U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C6H7NO.C4H6O6
Molecular Weight 259.2127
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NICOTINYL ALCOHOL TARTRATE

SMILES

OCC1=CN=CC=C1.O[C@H]([C@@H](O)C(O)=O)C(O)=O

InChI

InChIKey=NPORIZAYKBQYLF-LREBCSMRSA-N
InChI=1S/C6H7NO.C4H6O6/c8-5-6-2-1-3-7-4-6;5-1(3(7)8)2(6)4(9)10/h1-4,8H,5H2;1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1

HIDE SMILES / InChI
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
Metabolism of myosmine in Wistar rats.
2005 Nov
Reaction of the tobacco alkaloid myosmine with hydrogen peroxide.
2006 Jan
catena-Poly[[bis-[2-(2,3-dimethyl-anilino)benzoato-κO]cadmium(II)]-di-μ-3-pyridylmethanol-κN:O;κO:N].
2008 Feb 6
Improved synthesis of histone deacetylase inhibitors (HDIs) (MS-275 and CI-994) and inhibitory effects of HDIs alone or in combination with RAMBAs or retinoids on growth of human LNCaP prostate cancer cells and tumor xenografts.
2008 Mar 15
Oxidation of alcohols using a manganese (II) complex based on a pentakis benzimidazole amide ligand.
2009 Oct 1
Synthesis and Structural Characterization of a Metal Cluster and a Coordination Polymer Based on the [Mn(6)(mu(4)-O)(2)] Unit.
2010
The role of p53 in the cellular toxicity by active trans-platinum complexes containing isopropylamine and hydroxymethylpyridine.
2010 Jan
Patents

Sample Use Guides

25 mg tablet 4 times a daily
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
NICOTINYL ALCOHOL TARTRATE
JAN   MART.   VANDF  
Systematic Name English
NICOTINYL TARTRATE
INCI   WHO-DD  
INCI  
Official Name English
3-(HYDROXYMETHYL)PYRIDINE TARTRATE
Systematic Name English
NSC-147492
Code English
NICOTINYL TARTRATE [INCI]
Common Name English
NICOTINYL ALCOHOL D-TARTRATE [MI]
Common Name English
3-PYRIDINEMETHANOL, (R-(R*,R*))-2,3-DIHYDROXYBUTANEDIOATE (1:1) (SALT)
Common Name English
3-PYRIDYLMETHANOL-(RR)-HYDROGENTARTRATE
Common Name English
NICOTINYL ALCOHOL TARTRATE [MART.]
Common Name English
NICOTINYL ALCOHOL TARTRATE [VANDF]
Common Name English
3-PYRIDINEMETHANOL TARTRATE (1:1) SALT
Common Name English
NICOTINYL ALCOHOL D-TARTRATE
MI  
Systematic Name English
Nicotinyl tartrate [WHO-DD]
Common Name English
NICOTINYL ALCOHOL TARTRATE [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
Code System Code Type Description
RXCUI
235354
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY RxNorm
NSC
147492
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
MERCK INDEX
m7882
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY Merck Index
FDA UNII
5G605ZIE90
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
EVMPD
SUB14652MIG
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
228-199-1
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID90977232
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
NCI_THESAURUS
C77152
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
SMS_ID
100000079995
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
PUBCHEM
93578
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
CAS
6164-87-0
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY
ChEMBL
CHEMBL1235535
Created by admin on Fri Dec 15 15:26:18 GMT 2023 , Edited by admin on Fri Dec 15 15:26:18 GMT 2023
PRIMARY