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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H15N5O.C4H6O6
Molecular Weight 359.3351
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MINOXIDIL TARTRATE

SMILES

O[C@H]([C@@H](O)C(O)=O)C(O)=O.NC1=CC(=NC(N)=[N+]1[O-])N2CCCCC2

InChI

InChIKey=SNCJAEVKCLODRY-LREBCSMRSA-N
InChI=1S/C9H15N5O.C4H6O6/c10-7-6-8(12-9(11)14(7)15)13-4-2-1-3-5-13;5-1(3(7)8)2(6)4(9)10/h6H,1-5,10H2,(H2,11,12);1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1

HIDE SMILES / InChI

Molecular Formula C4H6O6
Molecular Weight 150.0868
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C9H15N5O
Molecular Weight 209.2483
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including https://www.drugs.com/pro/minoxidil.html

Minoxidil is an orally effective direct acting peripheral vasodilator that reduces elevated systolic and diastolic blood pressure by decreasing peripheral vascular resistance. Minoxidil is also used topically to treat androgenetic alopecia. Microcirculatory blood flow in animals is enhanced or maintained in all systemic vascular beds. In man, forearm and renal vascular resistance decline; forearm blood flow increases while renal blood flow and glomerular filtration rate are preserved. The predominant site of minoxidil action is arterial. Venodilation does not occur with minoxidil; thus, postural hypotension is unusual with its administration. The antihypertensive activity of minoxidil is due to its sulphate metabolite, minoxidil sulfate. Minoxidil is thought to promote the survival of human dermal papillary cells (DPCs) or hair cells by activating both extracellular signal-regulated kinase (ERK) and Akt and by preventing cell death by increasing the ratio of BCl-2/Bax. Minoxidil may stimulate the growth of human hairs by prolonging anagen through these proliferative and anti-apoptotic effects on DPCs. Minoxidil, when used as a vasodilator, acts by opening adenosine triphosphate-sensitive potassium channels in vascular smooth muscle cells. This vasodilation may also improve the viability of hair cells or hair follicles. Minoxidil is used for the treatment of severe hypertension and in the topical treatment (regrowth) of androgenic alopecia in males and females and stabilisation of hair loss in patients with androgenic alopecia.

Originator

Curator's Comment: Developed by then Upjohn Co. of Kalamazoo, Michigan, Minoxidil first came on the scene in 1960s

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.62 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Minoxidil

Approved Use

Because of the potential for serious adverse effects, Minoxidil tablets are indicated only in the treatment of hypertension that is symptomatic or associated with target organ damage and is not manageable with maximum therapeutic doses of a diuretic plus two other antihypertensive drugs. At the present time use in milder degrees of hypertension is not recommended because the benefit-risk relationship in such patients has not been defined.

Launch Date

1987
Primary
ROGAINE

Approved Use

Women’s ROGAINE® is for general thinning of hair on the top of the scalp

Launch Date

1988
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
2.13 ng/mL
50 mg 2 times / day multiple, topical
dose: 50 mg
route of administration: Topical
experiment type: MULTIPLE
co-administered:
MINOXIDIL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
37.2 ng/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MINOXIDIL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
18.71 ng × h/mL
50 mg 2 times / day multiple, topical
dose: 50 mg
route of administration: Topical
experiment type: MULTIPLE
co-administered:
MINOXIDIL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
55.1 ng × h/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MINOXIDIL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.27 h
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MINOXIDIL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: FASTED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
100%
MINOXIDIL plasma
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
PubMed

PubMed

TitleDatePubMed
Minoxidil accelerates heart failure development in rats with ascending aortic constriction.
1998-06
Age dependence of the cardiac lesions induced by minoxidil in the rat.
1996-06-17
Structural and functional consequences of minoxidil-induced cardiac hypertrophy.
1994-04
Effects of the arterial vasodilator minoxidil on cardiovascular structure and sympathetic activity in spontaneously hypertensive rats.
1993-12
Renin-angiotensin system and minoxidil-induced cardiac hypertrophy in rats.
1993-11
Hyperfiltration and conservation of renal function in hypertensive nephrosclerosis patients.
1993-04
Transcutaneous minoxidil in the treatment of erectile dysfunctions in spinal cord injured men.
1993-01-01
Severe hypertrichosis of the external ear canal during minoxidil therapy.
1988-08
Orthostatic hypotension occurring after discontinuation of long-term minoxidil therapy.
1988-08
Minoxidil induced pericardial effusion.
1988-05
Examination of minoxidil-induced acute cardiotoxicity in miniature swine.
1988-01
Minoxidil-associated pericardial effusion.
1987-09
[Minoxidil-induced pericardial effusion].
1987
Topical tretinoin for hair growth promotion.
1986-10
Prolonged hypotension after initial minoxidil dose.
1986-10
Minoxidil-associated pericarditis and fatal cardiac tamponade.
1985-10
Pericarditis after minoxidil reinstitution.
1985-10
Minoxidil in a once-a-day step-3 antihypertensive program.
1985-03
Cardiac morphologic alterations in acute minoxidil cardiotoxicity in miniature swine.
1984-08
Mode of antihypertensive action of nitrendipine.
1984
Pericarditis: a complication of minoxidil therapy.
1983-06
Bilateral optic neuritis following minoxidil administration.
1983-03
Minoxidil in severe and moderately severe hypertension, in association with methyldopa and chlortalidone.
1982-11
Effects of acute and chronic minoxidil administration on rest and exercise hemodynamics and clinical status in patients with severe, chronic heart failure.
1982-11
Vasodilators in the treatment of hypertension.
1982-11
[Pericardial effusion during long-term treatment with minoxidil].
1982-10
[Fluid retention with pericardial effusion in minoxidil therapy (author's transl)].
1982-06-25
Pleuropericardial effusion associated with minoxidil administration.
1982-05
Chest pain and abnormal electrocardiogram associated with minoxidil.
1982-05
Clinical experience of long-term treatment with minoxidil in severe arterial hypertension.
1982
Pericardial effusion associated with minoxidil therapy.
1981-11
Minoxidil and pericardial effusion: an idiosyncratic reaction.
1981-07
Minoxidil.
1981-01
Minoxidil in the management of intractable hypertension.
1981
Divergent effects of propranolol and furosemide pretreatment on acute cardiomyopathy induced by minoxidil in beagle dogs.
1981
Effect of minoxidil on sympathetic nervous activity in clonidine-treated hypertensive patients.
1981
Rebound hypertension following minoxidil withdrawal.
1980-04
Pericardial effusion associated with minoxidil therapy in dialyzed patients.
1980-01
Experiences with the antihypertensive drug minoxidil.
1980
Renal function in long-term minoxidil-treated patients.
1980
Long-term effects of minoxidil therapy on renal function of patients with refractory hypertension: the significance of albuminuria.
1980
Renal function and vascular resistance during long-term minoxidil treatment of severe hypertension.
1980
Hypertrichosis due to minoxidil.
1979-11
Reversible renal failure during treatment with captopril.
1979-09-08
Acute cardiomyopathy induced by the vasodilating antihypertensive agent minoxidil.
1979-03-15
Pericardial effusions associated with minoxidil.
1977-12-24
The outpatient treatment of refractory hypertension with minoxidil.
1977-07
Minoxidil in refractory hypertension: benefits, risks.
1977
The effect of minoxidil on blood pressure and plasma renin activity in patients with essential and renal hypertension.
1976-08-01
Clinical and haemodynamic effects of minoxidil in refractory hypertension.
1976
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: can also be used topically for hair loss treatment http://www.accessdata.fda.gov/drugsatfda_docs/label/2015/019501Orig1s029lbl.pdf
Usual Adult Dose for Hypertension Initial dose: 5 mg orally once a day. Maintenance dose: 10-40 mg in 1-2 divided doses.
Route of Administration: Oral
Minoxidil (0.1-100 uM) increased deer hair follicle growth
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:46:51 GMT 2025
Edited
by admin
on Mon Mar 31 21:46:51 GMT 2025
Record UNII
70J7ZH7ECA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,4-PYRIMIDINEDIAMINE, 6-(1-PIPERIDINYL)-, 3-OXIDE, (2R,3R)-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Preferred Name English
MINOXIDIL TARTRATE
Common Name English
Code System Code Type Description
FDA UNII
70J7ZH7ECA
Created by admin on Mon Mar 31 21:46:51 GMT 2025 , Edited by admin on Mon Mar 31 21:46:51 GMT 2025
PRIMARY
CAS
158473-55-3
Created by admin on Mon Mar 31 21:46:51 GMT 2025 , Edited by admin on Mon Mar 31 21:46:51 GMT 2025
PRIMARY
EPA CompTox
DTXSID60935925
Created by admin on Mon Mar 31 21:46:51 GMT 2025 , Edited by admin on Mon Mar 31 21:46:51 GMT 2025
PRIMARY
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