Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H30N2O5 |
| Molecular Weight | 402.484 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](N[C@@H](CCC1=CC=CC=C1)C(O)=O)C(=O)N2[C@H]3CCCC[C@@H]3C[C@H]2C(O)=O
InChI
InChIKey=AHYHTSYNOHNUSH-HXFGRODQSA-N
InChI=1S/C22H30N2O5/c1-14(23-17(21(26)27)12-11-15-7-3-2-4-8-15)20(25)24-18-10-6-5-9-16(18)13-19(24)22(28)29/h2-4,7-8,14,16-19,23H,5-6,9-13H2,1H3,(H,26,27)(H,28,29)/t14-,16+,17-,18-,19-/m0/s1
DescriptionSources: http://www.drugbank.ca/drugs/DB00519Curator's Comment: Description was created based on several sources, including
http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/020528s024lbl.pdf
Sources: http://www.drugbank.ca/drugs/DB00519
Curator's Comment: Description was created based on several sources, including
http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/020528s024lbl.pdf
Trandolapril is a non-sulhydryl prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications. It is metabolized to its biologically active diacid form, trandolaprilat, in the liver. Trandolaprilat inhibits 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). Trandolapril may be used to treat mild to moderate hypertension, to improve survival following myocardial infarction in clinically stable patients with left ventricular dysfunction, as an adjunct treatment for congestive heart failure, and to slow the rate of progression of renal disease in hypertensive individuals with diabetes mellitus and microalbuminuria or overt nephropathy. Trandolapril is marketed by Abbott Laboratories under the brand name Mavik.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19597068
Curator's Comment: trandolapril was classified as crossing the blood-brain barrier (centrally active)
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL1808 |
15.0 nM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | MAVIK Approved UseHypertension
MAVIK is indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive medication such as hydrochlorothiazide.
Heart Failure Post Myocardial Infarction or Left-Ventricular Dysfunction Post Myocardial Infarction
MAVIK is indicated in stable patients who have evidence of left-ventricular systolic dysfunction (identified by wall motion abnormalities) or who are symptomatic from congestive heart failure within the first few days after sustaining acute myocardial infarction. Launch Date1996 |
|||
| Primary | MAVIK Approved UseHypertension
MAVIK is indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive medication such as hydrochlorothiazide.
Heart Failure Post Myocardial Infarction or Left-Ventricular Dysfunction Post Myocardial Infarction
MAVIK is indicated in stable patients who have evidence of left-ventricular systolic dysfunction (identified by wall motion abnormalities) or who are symptomatic from congestive heart failure within the first few days after sustaining acute myocardial infarction. Launch Date1996 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
0.99 ng/mL |
1 mg single, oral dose: 1 mg route of administration: Oral experiment type: SINGLE co-administered: |
TRANDOLAPRILAT plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
1.3 ng/mL |
1 mg single, oral dose: 1 mg route of administration: Oral experiment type: SINGLE co-administered: |
TRANDOLAPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
9 ng/mL |
4 mg 1 times / day multiple, oral dose: 4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
TRANDOLAPRILAT plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
6.2 ng/mL |
4 mg 1 times / day multiple, oral dose: 4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
TRANDOLAPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
19.1 ng × h/mL |
1 mg single, oral dose: 1 mg route of administration: Oral experiment type: SINGLE co-administered: |
TRANDOLAPRILAT plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
1.8 ng × h/mL |
1 mg single, oral dose: 1 mg route of administration: Oral experiment type: SINGLE co-administered: |
TRANDOLAPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
101 ng × h/mL |
4 mg 1 times / day multiple, oral dose: 4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
TRANDOLAPRILAT plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
8.2 ng × h/mL |
4 mg 1 times / day multiple, oral dose: 4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
TRANDOLAPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
115 h |
4 mg 1 times / day multiple, oral dose: 4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
TRANDOLAPRILAT plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
