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
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
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.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2095219 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10858873 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Palliative | FLAVOXATE HYDROCHLORIDE Approved UseFlavoxate 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 Date2004 |
|||
Palliative | FLAVOXATE HYDROCHLORIDE Approved UseFlavoxate 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 Date2004 |
|||
Palliative | FLAVOXATE HYDROCHLORIDE Approved UseFlavoxate 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 Date2004 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
4.61 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/1026965 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/11232858/ |
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
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
4.02 mg × h/L/(mg dose/kg) EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/1026965 |
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) EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/1026965 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/11232858/ |
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
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
40.1 min EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/1026965 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/11232858/ |
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
Dose | Population | Adverse 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 Sources: Edema hands |
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
AE | Significance | Dose | Population |
---|---|---|---|
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: |
PubMed
Title | Date | PubMed |
---|---|---|
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 |
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4026456
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
Edited
Fri Dec 15 15:04:03 GMT 2023
by
admin
on
Fri Dec 15 15:04:03 GMT 2023
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Record UNII |
9C05J6089W
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29704
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114649
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SUB02201MIG
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C47533
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m5398
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100000091079
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PARENT -> SALT/SOLVATE | |||
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (TITRATION)
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