Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C24H30O6 |
| Molecular Weight | 414.4914 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)[C@@H]1CC2=CC(=O)CC[C@]2(C)[C@@]34O[C@@H]3C[C@@]5(C)[C@@H](CC[C@@]56CCC(=O)O6)[C@H]14
InChI
InChIKey=JUKPWJGBANNWMW-VWBFHTRKSA-N
InChI=1S/C24H30O6/c1-21-7-4-14(25)10-13(21)11-15(20(27)28-3)19-16-5-8-23(9-6-18(26)30-23)22(16,2)12-17-24(19,21)29-17/h10,15-17,19H,4-9,11-12H2,1-3H3/t15-,16+,17-,19+,21+,22+,23-,24-/m1/s1
| Molecular Formula | C24H30O6 |
| Molecular Weight | 414.4914 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: http://www.drugbank.ca/drugs/DB00700Curator's Comment: Description was created based on several sources, including
https://www.drugs.com/cdi/eplerenone.html
Sources: http://www.drugbank.ca/drugs/DB00700
Curator's Comment: Description was created based on several sources, including
https://www.drugs.com/cdi/eplerenone.html
Eplerenone, an aldosterone receptor antagonist similar to spironolactone, has been shown to produce sustained increases in plasma renin and serum aldosterone, consistent with inhibition of the negative regulatory feedback of aldosterone on renin secretion. The resulting increased plasma renin activity and aldosterone circulating levels do not overcome the effects of eplerenone. Eplerenone selectively binds to recombinant human mineralocorticoid receptors relative to its binding to recombinant human glucocorticoid, progesterone and androgen receptors. Eplerenone binds to the mineralocorticoid receptor and thereby blocks the binding of aldosterone (component of the renin-angiotensin-aldosterone-system, or RAAS). Aldosterone synthesis, which occurs primarily in the adrenal gland, is modulated by multiple factors, including angiotensin II and non-RAAS mediators such as adrenocorticotropic hormone (ACTH) and potassium. Aldosterone binds to mineralocorticoid receptors in both epithelial (e.g., kidney) and nonepithelial (e.g., heart, blood vessels, and brain) tissues and increases blood pressure through induction of sodium reabsorption and possibly other mechanisms. Used for improvement of survival of stable patients with left ventricular systolic dysfunction (ejection fraction <40%) and clinical evidence of congestive heart failure after an acute myocardial infarction.
Originator
Sources: http://adisinsight.springer.com/drugs/800007155
Curator's Comment: # Novartis
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL1994 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20672820 |
122.0 nM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | INSPRA Approved UseINSPRA is an aldosterone antagonist indicated for:
Improving survival of stable patients with LV systolic dysfunction (LVEF ≤40%) and CHF after an acute myocardial infarction.
Hypertension, alone or combined with other agents. Launch Date2002 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
2.49 μg/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/14570778 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
1641 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26262771/ |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE blood | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
797 ng/mL |
50 mg single, oral dose: 50 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
18.4 μg × h/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/14570778 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
10893 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26262771/ |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE blood | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
4017 ng × h/mL |
50 mg single, oral dose: 50 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
3.01 h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/14570778 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
4.5 h |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE blood | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
|
3 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26262771/ |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE blood | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
2.9 h |
50 mg single, oral dose: 50 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
38.2% EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/14570778 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
50% |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