8.4 h |
4 mg 1 times / day multiple, oral dose: 4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
TRANDOLAPRIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
8 mg 1 times / day multiple, oral Recommended Dose: 8 mg, 1 times / day Route: oral Route: multiple Dose: 8 mg, 1 times / day Sources: |
unhealthy, 55 |
Disc. AE: Diarrhea, Dizziness... AEs leading to discontinuation/dose reduction: Diarrhea Sources: Dizziness Elevated liver enzymes |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Diarrhea | Disc. AE | 8 mg 1 times / day multiple, oral Recommended Dose: 8 mg, 1 times / day Route: oral Route: multiple Dose: 8 mg, 1 times / day Sources: |
unhealthy, 55 |
| Dizziness | Disc. AE | 8 mg 1 times / day multiple, oral Recommended Dose: 8 mg, 1 times / day Route: oral Route: multiple Dose: 8 mg, 1 times / day Sources: |
unhealthy, 55 |
| Elevated liver enzymes | Disc. AE | 8 mg 1 times / day multiple, oral Recommended Dose: 8 mg, 1 times / day Route: oral Route: multiple Dose: 8 mg, 1 times / day Sources: |
unhealthy, 55 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Diagnosis of and therapy for renal hypertension]. | 2004-03-10 |
|
| [Therapeutic strategy for patients with stable-stage chronic kidney failure]. | 2004-03-10 |
|
| Endothelial dysfunction in congestive heart failure: ACE inhibition vs. angiotensin II antagonism. | 2004-03-01 |
|
| Significant target organs for hypertension and cardiac hypertrophy by angiotensin-converting enzyme inhibitors. | 2004-03 |
|
| [Effects of angiotensin II receptor blockers, angiotensin converting enzyme inhibitors, 3-hydroxy-3-methyl glutaryl (HMG) CoA reductase inhibitors, amlodipine and epalrestat on cultured basilar artery smooth muscle cell proliferation]. | 2004-03 |
|
| [Preventive therapy with ACE inhibitors for coronary patients]. | 2004-02-29 |
|
| [Induction of heat shock protein 70 in failing heart]. | 2004-02 |
|
| ACE-inhibition is superior to endothelin A receptor blockade in preventing abnormal capillary supply and fibrosis of the heart in experimental diabetes. | 2004-02 |
|
| Effects of bedtime vs. morning administration of the long-acting lipophilic angiotensin-converting enzyme inhibitor trandolapril on morning blood pressure in hypertensive patients. | 2004-01 |
|
| Effect of nolomirole on monocrotaline-induced heart failure. | 2004-01 |
|
| Pharmacological treatment and prevention of heart failure in the diabetic patient. | 2004 |
|
| A calcium antagonist vs a non-calcium antagonist hypertension treatment strategy for patients with coronary artery disease. The International Verapamil-Trandolapril Study (INVEST): a randomized controlled trial. | 2003-12-03 |
|
| The angiotensin converting enzyme inhibitor trandolapril has neutral effect on exercise tolerance or functional class in patients with myocardial infarction and reduced left ventricular systolic function. | 2003-12 |
|
| ACE inhibition limits chronic injury of kidney transplant even with treatment started when lesions are established. | 2003-12 |
|
| Aldosterone antagonism and myocardial infarction: from animals to man and back. | 2003-11-05 |
|
| Additive improvement of left ventricular remodeling and neurohormonal activation by aldosterone receptor blockade with eplerenone and ACE inhibition in rats with myocardial infarction. | 2003-11-05 |
|
| Differing anti-proteinuric action of candesartan and losartan in chronic renal disease. | 2003-11 |
|
| Submaximal dose of trandolapril in the COOPERATE trial? | 2003-11 |
|
| Angiotensin-converting enzyme inhibitor trandolapril does not affect C-reactive protein levels in myocardial infarction patients. | 2003-10-14 |
|
| Some recent randomized clinical trials in the management of atrial fibrillation. | 2003-10 |
|
| A study on the stereochemical purity of trandolapril and octahydro-1H-indole-2-carboxylic acid by HPLC method. | 2003-09-19 |
|
| Verapamil reverts acute renal functional impairment induced by angiotensin II converting enzyme inhibitors. | 2003-09 |
|
| Renal damage in the SHR/N-cp type 2 diabetes model: comparison of an angiotensin-converting enzyme inhibitor and endothelin receptor blocker. | 2003-09 |
|
| The BErgamo NEphrologic DIabetes Complications Trial (BENEDICT): design and baseline characteristics. | 2003-08 |
|
| ACE inhibitors and AT-1-receptor antagonists COOPERATE in non-diabetic renal disease. | 2003-07 |
|
| The verapamil versus amlodipine in nondiabetic nephropathies treated with trandolapril (VVANNTT) study. | 2003-07 |
|
| Role of L-type calcium channels in pacing-induced short-term and long-term cardiac memory in canine heart. | 2003-06-10 |
