Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H31N3O5.2H2O |
| Molecular Weight | 441.5185 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.NCCCC[C@H](N[C@@H](CCC1=CC=CC=C1)C(O)=O)C(=O)N2CCC[C@H]2C(O)=O
InChI
InChIKey=CZRQXSDBMCMPNJ-ZUIPZQNBSA-N
InChI=1S/C21H31N3O5.2H2O/c22-13-5-4-9-16(19(25)24-14-6-10-18(24)21(28)29)23-17(20(26)27)12-11-15-7-2-1-3-8-15;;/h1-3,7-8,16-18,23H,4-6,9-14,22H2,(H,26,27)(H,28,29);2*1H2/t16-,17-,18-;;/m0../s1
| Molecular Formula | H2O |
| Molecular Weight | 18.0153 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C21H31N3O5 |
| Molecular Weight | 405.4879 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Lisinopril is a potent, competitive inhibitor of angiotensin-converting enzyme (ACE). Lisinopril is marketed under the brand name ZESTRIL. ZESTRIL is indicated for the treatment of hypertension. It may be used alone as initial therapy
or concomitantly with other classes of antihypertensive agents. It is also indicated as adjunctive therapy in the management of heart failure in patients who
are not responding adequately to diuretics and digitalis. Lisinopril inhibits angiotensin-converting enzyme (ACE) in human subjects and animals. ACE
is a peptidyl dipeptidase that catalyzes the conversion of angiotensin I to the vasoconstrictor
substance, angiotensin II. Angiotensin II also stimulates aldosterone secretion by the adrenal
cortex. The beneficial effects of lisinopril in hypertension and heart failure appear to result
primarily from suppression of the renin-angiotensin-aldosterone system. Inhibition of ACE
results in decreased plasma angiotensin II which leads to decreased vasopressor activity and to
decreased aldosterone secretion. While the mechanism through which ZESTRIL lowers blood pressure is believed to be primarily
suppression of the renin-angiotensin-aldosterone system, ZESTRIL is antihypertensive even in
patients with low-renin hypertension.
CNS Activity
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL1808 |
0.36 nM [Ki] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | ZESTRIL Approved UseINDICATIONS & USAGE Hypertension Lisinopril tablets USP are indicated for the treatment of hypertension to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including lisinopril. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education ProgramJoint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC). Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. The largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly. Elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. Relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (for example, patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal. Some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in Black patients, and many antihypertensive drugs have additional approved indications and effects (e.g., on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy. Lisinopril tablets USP may be administered alone or with other antihypertensive agents. Heart Failure Lisinopril tablets USP are indicated as adjunctive therapy in the management of heart failure in patients who are not responding adequately to diuretics and digitalis. Acute Myocardial Infarction Lisinopril tablets USP are indicated for the treatment of hemodynamically stable patients within 24 hours of acute myocardial infarction, to improve survival. Patients should receive, as appropriate, the standard recommended treatments such as thrombolytics, aspirin and beta-blockers. In using lisinopril tablets USP, consideration should be given to the fact that another angiotensin-converting enzyme inhibitor, captopril, has caused agranulocytosis, particularly in patients with renal impairment or collagen vascular disease, and that available data are insufficient to show that lisinopril tablets USP do not have a similar risk (seeWARNINGS). In considering the use of lisinopril tablets USP, it should be noted that in controlled clinical trials, ACE inhibitors have an effect on blood pressure that is less in Black patients than in non-Blacks. In addition, ACE inhibitors have been associated with a higher rate of angioedema in Black than in non-Black patients (seeWARNINGS, Anaphylactoid and Possibly Related Reactions). Launch Date1987 |
|||
| Primary | ZESTRIL Approved UseHypertension
ZESTRIL is indicated for the treatment of hypertension. It may be used alone as initial therapy
or concomitantly with other classes of antihypertensive agents.
Heart Failure
ZESTRIL is indicated as adjunctive therapy in the management of heart failure in patients who
are not responding adequately to diuretics and digitalis.
Acute Myocardial Infarction
ZESTRIL is indicated for the treatment of hemodynamically stable patients within 24 hours of
acute myocardial infarction, to improve survival. Patients should receive, as appropriate, the
standard recommended treatments such as thrombolytics, aspirin and beta-blockers. Launch Date1987 |
|||
| Primary | ZESTRIL Approved UseHypertension
ZESTRIL is indicated for the treatment of hypertension. It may be used alone as initial therapy
or concomitantly with other classes of antihypertensive agents.
Heart Failure
ZESTRIL is indicated as adjunctive therapy in the management of heart failure in patients who
are not responding adequately to diuretics and digitalis.
Acute Myocardial Infarction
ZESTRIL is indicated for the treatment of hemodynamically stable patients within 24 hours of
acute myocardial infarction, to improve survival. Patients should receive, as appropriate, the
standard recommended treatments such as thrombolytics, aspirin and beta-blockers. Launch Date1987 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
95.62 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/14979604 |
20 mg single, oral dose: 20 mg route of administration: Oral experiment type: SINGLE co-administered: |
LISINOPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
61.11 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18368945 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
LISINOPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1264.94 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/14979604 |
20 mg single, oral dose: 20 mg route of administration: Oral experiment type: SINGLE co-administered: |
LISINOPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
906.97 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18368945 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
LISINOPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
6.554 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/14979604 |
20 mg single, oral dose: 20 mg route of administration: Oral experiment type: SINGLE co-administered: |
LISINOPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
10.03 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18368945 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
LISINOPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
100% |
LISINOPRIL serum | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Angiotensin-converting enzyme degrades Alzheimer amyloid beta-peptide (A beta ); retards A beta aggregation, deposition, fibril formation; and inhibits cytotoxicity. | 2001-12-21 |
|
| Pet ownership, but not ace inhibitor therapy, blunts home blood pressure responses to mental stress. | 2001-10 |
|
| Differential manipulation of the renin angiotensin system and epoietin requirements in maintenance haemodialysis patients. | 2001-09 |
|
| Angiotensin-converting enzyme inhibition induces apoptosis in erythroid precursors and affects insulin-like growth factor-1 in posttransplantation erythrocytosis. | 2001-09 |
|
| Norepinephrine induces alveolar epithelial apoptosis mediated by alpha-, beta-, and angiotensin receptor activation. | 2001-09 |
|
| Impact of postprandial hypertriglyceridemia on vascular responses in patients with coronary artery disease: effects of ACE inhibitors and fibrates. | 2001-09 |
|
| Cardiovascular critical event pathways for the progression of heart failure; a report from the ATLAS study. | 2001-09 |
|
| Prescribing patterns and cost of antihypertensive drugs in an internal medicine clinic. | 2001-08-23 |
|
| Renal tubular peptide catabolism in chronic vascular rejection. | 2001-08-14 |
|
| The effects of C-type natriuretic peptide on catecholamine release in the pacific spiny dogfish (Squalus acanthias). | 2001-08 |
|
| Lisinopril shows regression of myocardial fibrosis in patients with hypertensive heart disease. | 2001-07-28 |
|
| Simultaneous determination of hydrochlorothiazide and several inhibitors of angiotensin-converting enzyme by capillary electrophoresis. | 2001-07-27 |
|
| Reduction of left ventricular mass by lisinopril and nifedipine in hypertensive renal transplant recipients: a prospective randomized double-blind study. | 2001-07-15 |
|
| [Therapeutic perspectives: association of ACE inhibitors and angiotensin receptor blockers]. | 2001-07-10 |
|
| Fluorescence polarization studies of different forms of angiotensin-converting enzyme. | 2001-07 |
|
| The angiotensin II receptor antagonist candesartan cilexetil (TCV-116) ameliorates retinal disorders in rats. | 2001-07 |
|
| Does the antihypertensive response to angiotensin converting enzyme inhibition predict the antihypertensive response to angiotensin receptor antagonism? | 2001-07 |
|
| Better microvascular function on long-term treatment with lisinopril than with nifedipine in renal transplant recipients. | 2001-07 |
|
| Characterization of angiotensin-converting enzyme in canine testis. | 2001-07 |
|
| Sternal dehiscence after cardiac surgery and ACE inhibitors [correction of ACE type 1 inhibition]. | 2001-07 |
|
| Lisinopril improves endothelial function in chronic cigarette smokers. | 2001-07 |
|
| Multiple pathways of angiotensin I conversion and their functional role in the canine penile corpus cavernosum. | 2001-07 |
|
| Spectrophotometric and HPTLC-densitometric determination of lisinopril and hydrochlorothiazide in binary mixtures. | 2001-07 |
|
| Spectrophotometric, septrofluorimetric and LC determination of lisinopril. | 2001-07 |
|
| The quantitative determination of several inhibitors of the angiotensin-converting enzyme by CE. | 2001-07 |
|
| A prospective comparison of four antihypertensive agents in daily clinical practice. | 2001-06-30 |
|
| Possible roles of cardiac chymase after myocardial infarction in hamster hearts. | 2001-06 |
|
| ACE inhibition or angiotensin receptor blockade: impact on potassium in renal failure. | 2001-06 |
|
| A health perception score predicts cardiac events in patients with heart failure: results from the IMPRESS trial. | 2001-06 |
|
| Effects of various antihypertensive drugs on the function of osteoblast. | 2001-06 |
|
| Cardioprotective effect of propranolol from alcohol-induced heart muscle damage as assessed by plasma cardiac troponin-t. | 2001-06 |
|
| Possible interaction of clozapine and lisinopril. | 2001-06 |
|
| Pulse methylprednisolone, cyclosporine, and ace inhibitor therapy decreases proteinuria in two siblings with familial focal segmental glomerulosclerosis. | 2001-06 |
|
| Add-on angiotensin receptor blockade with maximized ACE inhibition. | 2001-06 |
|
| Effect of column temperature on the behaviour of some angiotensin converting enzyme inhibitors during high-performance liquid chromatographic analysis. | 2001-05-05 |
|
| Antihypertensive drug prescription trends at the primary health care centres in Bahrain. | 2001-05 |
|
| Update in pharmacologic treatment of hypertension. | 2001-05 |
|
| Trapped renal arteries: functional renal artery stenosis due to occlusion of the aorta in the arch and below the kidneys. | 2001-05 |
|
| Effect of antihypertensive therapy on renal artery structure in type 2 diabetic rats with hypertension. | 2001-05 |
|
| Lisinopril reduces albuminuria during exercise in low grade microalbuminuric type 1 diabetic patients: a double blind randomized study. | 2001-05 |
|
| Effect of angiotensin-converting enzyme inhibition on sympathetic tone in patients with mild to moderate heart failure. | 2001-05 |
|
| Reversal of pathophysiologic changes with long-term lisinopril treatment in isolated systolic hypertension. | 2001-05 |
|
| Effects of lisinopril on streptozotocin-induced diabetic neuropathy in rats. | 2001-04 |
|
| Circulating plasma vascular endothelial growth factor and microvascular complications of type 1 diabetes mellitus: the influence of ACE inhibition. | 2001-04 |
|
| The influence of dose of angiotensin I-converting enzyme inhibitor on systolic blood pressure variability in heart failure: a substudy of the Assessment of Treatment with Lisinopril and Survival in heart failure (ATLAS) trial. | 2001-04 |
|
| Characterization of bovine atrial angiotensin-converting enzyme. | 2001-04 |
|
| Early ACE-i intervention in microalbuminuric patients with type 1 diabetes: effects on albumin excretion, 24 h ambulatory blood pressure, and renal function. | 2001-04 |
|
| Ask the doctor. Recently, I read that the ACE inhibitor ramipril is very good at preventing heart problems, particularly in people with diabetes. I'm diabetic, and for years I have been on a different ACE inhibitor (lisinopril). Should I be taking ramipril instead? | 2001-04 |
|
| [Antihypertensive effect of enalapril and lisinopril administered in combination with nonsteroid anti-inflammatory agents]. | 2001 |
|
| Telmisartan: a review of its use in hypertension. | 2001 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/dosage/lisinopril.html
Usual Adult Dose for Hypertension
Initial dose: 10 mg orally once a day; 5 mg orally once a day
Maintenance dose: 20 to 40 mg orally once a day
Maximum dose: 80 mg orally once a day
Usual Adult Dose for Congestive Heart Failure
Initial dose: 2.5 to 5 mg orally once a day
Maintenance dose: Dosage should be increased as tolerated
Maximum dose: 40 mg orally once a day
Usual Adult Dose for Myocardial Infarction
Initial dose: 5 mg orally (within 24 hours of the onset of acute myocardial infarction)
Subsequent doses: 5 mg orally after 24 hours, then 10 mg orally after 48 hours.
Maintenance dose: 10 mg orally once a day. Dosing should continue for at least 6 weeks.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9594434
Lisinopril inhibited angiotensin converting enzyme from sheep serum with IC50 5.6 nM
| Substance Class |
Chemical
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| Record UNII |
E7199S1YWR
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Validated (UNII)
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| Classification Tree | Code System | Code | ||
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LIVERTOX |
NBK548860
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WHO-ATC |
C09BB03
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WHO-VATC |
QC09BA03
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FDA ORPHAN DRUG |
481915
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C09BA03
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C09AA03
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NCI_THESAURUS |
C247
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WHO-ATC |
C10BX07
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NDF-RT |
N0000175562
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QC09BB03
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FDA ORPHAN DRUG |
365512
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WHO-VATC |
QC09AA03
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SUB02939MIG
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100000091631
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758151
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83915-83-7
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Lisinopril
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C29159
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LISINOPRIL
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m6842
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (TITRATION)
EP
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PARENT -> SALT/SOLVATE |
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (HPLC)
USP
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ANHYDROUS->SOLVATE |
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TARGET -> INHIBITOR |
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| Related Record | Type | Details | ||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
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IMPURITY -> PARENT |
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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ACTIVE MOIETY |
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| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| ORAL BIOAVAILABILITY | PHARMACOKINETIC |
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| Tmax | PHARMACOKINETIC |
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| MAXIMUM TOLERATED DOSE | TOXICITY |
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ROUTE OF ADMINISTRATION |
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| MAXIMUM TOLERATED DOSE | TOXICITY |
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STAGE C REDUCED EJECTION FRACTION HEART FAILURE |
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| Biological Half-life | PHARMACOKINETIC |
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| Volume of Distribution | PHARMACOKINETIC |
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