Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H32N6O4S |
| Molecular Weight | 488.603 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC1=NC(C)=C2N1NC(=NC2=O)C3=C(OCC)C=CC(=C3)S(=O)(=O)N4CCN(CC)CC4
InChI
InChIKey=SECKRCOLJRRGGV-UHFFFAOYSA-N
InChI=1S/C23H32N6O4S/c1-5-8-20-24-16(4)21-23(30)25-22(26-29(20)21)18-15-17(9-10-19(18)33-7-3)34(31,32)28-13-11-27(6-2)12-14-28/h9-10,15H,5-8,11-14H2,1-4H3,(H,25,26,30)
| Molecular Formula | C23H32N6O4S |
| Molecular Weight | 488.603 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://www.drugbank.ca/drugs/DB00862Curator's Comment: Description was created based on several sources, including
http://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021400s017lbl.pdf
Sources: http://www.drugbank.ca/drugs/DB00862
Curator's Comment: Description was created based on several sources, including
http://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021400s017lbl.pdf
Vardenafil (Levitra) is an oral therapy for the treatment of erectile dysfunction. It is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5). Penile erection is a hemodynamic process initiated by the relaxation of smooth muscle in the corpus cavernosum and its associated arterioles. During sexual stimulation, nitric oxide is released from nerve endings and endothelial cells in the corpus cavernosum. Nitric oxide activates the enzyme guanylate cyclase resulting in increased synthesis of cyclic guanosine monophosphate (cGMP) in the smooth muscle cells of the corpus cavernosum. The cGMP in turn triggers smooth muscle relaxation, allowing increased blood flow into the penis, resulting in erection. The tissue concentration of cGMP is regulated by both the rates of synthesis and degradation via phosphodiesterases (PDEs). The most abundant PDE in the human corpus cavernosum is the cGMPspecific phosphodiesterase type 5 (PDE5); therefore, the inhibition of PDE5 enhances erectile function by increasing the amount of cGMP.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22426465
Curator's Comment: Vardenafil crossed the BBB
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL1827 Sources: http://www.drugbank.ca/drugs/DB00862 |
1.0 nM [Ki] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Levitra Approved UseLEVITRA is a phosphodiesterase 5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction. Launch Date2003 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
30.1 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27318021 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
VARDENAFIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
22.83 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27318021 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
VARDENAFIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
2.21 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27318021 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
VARDENAFIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
Doses
| Dose | Population | Adverse events |
|---|---|---|
2.4 mg 12 times / day multiple, respiratory Highest studied dose Dose: 2.4 mg, 12 times / day Route: respiratory Route: multiple Dose: 2.4 mg, 12 times / day Sources: |
healthy, 27.5 years (range: 24-31 years) Health Status: healthy Age Group: 27.5 years (range: 24-31 years) Sex: M+F Sources: |
|
120 mg single, oral Highest studied dose Dose: 120 mg Route: oral Route: single Dose: 120 mg Sources: |
healthy, adult Health Status: healthy Age Group: adult Sex: M Sources: |
Other AEs: Back pain, Myalgia... Other AEs: Back pain Sources: Myalgia Abnormal vision |
2.4 mg single, respiratory Highest studied dose Dose: 2.4 mg Route: respiratory Route: single Dose: 2.4 mg Sources: |
healthy, adult |
|
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
Disc. AE: Headache, Flushing... AEs leading to discontinuation/dose reduction: Headache (19 patients) Sources: Flushing (10 patients) Rhinitis (5 patients) Tachycardia (4 patients) Nausea (5 patients) Liver function test abnormal (4 patients) Dizziness (3 patients) Hypesthesia (3 patients) Abdominal pain (3 patients) Palpitations (3 patients) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Abnormal vision | 120 mg single, oral Highest studied dose Dose: 120 mg Route: oral Route: single Dose: 120 mg Sources: |
healthy, adult Health Status: healthy Age Group: adult Sex: M Sources: |
|
| Back pain | 120 mg single, oral Highest studied dose Dose: 120 mg Route: oral Route: single Dose: 120 mg Sources: |
healthy, adult Health Status: healthy Age Group: adult Sex: M Sources: |
|
| Myalgia | 120 mg single, oral Highest studied dose Dose: 120 mg Route: oral Route: single Dose: 120 mg Sources: |
healthy, adult Health Status: healthy Age Group: adult Sex: M Sources: |
|