|
| Addition of the selective aldosterone receptor antagonist eplerenone to ACE inhibition in heart failure: effect on endothelial dysfunction. | 2003-06-01 |
|
| Choosing a drug from within a class. | 2003-06 |
|
| ACE-inhibitors but not endothelin receptor blockers prevent podocyte loss in early diabetic nephropathy. | 2003-06 |
|
| Inhibition of platelet activation in congestive heart failure by aldosterone receptor antagonism and ACE inhibition. | 2003-06 |
|
| Tick-borne encephalitis with hemorrhagic syndrome, Novosibirsk region, Russia, 1999. | 2003-06 |
|
| Antihypertensive therapy with verapamil SR plus trandolapril versus atenolol plus chlorthalidone on glycemic control. | 2003-05 |
|
| Protective effects of quinaprilat and trandolaprilat, active metabolites of quinapril and trandolapril, on hemolysis induced by lysophosphatidylcholine in human erythrocytes. | 2003-05 |
|
| Trandolapril and endothelin antagonist LU-135252 in the treatment of the fructose-induced hypertensive, hyperinsulinemic, hypertriglyceridemic rat. | 2003-04 |
|
| The COOPERATE trial. | 2003-03-22 |
|
| The COOPERATE trial. | 2003-03-22 |
|
| [The effect of analysed hypotensive drugs on certain metabolic parameters]. | 2003-03 |
|
| Trandolapril: a newer angiotensin-converting enzyme inhibitor. | 2003-03 |
|
| Sustained activation of nuclear factor kappa B and activator protein 1 in chronic heart failure. | 2003-03 |
|
| Exercise testing in hypertensive patients taking different angiotensin-converting enzyme inhibitors. | 2003-02 |
|
| Combination treatment of angiotensin-II receptor blocker and angiotensin-converting-enzyme inhibitor in non-diabetic renal disease (COOPERATE): a randomised controlled trial. | 2003-01-11 |
|
| Trandolapril in left ventricular dysfunction after myocardial infarction: focus on the TRACE study. | 2003-01 |
|
| Combination treatment with an ET(A)-receptor blocker and an ACE inhibitor is not superior to the respective monotherapies in attenuating chronic transplant vasculopathy in different aorta allotransplantation rat models. | 2003-01 |
|
| Effect of endothelin blockade on early cardiovascular remodeling in the one-clip-two-kidney hypertension of the rat. | 2003 |
|
| Time-effect profile of antihypertensive agents assessed with trough/peak ratio, smoothness index and dose omission: an ambulatory blood pressure monitoring study with trandolapril vs. quinapril. | 2002-12 |
|
| Relative long-term effects of spironolactone in conjunction with an angiotensin-converting enzyme inhibitor on left ventricular mass and diastolic function in patients with essential hypertension. | 2002-11 |
|
| High-dose verapamil + trandolapril-induced thrombotic microangiopathy. | 2002 |
|
| [Clinical sequelae of tissue angiotensin converting enzyme inhibition: practicability of use in ischemic heart disease]. | 2002 |
|
| Trandolapril in hypertension: overview of a new angiotensin-converting enzyme inhibitor. | 1992-10-29 |
Patents
Sample Use Guides
The recommended initial dosage of MAVIK (Trandolapril) for patients not receiving a diuretic is 1 mg once daily in non-black patients and 2 mg in black patients.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10334975
Trandolapril at 10(-7) mol/l, significantly increased 11beta-HSD2 activity after pretreatment for 16 or 24 h of the human epithelial colon cell line SW-620
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NCI_THESAURUS |
C247
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NDF-RT |
N0000175562
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87679-71-8
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1546379
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100000077472
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DB14209
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CHEMBL1201387
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6370
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6455
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RR6866VL0O
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C061095
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SUB11213MIG
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m10999
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C72913
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5464097
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DTXSID101024709
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1672723
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ACTIVE MOIETY
PRODRUG (METABOLITE ACTIVE)