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

Details

Stereochemistry ACHIRAL
Molecular Formula C24H25NO4.ClH
Molecular Weight 427.921
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLAVOXATE HYDROCHLORIDE

SMILES

Cl.CC1=C(OC2=C(C=CC=C2C(=O)OCCN3CCCCC3)C1=O)C4=CC=CC=C4

InChI

InChIKey=XOEVKNFZUQEERE-UHFFFAOYSA-N
InChI=1S/C24H25NO4.ClH/c1-17-21(26)19-11-8-12-20(23(19)29-22(17)18-9-4-2-5-10-18)24(27)28-16-15-25-13-6-3-7-14-25;/h2,4-5,8-12H,3,6-7,13-16H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C24H25NO4
Molecular Weight 391.4596
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Flavoxate is a drug, indicated for symptomatic relief of dysuria, urgency, nocturia, suprapubic pain, frequency and incontinence as may occur in cystitis, prostatitis, urethritis, urethrocystitis/urethrotrigonitis. Flavoxate is not indicated for definitive treatment, but is compatible with drugs used for the treatment of urinary tract infections. It was approved for use in the United States in 1970 and continues to be used. Drug acts as a direct antagonist at muscarinic acetylcholine receptors in cholinergically innervated organs. Its anticholinergic-parasympatholytic action reduces the tonus of smooth muscle in the bladder, effectively reducing the number of required voids, facilitating increased volume per void. Common side effects are those of parasympathetic stimulation and include dryness of the mouth and eyes, decreased sweating, headache, visual blurring, constipation, urinary retention, impotence, tachycardia and palpitations, anxiety, restlessness and in some instances agitation and delusions.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
FLAVOXATE HYDROCHLORIDE

Approved Use

Flavoxate HCl tablets are indicated for symptomatic relief of dysuria, urgency, nocturia, suprapubic pain, frequency and incontinence as may occur in cystitis, prostatitis, urethritis, urethrocystitis/urethrotrigonitis. Flavoxate HCl tablets are not indicated for definitive treatment, but are compatible with drugs used for the treatment of urinary tract infections.

Launch Date

2004
Palliative
FLAVOXATE HYDROCHLORIDE

Approved Use

Flavoxate HCl tablets are indicated for symptomatic relief of dysuria, urgency, nocturia, suprapubic pain, frequency and incontinence as may occur in cystitis, prostatitis, urethritis, urethrocystitis/urethrotrigonitis. Flavoxate HCl tablets are not indicated for definitive treatment, but are compatible with drugs used for the treatment of urinary tract infections.

Launch Date

2004
Palliative
FLAVOXATE HYDROCHLORIDE

Approved Use

Flavoxate HCl tablets are indicated for symptomatic relief of dysuria, urgency, nocturia, suprapubic pain, frequency and incontinence as may occur in cystitis, prostatitis, urethritis, urethrocystitis/urethrotrigonitis. Flavoxate HCl tablets are not indicated for definitive treatment, but are compatible with drugs used for the treatment of urinary tract infections.

Launch Date

2004
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
4.61 mg/L
1.18 mg/kg single, intravenous
dose: 1.18 mg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
3-METHYLFLAVONE-8-CARBOXYLIC ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
14.4 μg/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
3-METHYLFLAVONE-8-CARBOXYLIC ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
4.02 mg × h/L/(mg dose/kg)
2.55 mg/kg single, oral
dose: 2.55 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
3-METHYLFLAVONE-8-CARBOXYLIC ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
4.49 mg × h/L/(mg dose/kg)
1.18 mg/kg single, intravenous
dose: 1.18 mg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
3-METHYLFLAVONE-8-CARBOXYLIC ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
27.85 μg × h/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
3-METHYLFLAVONE-8-CARBOXYLIC ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
40.1 min
1.18 mg/kg single, intravenous
dose: 1.18 mg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
3-METHYLFLAVONE-8-CARBOXYLIC ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
4.06 h
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
3-METHYLFLAVONE-8-CARBOXYLIC ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
200 mg 3 times / day multiple, oral
Dose: 200 mg, 3 times / day
Route: oral
Route: multiple
Dose: 200 mg, 3 times / day
Sources:
unhealthy, 26 years
n = 1
Health Status: unhealthy
Condition: urinary infection
Age Group: 26 years
Sex: F
Population Size: 1
Sources:
Disc. AE: Erythema, Edema hands...
AEs leading to
discontinuation/dose reduction:
Erythema
Edema hands
Sources:
1200 mg 1 times / day multiple, oral
Dose: 1200 mg, 1 times / day
Route: oral
Route: multiple
Dose: 1200 mg, 1 times / day
Sources:
unhealthy, 49.8 ± 9.7 years
Health Status: unhealthy
Condition: unstable bladder
Age Group: 49.8 ± 9.7 years
Sex: F
Sources:
AEs