EPLERENONE blood | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
200 mg 2 times / day multiple, oral Highest studied dose Dose: 200 mg, 2 times / day Route: oral Route: multiple Dose: 200 mg, 2 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
Other AEs: Arthralgia, Dizziness... Other AEs: Arthralgia (6%) Sources: Dizziness (6%) Leg cramps (6%) Infection respiratory (13%) Sinusitis (2%) Nausea (4%) |
400 mg 1 times / day multiple, oral Highest studied dose Dose: 400 mg, 1 times / day Route: oral Route: multiple Dose: 400 mg, 1 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
Other AEs: Dizziness, Nausea... |
50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
Other AEs: Palpitations, Diarrhoea... Other AEs: Palpitations (below serious, 1 patient) Sources: Diarrhoea (below serious, 1 patient) Fatigue (below serious, 2 patients) Vessel puncture site reaction (below serious, 1 patient) Fungal skin infection (below serious, 1 patient) Nasopharyngitis (below serious, 3 patients) Dizziness (below serious, 2 patients) Headache (below serious, 5 patients) Pollakiuria (below serious, 1 patient) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Infection respiratory | 13% | 200 mg 2 times / day multiple, oral Highest studied dose Dose: 200 mg, 2 times / day Route: oral Route: multiple Dose: 200 mg, 2 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
| Sinusitis | 2% | 200 mg 2 times / day multiple, oral Highest studied dose Dose: 200 mg, 2 times / day Route: oral Route: multiple Dose: 200 mg, 2 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
| Nausea | 4% | 200 mg 2 times / day multiple, oral Highest studied dose Dose: 200 mg, 2 times / day Route: oral Route: multiple Dose: 200 mg, 2 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
| Arthralgia | 6% | 200 mg 2 times / day multiple, oral Highest studied dose Dose: 200 mg, 2 times / day Route: oral Route: multiple Dose: 200 mg, 2 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
| Dizziness | 6% | 200 mg 2 times / day multiple, oral Highest studied dose Dose: 200 mg, 2 times / day Route: oral Route: multiple Dose: 200 mg, 2 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
| Leg cramps | 6% | 200 mg 2 times / day multiple, oral Highest studied dose Dose: 200 mg, 2 times / day Route: oral Route: multiple Dose: 200 mg, 2 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
| Dizziness | 2% | 400 mg 1 times / day multiple, oral Highest studied dose Dose: 400 mg, 1 times / day Route: oral Route: multiple Dose: 400 mg, 1 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
| Nausea | 5% | 400 mg 1 times / day multiple, oral Highest studied dose Dose: 400 mg, 1 times / day Route: oral Route: multiple Dose: 400 mg, 1 times / day Sources: |
unhealthy, 21-80 years Health Status: unhealthy Age Group: 21-80 years Sex: M+F Sources: |
| Diarrhoea | below serious, 1 patient | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
| Fungal skin infection | below serious, 1 patient | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
| Palpitations | below serious, 1 patient | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
| Pollakiuria | below serious, 1 patient | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
| Vessel puncture site reaction | below serious, 1 patient | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
| Dizziness | below serious, 2 patients | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
| Fatigue | below serious, 2 patients | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
| Nasopharyngitis | below serious, 3 patients | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
| Headache | below serious, 5 patients | 50 mg 1 times / day multiple, oral Dose: 50 mg, 1 times / day Route: oral Route: multiple Dose: 50 mg, 1 times / day Sources: |
healthy |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Page: 18.0 |
no [IC50 >300 uM] | |||
Page: 18.0 |
no [IC50 >300 uM] | |||
Page: 18.0 |
no [IC50 >300 uM] | |||
Page: 18.0 |
no [IC50 >300 uM] | |||
Page: 45.0 |
no | |||
Page: 18.0 |
no | |||
Page: 18.0 |
no | |||
Page: 41.0 |
weak |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Page: 9, 10, 15 |
major | yes (co-administration study) Comment: coadministered with ketoconazole increased elperenone AUC by 5.5-fold and Cmax by 1.7-fold and with erythromycin increased AUC by 1.8-fold and Cmax 61% Page: 9, 10, 15 |
||
Page: 18, 34 |
no | |||
Page: 10.0 |
