Details
Stereochemistry | RACEMIC |
Molecular Formula | C12H18N2O4.ClH |
Molecular Weight | 290.743 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.COC1=CC(C(O)CNC(=O)CN)=C(OC)C=C1
InChI
InChIKey=MGCQZNBCJBRZDT-UHFFFAOYSA-N
InChI=1S/C12H18N2O4.ClH/c1-17-8-3-4-11(18-2)9(5-8)10(15)7-14-12(16)6-13;/h3-5,10,15H,6-7,13H2,1-2H3,(H,14,16);1H
DescriptionSources: http://www.drugbank.ca/drugs/DB00211Curator's Comment: Description was created based on several sources, including
https://www.drugs.com/pro/midodrine.html
Sources: http://www.drugbank.ca/drugs/DB00211
Curator's Comment: Description was created based on several sources, including
https://www.drugs.com/pro/midodrine.html
Midodrine is a prodrug, i.e., the therapeutic effect of orally administered midodrine is due to the major metabolite desglymidodrine formed by deglycination of midodrine. Desglymidodrine diffuses poorly across the blood-brain barrier, and is therefore not associated with effects on the central nervous system. Administration of midodrine results in a rise in standing, sitting, and supine systolic and diastolic blood pressure in patients with orthostatic hypotension of various etiologies. Standing systolic blood pressure is elevated by approximately 15 to 30 mmHg at 1 hour after a 10-mg dose of midodrine, with some effect persisting for 2 to 3 hours. Midodrine has no clinically significant effect on standing or supine pulse rates in patients with autonomic failure. Midodrine forms an active metabolite, desglymidodrine, that is an alpha1-agonist, and exerts its actions via activation of the alpha-adrenergic receptors of the arteriolar and venous vasculature, producing an increase in vascular tone and elevation of blood pressure. Desglymidodrine does not stimulate cardiac beta-adrenergic receptors. Midodrine is used for the treatment of symptomatic orthostatic hypotension (OH). Midodrine is marketed under the brand names Amatine, ProAmatine, Gutron.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2452997
Curator's Comment: does not cross the blood-brain barrier
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL229 Sources: http://www.drugbank.ca/drugs/DB00211 |
|||
Target ID: CHEMBL232 Sources: http://www.drugbank.ca/drugs/DB00211 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | ORVATEN Approved Useindicated for the treatment of symptomatic orthostatic hypotension Launch Date2004 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
21 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26597181 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
MIDODRINE HYDROCHLORIDE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
2.2 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26597181 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
MIDODRINE HYDROCHLORIDE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
18.5 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26597181 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
MIDODRINE HYDROCHLORIDE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
2.5 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26597181 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
MIDODRINE HYDROCHLORIDE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
0.54 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26597181 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
MIDODRINE HYDROCHLORIDE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
0.6 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26597181 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
MIDODRINE HYDROCHLORIDE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
100% EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26597181 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
MIDODRINE HYDROCHLORIDE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
Doses
Dose | Population | Adverse events |
---|---|---|
350 mg single, oral Overdose |
unhealthy, 20 years n = 1 Health Status: unhealthy Age Group: 20 years Sex: F Population Size: 1 Sources: |
Other AEs: Hypertension, Bradycardia... Other AEs: Hypertension (severe, 1 patient) Sources: Bradycardia (1 patient) |
90 mg 1 times / day steady, oral Highest studied dose Dose: 90 mg, 1 times / day Route: oral Route: steady Dose: 90 mg, 1 times / day Sources: |
unhealthy, 49 years n = 1 Health Status: unhealthy Condition: hypotension Age Group: 49 years Sex: M Population Size: 1 Sources: |
|
2.5 mg single, intravenous Dose: 2.5 mg Route: intravenous Route: single Dose: 2.5 mg Sources: |
healthy, adult n = 12 Health Status: healthy Age Group: adult Sex: M Population Size: 12 Sources: |
|
205 mg single, oral Overdose Dose: 205 mg Route: oral Route: single Dose: 205 mg Sources: |
unknown n = 1 Health Status: unknown Population Size: 1 Sources: |
Other AEs: Lethargic... Other AEs: Lethargic (1 patient) Sources: |
250 mg single, oral Overdose Dose: 250 mg Route: oral Route: single Dose: 250 mg Sources: |
unknown n = 1 Health Status: unknown Population Size: 1 Sources: |
Other AEs: Blood pressure systolic increased... Other AEs: Blood pressure systolic increased (1 patient) Sources: |
10 mg 3 times / day steady, oral Recommended Dose: 10 mg, 3 times / day Route: oral Route: steady Dose: 10 mg, 3 times / day Sources: |
unhealthy n = 1 Health Status: unhealthy Population Size: 1 Sources: |
Disc. AE: Supine hypertension... AEs leading to discontinuation/dose reduction: Supine hypertension Sources: |
7.5 mg 1 times / day steady, oral Dose: 7.5 mg, 1 times / day Route: oral Route: steady Dose: 7.5 mg, 1 times / day Sources: |
unhealthy n = 2 |
Other AEs: Pancytopenia... |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Bradycardia | 1 patient | 350 mg single, oral Overdose |
unhealthy, 20 years n = 1 Health Status: unhealthy Age Group: 20 years Sex: F Population Size: 1 Sources: |
Hypertension | severe, 1 patient | 350 mg single, oral Overdose |
unhealthy, 20 years n = 1 Health Status: unhealthy Age Group: 20 years Sex: F Population Size: 1 Sources: |
Lethargic | 1 patient | 205 mg single, oral Overdose Dose: 205 mg Route: oral Route: single Dose: 205 mg Sources: |
unknown n = 1 Health Status: unknown Population Size: 1 Sources: |
Blood pressure systolic increased | 1 patient | 250 mg single, oral Overdose Dose: 250 mg Route: oral Route: single Dose: 250 mg Sources: |
unknown n = 1 Health Status: unknown Population Size: 1 Sources: |
Supine hypertension | Disc. AE | 10 mg 3 times / day steady, oral Recommended Dose: 10 mg, 3 times / day Route: oral Route: steady Dose: 10 mg, 3 times / day Sources: |
unhealthy n = 1 Health Status: unhealthy Population Size: 1 Sources: |
Pancytopenia | 2 patients | 7.5 mg 1 times / day steady, oral Dose: 7.5 mg, 1 times / day Route: oral Route: steady Dose: 7.5 mg, 1 times / day Sources: |
unhealthy n = 2 |
PubMed
Title | Date | PubMed |
---|---|---|
Treatment of Severe Intradialytic Hypotension With the Addition of High Dialysate Calcium Concentration to Midodrine and/or Cool Dialysate. | 2001 Feb |
|
Dysautonomia and neurocardiogenic syncope. | 2001 Mar |
|
Midodrine for the management of orthostatic hypotension in patients with spinal cord injury: A case report. | 2001 May |
|
Contingent negative variation in children with orthostatic dysregulation. | 2001 Oct |
|
Clinical case-based approach to understanding intradialytic hypotension. | 2001 Oct |
|
[Vasoconstrictors in the treatment of hepatorenal syndrome]. | 2002 |
|
Strategy for the management of vasovagal syncope. | 2002 |
|
Pandysautonomia associated with impaired ganglionic neurotransmission and circulating antibody to the neuronal nicotinic receptor. | 2002 Aug |
|
Treatment of orthostatic hypotension. | 2002 Dec |
|
[Lipothymia and syncope in adolescents]. | 2002 Dec |
|
[Syncope - a systematic overview of classification, pathogenesis, diagnosis and management]. | 2002 Feb |
|
Chronic hypotension in the dialysis patient. | 2002 Jul-Aug |
|
Orthostatic hypotension. | 2002 May |
|
A pilot randomized trial of induced blood pressure elevation: effects on function and focal perfusion in acute and subacute stroke. | 2003 |
|
Atrial septal aneurysm with right-to-left interatrial shunting. | 2003 |
|
Recurrent syncope in a patient after myocardial infarction. | 2003 Apr |
|
Acute renal failure in patients with cirrhosis: perspectives in the age of MELD. | 2003 Feb |
|
Efficacy and safety of midodrine in the treatment of dialysis-associated hypotension. | 2003 Jan |
|
Hepatorenal syndrome. | 2003 Jan-Mar |
|
[Results of midodrin treatment of vasovagal syncope]. | 2004 |
|
Postprandial hypotension treated with acarbose in a patient with type 1 diabetes mellitus. | 2004 Dec |
|
Clinical history. | 2004 Feb |
|
Midodrine, octreotide, albumin, and TIPS in selected patients with cirrhosis and type 1 hepatorenal syndrome. | 2004 Jul |
|
Chiral investigation of midodrine, a long-acting alpha-adrenergic stimulating agent. | 2004 Jul |
|
The in vitro metabolism of desglymidodrine, an active metabolite of prodrug midodrine by human liver microsomes. | 2004 Jul-Sep |
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Intestinal obstruction associated with oral midodrine. | 2004 Jun |
|
Synthesis and structure-activity studies on N-[5-(1H-imidazol-4-yl)-5,6,7,8-tetrahydro-1-naphthalenyl]methanesulfonamide, an imidazole-containing alpha(1A)-adrenoceptor agonist. | 2004 Jun 3 |
|
[Orthostatic hypotension and supine hypertension in pure autonomic failure]. | 2004 Nov |
|
New approaches to the treatment and prevention of neurally mediated reflex (neurocardiogenic) syncope. | 2004 Sep |
|
[Efficacy and safety of a herbal drug containing hawthorn berries and D-camphor in hypotension and orthostatic circulatory disorders/results of a retrospective epidemiologic cohort study]. | 2005 |
|
The effects of chronic treatment with octreotide versus octreotide plus midodrine on systemic hemodynamics and renal hemodynamics and function in nonazotemic cirrhotic patients with ascites. | 2005 Apr |
|
Fludrocortisone in patients with familial dysautonomia--assessing effect on clinical parameters and gene expression. | 2005 Aug |
|
Effects of therapy based on tilt testing results on the long-term outcome in patients with syncope. | 2005 Jul |
|
Adrenergic drugs for urinary incontinence in adults. | 2005 Jul 20 |
|
Consequences of cardiovascular adaptation to spaceflight: implications for the use of pharmacological countermeasures. | 2005 Jun |
|
Pregnancy in postural orthostatic tachycardia syndrome. | 2005 Jun |
|
Beneficial haemodynamic and renal sodium handling effects of combined midodrine and octreotide treatment in a cirrhotic patient with large hepatic hydrothorax and mild ascites. | 2005 Nov |
|
Effect of mineralocorticoids on interdialytic weight gain in hemodialysis patients with perdialytic hypotension. | 2005 Oct |
|
[Pharmacotherapy of stress incontinence]. | 2005 Oct 14 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/dosage/midodrine.html
10 mg orally three times a day. Do not give more frequently than every 3 hours, after the evening meal, or less than 4 hours before bedtime.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/61715
A decrease in atrial rate was elicited by high concentrations (above 10(-4) to 10(-3) M) of the sympathomimetic agent midodrine in guinea-pig right atrial preparation
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29709
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FDA ORPHAN DRUG |
7585
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31847
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U-33
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SUB03291MIG
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100000090278
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3092-17-9
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CHEMBL1201212
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m7533
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993491
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43218-56-0
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59JV96YTXV
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1443704
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C47620
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59JV96YTXV
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256-148-3
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ACTIVE MOIETY
SUBSTANCE RECORD