AEs

AESignificanceDosePopulation
Edema hands Disc. AE
200 mg 3 times / day multiple, oral
Dose: 200 mg, 3 times / day
Route: oral
Route: multiple
Dose: 200 mg, 3 times / day
Sources:
unhealthy, 26 years
n = 1
Health Status: unhealthy
Condition: urinary infection
Age Group: 26 years
Sex: F
Population Size: 1
Sources:
Erythema Disc. AE
200 mg 3 times / day multiple, oral
Dose: 200 mg, 3 times / day
Route: oral
Route: multiple
Dose: 200 mg, 3 times / day
Sources:
unhealthy, 26 years
n = 1
Health Status: unhealthy
Condition: urinary infection
Age Group: 26 years
Sex: F
Population Size: 1
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer




Drug as perpetrator​Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
no
PubMed

PubMed

TitleDatePubMed
Development of a high-performance liquid chromatographic method for bioequivalence study of flavoxate tablets.
2001 Feb 10
Drug therapy of urinary urge incontinence: a systematic review.
2002 Nov
Clinical pharmacokinetics of drugs used to treat urge incontinence.
2003
[The medical treatment of overactive bladder].
2003 May
Bladder training for urinary incontinence in adults.
2004
[Alpha-blockers and bioflavonoids in men with chronic nonbacterial prostatitis (NIH-IIIa): a prospective, placebo-controlled trial].
2004 Feb
The handling of urinary incontinence in Danish general practices after distribution of guidelines and voiding diary reimbursement: an observational study.
2004 Jun 29
Persistence and adherence of medications for chronic overactive bladder/urinary incontinence in the california medicaid program.
2005 Jul-Aug
Trospium chloride: an update on a quaternary anticholinergic for treatment of urge urinary incontinence.
2005 Jun
Activation of the rostral pontine reticular formation increases the spinal glycine level and inhibits bladder contraction in rats.
2005 May
The effects of flavoxate hydrochloride on voltage-dependent L-type Ca2+ currents in human urinary bladder.
2005 Sep
Canadian Urological Association guidelines on urinary incontinence.
2006 Jun
Conformational evaluation and detailed 1H and 13C NMR assignments of flavoxate, a urinary tract antispasmodic agent.
2006 May 3
Agents for treatment of overactive bladder: a therapeutic class review.
2007 Jul
Drug-induced acute cholestatic liver damage in a patient with mutation of UGT1A1.
2007 Jul
Anticholinergic drugs versus other medications for overactive bladder syndrome in adults.
2007 Jul 18
Effects of flavoxate hydrochloride on voltage-dependent Ba2+ currents in human detrusor myocytes at different experimental temperatures.
2007 Nov
Anticholinergic drugs versus other medications for overactive bladder syndrome in adults.
2007 Oct 17
Persistence, adherence, and switch rates among extended-release and immediate-release overactive bladder medications in a regional managed care plan.
2008 Apr
3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic acid.
2008 Apr 16
[Clinical evaluation of supplemental administration of flavoxate hydrochloride in benign prostatic hyperplasia patients with nocturia resistant to an alpha1-adrenoceptor blocker].
2008 Mar
[Summary of the practice guideline 'Urinary incontinence' (first revision) from the Dutch College of General Practitioners].
2008 Nov 22
Liquid chromatographic fingerprint of 3-methylflavone-8-carboxylic acid established for its synthesis control analysis.
2009 Mar 15
Acute myocardial infarction and Kounis syndrome.
2009 May 15
Oxybutynin extended release for the management of overactive bladder: a clinical review.
2009 Sep 21
Inappropriate prescribing in the hospitalized elderly patient: defining the problem, evaluation tools, and possible solutions.
2010 Apr 7
Liquid Chromatographic Determination of Flavoxate HCl in Pharmaceutical Formulation.
2010 Jul
Lipophilic cationic drugs increase the permeability of lysosomal membranes in a cell culture system.
2010 Jul
[Urinary incontinence and puppy coat due to spaying in the bitch. An overview of pathophysiology, diagnosis and therapy].
2010 Jun 8
New insights into molecular targets for urinary incontinence.
2010 Oct
Patents