yes | yes (co-administration study) Comment: coadminstration with fluconazole increased eplerenone AUC by 2.2-fold and Cmax by 1.4-fold Page: 10.0 |
Tox targets
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://pubmed.ncbi.nlm.nih.gov/21764470/ |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Pharmacokinetics and metabolism of [14C]eplerenone after oral administration to humans. | 2003-11 |
|
| Can renin status predict the antihypertensive efficacy of eplerenone add-on therapy? | 2003-11 |
|
| Two better than one. | 2003-10-14 |
|
| Aldosterone blockade in patients with systolic left ventricular dysfunction. | 2003-10-14 |
|
| Effects of eplerenone, enalapril, and eplerenone/enalapril in patients with essential hypertension and left ventricular hypertrophy: the 4E-left ventricular hypertrophy study. | 2003-10-14 |
|
| Ask the doctor. I am a 50-year-old man with congestive heart failure. My doctor has me on all the usual drugs, and a couple of years ago added spironolactone. I did okay with it for a while, but then began to notice that my breasts were getting bigger and began to hurt. My doctor agreed that I should stop taking spironolactone, but I wonder if I am missing out on something. | 2003-10 |
|
| Aldosterone receptor blockade and the role of eplerenone: evolving perspectives. | 2003-10 |
|
| RAAS escape: a real clinical entity that may be important in the progression of cardiovascular and renal disease. | 2003-10 |
|
| Eplerenone: a selective aldosterone receptor antagonist for hypertension and heart failure. | 2003-09-25 |
|
| Adjunctive treatment with eplerenone reduced morbidity and mortality in acute myocardial infarction. | 2003-09-05 |
|
| Aldosterone blockade after myocardial infarction. | 2003-09-02 |
|
| New developments in the management of hypertension. | 2003-09-01 |
|
| Long-term safety and efficacy of the selective aldosterone blocker eplerenone in patients with essential hypertension. | 2003-09 |
|
| Gateways to clinical trials. | 2003-09 |
|
| Should the aldosterone-receptor antagonist - eplerenone - be used after acute myocardial infarction with left ventricular dysfunction? | 2003-09 |
|
| [Anti-angiogenic effects of aldosterone antagonists in the fibrin chamber in rats]. | 2003-08-30 |
|
| Hyperkalemia, congestive heart failure, and aldosterone receptor antagonism. | 2003-08-26 |
|
| Aldosterone blockade and vascular calcification in hemodialysis patients. | 2003-08-15 |
|
| Aldosterone receptor antagonists in the treatment of heart failure. | 2003-08 |
|
| Primary aldosteronism - treatment options. | 2003-08 |
|
| Selective aldosterone blockade with eplerenone in patients with congestive heart failure. | 2003-08 |
|
| Symptoms and the distress they cause: comparison of an aldosterone antagonist and a calcium channel blocking agent in patients with systolic hypertension. | 2003-07-14 |
|
| Transgenic model of aldosterone-driven cardiac hypertrophy and heart failure. | 2003-07-11 |
|
| Eplerenone in patients with left ventricular dysfunction. | 2003-07-03 |
|
| Eplerenone in patients with left ventricular dysfunction. | 2003-07-03 |
|
| Eplerenone in patients with left ventricular dysfunction. | 2003-07-03 |
|
| Assessment of the novel selective aldosterone blocker eplerenone using ambulatory and clinical blood pressure in patients with systemic hypertension. | 2003-07-01 |
|
| Addition of the selective aldosterone receptor antagonist eplerenone to ACE inhibition in heart failure: effect on endothelial dysfunction. | 2003-06-01 |
|
| Gateways to clinical trials. | 2003-06 |
|
| Late breaking heart failure trials from the 2003 ACC meeting: EPHESUS and COMPANION. | 2003-06 |
|
| Update of clinical trials from the American College of Cardiology 2003. EPHESUS, SPORTIF-III, ASCOT, COMPANION, UK-PACE and T-wave alternans. | 2003-06 |
|
| Aldosterone resurgens--letter from EPHESUS. | 2003-06 |
|
| Inhibition of platelet activation in congestive heart failure by aldosterone receptor antagonism and ACE inhibition. | 2003-06 |
|
| Effect of eplerenone, a selective aldosterone blocker, on blood pressure, serum and macrophage oxidative stress, and atherosclerosis in apolipoprotein E-deficient mice. | 2003-06 |
|
| Aldosterone blockade in patients with acute myocardial infarction. | 2003-05-27 |
|
| Eplerenone: cardiovascular protection. | 2003-05-20 |
|
| Eplerenone (Inspra). | 2003-05-12 |
|
| Aldosterone antagonism and hypertension. | 2003-05 |
|