| Flushing | 10 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Headache | 19 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Abdominal pain | 3 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Dizziness | 3 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Hypesthesia | 3 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Palpitations | 3 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Liver function test abnormal | 4 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Tachycardia | 4 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Nausea | 5 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
| Rhinitis | 5 patients Disc. AE |
10 mg 1 times / day steady, oral Recommended Dose: 10 mg, 1 times / day Route: oral Route: steady Dose: 10 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/200179Orig1s000PharmR.pdf#page=19 Page: 19.0 |
major | yes (co-administration study) Comment: label: coadministration with ketoconazole (inhibitor) increased mean AUC and Cmax of vardenafil by 10-fold and 4-fold, respectively; coadministration with erythromycin (CYP3A4 substrate) increased mean AUC and Cmax of vardenafil, respectively; coadministration with indinavir (CYP3A4 inhibitor) increased mean AUC and Cmax of vardenafil by 16 fold and 7 fold, respectively; Ritonavir co-administered with vardenafil resulted in a 49-fold increase in vardenafil AUC and a 13 fold increase in vardenafil Cmax; Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/200179Orig1s000PharmR.pdf#page=19 Page: 19.0 |
||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/200179Orig1s000PharmR.pdf#page=19 Page: 19.0 |
minor | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/200179Orig1s000PharmR.pdf#page=19 Page: 19.0 |
minor | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/200179Orig1s000PharmR.pdf#page=19 Page: 19.0 |
minor | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/200179Orig1s000PharmR.pdf#page=19 Page: 19.0 |
minor | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/22775210/ Page: 7.0 |
yes | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/22775210/ Page: 7.0 |
yes | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/22775210/ Page: 7.0 |
yes |
Tox targets
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/200179Orig1s000PharmR.pdf#page=17 Page: 17.0 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Emerging oral drugs for erectile dysfunction. | 2004-05 |
|
| The efficacy and safety of flexible-dose vardenafil (levitra) in a broad population of European men. | 2004-05 |
|
| Erectile dysfunction: management update. | 2004-04-27 |
|
| [Comparison of efficacy and safety of phosphodiesterase type 5 inhibitors in the treatment of erectile dysfunction]. | 2004-04 |
|
| Tadalafil and vardenafil. | 2004-04 |
|
| Novel phosphodiesterase type 5 inhibitors: assessing hemodynamic effects and safety parameters. | 2004-04 |
|
| Phosphodiesterase type 5 inhibitor differentiation based on selectivity, pharmacokinetic, and efficacy profiles. | 2004-04 |
|
| Role of the cardiologist: clinical aspects of managing erectile dysfunction. | 2004-04 |
|
| Vardenafil: a novel type 5 phosphodiesterase inhibitor for the treatment of erectile dysfunction. | 2004-04 |
|
| Pills for erectile dysfunction: now there are three. | 2004-04 |
|
| Treatment of erectile dysfunction. | 2004-04 |
|
| Sustained efficacy and tolerability with vardenafil over 2 years of treatment in men with erectile dysfunction. | 2004-03 |
|
| Vardenafil--PDE5 inhibitor number 3. | 2004-03 |
|
| Pharmacokinetics, pharmacodynamics, and efficacy of phosphodiesterase type 5 inhibitors. | 2004-03 |
|
| Therapeutic options for patients returning to sexual activity. | 2004-03 |
|
| [Treatment of erectile dysfunction]. | 2004-02-29 |
|
| New tools 2003. | 2004-02-20 |
|
| Cialis is here. The soft sell. | 2004-02-02 |
|
| Tadalafil (Cialis) and vardenafil (Levitra) recently approved drugs for erectile dysfunction. | 2004-02 |
|
| [Erectile dysfunction. Epidemiology, physiology, etiology, diagnosis and therapy]. | 2004-02 |
|
| Drug approval highlights for 2003. | 2004-02 |
|
| Cardioprotection with phosphodiesterase-5 inhibition--a novel preconditioning strategy. | 2004-02 |
|
| Vardenafil treatment for erectile dysfunction. | 2004-01 |
|
| Are they better than Viagra? Two new drugs for erectile dysfunction work like Viagra and carry similar risks and benefits. Their subtle differences, however, may make a difference for some men. | 2004-01 |
|
| Spotlight on vardenafil in erectile dysfunction. | 2004 |
|
| FDA approves new drug for treatment of erectile dysfunction in men. | 2003-12-12 |
|
| Novel PDE5 inhibitors for the treatment of male erectile dysfunction. | 2003-12-06 |
|
| Oral drug treatment of erectile dysfunction. | 2003-12 |
|
| Pro-erectile effect of vardenafil: in vitro experiments in rabbits and in vivo comparison with sildenafil in rats. | 2003-12 |
|
| Vardenafil: a new approach to the treatment of erectile dysfunction. | 2003-12 |
|
| Molecular mechanisms and pharmacokinetics of phosphodiesterase-5 antagonists. | 2003-12 |
|
| Overview of phosphodiesterase 5 inhibition in erectile dysfunction. | 2003-11-06 |
|
| Switching patients with erectile dysfunction from sildenafil citrate to tadalafil: results of a European multicenter, open-label study of patient preference. | 2003-11 |
|
| New drugs and dosage forms. | 2003-10-01 |
|
| [Drug therapy of erectile dysfunction--the current status]. | 2003-10 |
|
| Phosphodiesterase type 5 inhibitors: a biochemical and clinical correlation survey. | 2003-10 |
|
| Safety and efficacy of vardenafil for the treatment of men with erectile dysfunction after radical retropubic prostatectomy. | 2003-10 |
|
| Vardenafil (levitra) for erectile dysfunction. | 2003-09-29 |
|
| Therapy of ED: PDE-5 Inhibitors. | 2003-09-15 |
|
| Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules. | 2003-09-04 |
|
| [Medication of the month. Vardenafil (Levitra)]. | 2003-09 |
|
| Efficacy and tolerability of vardenafil for treatment of erectile dysfunction in patient subgroups. | 2003-09 |
|
| Phosphodiesterase 5 inhibitors in male sexual dysfunction. | 2003-09 |
|
| US advertising campaign begins for alternative to sildenafil. | 2003-08-30 |
|
| Hypogonadism and erectile dysfunction: the role for testosterone therapy. | 2003-08 |
|
| Erectile dysfunction in the cardiac patient: how common and should we treat? | 2003-08 |
|
| [New PDE-5 inhibitor for treatment of impotence. 9 out of 10 have erections again]. | 2003-06-26 |
|
| [Conservative treatment of erectile dysfunction]. | 2003-06-01 |
|
| New phosphodiesterase type 5 inhibitors in the management of erectile dysfunction. | 2003-06 |
|
| Vardenafil: a review of its use in erectile dysfunction. | 2003 |
Sample Use Guides
For most patients, the starting dose is 10 mg, up to once daily. Increase to 20 mg or decrease to 5 mg based on efficacy/tolerability.
A starting dose of 5 mg LEVITRA should be considered in patients ≥ 65
years of age.
LEVITRA is taken orally, approximately 60 minutes before sexual
activity.
The maximum recommended dosing frequency is one tablet per day.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25736325
Treatment with vardenafil at concentrations of 50, 100, and 250 umol/L increased expression of PlGF in a dose-dependent manner in human umbilical vein endothelial cells.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:07:13 GMT 2025
by
admin
on
Mon Mar 31 18:07:13 GMT 2025
|
| Record UNII |
UCE6F4125H
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
EMA ASSESSMENT REPORTS |
LEVITRA (AUTHORIZED: ERECTILE DYSFUNCTIONS)
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
||
|
NDF-RT |
N0000020026
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
||
|
FDA ORPHAN DRUG |
679319
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
||
|
WHO-ATC |
G04BE09
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
||
|
WHO-VATC |
QG04BE09
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
||
|
LIVERTOX |
NBK548920
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
||
|
NCI_THESAURUS |
C2127
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
||
|
NDF-RT |
N0000175599
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
||
|
EMA ASSESSMENT REPORTS |
VIVANZA (AUTHORIZED: ERECTILE DYSFUNCTIONS)
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
UCE6F4125H
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
7950
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
C426063
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
NN-53
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
VARDENAFIL
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
100000089525
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
C66650
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
7304
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
7320
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
Vardenafil
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
306674
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | RxNorm | ||
|
135400189
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
DTXSID3048318
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
CHEMBL1520
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
224785-90-4
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
DB00862
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
UCE6F4125H
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
2809
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | |||
|
m11394
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY | Merck Index | ||
|
SUB20047
Created by
admin on Mon Mar 31 18:07:13 GMT 2025 , Edited by admin on Mon Mar 31 18:07:13 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
TRANSPORTER -> INHIBITOR | |||
|
METABOLIC ENZYME -> SUBSTRATE | |||
|
BINDER->LIGAND |
BINDING
|
||
|
|
SALT/SOLVATE -> PARENT | |||
|
|
SALT/SOLVATE -> PARENT | |||
|
METABOLIC ENZYME -> SUBSTRATE |
MAJOR
|
||
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
METABOLITE -> PARENT |
FECAL; PLASMA
|
||
|
METABOLITE -> PARENT |
CYP2C9 also contributes to the metabolism of vardenafil.
MINOR
FECAL; PLASMA; URINE
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| Tmax | PHARMACOKINETIC |
|
FASTED STATE |
|
||
| Volume of Distribution | PHARMACOKINETIC |
|
|
|||
| Biological Half-life | PHARMACOKINETIC |
|
|
|||