Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H31N3O5 |
Molecular Weight | 405.4879 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NCCCC[C@H](N[C@@H](CCC1=CC=CC=C1)C(O)=O)C(=O)N2CCC[C@H]2C(O)=O
InChI
InChIKey=RLAWWYSOJDYHDC-BZSNNMDCSA-N
InChI=1S/C21H31N3O5/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)/t16-,17-,18-/m0/s1
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 |
PubMed
Title | Date | PubMed |
---|---|---|
[Impossibility of intubation due to angioedema secondary to an angiotensin-converting enzyme inhibitor]. | 1999 Feb |
|
Reduced bcl-2 concentrations in hypertensive patients after lisinopril or nifedipine administration. | 1999 Jan |
|
[Antihypertensive effect of enalapril and lisinopril administered in combination with nonsteroid anti-inflammatory agents]. | 2001 |
|
Early ACE-i intervention in microalbuminuric patients with type 1 diabetes: effects on albumin excretion, 24 h ambulatory blood pressure, and renal function. | 2001 Apr |
|
Are angiotensin-converting enzyme (ACE) inhibitors effective in preventing migraine in nonhypertensive patients? | 2001 Apr |
|
The effects of C-type natriuretic peptide on catecholamine release in the pacific spiny dogfish (Squalus acanthias). | 2001 Aug |
|
Angiotensin-converting enzyme degrades Alzheimer amyloid beta-peptide (A beta ); retards A beta aggregation, deposition, fibril formation; and inhibits cytotoxicity. | 2001 Dec 21 |
|
[Clinical study of the month. The CALM study assessing the combination of an angiotensin-converting enzyme inhibitor and an angiotensin II receptor antagonist in the treatment of diabetic nephropathy]. | 2001 Feb |
|
Disparate results of ACE inhibitor dosage on exercise capacity in heart failure: a reappraisal of vasodilator therapy and study design. | 2001 Feb |
|
In vivo protein synthetic rates of atrial, ventricular, and pulmonary tissue proteins in aortic constriction, goldblatt, and bromoethylamine models of hypertension. | 2001 Feb |
|
Angiotensin I-converting enzyme transition state stabilization by HIS1089: evidence for a catalytic mechanism distinct from other gluzincin metalloproteinases. | 2001 Feb 16 |
|
[Comparison of vasopeptidase inhibitor, omapatrilat, and lisinopril on exercise tolerance and morbidity in patients with heart failure]. | 2001 Jan |
|
In vitro degradation of the Neb-Trypsin modulating oostatic factor (Neb-TMOF) in gut luminal content and hemolymph of the grey fleshfly, Neobellieria bullata. | 2001 Jan |
|
Fluorescence polarization studies of different forms of angiotensin-converting enzyme. | 2001 Jul |
|
Does the antihypertensive response to angiotensin converting enzyme inhibition predict the antihypertensive response to angiotensin receptor antagonism? | 2001 Jul |
|
Spectrophotometric and HPTLC-densitometric determination of lisinopril and hydrochlorothiazide in binary mixtures. | 2001 Jul |
|
Spectrophotometric, septrofluorimetric and LC determination of lisinopril. | 2001 Jul |
|
The quantitative determination of several inhibitors of the angiotensin-converting enzyme by CE. | 2001 Jul |
|
Simultaneous determination of hydrochlorothiazide and several inhibitors of angiotensin-converting enzyme by capillary electrophoresis. | 2001 Jul 27 |
|
ACE inhibition or angiotensin receptor blockade: impact on potassium in renal failure. | 2001 Jun |
|
Familial factors in the antihypertensive response to lisinopril. | 2001 Mar |
|
Late escape from the antiproteinuric effect of ace inhibitors in nondiabetic renal disease. | 2001 Mar |
|
Combination treatment effective option for hypertensive, diabetic patients with microalbuminuria. | 2001 Mar 20 |
|
Antihypertensive drug prescription trends at the primary health care centres in Bahrain. | 2001 May |
|
Trapped renal arteries: functional renal artery stenosis due to occlusion of the aorta in the arch and below the kidneys. | 2001 May |
|
Effect of antihypertensive therapy on renal artery structure in type 2 diabetic rats with hypertension. | 2001 May |
|
Lisinopril reduces albuminuria during exercise in low grade microalbuminuric type 1 diabetic patients: a double blind randomized study. | 2001 May |
|
Effect of Lisinopril on the progression of renal insufficiency in mild proteinuric non-diabetic nephropathies. | 2001 May |
|
RXP 407, a selective inhibitor of the N-domain of angiotensin I-converting enzyme, blocks in vivo the degradation of hemoregulatory peptide acetyl-Ser-Asp-Lys-Pro with no effect on angiotensin I hydrolysis. | 2001 May |
|
Renal tubular peptide catabolism in chronic vascular rejection. | 2001 May-Jul |
|
Pet ownership, but not ace inhibitor therapy, blunts home blood pressure responses to mental stress. | 2001 Oct |
|
Differential manipulation of the renin angiotensin system and epoietin requirements in maintenance haemodialysis patients. | 2001 Sep |
|
Angiotensin-converting enzyme inhibition induces apoptosis in erythroid precursors and affects insulin-like growth factor-1 in posttransplantation erythrocytosis. | 2001 Sep |
|
Cardiovascular critical event pathways for the progression of heart failure; a report from the ATLAS study. | 2001 Sep |
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 |
7Q3P4BS2FD
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SOLVATE->ANHYDROUS |
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SUBSTANCE->BASIS OF STRENGTH |
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TARGET -> INHIBITOR |
Enzymatic Assay
IC50
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TARGET -> INHIBITOR |
Ki
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ACTIVE MOIETY |
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Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Biological Half-life | PHARMACOKINETIC |
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Elimination PHARMACOKINETIC |
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