| More hope for heart failure. Findings suggest expanded use of aldosterone-blockers. | 2003-05 |
|
| New developments in the pharmacological treatment of chronic heart failure. | 2003-05 |
|
| Effects of the selective aldosterone blocker eplerenone versus the calcium antagonist amlodipine in systolic hypertension. | 2003-05 |
|
| Aldosterone and aldosterone antagonism in cardiovascular disease: focus on eplerenone (Inspra). | 2003-04-26 |
|
| Aldosterone receptor blockade: a therapy resurrected. | 2003-04-26 |
|
| Hypertension, angiotensin II, aldosterone, and race. | 2003-04-02 |
|
| Aldosterone antagonism in addition to angiotensin-converting enzyme inhibitors in heart failure. | 2003-04 |
|
| Eplerenone. Pharmacia. | 2003-03 |
|
| Aldosterone as a target in congestive heart failure. | 2003-03 |
|
| [Efficacy of an aldosterone receptor blocker eplerenone in high risk survivors of acute myocardial infarction with signs of heart failure: results of EPHESUS]. | 2003 |
|
| Aldosterone receptor antagonists for hypertension: what do they offer? | 2003 |
|
| Eplerenone: a selective aldosterone blocker. | 2003 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/cdi/eplerenone.html
Congestive heart failure post-myocardial infarction:
Initial dosage: 25 mg orally once daily. Dosage should titrated to the target dose of 50 mg once daily preferably within 4 weeks.
Usual Adult Dose for Hypertension
50 mg orally once daily. Patients with an inadequate blood pressure response should be increased to 50 mg twice a day.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27153999
Eplerenone (10uM) significantly decreased corticosterone- (0.81 fold compared to treatment with corticosterone alone) and 11-DHC-driven (0.64 fold compared to treatment with 11-DHC alone) mouse VSMC calcification
| Substance Class |
Chemical
Created
by
admin
on
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| Record UNII |
6995V82D0B
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Validated (UNII)
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QC03DA04
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NBK547930
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C270
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C03DA04
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C843
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| Related Record | Type | Details | ||
|---|---|---|---|---|
|
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TARGET -> INHIBITOR |
|
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EXCRETED UNCHANGED |
FECAL; URINE
|
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BINDER->LIGAND |
BINDING
|
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METABOLIC ENZYME -> SUBSTRATE |
MAJOR
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
METABOLITE -> PARENT |
MINOR
FECAL; URINE
|
||
|
|
METABOLITE -> PARENT |
MINOR
PLASMA
|
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|
METABOLITE -> PARENT |
MINOR
FECAL
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METABOLITE -> PARENT |
Primarily mediated via CYP3A4. No active metabolites of eplerenone have been identified in human plasma
MINOR
FECAL; PLASMA; URINE
|
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METABOLITE -> PARENT |
Primarily mediated via CYP3A4. No active metabolites of eplerenone have been identified in human plasma
MAJOR
PLASMA; URINE
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METABOLITE -> PARENT |
MINOR
FECAL
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||
|
METABOLITE -> PARENT |
Primarily mediated via CYP3A4. No active metabolites of eplerenone have been identified in human plasma
MINOR
FECAL; URINE
|
||
|
METABOLITE -> PARENT |
Major in fecal and urine; Primarily mediated via CYP3A4. No active metabolites of eplerenone have been identified in human plasma
MAJOR
FECAL; PLASMA; URINE
|
||
|
METABOLITE -> PARENT |
Primarily mediated via CYP3A4. No active metabolites of eplerenone have been identified in human plasma
MINOR
FECAL
|
||
|
METABOLITE -> PARENT |
Primarily mediated via CYP3A4. No active metabolites of eplerenone have been identified in human plasma
MINOR
FECAL; PLASMA; URINE
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|
| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| Tmax | PHARMACOKINETIC |
|
ORAL ADMINISTRATION |
|
||
| Volume of Distribution | PHARMACOKINETIC |
|
AT STEADY-STATE |
|
||
| Biological Half-life | PHARMACOKINETIC |
|
|
|||