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Details

Stereochemistry ACHIRAL
Molecular Formula C34H32N4O9
Molecular Weight 640.6393
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NICOMOL

SMILES

OC1C(COC(=O)C2=CN=CC=C2)(COC(=O)C3=CN=CC=C3)CCCC1(COC(=O)C4=CN=CC=C4)COC(=O)C5=CN=CC=C5

InChI

InChIKey=VRAHPESAMYMDQI-UHFFFAOYSA-N
InChI=1S/C34H32N4O9/c39-28(24-6-1-12-35-16-24)44-20-33(21-45-29(40)25-7-2-13-36-17-25)10-5-11-34(32(33)43,22-46-30(41)26-8-3-14-37-18-26)23-47-31(42)27-9-4-15-38-19-27/h1-4,6-9,12-19,32,43H,5,10-11,20-23H2

HIDE SMILES / InChI

Molecular Formula C34H32N4O9
Molecular Weight 640.6393
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 http://www.genome.jp/dbget-bin/www_bget?D01291

Hypolipidemic agent, Nicomol is an ingredient of Cholexamin in Japan. Cholexamin, a lipid metabolism and peripheral circulation improving agent, was launched by KYORIN Pharmaceutical in 1971. It is indicated for the treatment of hyperlipemia, improvement in peripheral circulatory disorder resulting from the following diseases Chilblain, limb arterial occlusive disease (obstructive thromboarteritis and arteriosclerosis obliterans), Raynaud syndrome.

Originator

Curator's Comment: Was launched in 1971

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q704S8
Gene ID: 311849.0
Gene Symbol: Crat
Target Organism: Rattus norvegicus (Rat)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Unknown

Approved Use

Unknown
Primary
Cholexamin

Approved Use

INDICATIONS: Hyperlipemia Improvement in peripheral circulatory disorder resulting from the following diseases Chilblain, limb arterial occlusive disease (obstructive thromboarteritis and arteriosclerosis obliterans), Raynaud syndrome

Launch Date

1970
Primary
Cholexamin

Approved Use

INDICATIONS: Hyperlipemia Improvement in peripheral circulatory disorder resulting from the following diseases Chilblain, limb arterial occlusive disease (obstructive thromboarteritis and arteriosclerosis obliterans), Raynaud syndrome

Launch Date

1969
Primary
Cholexamin

Approved Use

Hyperlipemia Improvement in peripheral circulatory disorder resulting from the following diseases Chilblain, limb arterial occlusive disease (obstructive thromboarteritis and arteriosclerosis obliterans), Raynaud syndrome

Launch Date

1970
Doses

Doses

DosePopulationAdverse events​
1200 mg 3 times / day multiple, oral
Highest studied dose
Dose: 1200 mg, 3 times / day
Route: oral
Route: multiple
Dose: 1200 mg, 3 times / day
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: FASTED
Sources:
PubMed

PubMed

TitleDatePubMed
Effects of some hypolipidemic drugs on biochemical values and on hepatic peroxisomal enzymes of normolipemic rat.
1981-10
Effect of nicomol on high density lipoprotein (HDL) subfractions, HDL2e and HDL3e, separated by electrophoresis.
1981-04
Effect of nicomol on HDL cholesterol level.
1979-08
Arrhythmogenic effects of acute free fatty acid mobilization on ischemic heart.
1976-05-26
Patents

Sample Use Guides

The usual adult dosage of this product for oral use is 200 to 400 mg of Nicomol three times daily after meals.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:14:47 GMT 2025
Edited
by admin
on Mon Mar 31 18:14:47 GMT 2025
Record UNII
215U8X2R44
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHOLEXAMIN
Preferred Name English
NICOMOL
INN   MART.   MI   WHO-DD  
INN  
Official Name English
NICOMOL [MART.]
Common Name English
NICOMOL [MI]
Common Name English
Nicomol [WHO-DD]
Common Name English
nicomol [INN]
Common Name English
NICOMOL [JAN]
Common Name English
2-HYDROXY-1,1,3,3-CYCLOHEXANETETRAMETHANOL 1,1,3,3-TETRANICOTINATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C98151
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
Code System Code Type Description
MESH
C008612
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
PUBCHEM
34081
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
NCI_THESAURUS
C84011
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
INN
2880
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
EPA CompTox
DTXSID9048722
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
ChEMBL
CHEMBL2103919
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
CAS
27959-26-8
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
EVMPD
SUB09240MIG
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
SMS_ID
100000084416
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
ECHA (EC/EINECS)
248-748-9
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
FDA UNII
215U8X2R44
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
DRUG CENTRAL
1917
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY
MERCK INDEX
m844
Created by admin on Mon Mar 31 18:14:47 GMT 2025 , Edited by admin on Mon Mar 31 18:14:47 GMT 2025
PRIMARY Merck Index
Related Record Type Details
ACTIVE MOIETY