Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C23H32N2O5 |
Molecular Weight | 416.5106 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CCC[C@]1([H])N([C@@H](C2)C(O)=O)C(=O)[C@H](C)N[C@@H](CCC3=CC=CC=C3)C(=O)OCC
InChI
InChIKey=HDACQVRGBOVJII-JBDAPHQKSA-N
InChI=1S/C23H32N2O5/c1-3-30-23(29)18(13-12-16-8-5-4-6-9-16)24-15(2)21(26)25-19-11-7-10-17(19)14-20(25)22(27)28/h4-6,8-9,15,17-20,24H,3,7,10-14H2,1-2H3,(H,27,28)/t15-,17-,18-,19-,20-/m0/s1
DescriptionCurator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/16398929
Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/16398929
Ramipril (sold under the brand name Altace ) is a prodrug belonging to the angiotensin-converting enzyme (ACE) inhibitors. It is metabolized to ramiprilat in the liver and, to a lesser extent, kidneys. Ramiprilat is a potent, competitive inhibitor of ACE, the enzyme responsible for the conversion of angiotensin I (ATI) to angiotensin II (ATII). ATII regulates blood pressure and is a key component of the renin-angiotensin-aldosterone system (RAAS). Ramipril is indicated for the treatment of hypertension, to lower blood pressure; also used to reduce the risk of myocardial infarction, stroke, or death from cardiovascular causes; in addition, this drug is used to reduce the rate of death, myocardial infarction and stroke in individuals at high risk of cardiovascular events.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL1808 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16398929 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | ALTACE Approved UseReduction in Risk of Myocardial Infarction, Stroke, and Death from Cardiovascular Causes Ramipril capsules are indicated in patients 55 years or older at high risk of developing a major cardiovascular event because of a history of coronary artery disease, stroke, peripheral vascular disease, or diabetes that is accompanied by at least one other cardiovascular risk factor (hypertension, elevated total cholesterol levels, low HDL levels, cigarette smoking, or documented microalbuminuria), to reduce the risk of myocardial infarction, stroke, or death from cardiovascular causes. Ramipril capsules can be used in addition to other needed treatment (such as antihypertensive, antiplatelet or lipid-lowering therapy). Hypertension Ramipril capsules are indicated for the treatment of hypertension. It may be used alone or in combination with thiazide diuretics. In using ramipril capsules, 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. Available data are insufficient to show that ramipril capsules do not have a similar risk. (See WARNINGS.) In considering use of ramipril capsules, it should be noted that in controlled trials ACE inhibitors have an effect on blood pressure that is less in black patients than in non-blacks. In addition, ACE inhibitors (for which adequate data are available) cause a higher rate of angioedema in black than in non-black patients. (See WARNINGS, Angioedema.) Launch Date1991 |
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Preventing | ALTACE Approved UseReduction in Risk of Myocardial Infarction, Stroke, and Death from Cardiovascular Causes Ramipril capsules are indicated in patients 55 years or older at high risk of developing a major cardiovascular event because of a history of coronary artery disease, stroke, peripheral vascular disease, or diabetes that is accompanied by at least one other cardiovascular risk factor (hypertension, elevated total cholesterol levels, low HDL levels, cigarette smoking, or documented microalbuminuria), to reduce the risk of myocardial infarction, stroke, or death from cardiovascular causes. Ramipril capsules can be used in addition to other needed treatment (such as antihypertensive, antiplatelet or lipid-lowering therapy). Hypertension Ramipril capsules are indicated for the treatment of hypertension. It may be used alone or in combination with thiazide diuretics. In using ramipril capsules, 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. Available data are insufficient to show that ramipril capsules do not have a similar risk. (See WARNINGS.) In considering use of ramipril capsules, it should be noted that in controlled trials ACE inhibitors have an effect on blood pressure that is less in black patients than in non-blacks. In addition, ACE inhibitors (for which adequate data are available) cause a higher rate of angioedema in black than in non-black patients. (See WARNINGS, Angioedema.) Launch Date1991 |
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Primary | ALTACE Approved UseReduction in Risk of Myocardial Infarction, Stroke, and Death from Cardiovascular Causes Ramipril capsules are indicated in patients 55 years or older at high risk of developing a major cardiovascular event because of a history of coronary artery disease, stroke, peripheral vascular disease, or diabetes that is accompanied by at least one other cardiovascular risk factor (hypertension, elevated total cholesterol levels, low HDL levels, cigarette smoking, or documented microalbuminuria), to reduce the risk of myocardial infarction, stroke, or death from cardiovascular causes. Ramipril capsules can be used in addition to other needed treatment (such as antihypertensive, antiplatelet or lipid-lowering therapy). Hypertension Ramipril capsules are indicated for the treatment of hypertension. It may be used alone or in combination with thiazide diuretics. In using ramipril capsules, 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. Available data are insufficient to show that ramipril capsules do not have a similar risk. (See WARNINGS.) In considering use of ramipril capsules, it should be noted that in controlled trials ACE inhibitors have an effect on blood pressure that is less in black patients than in non-blacks. In addition, ACE inhibitors (for which adequate data are available) cause a higher rate of angioedema in black than in non-black patients. (See WARNINGS, Angioedema.) Launch Date1991 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
43.8 ng/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/2533075 |