Sample Use Guides

Adults and children over 12 years of age: one or two 100 mg tablets 3 or 4 times a day. With improvement of symptoms, the dose may be reduced. This drug cannot be recommended for infants and children under 12 years of age because safety and efficacy have not been demonstrated in this age group.
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: The antispasmodic effects of the flavone compounds flavoxate hydrochloride on the human detrusor, prostatic adenoma, prostatic capsule, and bladder neck, were studied by the in vitro isometric method. Flavoxate showed a slightly greater activity than the other compounds in the prostatic and bladder neck tissues. The relaxant effect on the prostatic tissues suggests a potential use for these compounds in benign prostatic obstruction.
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:04:03 GMT 2023
Edited
by admin
on Fri Dec 15 15:04:03 GMT 2023
Record UNII
9C05J6089W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLAVOXATE HYDROCHLORIDE
EP   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN  
Official Name English
FLAVOXATE HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
4H-1-BENZOPYRAN-8-CARBOXYLIC ACID, 3-METHYL-4-OXO-2-PHENYL-, 2-(1-PIPERIDINYL)ETHYL ESTER, HYDROCHLORIDE
Common Name English
FLAVOXATE HYDROCHLORIDE [USAN]
Common Name English
FLAVOXATE HYDROCHLORIDE [MART.]
Common Name English
FLAVOXATE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
DW-61
Code English
FLAVOXATE HYDROCHLORIDE [EP IMPURITY]
Common Name English
2-Piperidinoethyl 3-methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-carboxylate hydrochloride
Systematic Name English
FLAVOXATE HCL
Common Name English
Flavoxate hydrochloride [WHO-DD]
Common Name English
FLAVOXATE HYDROCHLORIDE [JAN]
Common Name English
FLAVOXATE HYDROCHLORIDE [MI]
Common Name English
FLAVOXATE HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
FLAVOXATE HYDROCHLORIDE [USP-RS]
Common Name English
NSC-114649
Code English
URISPAS
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C29704
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
Code System Code Type Description
NSC
114649
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
EVMPD
SUB02201MIG
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
NCI_THESAURUS
C47533
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
DRUG BANK
DBSALT000407
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
ECHA (EC/EINECS)
223-066-4
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
CHEBI
5089
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
FDA UNII
9C05J6089W
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
ChEMBL
CHEMBL1493
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
RS_ITEM_NUM
1270708
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
RXCUI
142437
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY RxNorm
CAS
3717-88-2
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
EPA CompTox
DTXSID1047784
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
DAILYMED
9C05J6089W
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
PUBCHEM
441345
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
MERCK INDEX
m5398
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY Merck Index
SMS_ID
100000091079
Created by admin on Fri Dec 15 15:04:03 GMT 2023 , Edited by admin on Fri Dec 15 15:04:03 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
EP
Related Record Type Details
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY