
Health Status: healthy
Age Group: 24-65
Sex: M+F
Population Size: 10
Sources:
8 g 1 times / day multiple, oral
Overdose
Dose: 8 g, 1 times / day
Route: oral
Route: multiple
Dose: 8 g, 1 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Urinary tract infections
Sources:
Other AEs: Bladder irritation, Micturition painful...
Other AEs:
Bladder irritation
Micturition painful
Micturition frequency
Albuminuria
Hematuria
Sources:
AEs

AEs

AESignificanceDosePopulation
Albuminuria
8 g 1 times / day multiple, oral
Overdose
Dose: 8 g, 1 times / day
Route: oral
Route: multiple
Dose: 8 g, 1 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Urinary tract infections
Sources:
Bladder irritation
8 g 1 times / day multiple, oral
Overdose
Dose: 8 g, 1 times / day
Route: oral
Route: multiple
Dose: 8 g, 1 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Urinary tract infections
Sources:
Hematuria
8 g 1 times / day multiple, oral
Overdose
Dose: 8 g, 1 times / day
Route: oral
Route: multiple
Dose: 8 g, 1 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Urinary tract infections
Sources:
Micturition frequency
8 g 1 times / day multiple, oral
Overdose
Dose: 8 g, 1 times / day
Route: oral
Route: multiple
Dose: 8 g, 1 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Urinary tract infections
Sources:
Micturition painful
8 g 1 times / day multiple, oral
Overdose
Dose: 8 g, 1 times / day
Route: oral
Route: multiple
Dose: 8 g, 1 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Urinary tract infections
Sources:
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
High-throughput reverse genetics: RNAi screens in Caenorhabditis elegans.
2001
The unpredictability of seal after post space preparation: a fluid transport study.
2001 Apr
Disseminated histoplasmosis presenting as pyoderma gangrenosum-like lesions in a patient with acquired immunodeficiency syndrome.
2001 Aug
Developmental changes in the fine structure and histochemical properties of mucous cells in the parotid gland of the infant Japanese macaque.
2001 Dec
Wnt/Frizzled activation of Rho regulates vertebrate gastrulation and requires a novel Formin homology protein Daam1.
2001 Dec 28
Localization of a mammalian homolog of diaphanous, mDia1, to the mitotic spindle in HeLa cells.
2001 Feb
Effect of ultrasonic vibration and various sealer and cement combinations on titanium post removal.
2001 Jan
Toward designed assembly of microporous coordination networks constructed from silver(I)-hexamethylenetetramine layers.
2001 Jul 2
A distinctive pediatric renal neoplasm characterized by epithelioid morphology, basement membrane production, focal HMB45 immunoreactivity, and t(6;11)(p21.1;q12) chromosome translocation.
2001 Jun
Formin-2, polyploidy, hypofertility and positioning of the meiotic spindle in mouse oocytes.
2002 Dec
A Formin Homology protein and a profilin are required for cytokinesis and Arp2/3-independent assembly of cortical microfilaments in C. elegans.
2002 Dec 23
Dramatic rate acceleration of the Baylis-Hillman reaction in homogeneous medium in the presence of water.
2002 Dec 26
Formin' actin filament bundles.
2002 Feb
Delphilin: a novel PDZ and formin homology domain-containing protein that synaptically colocalizes and interacts with glutamate receptor delta 2 subunit.
2002 Feb 1
Evaluation of lectin staining in the diagnosis of fungal keratitis in an experimental rabbit model.
2002 Jan 25
Primary evaluation of methenamine as a NPN compound with probable effects on increasing ruminal escaped protein.
2002 Jun
Formins direct Arp2/3-independent actin filament assembly to polarize cell growth in yeast.
2002 Mar
Dimethylsilane polyamines: cytostatic compounds with potentials as anticancer drugs. II. Uptake and potential cytotoxic mechanisms.
2002 Nov-Dec
Degeneration of Pick bodies visualized by methenamine-silver staining and immunohistochemistry.
2002 Sep
Activation of adriamycin by the pH-dependent formaldehyde-releasing prodrug hexamethylenetetramine.
2003 Feb
ForC, a novel type of formin family protein lacking an FH1 domain, is involved in multicellular development in Dictyostelium discoideum.
2003 Feb 15
Crystallographic analysis of the thermal motion of the inclusion complex of cyclomaltoheptaose (beta-cyclodextrin) with hexamethylenetetramine.
2003 Feb 7
Adducts of hexamethylenetetramine with ferrocenecarboxylic acid and ferrocene-1,1'-dicarboxylic acid: multiple disorder in space groups Fmm2 and Cmcm.
2003 Jul
Gremlin is the BMP antagonist required for maintenance of Shh and Fgf signals during limb patterning.
2003 Jul
Formins: signaling effectors for assembly and polarization of actin filaments.
2003 Jul 1
Immunofluorescence of the epizootic ulcerative syndrome pathogen, Aphanomyces invadans, using a monoclonal antibody.
2003 Jun 20
Glomerular lesions in dogs infected with Leishmania organisms.
2003 May
Measuring gluconeogenesis using a low dose of 2H2O: advantage of isotope fractionation during gas chromatography.
2003 May
Activation of the Rac-binding partner FHOD1 induces actin stress fibers via a ROCK-dependent mechanism.
2003 Oct 3
Patents

Sample Use Guides

One tablet (1 g) twice daily for adults and children over 12 years of age. One-half tablet or one tablet (0.5 or 1 g) twice daily for children 6 to 12 years of age.
Route of Administration: Oral
In Vitro Use Guide
The antibacterial activity of methenamine and two of its organic acid salts was compared by continuous turbidimetric monitoring of static cultures exposed to the drugs and in an in vitro model of the treatment of bacterial cystitis. At pH 5.5, concentrations of 32 to 125 mg methenamine per 1 caused some inhibition of bacterial growth (Klebsiella aerogenes), but 250 to 500 mg/l were needed to suppress growth overnight. Methenamine hippurate was found to be less active than methenamine itself, whereas methenamine mandelate was as active as the parent compound.
Name Type Language
METHENAMINE DIPHOSPHATE
Common Name English
1,3,5,7-TETRAAZATRICYCLO(3.3.1.13,7)DECANE, PHOSPHATE (1:2)
Systematic Name English
HEXAMETHYLENETETRAMINE DIPHOSPHORIC ACID
Common Name English
DI(HEXAMETHYLENETETRAMINE) TRIPHOSPHORIC ACID
Common Name English
Code System Code Type Description
PUBCHEM
92135816
Created by admin on Sat Dec 16 10:11:37 GMT 2023 , Edited by admin on Sat Dec 16 10:11:37 GMT 2023
PRIMARY
CAS
72962-49-3
Created by admin on Sat Dec 16 10:11:37 GMT 2023 , Edited by admin on Sat Dec 16 10:11:37 GMT 2023
PRIMARY
FDA UNII
IZP83XSR30
Created by admin on Sat Dec 16 10:11:37 GMT 2023 , Edited by admin on Sat Dec 16 10:11:37 GMT 2023
PRIMARY
CAS
13325-31-0
Created by admin on Sat Dec 16 10:11:37 GMT 2023 , Edited by admin on Sat Dec 16 10:11:37 GMT 2023
NON-SPECIFIC STOICHIOMETRY
DRUG BANK
DBSALT002249
Created by admin on Sat Dec 16 10:11:37 GMT 2023 , Edited by admin on Sat Dec 16 10:11:37 GMT 2023
PRIMARY