5 mg 1 times / day steady-state, oral dose: 5 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
RAMIPRIL plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
24 ng/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/6097458 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RAMIPRILAT unknown | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
197 ng × h/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/2533075 |
5 mg 1 times / day steady-state, oral dose: 5 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
RAMIPRIL plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
414 μg × h/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/6097458 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RAMIPRILAT unknown | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
Doses
Dose | Population | Adverse events |
---|---|---|
10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Other AEs: Headache, Cough... Other AEs: Headache (13%) Sources: Cough (33%) Dizziness (13%) Asthenia (19%) Cramps (4%) Diarrhea (4%) Nausea (8%) Palpitations (1%) Dyspnea (1%) Tinnitus (1%) Malaise (3%) Pruritus (1%) Dry mouth (1%) Polyuria (3%) |
20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Other AEs: Dizziness, Vertigo... Other AEs: Dizziness (6%) Sources: Vertigo (6%) Asthenia (4%) Nausea (3%) Headache (2%) Abdominal pain (1%) Gastrointestinal disorder (1%) Rash (1%) Cough increased (1%) |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Dry mouth | 1% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Dyspnea | 1% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Palpitations | 1% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Pruritus | 1% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Tinnitus | 1% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Dizziness | 13% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Headache | 13% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Asthenia | 19% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Malaise | 3% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Polyuria | 3% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Cough | 33% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Cramps | 4% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Diarrhea | 4% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Nausea | 8% | 10 mg 1 times / day multiple, oral (max) Recommended Dose: 10 mg, 1 times / day Route: oral Route: multiple Dose: 10 mg, 1 times / day Sources: |
unhealthy, 18-75 n = 661 Health Status: unhealthy Condition: Hypertension Age Group: 18-75 Sex: M+F Population Size: 661 Sources: |
Abdominal pain | 1% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Cough increased | 1% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Gastrointestinal disorder | 1% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Rash | 1% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Headache | 2% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Nausea | 3% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Asthenia | 4% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Dizziness | 6% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Vertigo | 6% | 20 mg 1 times / day multiple, oral (max) Recommended Dose: 20 mg, 1 times / day Route: oral Route: multiple Dose: 20 mg, 1 times / day Co-administed with:: hydrochlorothiazide(25 mg; 1/day) Sources: |
unhealthy, 55.7 years (range: 21-88 years) n = 555 Health Status: unhealthy Condition: Essential hypertension Age Group: 55.7 years (range: 21-88 years) Sex: M+F Population Size: 555 Sources: |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Sources: https://pubmed.ncbi.nlm.nih.gov/18713951/ |
yes | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18713951/ |
yes |
Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
no | ||||
yes |
PubMed
Title | Date | PubMed |
---|---|---|
Mechanical vs intrinsic components in the improvement of brachial arterial compliance. Comparison of the effects of atenolol versus ramipril in hypertensive patients. | 2001 |
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[Activity of the renin-angiotensin-aldosterone system and its impact on the effectiveness of treatment of chronic heart failure in patients with pulmonary tuberculosis]. | 2001 |
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Cost effectiveness of ramipril in patients with non-diabetic nephropathy and hypertension: economic evaluation of Ramipril Efficacy in Nephropathy (REIN) Study for Germany from the perspective of statutory health insurance. | 2001 |
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Differential regulation of cathepsin B and prorenin gene expression in renal juxtaglomerular cells. | 2001 |
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An ACE inhibitor to coronary patients: ramipril reduces mortality according to HOPE trial. | 2001 Apr |
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Use of 7-fluoro-4-nitrobenzo-2-oxo-1,3-diazole (NBD-F) for the determination of ramipril in tablets and spiked human plasma. | 2001 Apr |
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Study at up to 700 sites will build on landmark HOPE trial. | 2001 Apr-May |
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[Effect of a non-antihypertensive dose of ramipril on the plasma and tissue renin-angiotensin system in 27 TGR (mRen2) rats]. | 2001 Aug |
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HOPE for patients with Type 2 diabetes: an application of the findings of the MICRO-HOPE substudy in a British hospital diabetes clinic. | 2001 Aug |
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The HOPE study: comparison with other trials of secondary prevention. | 2001 Aug |
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Impaired angiotensin II regulation of renal C-type natriuretic peptide mRNA expression in experimental diabetes mellitus. | 2001 Aug 15 |
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Cardioprotective effects of ramipril and losartan in right ventricular pressure overload in the rabbit: importance of kinins and influence on angiotensin II type 1 receptor signaling pathway. | 2001 Aug 21 |
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[Diabetic nephropathy. Smoking also damages the kidney]. | 2001 Aug 23 |
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Changes in vasoconstrictive hormones, natriuretic peptides, and left ventricular remodeling soon after anterior myocardial infarction. | 2001 Dec |
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Diabetes and the HOPE study: implications for macrovascular and microvascular disease. | 2001 Jan |
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Future perspectives and implications. | 2001 Jan |
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Pharmacoeconomic impact of HOPE. | 2001 Jan |
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Modifying the natural history of atherosclerosis: the SECURE trial. | 2001 Jan |
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Podocyte foot process broadening in experimental diabetic nephropathy: amelioration with renin-angiotensin blockade. | 2001 Jul |
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Right atrial function in hypertensive patients: effects of antihypertensive therapy. | 2001 Jul |
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Potentiation of kinin analogues by ramiprilat is exclusively related to their degradation. | 2001 Jul |
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Bradykinin metabolism in the isolated perfused rabbit heart. | 2001 Jul |
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Simultaneous determination of hydrochlorothiazide and several inhibitors of angiotensin-converting enzyme by capillary electrophoresis. | 2001 Jul 27 |
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Effects of ramipril on coronary events in high-risk persons: results of the Heart Outcomes Prevention Evaluation Study. | 2001 Jul 31 |
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Prospective randomized controlled multicenter trial on steroids plus ramipril in proteinuric IgA nephropathy. | 2001 Jul-Aug |
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Renal insufficiency predicts cardiovascular disease in high-risk individuals: the benefit of ramipril in the HOPE study. Heart Outcomes and Prevention Evaluation. | 2001 Jul-Aug |
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The African American Study of Kidney Disease and Hypertension (AASK): new findings. | 2001 Jul-Aug |
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[Decreased platelet aggregation during angiotensin-converting enzyme inhibitor therapy. Results of a pilot study]. | 2001 Jun 15 |
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Differential effects of angiotensin AT1 and AT2 receptors on the expression, translation and function of the Na+-H+ exchanger and Na+-HCO3- symporter in the rat heart after myocardial infarction. | 2001 Jun 15 |
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[Therapeutic perspectives: association of ACE inhibitors and angiotensin receptor blockers]. | 2001 Mar-Apr |
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ACE inhibitor inhibits atherosclerosis. | 2001 May |
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[Severe hypoglycemia secondary to angiotensin-converting-enzyme inhibitors in the absence of diabetes mellitus. Report of a case]. | 2001 May-Jun |
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Prevention, protection, and the intrarenal renin-angiotensin systems. | 2001 Nov |
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The effects of an ACE inhibitor and a calcium antagonist on the progression of renal disease: the Nephros Study. | 2001 Nov |
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Simvastatin reverses impaired regulation of renal oxygen consumption in congestive heart failure. | 2001 Nov |
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Clinical trials report. The effect of Ramipril versus Amlodipine on renal outcomes in hypertension nephrosclerosis. | 2001 Oct |
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Ramipril and the development of diabetes. | 2001 Oct 17 |
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Reduction of cardiovascular risk by regression of electrocardiographic markers of left ventricular hypertrophy by the angiotensin-converting enzyme inhibitor ramipril. | 2001 Oct 2 |
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[Atherosclerosis. High ACE activity in plaque: risk of rupture!]. | 2001 Oct 25 |
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Inhibition of cyclooxygenase-2 attenuates urinary prostanoid excretion without affecting renal renin expression. | 2001 Sep |
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What is the best treatment for slowing the progression to end-stage renal disease (ESRD) in African Americans with hypertensive nephropathy? | 2001 Sep |
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What is the relevance of the HOPE study in general practice? | 2001 Sep |
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Enantioseparation of the anticoagulant drug phenprocoumon in capillary electrophoresis with UV and laser-induced fluorescence detection and application of the method to urine samples. | 2001 Sep |
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Apstatin, a selective inhibitor of aminopeptidase P, reduces myocardial infarct size by a kinin-dependent pathway. | 2001 Sep |
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Inhibitors of bradykinin-inactivating enzymes decrease myocardial ischemia/reperfusion injury following 3 and 7 days of reperfusion. | 2001 Sep |
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The Heart Outcomes Prevention Evaluation study: angiotensin-converting enzyme inhibitors: are their benefits a class effect or do individual agents differ? | 2001 Sep |
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Can ACE inhibitor therapy prevent end-stage renal failure? | 2001 Sep 3 |
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[Ramipril can do more. Halting progression of atherosclerosis]. | 2001 Sep 6 |
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[Achieving vascular protection. ACE inhibitor lowers not only blood pressure]. | 2001 Sep 6 |
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Blacks with hypertension, renal insufficiency, and baseline proteinuria benefit more from ACE inhibition than from calcium channel blockade. | 2001 Sep-Oct |
Patents
Sample Use Guides
Hypertension: The recommended initial dose for patients not receiving a diuretic is 2.5 mg once a day. Adjust dose according to blood pressure response. The usual maintenance dosage range is 2.5 mg to 20 mg per day administered as a single dose or in two.
Myocardial Infarction, Stroke, and Death from Cardiovascular Causes: Initiate dosing at 2.5 mg once daily for 1 week, 5 mg once daily for the next 3 weeks, and then increase as tolerated, to a maintenance dose of 10 mg once daily.
equally divided doses. In some patients treated once daily, the antihypertensive effect may diminish toward the end of the dosing interval.
Heart Failure Post-Myocardial Infarction: the recommended starting dose is 2.5 mg twice daily (5 mg per day). A patient who becomes hypotensive at this dose may be switched to 1.25 mg twice daily. After one week at the starting dose, increase dose (if tolerated) toward a target dose of 5 mg twice daily, with dosage increases being about 3 weeks apart.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10352363
Curator's Comment: The effect of ramipril on DNA synthesis, cell proliferation and PDGF A and B chain gene expression in fetal calf serum (FCS)-activated cultured human glomerular mesangial cells was investigated. Ramipril significantly reduced FCS-induced PDGF A and B chain gene expression, completely abolished the PDGF A and B chain gene expression induced by phorbol 12-myristate 13-acetate, a specific protein kinase C activator, suggesting a site of action downstream of this enzyme in the mitogenic signal transduction pathway.
Unknown
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Classification Tree | Code System | Code | ||
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WHO-ATC |
C09BB07
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-VATC |
QC09BB05
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-ATC |
C09BB05
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-VATC |
QC09BA05
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-VATC |
QC09BB07
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-ATC |
C10BX04
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-VATC |
QC09AA05
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-ATC |
C09BA05
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-ATC |
C09BX03
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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NDF-RT |
N0000000181
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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LIVERTOX |
NBK548689
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-VATC |
QC10BX04
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-ATC |
C09AA05
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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WHO-ATC |
C10BX06
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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NDF-RT |
N0000175562
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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NCI_THESAURUS |
C247
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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Code System | Code | Type | Description | ||
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CHEMBL1168
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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5561
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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RAMIPRIL
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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2356
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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8774
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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DB00178
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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100000092240
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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SUB10248MIG
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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87333-19-5
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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L35JN3I7SJ
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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L35JN3I7SJ
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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C29411
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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D017257
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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1598303
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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758933
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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Ramipril
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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35296
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | RxNorm | ||
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X-65
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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6339
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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DTXSID8023551
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | |||
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m9491
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY | Merck Index | ||
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5362129
Created by
admin on Fri Dec 15 15:04:06 GMT 2023 , Edited by admin on Fri Dec 15 15:04:06 GMT 2023
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD