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Details

Stereochemistry RACEMIC
Molecular Formula C6H7NO.C4H6O5
Molecular Weight 243.2133
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0
Stereo Comments Assumed racemic

SHOW SMILES / InChI
Structure of NICOTINYL ALCOHOL MALATE

SMILES

OCC1=CN=CC=C1.OC(CC(O)=O)C(O)=O

InChI

InChIKey=ZTFZMPGWBKSBSL-UHFFFAOYSA-N
InChI=1S/C6H7NO.C4H6O5/c8-5-6-2-1-3-7-4-6;5-2(4(8)9)1-3(6)7/h1-4,8H,5H2;2,5H,1H2,(H,6,7)(H,8,9)

HIDE SMILES / InChI

Molecular Formula C4H6O5
Molecular Weight 134.0874
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula C6H7NO
Molecular Weight 109.1259
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Nicotinyl alcohol is a direct-acting vasolidator, that may decrease the blood pressure and it is a cholesterol-lowering agent. Nicotinyl alcohol as a tartrate salt led to the efficiency improvements in patients with intermittent claudication. In addition, nicotinyl alcohol alone or associated with other drugs was studied in the treatment of radicular syndromes; and was shown, that the effect had not been due to mechanical compression.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ronicol

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Doses

Doses

DosePopulationAdverse events​
600 mg 2 times / day steady, oral
Recommended
Dose: 600 mg, 2 times / day
Route: oral
Route: steady
Dose: 600 mg, 2 times / day
Sources:
unhealthy, 30 - 66 years
n = 20
Health Status: unhealthy
Condition: hyperlipoproteinemia
Age Group: 30 - 66 years
Sex: M+F
Population Size: 20
Sources:
Other AEs: Increased appetite, Skin rash...
Other AEs:
Increased appetite (15%)
Skin rash (36%)
Itching (37%)
Flushing (68%)
Nausea (50%)
Abdominal pain (15%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Abdominal pain 15%
600 mg 2 times / day steady, oral
Recommended
Dose: 600 mg, 2 times / day
Route: oral
Route: steady
Dose: 600 mg, 2 times / day
Sources:
unhealthy, 30 - 66 years
n = 20
Health Status: unhealthy
Condition: hyperlipoproteinemia
Age Group: 30 - 66 years
Sex: M+F
Population Size: 20
Sources:
Increased appetite 15%
600 mg 2 times / day steady, oral
Recommended
Dose: 600 mg, 2 times / day
Route: oral
Route: steady
Dose: 600 mg, 2 times / day
Sources:
unhealthy, 30 - 66 years
n = 20
Health Status: unhealthy
Condition: hyperlipoproteinemia
Age Group: 30 - 66 years
Sex: M+F
Population Size: 20
Sources:
Skin rash 36%
600 mg 2 times / day steady, oral
Recommended
Dose: 600 mg, 2 times / day
Route: oral
Route: steady
Dose: 600 mg, 2 times / day
Sources:
unhealthy, 30 - 66 years
n = 20
Health Status: unhealthy
Condition: hyperlipoproteinemia
Age Group: 30 - 66 years
Sex: M+F
Population Size: 20
Sources:
Itching 37%
600 mg 2 times / day steady, oral
Recommended
Dose: 600 mg, 2 times / day
Route: oral
Route: steady
Dose: 600 mg, 2 times / day
Sources:
unhealthy, 30 - 66 years
n = 20
Health Status: unhealthy
Condition: hyperlipoproteinemia
Age Group: 30 - 66 years
Sex: M+F
Population Size: 20
Sources:
Nausea 50%
600 mg 2 times / day steady, oral
Recommended
Dose: 600 mg, 2 times / day
Route: oral
Route: steady
Dose: 600 mg, 2 times / day
Sources:
unhealthy, 30 - 66 years
n = 20
Health Status: unhealthy
Condition: hyperlipoproteinemia
Age Group: 30 - 66 years
Sex: M+F
Population Size: 20
Sources:
Flushing 68%
600 mg 2 times / day steady, oral
Recommended
Dose: 600 mg, 2 times / day
Route: oral
Route: steady
Dose: 600 mg, 2 times / day
Sources:
unhealthy, 30 - 66 years
n = 20
Health Status: unhealthy
Condition: hyperlipoproteinemia
Age Group: 30 - 66 years
Sex: M+F
Population Size: 20
Sources:
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Importance of free fatty acids as a determinant of myocardial oxygen consumption and myocardial ischemic injury during norepinephrine infusion in dogs.
1974 May
Reaction of the tobacco alkaloid myosmine with hydrogen peroxide.
2006 Jan
Picolinyl ester fragmentation mechanism studies with application to the identification of acylcarnitine acyl groups following transesterification.
2006 Nov
Enzymatic oxidation of NADP+ to its 4-oxo derivative is a side-reaction displayed only by the adrenodoxin reductase type of ferredoxin-NADP+ reductases.
2007 Aug
catena-Poly[[tetrakis(mu-propionato-kappa(2)O:O')dicopper(II)]-mu-3-pyridylmethanol-kappa(2)N:O-[bis(propionato-kappaO)bis(3-pyridylmethanol-kappaN)copper(II)]-mu-3-pyridylmethanol-kappaO:N].
2007 Mar
catena-Poly[[bis-[2-(2,3-dimethyl-anilino)benzoato-κO]cadmium(II)]-di-μ-3-pyridylmethanol-κN:O;κO:N].
2008 Feb 6
Equilibria of 3-pyridylmethanol with copper(II). A comparative electron spin resonance study by the decomposition of spectra in liquid and frozen solutions.
2008 Oct 16
A rapid and sensitive method for the simultaneous analysis of aliphatic and polar molecules containing free carboxyl groups in plant extracts by LC-MS/MS.
2009 Nov 25
Synthesis and Structural Characterization of a Metal Cluster and a Coordination Polymer Based on the [Mn(6)(mu(4)-O)(2)] Unit.
2010
Noncovalent synthesis of hierarchical zinc phosphates from a single Zn(4)O(12)P(4) double-four-ring building block: dimensionality control through the choice of auxiliary ligands.
2010 Jan 18
Copper (II) complexes of the anti-inflammatory drug naproxen and 3-pyridylmethanol as auxiliary ligand. Characterization, superoxide dismutase and catecholase--mimetic activities.
2010 Sep
Patents

Sample Use Guides

25 mg tablet 4 times a daily
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:35:58 GMT 2023
Edited
by admin
on Fri Dec 15 15:35:58 GMT 2023
Record UNII
W6T0WO5LEJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NICOTINYL ALCOHOL MALATE
Common Name English
3-PYRIDINEMETHANOL, HYDROXYBUTANEDIOATE (SALT)
Systematic Name English
BUTANEDIOIC ACID, HYDROXY-, COMPD. WITH 3-PYRIDINEMETHANOL
Systematic Name English
Code System Code Type Description
PUBCHEM
137321938
Created by admin on Fri Dec 15 15:35:59 GMT 2023 , Edited by admin on Fri Dec 15 15:35:59 GMT 2023
PRIMARY
CAS
181074-82-8
Created by admin on Fri Dec 15 15:35:59 GMT 2023 , Edited by admin on Fri Dec 15 15:35:59 GMT 2023
NON-SPECIFIC STOICHIOMETRY
FDA UNII
W6T0WO5LEJ
Created by admin on Fri Dec 15 15:35:59 GMT 2023 , Edited by admin on Fri Dec 15 15:35:59 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE